- Open Access
β-Lapachone induces heart morphogenetic and functional defects by promoting the death of erythrocytes and the endocardium in zebrafish embryos
Journal of Biomedical Science volume 18, Article number: 70 (2011)
β-Lapachone has antitumor and wound healing-promoting activities. To address the potential influences of various chemicals on heart development of zebrafish embryos, we previously treated zebrafish embryos with chemicals from a Sigma LOPAC1280™ library and found several chemicals including β-lapachone that affected heart morphogenesis. In this study, we further evaluated the effects of β-lapachone on zebrafish embryonic heart development.
Embryos were treated with β-lapachone or dimethyl sulfoxide (DMSO) at 24 or 48 hours post fertilization (hpf) for 4 h at 28°C. Heart looping and valve development was analyzed by whole-mount in situ hybridization and histological analysis. For fractional shortening and wall shear stress analyses, AB and Tg (gata1:DsRed) embryos were recorded for their heart pumping and blood cell circulations via time-lapse fluorescence microscopy. Dextran rhodamine dye injection into the tail reticular cells was used to analyze circulation. Reactive oxygen species (ROS) was analyzed by incubating embryos in 5-(and 6-)-chloromethyl-2',7'-dichloro-dihydrofluorescein diacetate (CM-H2DCFDA) and recorded using fluorescence microscopy. o-Dianisidine (ODA) staining and whole mount in situ hybridization were used to analyze erythrocytes. TUNEL assay was used to examine DNA fragmentation.
We observed a linear arrangement of the ventricle and atrium, bradycardia arrhythmia, reduced fractional shortening, circulation with a few or no erythrocytes, and pericardial edema in β-lapachone-treated 52-hpf embryos. Abnormal expression patterns of cmlc2, nppa, BMP4, versican, and nfatc1, and histological analyses showed defects in heart-looping and valve development of β-lapachone-treated embryos. ROS production was observed in erythrocytes and DNA fragmentation was detected in both erythrocytes and endocardium of β-lapachone-treated embryos. Reduction in wall shear stress was uncovered in β-lapachone-treated embryos. Co-treatment with the NQO1 inhibitor, dicoumarol, or the calcium chelator, BAPTA-AM, rescued the erythrocyte-deficiency in circulation and heart-looping defect phenotypes in β-lapachone-treated embryos. These results suggest that the induction of apoptosis of endocardium and erythrocytes by β-lapachone is mediated through an NQO1- and calcium-dependent pathway.
The novel finding of this study is that β-lapachone affects heart morphogenesis and function through the induction of apoptosis of endocardium and erythrocytes. In addition, this study further demonstrates the importance of endocardium and hemodynamic forces on heart morphogenesis and contractile performance.
The heart is the first organ to form during vertebrate embryonic development. An embryonic heart tube is composed of outer myocardial and inner endocardial layers. After chamber formation, cardiac valves are formed from the endocardial cushion which is derived from the endocardium located at the atrioventricular boundary through an epithelial-to-mesenchymal transition . The interaction between the myocardium and endocardium was shown to be important for developing a heart with normal functions. Bartman et al. demonstrated that reduced myocardial function can cause defects in endocardial cushion development via both sih and cfk zebrafish mutants associated with mutations in cardiac troponin T and a sarcomeric actin . Similarly, a dysmorphic heart containing a compact ventricle and enlarged atrium with reduced contractility was observed in zebrafish cloche mutants with defects in the differentiation of all endothelial cells .
Blood circulation occurs early in the linear heart tube stage when diffuse oxygen is still sufficient to support various physiological processes, suggesting that blood circulation is required for heart morphogenesis . The proper formation of a heart with normal functions is regulated by both a genetic program cascade and epigenetic factors (e.g., blood fluidic shear stresses) [5–7]. Fluidic shear stress is the frictional force derived from blood flow and plays an important role in embryonic vascular remodeling and cardiac morphogenesis [7–10]. In both mlc2a-null mice and wea zebrafish mutants (i.e., either a mutation in the atrial myosin light chain 2 or atrial myosin heavy chain gene), the mutation caused enlarged atria as well as a compact ventricle with underdeveloped trabeculae and a narrow lumen [11, 12]. Since only atrial cardiomyoctyes completely lack myofibril organization, alteration of ventricle morphogenesis is likely attributable to changes in hemodynamic forces. Additionally, intracardiac fluidic forces were shown to be one of the essential factors for heart-looping and valve development in zebrafish embryos through blocking either the cardiac inflow or outflow by inserting glass beads .
β-Lapachone (3,4-dihydro-2,2-dimethyl-2H- naphthol[1,2-b] pyran-5,6-dione), a lipophilic ortho-naphthoquinone, was originally isolated from the lapacho tree (Tabebuia avellanedae) of South America . β-Lapachone has antibacterial, antifungal, antiviral, anti-trypanosomal, and antitumor activities [14–18]. In a number of tumors (e.g., breast, colon, pancreatic, and lung cancers) with high expression levels of NAD(P)H:quinone oxidoreductase (NQO1), β-lapachone activates a novel apoptotic response [19–21]. In those tumors, NQO1 utilizes NAD(P)H as an electron donor to catalyze the two-electron reduction of β-lapachone to hydroquinone and a semiquinone intermediate in a futile cycle, resulting in the formation of reactive oxygen species (ROS) such as superoxide [21, 22]. ROS can cause DNA damage, hyperactivation of poly(ADP-ribose) polymerase (PARP)-1 which depletes NAD+ and ATP pools, that respectively result in an increase of the intracellular cytosolic Ca2+ concentration, and activation of μ-calpain cysteine protease activity [23–25]. Treatment with dicoumarol (an NQO1 inhibitor) or BAPTA-AM (a Ca2+ chelator) can inhibit cell death induced by β-lapachone [26, 27].
