Myosin VI contributes to maintaining epithelial barrier function
© Liao et al.; licensee BioMed Central Ltd. 2013
Received: 20 June 2013
Accepted: 10 September 2013
Published: 13 September 2013
Epithelial barrier dysfunction is associated with the pathogenesis of a number of immune inflammations; the etiology is not fully understood. The fusion of endosome/lysosome is a critical process in the degradation of endocytic antigens in epithelial cells. Recent reports indicate that myosin VI (myo6) is involved in the activities of endosomes. The present study aims to investigate the role of myo6 in epithelial barrier dysfunction.
The endosome accumulation was observed in myo6-deficient Rmcs. More than 80% endosomes were fused with lysosomes in naïve Rmcs while less than 30% endosomes were fused with lysosomes in the myo6-deficient Rmcs. The myo6-deficient Rmc monolayers showed high permeability to a macromolecular antigen, ovalbumin, the latter still conserved the antigenicity, which induced strong T cell activation.
We conclude that myo6 plays a critical role in the fusion of endosome/lysosome in Rmc epithelial cells. Deficiency of myo6 compromises the epithelial barrier function.
The epithelial barrier is formed by epithelial cell bodies and the tight junctions around the top of each epithelial cell. Such a barrier separates the body tissue from the external environment. Under the physiological states, the epithelial barrier only allows water and substances with small molecular weight to pass through . Pathogens and macromolecular antigens are generally prevented from entering into the deep tissue by the epithelial barrier . However, under the states of epithelial barrier dysfunction, the macromolecular antigens do enter the deep tissue in the body to interact with immune cells and induce skewed immune responses and cause immune inflammations [3, 4]. The pathogenesis of epithelial barrier dysfunction is to be further understood.
Protein antigens can pass the dysfunctional epithelial barrier via paracellular pathways  or intracellular pathways  to enter the deep regions of tissue. The paracellular pathway is sealed by the tight junctions under normal physiological conditions . In harsh conditions, such as psychological stress, the paracellular pathway may be opened to allow noxious substances to be absorbed . Alternatively, antigens can be also transported across the epithelial barrier via the intracellular pathways . In the process of via the intracellular pathways, the antigens are firstly wrapped by the plasma membranes to form endosomes, and then to be transported to the subepithelial region . Theoretically, the endosomes can fuse with lysosomes within epithelial cells . The endocytosed antigens should be degraded by the acidic hydrolases of lysosomes . However, according to previous reports, the antigen-carrying endosomes can be transported across the epithelial barrier to be delivered into the deeper regions of tissue . The phenomenon implies that the fusion of endosome and lysosome may be disturbed in the case of epithelial barrier dysfunction; the underlying mechanism needs to be further investigated.
Recent reports suggest that myosin VI (myo6) is involved in the activities of endosome and lysosome  in body cells. Myo6 belong to the myosin family that is composed by the ATP-dependent motor proteins, which play a role in muscle contraction and are involved in a wide range of other eukaryotic motility processes. After engulfing by epithelial cells, antigens can be wrapped to form endosomes. Previous studies observed that the endosomes in intestinal epithelial cells could move from the luminal side to the bottom side . Thus, we hypothesized that myo6 may be involved in the movement of the endosomes. In this study, we knocked down the gene of myo6 from epithelial cells and found that the myo6-deficient epithelial cells showed endosome accumulation, less frequency of the fused endosome and lysosome and the endocytic protein antigens were transported across the epithelial barrier.
The antibodies of EEA1, LAMP2, myosin VI and shRNA (sc-37133-SH) of myo6 were purchased from Santa Cruz Biotech (Shanghai, China). The 51Cr-EDTA was purchased from Chemindustry (Shanghai, China). Ovalbumin (OVA) and bovine serum albumin (BSA) were purchased from Sigma Aldrich (Shanghai, China). The ELISA kit of OVA was purchased from the AlphaDiagnosis (Hangzhou, China). Reagents of real time RT-PCR were purchased from Invitrogen China (Shanghai, China). The reagents of immune cell purification were purchased from Miltenyi Bioltech (Shanghai, China).
