- Open Access
Induction of apoptosis and inhibition of cell growth by tbx5 knockdown contribute to dysmorphogenesis in Zebrafish embryos
- Jenher Lu†1, 2Email author,
- Tzuchun Tsai2, 3,
- Sielin Choo4,
- Shuyu Yeh4,
- Renbing Tang1, 2,
- Anhang Yang1, 2,
- Hsinyu Lee5 and
- Jennkan Lu†4
© Lu et al; licensee BioMed Central Ltd. 2011
Received: 22 May 2011
Accepted: 8 October 2011
Published: 8 October 2011
The tbx5 mutation in human causes Holt-Oram syndrome, an autosomal dominant condition characterized by a familial history of congenital heart defects and preaxial radial upper-limb defects. We report aberrant apoptosis and dormant cell growth over head, heart, trunk, fin, and tail of zebrafish embryos with tbx5 deficiency correspond to the dysmorphogenesis of tbx5 morphants.
Wild-type zebrafish embryos at the 1-cell stage were injected with 4.3 nl of 19.4 ng of tbx5 morpholino or mismatch-tbx5-MO respectively in tbx5 morphants and mismatched control group. Semi-quantitative RT-PCR was used to for expression analysis of apoptosis and cell cycle-related genes. TUNEL and immunohistochemical assay showed the apoptosis spots within the local tissues. Ultra-structure of cardiac myocardium was examined by transmission electron microscope.
Apoptosis-related genes (bad, bax, and bcl2), and cell cycle-related genes (cdk2, pcna, p27, and p57) showed remarkable increases in transcriptional level by RT-PCR. Using a TUNEL and immnuohistochemical assay, apoptosis was observed in the organs including the head, heart, pectoral fins, trunk, and tail of tbx5 knockdown embryos. Under transmission electron microscopic examination, mitochondria in cardiomyocytes became swollen and the myocardium was largely disorganized with a disarrayed appearance, compatible with reduced enhancement of myosin in the cardiac wall. The ATP level was reduced, and the ADP/ATP ratio as an apoptotic index significantly increased in the tbx5 deficient embryos.
Our study highlighted that tbx5 deficiency evoked apoptosis, distributed on multiple organs corresponding to dysmorphogenesis with the shortage of promising maturation, in tbx5 knockdown zebrafish embryos. We hypothesized that mesenchymal cell apoptosis associated with altered TBX5 level may subsequently interfered with organogenesis and contributed to dysmorphogenesis in tbx5 deficiency zebrafish embryos.
Tbx5 belongs to the T-box family of transcription factors and is required for the embryonic development of the heart and forelimbs [1, 2]. Tbx5 mutations in humans cause Holt-Oram syndrome (HOS), an autosomal dominant condition characterized by a familial history of congenital heart defects and preaxial radial ray upper-limb defects [3, 4]. The phenotypic manifestations of tbx5 deficiency in different vertebrates are quite similar. Tbx5 deficiency in zebrafish causes multiple organ defects during organogenesis, including a shortened trunk, failure of cardiac looping formation, and hypogenesis or agenesis of the pectoral fins [5, 6]. Either the type of mutation or the location of a mutation is predictive for the severity of heart or limb malformations in Holt-Oram syndrome patients. That is, there is no correlation between the tbx5 genotype and phenotype.
Since tbx5 encodes a transcription factor, tbx5 deficiency is presumed to disrupt development by altering the transcriptional function of the TBX5 protein, thereby affecting downstream target gene expressions, particularly affiliation binding proteins or transcription factors [7–9]. Though TBX5 is an important developmental regulator in normal development and disease, which TBX5 functions or whether the TBX5 protein plays a role as trasnscriptional activator or repressor, even divergent in different condition, is still relatively unclear.
The syndrome caused by mutations in T-box transcription factor 5 (TBX5) was described as "premature stops" or "developmental delay" in embryogenesis, though the mechanism how to delay or stop the development of the embryo, especially the cardiogenesis, remained indistinct . Some revealed that the depletion of tbx5 leading to cardiac cell cycle arrest have been proved to elicit defect in cardiac sacromere formation and decreased cardiac cell number .
Apoptosis is a key event in many biological processes including embryogenesis and occurs in a variety of circumstance in specific time window in embryos. Zebrafish undergoes different levels of developmental cell death throughout embryonic stages precisely, including brain, spinal cord, ear, eyes, germ cells, tail bud and excretory system . Apoptosis partakes in the complicate orchestration cell-cell interaction during organogenesis, such as cell differentiation in heart myocardium and the endocardial cushions during specific time . Some postulated that anomalous apoptosis due to insufficient or improper induction of organogenesis specific factors leads to particular congenital diseases .