In addition to being a model organism for probing vertebrate genetics and development, zebrafish have also proven to be ideal for screening small-molecule libraries to identify new therapeutic drugs [28, 29]. To address the potential influences of various chemicals on the heart development of zebrafish embryos, we previously treated zebrafish embryos with chemicals from a Sigma LOPAC1280™ library and found several chemicals including β-lapachone that affected heart morphogenesis. In this study, we further evaluated the effects of β-lapachone on zebrafish embryonic heart development. We detected reduced fractional shortening, defects in heart-looping and valve development in β-lapachone-treated embryos. DNA fragmentation was also detected in both erythrocytes and the endocardium of β-lapachone-treated embryos. Furthermore, we demonstrated that the induction of apoptosis of the endocardium and erythrocytes by β-lapachone is mediated through an NQO1- and calcium-dependent pathway. This study, we believe, further demonstrates the importance of the endocardium and hemodynamic forces on heart morphogenesis and contractile performance in zebrafish embryos as a model system.
Materials and methods
Fish maintenance and collection of embryos
Adult zebrafish (Danio rerio) were raised at the zebrafish facility of the Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan. The fish were maintained in 20-L aquariums supplied with filtered fresh water and aeration under a 14-h light: 10-h dark photoperiod. Different developmental stages were determined based on previously described morphological criteria .
Embryos were treated with β-lapachone (Sigma-Aldrich, St. Louis, MO, USA) at a final concentration of 2 μM diluted with egg water at 24 or 48 hpf for 4 h at 28°C. Embryos from the same developmental stage treated with 0.2% DMSO for 4 h were used as the control.
Whole-mount in situ hybridization
Whole-mount in situ hybridization was performed on embryos treated with 0.003% phenylthiocarbamide using digoxigenin-labeled antisense RNA probes and alkaline phosphatase-conjugated anti-digoxigenin antibodies as described previously . Various templates were linearized, and antisense RNA probes were generated as follows: BMP4 (Not I/T7), cmlc2 (Nco I/SP6), hbae1 (Not I/T7), nfatc1 (Spe I/T7), nppa (Nco I/SP6), and versican (Nco I/SP6).
o-Dianisidine (ODA) staining
Embryos were fixed with 4% paraformaldehyde overnight at 4°C. After several washes with PBST (1 × PBS and 0.1% Tween-20), β-lapachone- and DMSO-treated 48-hpf embryos were incubated in H2O2 (20 μl/ml)-activated ODA staining buffer (0.6 mg/ml ODA (Sigma-Aldrich, St. Louis, MO, USA) in 10 mM sodium acetate (pH 5.2) and 4% ethanol) for 15 min in the dark at room temperature and then washed with PBST several times.
β-Lapachone- and DMSO-treated embryos were incubated in 5-(and 6-)-chloromethyl-2',7'-dichloro-dihydrofluorescein diacetate (CM-H2DCFDA) (Invitrogen, Carlsbad, CA, USA) at a final concentration of 500 ng/ml for 1 h in the dark at room temperature. After rinsing with egg water, embryos were examined using fluorescence microscopy equipped with a green fluorescent protein (GFP) filter.
TUNEL assay and histological analysis
For the TUNEL assay to analyze apoptosis in the heart and erythrocytes, 48-hpf embryos were treated with either β-lapachone or DMSO for 4 h and then fixed at 52 hpf for ODA staining. Subsequently ODA-stained DMSO- and β-lapachone-treated 52-hpf embryos were fixed in 4% paraformaldehyde overnight at 4°C and embedded in paraffin according to standard procedures. Paraffin sections (5 μm) were dewaxed and rehydrated in PBST through an ethanol series. They were treated with 10 μg/ml proteinase K for 15 min at room temperature before DNA breaks were labeled with terminal deoxynucleotidyl transferase and fluorescein-dUTP according to protocols provided by the manufacturer (Roche Applied Bioscience, Mannheim, Germany). Nuclei were stained with DAPI. For the histological analysis, paraffin sectioning and hematoxylin (Vector, Burlingame, CA, USA) and eosin (Muto Pure Chemical, Tokyo, Japan) staining were performed according to standard procedures.
Dextran rhodamine dye injection and photography
Diluted dextran rhodamine was injected into tail reticular cells of 48-hpf embryos using an IM300 microinjector (Narishigi, Tokyo, Japan). Images of embryos from various analyses were taken using an RT color digital camera (SPOT, Mchenry, IL, USA) on either a Zeiss Axioplan 2 microscope (Göttingen, Germany) or a Leica Z16 APO microscope (Wetzlar, Germany) equipped DIC or FITC mode.
Wall shear stress and fractional shortening (FS) measurements
For wall shear stress and the FS analyses, 24-hpf Tg (gata1:DsRed) and 48-hpf AB embryos were treated with either β-lapachone or DMSO for 4 h, and then their blood cell circulations and heart pumping were recorded at 30 and 52 hpf, respectively, via time-lapse fluorescence microscopy using an AxioCam HRC camera with a high-speed recording mode (50 frames/s) under a Zeiss Axio Imager M1 microscope (Göttingen, Germany) with a tetramethylrhodamine isothiocyanate (TRITC; corresponding to pseudo-colored red) filter set.
Real-Time Quantitative (Q) Reverse-Transcription (RT)-PCR
Q-RT-PCR was conducted and analyzed as described . The primer pair for nppa was F-GGCAACAGAAGAGGCATCAGAG and R-GGAGCTGCTGCTTCCTCTCGGTC. The primer pair for β-actin was F-CCATTGGCAATGAGAGGTTCAG and R-TGATGGAGTTGAAAGTGGTCTCG.