The RPMI 2650 cells (Rmc, in short; a Human nasal epithelial cell line) were purchased from ATCC (Manassas, VA) and grown in Eagle’s minimal essential medium (MEM) supplemented with 100 U/ml penicillin, 100 μg/ml streptomycin and 10% fetal bovine serum (FBS) in a humidified incubator at 37°C with 5% CO2. The cells were further cultured in Transwells (polycarbonate membrane, 0.4 μm pore size, 1.12 cm2 surface area, Corning Costar Co., USA) to form monolayers to be used in further experiments.
Permeability of Rmc monolayer assessment
Rmcs were cultured for 2 weeks in Transwell inserts to confluence (TER ≥500 Ohm/cm2). Two types of tracers were tested. For the macromolecular tracer, OVA (10 μg/ml) was added to the apical chambers of Transwells. Samples were taken from the basal chambers and analyzed the levels of OVA by ELISA. For the small molecular tracer, 51Cr-EDTA (Ethylenediaminetetraacetic acid; 1 μCi) was added to the apical chambers of Transwells. The [51Cr]- radioactivity was counted using a γ-counter. The permeability was expressed as the ratio between the original amount added to the apical chambers and the recovered amount from the basal chambers.
Recording transepithelial resistance (TER)
The TER of Rmc monolayer was recorded using the Millicell ERS apparatus (Millipore, Bedford, Massachusetts, USA).
Enzyme-linked immunoassay (ELISA)
The levels of OVA in the basal chambers of Transwells were determined by ELISA with commercial reagent kits following the manufacturer’s instruction.
Total proteins were extracted from the cells. The protein extracts were fractioned in sodium dodecyl sulfate polyacrylamide gel electrophoresis and transferred onto nitrocellulose membrane. The membrane was incubated with primary antibodies (100 ng/ml) at 4°C overnight. After washing with TBST (Tris-buffered saline with Tween-20), the membrane was incubated with HRP-labeled secondary antibodies (50 ng/ml). The immune blots were developed with the ECL Western Blotting Reagent (Amersham; Shanghai, China).
RNA interference of myo6
Following published procedures with modifications , endosomes and lysosomes were stained in Rmcs. The cells were fixed with 2% paraformaldehyde for 2 h at room temperature, incubated with the primary antibodies (0.5 μg/ml) for 1 h at room temperature and followed by incubating with fluorescence-labeled secondary antibodies (0.5 μg/ml) for 1 h at room temperature. The cells were smeared onto a slide and observed under a confocal microscope with the × 630 objective. When the positive staining of interest was identified, the images were further enlarged using the built-in enlarging software feature. Thirty images were photographed from experimental each group. The total number of positive stained particles in the cells was counted on each image. The OVA+/EEA1+ and OVA+/EEA1+/LAMP1+ particles were counted respectively.
Preparation of immune cells
The CD3+ CD4+ CD25- T cells (Th0) and dendritic cells (DC) were isolated from the spleen of OVA-TCR transgenic DO11.10 mice (purchased from Beijing Experimental Animal Center; Beijing, China) by the magnetic cell sorting with commercial reagent kits following the manufacturer’s instruction (the cell purity was more than 95% as checked by flow cytometry. The cells were cultured in RPMI1640 medium for further experiments. The using animal in the study was approved by the Animal Ethic Committee at our university.
The isolated Th0 cells were labeled with CFSE (Carboxyfluorescein succinimidyl ester) and cultured with DC (T cell: DC = 10:1; 105 cells/ml) in the presence of OVA (10 μg/ml; BSA was used as an irrelevant control protein) or sample protein (from the basal chamber medium) in culture medium for 3 days. The CFSE-dilution assay was performed with a flow cytometer (FACSCanto, BD Bioscience, San Jose, CA).
The data were presented as mean ± SD. Differences between two groups were determined by Student t test. p < 0.05 was set as the significant criterion.
Deficiency of myo6 results in an accumulation of endosomes in epithelial cells
Published data indicate that the intracellular transport pathway plays a role in the pathogenesis of epithelial barrier dysfunction . The process by which epithelial cells transport antigens across the epithelial barrier remains largely unknown. Recent studies indicate that the endosome/lysosome system and myo6 in epithelial cells plays a critical role in the transporting endocytic cargo [12, 14, 15]. Thus, we firstly observed the role of myo6 in the endosome metabolism in epithelial cells. We cultured an airway epithelial monolayer with or without the myo6 gene knockdown (Figure 1A). The epithelial cells were then processed for determining the levels of EEA1, a protein marker of endosome . As shown by Western blotting, EEA1 protein was detected in naïve epithelial cells, which was markedly increased in myo6-deficient epithelial cells (Figure 1B). The results were confirmed by morphological study; the immunocytochemical staining showed much more non-fused endosomes and EEA1 staining in the myo6-deficient epithelial cells than that in control cells (Figure 1C-D). The results indicate that myo6 plays a critical role in the metabolism of endosomes in epithelial cells.