In this study, we reported that aberrant apoptosis and cell cycle arrest are increasing in zebrafish embryos with tbx5 deficiency; meanwhile, the excessive apoptosis is in coincidence with the dysmorphogenesis in individuals with tbx5 deficiency.
Materials and methods
The approval of this study was granted by the National Taiwan Ocean University Aquaculture Animal ethics review board with annual evaluation.
Maintenance of zebrafish
Zebrafish were maintained in 45-liter aquaria heated to 28.5°C with 25 fish per tank. The water was filtered, and about half of the water was replaced at least once a week. Adult zebrafish were fed 1 or 2 times per day with a variety of food, and the tank was cleaned by siphoning off any excess food after the second daily feeding. The day-night cycle was controlled with an automatic timer (14 h light/10 h dark).
Breeding of zebrafish
Zebrafish reach sexual maturity in 10~12 weeks, but breeding fish should be between 7 and 18 months of age for maximum embryo production. The day before breeding, 1/3 of the water was replaced and the tank was cleaned after feeding (1~2 h before the end of the light period). Finally, a collection box was placed at the bottom of the tank and preparation was made to collect the embryos the next day.
When the light came on, we removed the collection box and placed the collected embryos into an incubator maintained at a temperature of 28.5°C.
Total RNA was isolated from 50 embryos using the guanidine isothiocyanate-based TRIzol solution. RNA samples were resuspended in DEPC-treated water and quantified spectrophotometrically at 260 nm. The RNA quality was then checked by 1.2% agarose gel electrophoresis, after staining with 1 μg/ml ethidium bromide. The RNA stock was stored at -80°C.
Semi-quantitative Reverse-Transcriptase Polymerase Chain Reaction
Total RNA was prepared from 50 morpholino (MO) injected or normal embryos (Invitrogen Corporation, Carlsbad, CA, USA). Three microliters of 1st-strand cDNA was amplified. Amplification primers for each specific mRNA were deduced from published sequences and included bcl2 (P1: 5'-GTTCCACCCGTTTTCA-3', P2: 5'-GCGAGTCCTCATTCTGT-3'), bad (P1: 5'-CAAGCCTGGATAAACAC-3', P2: 5'-GGCAGATTGAAAGAAAG-3'), and bax (P1: 5'-AAGCATTGAGAGGTG-3', P2: 5'-AGAGGAAGTGAGGAGAA-3'), p27 (P1: 5'-GTTCGCTTGTCTAATGG-3', P2: 5'-GTCGGACTCAATGGTT-3'), p57 (P1: 5'-AGATTACGAGTGGGAGG-3', P2: 5'-TGAGTTCAGAGAGAAAGGG-3'), and pcna (P1: 5'-GCTCGCGGGATTTCT-3', P2: 5'-CAGCGGAGTGGCTTTGG-3'), cdk2 (P1: 5'-CAAGAGTTTCAGTCGC-3', P2: 5'-TAAGTCCGCACAGGTA -3'). PCR conditions were as follows: denaturation at 95°C for 3 min, followed by 50 cycles of amplification (95°C for 20 s, 59°C for 15 s, and 72°C for 20 s). Quantification of PCR product was performed on an electrophoresis agarose gel using Kodak image 3.5 software. All measurements were performed in triplicate (n = 3).
Microinjection and morpholino treatment
The morpholino antisense oligonucleotide, tbx5-MO (5 GAAAGGTGTCTTCACTGTCCGCCAT-3), was designed against the tbx5 translational start site (Gene Tools LLC, Philomath, OR, USA) and a mismatch tbx5-MO (5'-GTCTCTTGACTCTCCGCGATCTCGG-3') was designed for control (Gene Tools LLC, Philomath, OR, USA). Wild-type embryos primarily at the 1-cell stage with the chorion intact were injected with 19.4 ng/4.3 nl of stock morpholino diluted in Danieau's solution. The injected embryos were raised at 28.5°C. Embryos used for analyzing the expression of various markers were fixed with 4% paraformaldehyde. Otherwise, embryos were scored after 2 days of development for late effects. In our previous study, three control groups, including 3' end of tbx5-MO(2) (5'-GCCTGTACGATGTCTACCGTGAGGC-3') and embryos with blank microinjection and wild-type ones without microinjection, were included to identify the specific blockage of tbx5 mRNA translation effect of tbx5-MO.6 In order to examine the knockdown effectiveness of the tbx5-MO, a tbx5-GFP construct was generated by fusing a 468-bp fragment of tbx5, which included the morpholino target side into a GFP producing vector. Tbx5-MO at 19.4 ng and tbx5-GFP DNA at 150 μg were co-injected into 1-cell stage embryos. In control group, only 150 μg of tbx5-GFP was microinjected into 1-cell stage embryos .