Phenotypes of β-lapachone-treated embryos
Embryos at 6 hpf were first treated with different concentrations (2, 5, 10, and 50 μM) of β-lapachone overnight; then the death of embryos was observed in all treatments (data not shown). Subsequently, 24-hpf embryos were treated with 2 μM β-lapachone for different time periods to evaluate its effect on heart development (data not shown). We then treated 24-hpf embryos with 2 μM β-lapachone for 4 h and found that β-lapachone-treated 30-hpf embryos showed pericardial edema compared to DMSO-treated embryos (Figure 1A & 1B). Pronounced pericardial edema accompanied by a linear arrangement of the ventricle and atrium which underwent bradycardia arrhythmia and the presence of only a few or no erythrocytes in the blood circulation were observed in β-lapachone-treated 52- and 72-hpf embryos (Figure 1C-J). Severe pericardial and yolk edema accompanied by the linear arrangement of the heart chambers and a lack of blood circulation were observed in β-lapachone-treated 96-hpf embryos compared to DMSO-treated embryos (Figure 1K & 1L). A blood circulation defect was further confirmed by injecting dextran rhodamine into both β-lapachone- and DMSO-treated 48-hpf embryos. The injected dextran rhodamine dye was readily observed in all vasculature of DMSO-treated embryos 2 min after the injection, while in β-lapachone-treated embryos, the dye remained in the yolk extension region close to the injection point for at least 16 min (Figure 1M-P).
Defects in heart-looping and valve development and decreased cardiac output were recorded in β-lapachone-treated embryos
To clarify the role of β-lapachone treatment in heart chamber morphogenesis, we treated 24-hpf embryos with either DMSO or β-lapachone for 4 h and then fixed them at 48 and 72 hpf for whole-mount in situ hybridization using nppa and cmlc2 as RNA probes. In DMSO-treated 48- and 72-hpf embryos, nppa expression was restricted to the outer curvature of the ventricle and atrium , whereas nppa was intensively expressed in the entire ventricle and atrium in β-lapachone-treated 48-hpf embryos (n > 50), and decreased nppa expression was later shown in β-lapachone-treated 72-hpf embryos (n > 50) (Figure 2A). Quantitative real time-RT-PCR analyses of the nppa expression level further confirmed the whole-mount in situ hybridization results (panel i in Figure 2A). In DMSO-treated 48- and 72-hpf embryos, cmlc2 was mainly expressed in looped ventricle and to some extent in the atrium, While, similar level of cmlc2 expression in the linearly arranged atrium and ventricle was found in β-lapachone-treated 48- and 72-hpf embryos (n > 50) (Figure 2A).
Furthermore, in order to evaluate the influence of β-lapachone treatment on cardiac output, we treated 48-hpf embryos with either DMSO or β-lapachone for 4 h and then recorded their heart pumping at 52 hpf (panel a-c' in Figure 2B). We grouped β-lapachone-treated embryos into either embryos containing few erythrocytes (n = 6) or no erythrocytes (n = 8). We found that the fractional shortening (FS) of both the atrium and ventricle was significantly decreased in both groups of β-lapachone-treated 52-hpf embryos compared to DMSO-treated embryos (n = 9) (panel d in Figure 2B).
During heart valve development, BMP signals from the myocardium promote the endocardial cushion to undergo the epithelial-mesenchymal transition [33, 34]. Nfatc1 expression in the endocardial cushion is essential for its growth and subsequent valve remodeling . Versican is an extracellular matrix component in the heart that is required for the development of endocardial cushion swelling . Therefore, we selected BMP4, versican, and nfatc1 as RNA probes for whole-mount in situ hybridization to investigate heart valve development of zebrafish embryos treated with β-lapachone. We treated 24-hpf embryos with either DMSO or β-lapachone for 4 h and then fixed them at 48 and 72 hpf to perform whole-mount in situ hybridization. In DMSO-treated 48-hpf embryos, BMP4 was expressed in the myocardium located at the ventriculobulbal (VB) and atrioventricular (AV) junctions, whereas both versican and nfatc1 were mainly respectively expressed in the myocardium and endocardium at the AV junction of the heart in both DMSO-treated 48- and 72-hpf embryos (Figure 2C). Ectopic expressions of BMP4 (n > 50), versican (n > 50), and nfatc1 (n > 50) in both the ventricle and atrium were observed in β-lapachone-treated 48- and 72-hpf embryos compared to DMSO-treated control embryos (Figure 2C). Histological analyses further demonstrated the respective impairment of endocardial cushion formation and valve development in β-lapachone-treated 72- (N = 4, n = 20) and 96-hpf (N = 4, n = 20) embryos (Figure 2D). These results indicate that heart morphogenesis including heart-looping, formation of the heart chamber curvature and valve, and cardiac output were affected by β-lapachone treatment.
β-Lapachone treatment induces the death of erythrocytes and endocardium
Embryos at 24 hpf were treated with either DMSO or β-lapachone for 4 h and then fixed at 30 and 48 hpf to analyze the presence of erythrocytes by whole-mount in situ hybridization using hbae1 (hemoglobin α embryonic 1) as a probe and hemoglobin staining with ODA (Figure 3A). In DMSO-treated 30- and 48-hpf embryos, hbae1-hybridized erythrocytes were readily observed in the dorsal aorta, posterior cardinal vein, and common cardinal vein. Relatively few hbae1-hybridized erythrocytes were observed in β-lapachone-treated 30-hpf embryos (n > 50), and no hbae1 hybridization was detected in β-lapachone-treated 48-hpf embryos (n > 50) (Figure 3A). Similarly ODA-stained hemoglobin was readily observed in both the dorsal aorta and posterior cardinal vein of DMSO-treated 48-hpf embryos; however, no ODA-stained hemoglobin was detected in β-lapachone-treated embryos (n > 50) (Figure 3A). Quantitative real time-RT-PCR analyses further confirmed the presence of very low expression levels of both hbae1 and hbbe1 (hemoglobin β embryonic 1) in β-lapachone-treated 48-hpf embryos (data not shown).
