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首页> 外文期刊>Journal of Neuroscience Methods >Isolation, growth and differentiation of hair cell progenitors from the newborn rat cochlear greater epithelial ridge.
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Isolation, growth and differentiation of hair cell progenitors from the newborn rat cochlear greater epithelial ridge.

机译:新生大鼠耳蜗较大上皮ridge的毛细胞祖细胞的分离,生长和分化。

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Mammalian cochlear hair cell loss is irreversible and leads to permanent hearing loss. To restore hearing physiologically, it is necessary to generate new functional hair cells either from endogenous cells or from exogenously transplanted hair cells/progenitors. Previous studies suggest that cochlear greater epithelial ridge (GER) and lesser epithelial ridge (LER) cells are capable of differentiating into hair cells. While it was recently possible to obtain and culture pure LER progenitors, isolation of pure GER progenitors has not been reported. Here we describe a method that allows isolation of pure GER cells from neonatal rat cochleae. The cochlear epithelial sheet (CES) containing GER progenitor cells was mechanically separated from the underlying mesenchymal tissue after digestion with thermolysin. The GER area could then be dissected following mechanical removal of organ of Corti as well as all the lateral area. The isolated GER cells showed significant proliferation and expressed markers for GERcells but not markers for hair cells or LER. When the GER cells were cultured in serum-free medium containing epidermal growth factor, spheres were formed where they continued to proliferate. Furthermore, when GER cells were induced to express Hath1 or co-cultured with mesenchymal cells prepared from neonate rat cochleae, they showed the potential to differentiate into hair cell-like cells. Successful isolation, culture and differentiation of GER hair cell progenitors will shed additional light on the mechanism of hair cell differentiation and potential hair cell replacement.
机译:哺乳动物的耳蜗毛细胞丧失是不可逆的,并导致永久性听力丧失。为了恢复生理听觉,有必要从内源性细胞或从外源移植的毛细胞/祖细胞产生新的功能性毛细胞。先前的研究表明,耳蜗较大的上皮(GER)和较小的上皮(LER)细胞能够分化为毛细胞。尽管最近有可能获得和培养纯LER祖细胞,但尚未报道纯GER祖细胞的分离。在这里,我们描述了一种允许从新生大鼠耳蜗中分离纯GER细胞的方法。用嗜热菌蛋白酶消化后,将含有GER祖细胞的耳蜗上皮薄片(CES)与下面的间充质组织机械分离。机械切除Corti器官以及所有侧面区域后,即可解剖GER区域。分离的GER细胞显示出显着的增殖,并表达了GER细胞的标志物,但没有表达毛细胞或LER的标志物。当GER细胞在含有表皮生长因子的无血清培养基中培养时,会形成球体并继续增殖。此外,当GER细胞被诱导表达Hath1或与新生大鼠耳蜗制备的间充质细胞共培养时,它们显示出分化为毛细胞样细胞的潜力。 GER毛细胞祖细胞的成功分离,培养和分化将进一步阐明毛细胞分化的机制和潜在的毛细胞置换。

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