Zebrafish embryos were fixed with 4% paraformaldehyde in phosphate-buffered saline (PBS). Deparaffinized sections (3 μm) of zebrafish embryo tissues were placed on slides and processed for immunohistochemistry. After blocking with a biotin blocking system (Dako A/S, Glostrup, Denmark) for 30 min, sections were incubated with target-purified rabbit primary antibodies, including BCL2 (Anaspec Inc., Fremont, CA, USA), BAD (Anaspec Inc., Fremont, CA, USA), CASPASE-3 (Anaspec Inc., Fremont, CA, USA), CASPASE-8 (Anaspec Inc., Fremont, CA, USA),
CDK2 (Anaspec Inc., Fremont, CA, USA), P27 (Anaspec Inc., Fremont, CA, USA) and MF20 (Developmental Studies Hybridoma Bank, Iowa City, IA, USA), washed in PBS, and then incubated with a rhodamine-conjugated secondary antibody: goat anti-rabbit immunoglobulin G (IgG). After washing in PBS, sections were incubated with mounting medium and kept at 4°C.
Transmission electron microscopic examinations
Embryos were fixed at 48 h post-fertilization (hpf) with 2.5% glutaraldehyde in Sorenson's phosphate buffer, postfixed with 1% OsO4 in Sorenson's phosphate buffer followed by dehydration through a graded series of ethanol washes, and embedded in Spurr's EPON. Blocks were heated in an oven for 8 h at 70°C. Semithin (1-μm) sections were cut and stained with toluidine blue for adequate preview under a microscope. Ultrathin sections (900 Å) were cut with a diamond knife, stained with uranyl acetate and lead citrate, and examined with an electron microscope.
Both whole mount and sectioned TdT-UTP nick end labeling (TUNEL) assays were performed using an ApopTag kit (Chemicon, Heule, Belgium). Briefly, zebrafish embryos were fixed with 4% paraformaldehyde in PBS. Proteinase K-treated whole embryos or deparaffinized sections (5 μm) of embryos were incubated with the TdT enzyme followed by anti-digoxigenin. Finally, embryos or slides were stained with DAB for 5 min.
Western blot analysis
Embryos were homogenized on ice in lysis buffer (Sigma-Aldrich, St. Louis, MO, USA). Then, cellular debris was pelleted by centrifugation at 12,000 rpm for 20 min, and the supernatant was collected and measured. Proteins were mixed with sample buffer before separating in 10% sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE) gels. The SDS-PAGE was then transferred onto nitrocellulose membranes at 100 V for 1 h. Membranes were blocked with blocking buffer (5% bovine serum albumin (BSA)) at room temperature for 1 h. The TBX5 primary antibody (Aviva Systems Biology LLC, San Diego, CA, USA) was incubated overnight at 4°C using the appropriate dilution (1: 1000). The nitrocellulose membranes were washed with PBST followed by incubating with a horseradish peroxidase (HRP)-conjugated secondary antibody (1: 5000) for 1 h at room temperature before the images were digitized.
ATP and ADP/ATP ratio assay were performed using an ApoSENSOR™ ADP/ATP Ratio Assay Kit (Biovision, Mountain View, CA, USA). Ten embryos (n = 10 in each subgroup) were separately placed in 96-well round-bottomed, flat, white plates for detection. The RLU (relative luminescence unit) value was detected using the PARADIGM™ Detection Platform (Beckman Coulter Inc., Brea, CA, USA).
Results are given as the mean ± S.D. Where applicable, a t-test was performed. Statistical significance was accepted at p < 0.05.