Since proerythroblasts from the intermediate cell mass expressing embryonic globins began to enter the circulation at 24 hpf, and hematopoiesis shifted from a primitive to a definitive wave at around 30 hpf, we also analyzed these two transcriptional factors which are important for definitive hematopoiesis . Similar expression patterns and levels of c-myb (n > 50) and ikaros (n > 50) were found in DMSO- and β-lapachone-treated 30-hpf embryos, indicating that definitive hematopoiesis was not affected by β-lapachone treatment (Additional file, Fig. S1).
Since the incubation of β-lapachone with Trypanosoma cruzi preferentially causes the inhibition of DNA synthesis and DNA damage from the generation of oxygen radicals , we also evaluated whether ROS were generated in β-lapachone-treated embryos . In the presence of peroxyl radicals (a type of ROS), CM-H2DCFDA is converted to the fluorescent dichlorofluorescein (DCF). We treated 24-hpf embryos with either DMSO or β-lapachone for 4 h and then incubated them with CM-H2DCFDA for 1 h at 29 hpf. Erythrocytes with green fluorescence were detected flowing from the common cardinal vein to the atrium of β-lapachone-treated 30-hpf embryos (N = 4, n > 50) but not in the respective DMSO-treated control embryos (Figure 3B).
Unlike mammals, zebrafish erythrocytes possess nuclei. Therefore, we treated 48-hpf embryos with either DMSO or β-lapachone for 4 h and fixed them at 52 hpf for ODA staining. These ODA-stained embryos were then used for the TUNEL assay. In DMSO-treated control embryos, a group of ODA-stained erythrocytes were detected in the tail blood island but fail to be labeled by fluorescein-dUTP (panel a-d in Figure 3C). In contrast, fluorescein-dUTP-labeled erythrocytes were found close to several ODA-stained erythrocytes in the tail blood island of β-lapachone-treated 52-hpf embryos (panel e-h in Figure 3C; N = 3, n = 15). However, ODA-stained erythrocytes did not show DNA fragmentation, indicating that fluorescein-dUTP-labeled erythrocytes had already lost their hemoglobin in the cytoplasm.
Although we did not detect ROS in the hearts of β-lapachone-treated 30-hpf embryos incubated with CM-H2DCFDA, TUNEL staining of paraffin sections revealed the presence of fluorescein-dUTP-labeled cells in the endocardium of the atrium and ventricle of β-lapachone-treated 52-hpf embryos (N = 3, n = 17), but not in DMSO-treated control embryos (Figure 3D). In addition, fluorescein-dUTP-labeled erythrocytes were observed in the yolk near the heart probably in the common cardinal vein (panels f & j in Figure 3D). These results indicated that β-lapachone treatment caused the occurrence of ROS in erythrocytes and DNA fragmentation in the endocardium and erythrocytes of zebrafish embryos.
Decreased wall shear stress was identified in β-lapachone-treated embryos
Both the velocity gradient and blood viscosity when blood flows in a blood vessel are major physical factors determining the fluidic shear stress, and one of the major factors influencing the blood viscosity is hematocrit [38, 39]. Since we observed a decreased number of erythrocytes in β-lapachone-treated embryos, we then evaluated the effect of β-lapachone treatment on the wall shear stress in the caudal artery of embryos. We treated 24-hpf Tg(gata1:DsRed) embryos with β-lapachone for 4 h and recorded the blood cell circulation at 30 hpf. Here, we used the formula 4 μQ/πR3 to determine the wall shear stress, where μ is viscosity, Q is the flow rate, and R is the blood vessel diameter . We first measured the average diameter of the caudal artery in DMSO- (20 μm) and β-lapachone-treated embryos (17 μm) and obtained the velocity of several individual DsRed-labeled erythrocyte in the caudal artery of DMSO- and β-lapachone-treated embryos by tracing the distance they traveled in a fixed period of time via time-lapse fluorescence microscopy. Flow rate (Q) was then calculated based on the average diameter of the caudal artery and average velocity of erythrocytes in both DMSO- (0.000533 μm/s) and β-lapachone-treated (0.000329 μm/s) embryos. We then estimated the relative shear stress using the viscosity value (0.008 Nt·s/m2) measured in oxygenated trout cannula blood at 26% hematocrit and a 90/s shear rate . As shown in Figure 4, the wall shear stress (τ) significantly decreased in β-lapachone-treated (1.24 Nt/m2) 30-hpf embryos (n = 14) compared to DMSO-treated (1.55 Nt/m2) control embryos (n = 10).
Co-treatment with either dicoumarol or BAPTA-AM and β-lapachone rescued both the heart-looping defect and erythrocyte-deficiency in circulation phenotypes
Since β-lapachone treatment induces NQO1- and μ-calpain-mediated apoptosis in a number of tumors [26, 27], we evaluated whether the erythrocyte-deficiency in circulation and heart-looping defect phenotypes in zebrafish embryos induced by β-lapachone also adopted a similar mechanism. Dicoumarol, an inhibitor of NQO1, and BAPTA-AM, a Ca2+ ion chelator which can affect the activity of calcium-dependent μ-calpain, were used [41, 24]. We treated 24-hpf embryos with either 2 μM β-lapachone (n = 318 and 627) alone or together with either 5 μM dicoumarol (n = 215) or 50 μM BAPTA-AM (n = 557) for 4 h and fixed them at 48 hpf. In β-lapachone-treated 48-hpf embryos, a linear arrangement of the ventricle and atrium, ectopic nppa expression, and no ODA-stained erythrocytes were observed compared to DMSO- (n = 243) and dicoumarol-treated (n = 193) control embryos (Figure 5A-F). However, approximately 76% of 48-hpf embryos treated with both β-lapachone and dicoumarol showed levels of ODA-stained erythrocytes in circulation and a normal heart chamber morphology as assayed by nppa expression patterns, compared to those of control embryos (Figure 5G-I). Similarly, co-treatment with BAPTA-AM also rescued the β-lapachone-induced heart-looping defect and erythrocyte-deficiency in circulation phenotypes (data not shown). Approximately 81% of 48-hpf embryos treated with both β-lapachone and BAPTA-AM exhibited levels of ODA-stained erythrocytes in circulation and a normal heart chamber morphology, compared to DMSO- (n = 216) and BAPTA-AM-treated (n = 239) control embryos (Figure 5J). Collectively, these results indicate that the heart-looping defect and erythrocyte-deficiency in circulation phenotypes observed in β-lapachone-treated embryos were both induced by an NQO1- and calcium-mediated pathway.
