A.V. Zhirmunsky Institute of Marine Biology, Far Eastern Branch of the Russian Academy of Sciences, Palchevsky St. 17, 690059, Vladivostok, Russia,
Cytotechnology. 2013 Oct;65(5):725-35. doi: 10.1007/s10616-013-9577-z. Epub 2013 May 9.
Components of the extracellular matrix may modulate the growth factor effects that play important roles in the proliferation and differentiation of precursor cells. We developed an in vitro cultivation protocol for cells of the larval marine bivalve Mytilus trossulus to study the role that extracellular matrix components may play in myodifferentiation and replication-mediated DNA synthesis using immunofluorescence and confocal laser scanning microscopy. Here, we demonstrate that the extracellular matrix regulates the expression of muscle proteins, leading to their assembly and the terminal muscle differentiation of larval cells during cultivation. We further show that the myogenesis process progresses in cells cultivated on fibronectin, carbon or poly-L-lysine but is inhibited in cells grown on a collagen carpet. Consistent with a decrease in muscle protein expression in cells cultivated on collagen, we demonstrate an increase in the number of BrdU-positive cells in comparison with cells cultured on other substrates during the entire cultivation period. Moreover, we demonstrate that the matrix-dependent myogenic differentiation of larval mussel cells is reversible. Round-shaped cells cultivated on collagen were able to differentiate into muscle cells after reseeding on fibronectin, carbon or poly-L-lysine. In addition, cells cultured on collagen and then transplanted to fibronectin exhibited distinct cross-striation and contractile activity. Taken together, our data suggest that the extracellular matrix participates in the regulation of the proliferation and myodifferentiation of mussel trochophore progenitor cells and validate novel approaches for successfully culturing cells from bivalves over extended periods.
细胞外基质的成分可能调节生长因子的作用,这些生长因子在祖细胞的增殖和分化中起着重要作用。我们开发了一种用于幼虫海洋双壳类贻贝 Mytilus trossulus 细胞的体外培养方案,以使用免疫荧光和共聚焦激光扫描显微镜研究细胞外基质成分在肌分化和复制介导的 DNA 合成中可能发挥的作用。在这里,我们证明细胞外基质调节肌肉蛋白的表达,导致它们在培养过程中的组装和幼虫细胞的终末肌肉分化。我们进一步表明,在纤维连接蛋白、碳或聚-L-赖氨酸上培养的细胞中,肌发生过程进展,但在胶原蛋白地毯上生长的细胞中受到抑制。与在胶原蛋白上培养的细胞中肌肉蛋白表达减少一致,我们证明在整个培养期间,与在其他底物上培养的细胞相比,BrdU 阳性细胞的数量增加。此外,我们证明幼虫贻贝细胞的基质依赖性肌生成分化是可逆的。在胶原蛋白上培养的圆形细胞在重新接种到纤维连接蛋白、碳或聚-L-赖氨酸上后能够分化为肌肉细胞。此外,在胶原蛋白上培养然后移植到纤维连接蛋白上的细胞表现出明显的横纹和收缩活性。总之,我们的数据表明,细胞外基质参与贻贝担轮祖细胞的增殖和肌分化的调节,并验证了成功培养贝类细胞的新方法,以延长培养时间。