Morphological characteristics of tbx5 knockdown embryos
TUNEL assay of tbx5 knockdown embryos
We examined apoptosis using a TUNEL assay. Aberrant poptosis was present in the entire paravertebral mesenchymal zone of tbx5 knockdown embryos (Figure 1H, Q). Apoptosis was noted in the heart (Figure 1D), tail (Figure 1L), bilateral paravertebral mesenchymal region (Figure 1H) and trunk (Figure 1Q) of tbx5 knockdown embryos. Apoptosis also slightly noted in the pericardium (Figure 1C), tail (Figure 1K), bilateral paravertebral mesenchymal region (Figure 1G) and trunk (Figure 1O) of WT embryos. Furthermore, there was no significant difference between WT and mismatch-tbx5-MO treated embryos (Figure 1P).
Molecular characteristics of tbx5 knockdown embryos
We tested the expressions of apoptosis-related genes at 3 important developmental periods in both WT and MO-treated zebrafish embryos: heart tube formation at 24 hpf, looping formation at 30 hpf, and chamber formation at 48 hpf. Cell apoptosis-related genes, including bad, bax, and bcl2, showed remarkable increases in tbx5 morphants in all studied periods but not in embryos injected with mismatch-tbx5-MO, which has no significant different with the wild-type and control mismatch (Figure 2B-D).
Ultrastructural changes in mitochondria
Ultrastructural changes in cardiac myofibrils
Normal cardiac myofibrils were well organized as the Z-disc and M-lines in WT embryos at 48 hpf (Figure 7C). In contrast, the ultrastructure of the myocardium appeared largely disorganized in tbx5 knockdown embryos. In addition, myofibrils appeared to be disarrayed (Figure 7D). Furthermore, cardiocytes were disaggregated and failed to develop a tight junction to each other. (Figure 7A-B) The myofibril layer in the cardiac chamber wall had become very thin with a disarrayed arrangement (data not shown).
Changes in the ADP/ATP ratio
Organogenesis is a vital process during embryonic development and is often accompanied by apoptosis in certain time windows. Vertebrate embryos, including those of zebrafish, undergo programmed cell death throughout the development process [15, 16]. Development of an organ or tissue is often preceded by the extensive proliferation and differentiation of a particular cell; the resultant mass is then "pruned" into the correct form by apoptosis. Therefore, embryonic development is strictly regulated by processes including cell proliferation, migration, differentiation, and apoptosis. Dysregulation of any of the processes can cause congenital diseases and anomalies. Previous evidence showed the important roles of apoptosis in embryonic cardiac development. Poelmann et al. reviewed how apoptosis occurs in the myocardium of the outflow tract and in the formation of the atrioventricular cushion, pulmonary trunk, semilunar valves, and even vascular remodeling . Aberrant patterns, overactivation, or disruption of apoptosis can cause congenital malformations. For example, disorder of the apoptosis process impelled the regression of four-arch segments and interrupted aortic arch type B in tumor growth factor (TGF)-β2-deficient mice .
Our data revealed activation of apoptosis and inhibition of cell growth in embryonic tbx5 morphants at 36 hpf by transcriptional and translational levels. By RT-PCR, the members of BCL-2 family genes and cell cycle-related genes were overexpressed in specific time window during zebrafish embryonic development. All apoptosis related genes either anti-apoptosis related gene (bcl-2) or pro-apoptosis related genes (bad and bax) were all transcriptionally activated, and so were the cell proliferation markers (cdk2 and pcna) and cyclin kinase inhibitors (p27 and p57). In protein level, remarkably plentiful production of apoptosis-related proteins including CASPASE-3, CASPASE-8, and BAD were proved by immunohistochemistry These data disclose that a deficiency of tbx5, a transcription factor, in zebrafish embryos may trigger multiple signal pathways including promoting or inhibiting molecules and eventually come to the end sequel of apoptosis and cease of cell growth.
Besides, the distribution of aberrant apoptosis and deviant cell cycle caused by a deficiency of tbx5 in the embryos might be associated with the dysmorphogenesis, especially engendering the string-like heart, short fins, and malformed trunk during zebrafish embryonic development.
There are two main apoptosis pathways including cell-intrinsic (mitochondrial) pathway and cell-extrinsic (death receptor) pathway; the intrinsic pathway is largely regulated by mitochondria, whereas the extrinsic pathway interacts with death receptors . Mitochondria play fundamental roles in both life and death to provide factories of bio-energy and also gates of apoptosis for cells . There is no exception in embryonic development. Mitochondria supply energy to embryos from the beginning of fertilization to ensure that the progressive development of an embryo is clearly documented [20, 21]. The synthesis of ATP which is compulsory for maintaining regular cellular function was impaired during the mitochondrial apoptotic process and diminished cell viability [22–24]. In addition, resynthesis of ATP decreased in the mitochondria of apoptotic cells, and a relatively low ratio of ATP to ADP can be used to monitor apoptosis. The decreased ATP level suggests an inadequate energy supplement; furthermore, conversion of the ADP/ATP ratio indicates energetic exhaustion as a result of an apoptotic process in tbx5-deficient embryos at the late stage of organogenesis [25, 26].