β-Lapachone is currently in phase II clinical trials for treating pancreatic adenocarcinomas due to its antitumor activity . It was also shown to have potential therapeutic use due to its wound healing-promoting activity . In our study, we evaluated the potential effects of β-lapachone on heart development using zebrafish as the model organism.
β-Lapachone treatment induces apoptosis of the endocardium and erythrocytes which in turn affect heart morphogenetic development and function
We observed a linear arrangement of the ventricle and atrium, bradycardia arrhythmia, reduced FS, and circulation with only a few or no blood cells in β-lapachone-treated 48-hpf embryos (Figure 1). Abnormal expression patterns of cmlc2, nappa, BMP4, versican, and nfatc1 and histological analyses demonstrated that there were defects in heart-looping and valve development in β-lapachone-treated embryos (Figure 2). Furthermore, we detected the presence of ROS in erythrocytes and DNA fragmentation in both the endocardium and erythrocytes of β-lapachone-treated embryos (Figure 3). These results indicate that defects in heart morphogenetic development and function can be attributed to apoptosis of the endocardium and erythrocytes induced by β-lapachone treatment.
An integral endocardium is essential for cardiac valve development because it gives rise to the endocardial cushion through an epithelial-to-mesenchymal transition process . In addition, integral cardiac endocardial and myocardial interaction is required for proper heart development and contractile function . Neuregulin-1 is a paracrine factor produced by endocardium endothelial cells. Mice possessing a homozygous mutation in Neuregulin-1 showed a heart that lacked trabecular formation in the ventricular wall, and slower contractions of the atrium and ventricle . Similarly, Neuregulin/ErbB signaling was shown to be essential for ventricle trabeculation in zebrafish embryos, and knockdown Neuregulin-1 expression in zebrafish also resulted in heart development defects especially in the conducting system [46, 47]. Therefore, our results further demonstrate the importance of the endocardium in cardiac structural and functional development.
As hematocrit influences the blood viscosity, which is one of the main physical factors affecting blood fluidic shear stress on the blood vessel wall [7, 39], our relative wall shear stress approach also indicated a significant decrease in the wall shear stress in β-lapachone-treated embryos due to relatively few erythrocytes in the circulation (Figure 4). A decreased wall shear stress produced decreased hemodynamic forces which further impacted heart development and function in β-lapachone-treated embryos.
Both the endothelium and erythrocytes are regulated by oxidative stress
Oxidative stress was shown to regulate the growth, survival, and apoptosis of vascular smooth muscle and endothelial cells . Cytokines and growth factors (e.g., tumor necrosis factor-α, interleukin 1β, and angiotensin II) were shown to promote the generation of superoxide in endothelial cells by activating NADPH oxidase [49, 50]. ROS then cause the release of cytochrome C from mitochondria to activate caspase, resulting in phosphatidylserine exposure, DNA fragmentation, and cell morphological changes . A study on human umbilical vein endothelial cells further demonstrated that the activities of both caspase 3 and c-Jun N-terminal kinases (JNKs) were stimulated due to an increase in intracellular ROS levels .
The function and fate of erythrocytes are under redox control . Although the presence of a high iron concentration, hemoglobin, and both non-enzymatic and enzymatic antioxidants provide erythrocytes with an antioxidant capacity, erythrocytes can become the target of xenobiotics or ROS produced by nearby tissues, thus accumulating oxidative damage and then being removed. Several components of the apoptotic machinery found in nucleated cells were identified to be upregulated in mammalian erythrocytes under oxidative stress. Procaspase 3 was found in mature human erythrocytes and is activated under oxidative stress upon t-butylhydroperoxide treatment leading to impairment of aminophospholipid flippase activity, phosphatidylserine externalization, and increased erythrophagocytosis . Components of the extrinsic apoptotic pathway including FasL, the Fas-associated death domain, and caspase 8 were shown to form complexes in membrane rafts of aged and oxidatively stressed erythrocytes. A previous study also showed that oxidative stress can activate Ca2+-permeable cation channels, cause increased cytosolic calcium concentrations, and trigger erythrocyte apoptosis .
Induction of cell death of erythrocytes and the endocardium in zebrafish embryos by β-lapachone is mediated through an NQO1- and calcium-dependent pathway
The linear arrangement of the ventricle and atrium and the presence of only a few or no erythrocytes in circulation were observed in β-lapachone-treated 52-, 72-, and 96-hpf embryos (Figure 1). In addition, β-lapachone treatment caused the occurrence of ROS in erythrocytes and DNA fragmentation in erythrocytes and the endocardium of zebrafish embryos (Figure 3). In a number of tumors which possess high expression levels of NQO1, β-lapachone can be reduced by NQO1 and leads to a futile cycle between quinone and hydroquinone, accompanied by depletion of NAD(P)H and the generation of ROS. ROS can cause DNA damage, hyperactivation of PARP-1, which depletes NAD+ and ATP pools that results in increased intracellular cytosolic Ca2+ concentrations, and the activation of μ-calpain cysteine protease activity [23–25]. We also showed that both the heart-looping defect and erythrocyte-deficiency in circulation phenotypes could be rescued by co-incubation of β-lapachone with either dicoumarol, an NQO1 inhibitor, or BAPTA-AM, a Ca2+ chelator (Figure 5). These results indicate that the induction of cell death of erythrocytes and the endocardium in zebrafish embryos by β-lapachone is mediated through an NQO1- and calcium-dependent pathway.