Myo6 Facilitates fusion of endosome and lysosome
Positively stained granules in epithelial cells
Deficiency of myo6 promotes intracellular antigen transport across epithelial barrier
Antigens passed through the myo6-deficient epithelial monolayers conserve antigenicity
In this study, we found that endosomes accumulated in the myo6-deficient epithelial cells. Myo6 was required in the process of the fusion of endosome and lysosome in epithelial cells. The knockdown of myo6 gene compromised the epithelial barrier function manifesting the increase in the permeability to macromolecular protein antigens. After passing the myo6-deficient epithelial barrier, the antigens still conserved the antigenicity.
The epithelial barrier function plays a critical role in the maintenance of the homeostasis of the body. The pathogenesis of a number of diseases, such as allergic diseases  and chronic immune inflammation , are associated with the epithelial barrier dysfunction. Various factors, such as psychological stress, microbial infection and radiations, are suggested associated with the epithelial barrier dysfunction. The present data have added a piece of novel information to this area; the myo6 plays a critical role in the maintenance of the epithelial barrier function. The data indicate that the myo6-deficiency-induced epithelial barrier hyperpermeability is via the intracellular pathway since the TER, the indicator of the paracellular functional state, is not altered in the epithelial monolayers. Myo6 is thought to transport endocytic vesicles into the cell, functions in a variety of intracellular processes such as vesicular membrane traffic, cell migration, and mitosis . The present data indicate that myo6 is also involved in the fusion of endosome/lysosome. Inhibition of myo6 results in accumulation of endosomes in the cytoplasm as we observed in the present study. The phenomenon implicate that myo6 is required in the fusion of endosome/lysosome to render the endocytic cargo to be digested by the enzymes in lysosome. Shorting of myo6 may drive the endosomes with endocytic cargo, such as macromolecular antigens, to be transported to the subepithelial region to contact immune cells; some of the antigens may induce unwanted immune responses.
The sub-cellular pathology of this study showed that the myo6-deficient epithelial cells had the endosome accumulation. Under physiological states, the early endosomes form late endosomes, and then, fuse with lysosomes. The acidic hydrolases in lysosomes can degrade the endocytic cargo in endosomes. The accumulation of endosomes in the myo6-deficient epithelial cells implies the metabolism of the endosomes may be disturbed. The inference is supported by the subsequent data; much less endosome/lysosome fusion was observed in the myo6-deficient epithelial cells. The data are in line with others’ findings. Chen et al  reported that the ubiquitin TNFAIP3-deficient epithelial cells had less fusion of endosome/lysosome; the cells showed less ability to degrade the endocytic microbial products. Huang et al  suggested that ubiquitin myo6-deficient Caco-2 monolayers had disturbed fusion of endosome/lysosome.
The permeability is an important aspect to mirror the epithelial barrier function. In the present study, we observed marked increases in the permeability of the myo6-deficient epithelial monolayers; abundant protein antigens were transported across the epithelial monolayers to arrive the basal chambers of Transwells. The Transwell system is a mimic of epithelial barrier; the basal chambers are somewhat similar to the subepithelial region in the mucosa. The transported antigens have the opportunity to interact with immune cells in the subepithelial region. Thus, whether the antigens still conserve the antigenicity is of significance. Our further results corroborate the reasoning by showing that the transported antigens have strong antigenicity to induce T cell proliferation. Similar results were also reported recently; Song et al  found that antigens passed through the 20-deficient epithelial monolayers could activate antigen specific T cells.
Taken together, the data indicate that the fusion of endosome/lysosome plays a critical role in the maintenance of the epithelial barrier function. The deficiency of myo6 can compromise the epithelial barrier function by increasing the intracellular permeability to macromolecular protein antigens.
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