The mitochondrial apoptotic process causes the outer membrane of mitochondria to release proapoptotic proteins and eventually gives rise to swollen mitochondria [27, 28]. Our ultrastructural findings by TEM revealed that mitochondria were swollen and loose in the hearts of tbx5 knockdown embryos, rather than small and dense in WT embryos. This phenomenon is compatible with the morphological changes of mitochondria during apoptosis, which culminates in permeabilization of the mitochondrial outer membrane and release of soluble proteins from the mitochondrial intermembrane space. Once the mitochondrial permeability transition pore is opened, proapoptotic proteins are released, and the membrane potential collapses, which results in swelling of mitochondria. The number of mitochondria in tbx5 deficiency embryos also increased in addition to their size. Although a similar phenomenon was described during apoptosis induced by anticancer drugs in colon cancer cells and apoptosis in mitochondrial myopathy, mitochondrial proliferation accompanied by mitochondrial swelling was first reported in apoptosis of zebrafish embryos with tbx5 deficiency . Until now, the role of mitochondrial proliferation linked to apoptosis has remained unexplained.
Under TEM, the ultrastructure of the myocardium in tbx5 knockdown embryos appeared eminently disorganized. The myofibrils were quantitatively diminished at both the atrial and ventricular levels. We used MF20, an anti-myosin antibody, to prove a decrease in cardiac myosin. This result is in accordance with conclusion of our previous study that cardiomyogenesis-related genes were perturbed in tbx5 knockdown embryos .
The TUNEL assay showed that a shortage of tbx5 activated aberrant apoptosis and dormant cell growth in the head, heart, fins, and trunk. Although abnormal apoptosis-related genes were expressed throughout the entire process of organogenesis in tbx5 knockdown embryos, the degree and distribution of apoptosis varied in different locations at 48 hpf. Such aberrant apoptosis may contribute to consequent morphologic anomalies including a string-like heart, a curled trunk, and hypogenesis of the pectoral fins, but it did not interfere with the migration and differentiation of progenitor cells during early development. For example, no ectopic fin was found in embryos, although hypogenesis or agenesis of the pectoral fin was frequently observed in tbx5 morphants, as was the string-like heart. We hypothesized that the aberrant apoptosis may play a role in the interruption of cardiac looping, chamber formation, and growth of pectoral fins in zebrafish. Nevertheless, mutations in tbx5 gene underlie Holt-Oram syndrome, the majority of which is assumed as sequel "premature stops" or "developmental delay", may induce inappropriate apoptotic processes during embryogenesis and lead to the dysmorphogenesis including cardiac and limb malformation.
From a genomic analysis, dozens of genes were related to the underlying causes of isolated congenital heart disease and genetic syndrome associated with cardiac anomalies. However, genotype-phenotype distinctions exist. The discrepancy was frequently related to multiple genetic pathways, the size of the deletion, different allele/loci, point mutations, or a haploinsufficiency. Our observation presumed that the genotype-phenotype distinction might be a consequence of variable degrees of apoptosis in progenitor cells.
Some study declared that exogenous TBX5 could induce apoptosis and inhibit cell proliferation in vitro . Our results revealed tbx5 insufficiency ultimately resulted in activation of apoptosis and inhibition of cell growth in whole individual of zebrafish embryo, though knockdown of TBX5 leads to overexpression of both anti-apoptotic and pro-apoptotic gene than wild type embryos and the controls. Those data implied that abnormal tbx5 level play a role in aberrant apoptosis and cell growth contributing to dysmorphogenesis.
In summary, abnormal appearances in zebrafish embryos with tbx5 deficiency including string-like heart, curled trunk, curled tail, and pectoral fins might be a consequence of aberrant apoptosis and dormant cell growth in early embryonic development, which affected late differentiation and growth of organs as well as maturation.
The MF20 antibody developed by D.A. Fischman was obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by the University of Iowa, Department of Biological Sciences, Iowa City, IA 52242.
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