A recent study also showed that oral treatment of rats with β-lapachone induced anemia that was attributed to increased phosphatidylserine externalization and erythrophagocytosis induced by ROS . However, the extents of reduction in erythrocyte cell numbers in adult rats (22%~26%) and zebrafish embryos (75%~90%) upon β-lapachone treatment greatly differed. This discrepancy may have been due to the presence of mitochondria in mature fish erythrocytes but not in mature mammalian erythrocytes . It was shown that over 60 moles of NAD(P)H are used by NQO1 to react with each mole of β-lapachone. Since the citric acid cycle in mitochondria can produce more NADH than glycolysis in the cytosol, we suggest that more ROS can be generated in zebrafish erythrocytes than in rat erythrocytes upon β-lapachone treatment. ROS then cause DNA damage, an increased cytosolic Ca2+ concentration either from endoplasmic reticulum release or entry from Ca2+-permeable cation channels, loss of ATP and NAD+, and inhibition of DNA repair, leading to cell death .
Our study indicates that β-lapachone treatment causes death of the endocardium and erythrocytes in zebrafish embryos resulting in defects in heart-looping, valve formation, and cardiac output. The induction of apoptosis of the endocardium and erythrocytes by β-lapachone is mediated through an NQO1- and calcium-dependent pathway. This study further demonstrated the importance of the endocardium and hemodynamic forces to heart morphogenesis and contractile performance.
hours post fertilization
differential interference contrast
Stainier DY: Zebrafish genetics and vertebrate heart formation. Nat Rev Genet. 2001, 2: 39-48. 10.1038/35047564.
Bartman T, Walsh EC, Wen KK, McKane M, Ren J, Alexander J, Rubenstein PA, Stainier DY: Early myocardial function affects endocardial cushion development in zebrafish. PLoS Biol. 2004, 2: E129-10.1371/journal.pbio.0020129.
Stainier DY, Weinstein BM, Detrich HW, Zon LI, Fishman MC: Cloche, an early acting zebrafish gene, is required by both the endothelial and hematopoietic lineages. Development. 1995, 121: 3141-3150.
Pelster B, Burggren WW: Disruption of hemoglobin oxygen transport does not impact oxygen-dependent physiological processes in developing embryos of zebra fish (Danio rerio). Circ Res. 1996, 79: 358-362.
Yelon D: Cardiac patterning and morphogenesis in zebrafish. Dev Dyn. 2001, 222: 552-563. 10.1002/dvdy.1243.
Bruneau BG: Transcriptional regulation of vertebrate cardiac morphogenesis. Circ Res. 2002, 90: 509-519. 10.1161/01.RES.0000013072.51957.B7.
Hierck BP, Van der Heiden K, Poelma C, Westerweel J, Poelmann RE: Fluid shear stress and inner curvature remodeling of the embryonic heart. Choosing the right lane!. ScientificWorldJournal. 2008, 8: 212-222.
Hove JR, Koster RW, Forouhar AS, Acevedo-Bolton G, Fraser SE, Gharib M: Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis. Nature. 2003, 421: 172-177. 10.1038/nature01282.
Jones EA, le Noble F, Eichmann A: What determines blood vessel structure? Genetic prespecification vs. hemodynamics. Physiology (Bethesda). 2006, 21: 388-395. 10.1152/physiol.00020.2006.
Auman HJ, Coleman H, Riley HE, Olale F, Tsai HJ, Yelon D: Functional modulation of cardiac form through regionally confined cell shape changes. PLoS Biol. 2007, 5: e53-10.1371/journal.pbio.0050053.
Berdougo E, Coleman H, Lee DH, Stainier DY, Yelon D: Mutation of weak atrium/atrial myosin heavy chain disrupts atrial function and influences ventricular morphogenesis in zebrafish. Development. 2003, 130: 6121-6129. 10.1242/dev.00838.
Huang C, Sheikh F, Hollander M, Cai C, Becker D, Chu PH, Evans S Chen J: Embryonic atrial function is essential for mouse embryogenesis, cardiac morphogenesis and angiogenesis. Development. 2003, 130: 6111-6119. 10.1242/dev.00831.
Schaffner-Sabba K, Schmidt-Ruppin KH, Wehrli W, Schuerch AR, Wasley JW: beta-Lapachone: synthesis of derivatives and activities in tumor models. J Med Chem. 1984, 27: 990-994. 10.1021/jm00374a010.
Don MJ, Chang YH, Chen KK, Ho LK, Chau YP: Induction of CDK inhibitors (p21(WAF1) and p27(Kip1)) and Bak in the beta-lapachone-induced apoptosis of human prostate cancer cells. Mol Pharmacol. 2001, 59: 784-794.
Goijman SG, Stoppani AO: Effects of beta-lapachone, a peroxide-generating quinone, on macromolecule synthesis and degradation in Trypanosoma cruzi. Arch Biochem Biophys. 1985, 240: 273-280. 10.1016/0003-9861(85)90033-5.
Guiraud P, Steiman R, Campos-Takaki GM, Seigle-Murandi F, Simeon de Buochberg M: Comparison of antibacterial and antifungal activities of lapachol and beta-lapachone. Planta Med. 1994, 60: 373-374. 10.1055/s-2006-959504.
Li YZ, Li CJ, Pinto AV, Pardee AB: Release of mitochondrial cytochrome C in both apoptosis and necrosis induced by beta-lapachone in human carcinoma cells. Mol Med. 1999, 5: 232-239.
Schuerch AR, Wehrli W: beta-Lapachone, an inhibitor of oncornavirus reverse transcriptase and eukaryotic DNA polymerase-alpha. Inhibitory effect, thiol dependence and specificity. Eur J Biochem. 1978, 84: 197-205. 10.1111/j.1432-1033.1978.tb12157.x.
Logsdon CD, Simeone DM, Binkley C, Arumugam T, Greenson JK, Giordano TJ, Misek DE, Kuick R, Hanash S: Molecular profiling of pancreatic adenocarcinoma and chronic pancreatitis identifies multiple genes differentially regulated in pancreatic cancer. Cancer Res. 2003, 63: 2649-2657.
Malkinson AM, Siegel D, Forrest GL, Gazdar AF, Oie HK, Chan DC, Bunn PA, Mabry M, Dykes DJ, Harrison SD: Elevated DT-diaphorase activity and messenger RNA content in human non-small cell lung carcinoma: relationship to the response of lung tumor xenografts to mitomycin Cl. Cancer Res. 1992, 52: 4752-4757.
Pink JJ, Planchon SM, Tagliarino C, Varnes ME, Siegel D, Boothman DA: NAD(P)H:Quinone oxidoreductase activity is the principal determinant of beta-lapachone cytotoxicity. J Biol Chem. 2000, 275: 5416-5424. 10.1074/jbc.275.8.5416.
Ross D, Siegel D: NAD(P)H:quinone oxidoreductase 1 (NQO1, DT-diaphorase), functions and pharmacogenetics. Methods Enzymol. 2004, 382: 115-144.
Bey EA, Wuerzberger-Davis SM, Pink JJ, Yang CR, Araki S, Reinicke KE, Bentle MS, Dong Y, Cataldo E, Criswell TL, Wagner MW, Li L, Gao J, Boothman DA: Mornings with Art, lessons learned: feedback regulation, restriction threshold biology, and redundancy govern molecular stress responses. J Cell Physiol. 2006, 209: 604-610. 10.1002/jcp.20783.
Tagliarino C, Pink JJ, Dubyak GR, Nieminen AL, Boothman DA: Calcium is a key signaling molecule in beta-lapachone-mediated cell death. J Biol Chem. 2001, 276: 19150-19159. 10.1074/jbc.M100730200.
Tagliarino C, Pink JJ, Reinicke KE, Simmers SM, Wuerzberger-Davis SM, Boothman DA: Mu-calpain activation in beta-lapachone-mediated apoptosis. Cancer Biol Ther. 2003, 2: 141-152.
Ough M, Lewis A, Bey EA, Gao J, Ritchie JM, Bornmann W, Boothman DA, Oberley LW, Cullen JJ: Efficacy of beta-lapachone in pancreatic cancer treatment: exploiting the novel, therapeutic target NQO1. Cancer Biol Ther. 2005, 4: 95-102. 10.4161/cbt.4.1.1382.
Pardee AB, Li YZ, Li CJ: Cancer therapy with beta-lapachone. Curr Cancer Drug Targets. 2002, 2: 227-242. 10.2174/1568009023333854.
Goldsmith P: Zebrafish as a pharmacological tool: the how, why and when. Curr Opin Pharmacol. 2004, 4: 504-512. 10.1016/j.coph.2004.04.005.
MacRae CA, Peterson RT: Zebrafish-based small molecule discovery. Chem Biol. 2003, 10: 901-908. 10.1016/j.chembiol.2003.10.003.
Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF: Stages of embryonic development of the zebrafish. Dev Dyn. 1995, 203: 253-310. 10.1002/aja.1002030302.
Peng MY, Wen HJ, Shih LJ, Kuo CM, Hwang SPL: Myosin heavy chain expression in cranial, pectoral fin, and tail muscle regions of zebrafish embryos. Mol Reprod Dev. 2002, 63: 422-429. 10.1002/mrd.10201.
Chen YH, Lu YF, Ko TY, Tsai MY, Lin CY, Lin CC, Hwang SPL: Zebrafidh cdx1b regulates differentiation of various intestinal cell lineages. Dev Dyn. 2009, 238: 1021-1032. 10.1002/dvdy.21908.
Combs MD, Yutzey KE: Heart valve development: regulatory networks in development and disease. Circ Res. 2009, 105: 408-421. 10.1161/CIRCRESAHA.109.201566.
Ma L, Lu MF, Schwartz RJ, Martin JF: Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning. Development. 2005, 132: 5601-5611. 10.1242/dev.02156.
Mjaatvedt CH, Yamamura H, Capehart AA, Turner D, Markwald RR: The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation. Dev Biol. 1998, 202: 56-66. 10.1006/dbio.1998.9001.
Hsia N, Zon LI: Transcriptional regulation of hematopoietic stem cell development in zebrafish. Exp Hematol. 2005, 33: 1007-1014. 10.1016/j.exphem.2005.06.013.
Hermann AC, Millard PJ, Blake SL, Kim CH: Development of a respiratory burst assay using zebrafish kidneys and embryos. J Immunol Methods. 2004, 292: 119-129. 10.1016/j.jim.2004.06.016.
Lipowsky HH, Usami S, Chien S: In vivo measurements of "apparent viscosity" and microvessel hematocrit in the mesentery of the cat. Microvasc Res. 1980, 19: 297-319. 10.1016/0026-2862(80)90050-3.
Papaioannou TG, Stefanadis C: Vascular wall shear stress: basic principles and methods. Hellenic J Cardiol. 2005, 46: 9-15.
Sorensen B, Weber RE: Effects of oxygenation and the stress hormones adrenaline and cortisol on the viscosity of blood from the trout oncorhynchus mykiss. J Exp Biol. 1995, 198: 953-959.
Planchon SM, Wuerzberger S, Frydman B, Witiak DT, Hutson P, Church DR, Wilding G, Boothman DA: Beta-lapachone-mediated apoptosis in human promyelocytic leukemia (HL-60) and human prostate cancer cells: a p53-independent response. Cancer Res. 1995, 55: 3706-3711.
Bey EA, Bentle MS, Reinicke KE, Dong Y, Yang CR, Girard L, Bornmann WG, Gao J, Boothman DA: An NQO1- and PARP-1-mediated cell death pathway induced in non-small-cell lung cancer cells by β-lapachone. Proc Natl Acad Sci USA. 2007, 104: 11832-11837. 10.1073/pnas.0702176104.
Kung HN, Yang MJ, Chang CF, Chau YP, Lu KS: In vitro and in vivo wound healing-promoting activities of beta-lapachone. Am J Physiol Cell Physiol. 2008, 295: C931-943. 10.1152/ajpcell.00266.2008.
Brutsaert DL: Cardiac endothelial-myocardial signaling: its role in cardiac growth, contractile performance, and rhythmicity. Physiol Rev. 2003, 83: 59-115.
Lemke G: Neuregulins in development. Mol Cell Neurosci. 1996, 7 (4): 247-262. 10.1006/mcne.1996.0019.
Milan DJ, Giokas AC, Serluca FC, Peterson RT, MacRae CA: Notch1b and neuregulin are required for specification of central cardiac conduction tissue. Development. 2006, 133: 1125-1132. 10.1242/dev.02279.
Peshkovsky C, Totong R, Yelon D: Dependence of cardiac trabeculation on neuregulin signaling and blood flow in zebrafish. Dev Dyn. 2011, 240: 446-456. 10.1002/dvdy.22526.
Irani K: Oxidant signaling in vascular cell growth, death, and survival: a review of the roles of reactive oxygen species in smooth muscle and endothelial cell mitogenic and apoptotic signaling. Circ Res. 2000, 87: 179-183.
Kunsch C, Medford RM: Oxidative stress as a regulator of gene expression in the vasculature. Circ Res. 1999, 85: 753-766.
Deshpande SS, Angkeow P, Huang J, Ozaki M, Irani K: Rac1 inhibits TNF-alpha-induced endothelial cell apoptosis: dual regulation by reactive oxygen species. FASEB J. 2000, 14: 1705-1714. 10.1096/fj.99-0910com.
Hampton MB, Orrenius S: Redox regulation of apoptotic cell death in the immune system. Toxicol Lett. 1998, 102-103: 355-358.
Li AE, Ito H, Kim KS, Takeda K, Yu ZY, Ferrans VJ, Finkel T: A role for reactive oxygen species in endothelial cell anoikis. Circ Res. 1999, 85: 304-310.
Minetti M, Malorni W: Redox control of red blood cell biology: the red blood cell as a target and source of prooxidant species. Antioxid Redox Signal. 2006, 8: 1165-1169. 10.1089/ars.2006.8.1165.
Mandal D, Moitra PK, Saha S, Basu J: Caspase 3 regulates phosphatidylserine externalization and phagocytosis of oxidatively stressed erythrocytes. FEBS Lett. 2002, 513: 184-188. 10.1016/S0014-5793(02)02294-9.
Lang KS, Duranton C, Poehlmann H, Myssina S, Bauer C, Lang F, Wieder T, Huber SM: Cation channels trigger apoptotic death of erythrocytes. Cell Death Differ. 2003, 10: 249-256. 10.1038/sj.cdd.4401144.
Noh JY, Park JS, Lim KM, Kim KY, Bae ON, Chung SM, Shin S, Chung JH: A naphthoquinone derivative can induce anemia through phosphatidylserine exposure mediated erythrophagocytosis. J Pharmacol Exp Ther. 2010, 333: 414-420. 10.1124/jpet.109.164608.
Moyes CD, Sharma ML, Lyons C, Leary SC, Leon M, Petrie A, Lund SG, Tufts BL: Origins and consequences of mitochondrial decline in nucleated erythrocytes. Biochim Biophys Acta. 2002, 1591: 11-20. 10.1016/S0167-4889(02)00224-0.
This study was supported by grants from Academia Sinica (# 94M011 and AS-99-TP-B08) to SPLH. We would like to thank Dr. Han-Jia Lin, Dr. Chin-Hwa Hu, and Dr. Yi-Chuan Cheng for their helpful discussions and advice. The authors thank Ms. Wun-Hsiang Yu for her maintenance of the fish room. We thank the Core Facility of the Institute of Cellular and Organismic Biology, Academia Sinica, for assistance with DNA sequencing. We thank Taiwan Zebrafish Core at Academia Sinica (ZCAS), funded by the National Science Council (NSC 100-2321-B-001-030) for providing Tg(gata1:DsRed) transgenic fish.
The authors declare that they have no competing interests.
YTW conducted the drug treatment, whole-mount in situ hybridization, histological sectioning, TUNEL assay, and interpretation of data. LCY participated in the ROS, fractional shortening, rhodamine dye injection, and wall shear stress measurement. MYT carried out the whole-mount in situ hybridization and interpretation of data. YHC participated in the initial drug screening and histological sectioning. YFL carried out the histological sectioning and TUNEL assay. CJH participated in the contribution of reagents and interpretation of data. CMC participated in the interpretation of data and helped to draft the manuscript. SPLH participated in the design of this study, performed statistical analysis, interpretation of data and draft the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: c-myb and ikaros. Embryos were treated with DMSO or β-lapachone at 24 hours post-fertilization (hpf) for 4 h and fixed at 30 hpf for whole-mount in situ hybridization using either c-myb (A, B) or ikaros (C, D) as RNA probes. Scale bars represent 100 μm. (TIFF 1 MB)
About this article
Cite this article
Wu, Y., Lin, C.Y., Tsai, M. et al. β-Lapachone induces heart morphogenetic and functional defects by promoting the death of erythrocytes and the endocardium in zebrafish embryos. J Biomed Sci 18, 70 (2011). https://doi.org/10.1186/1423-0127-18-70
- heart morphogenesis
- erythrocyte deficiency