Baird R A, Burton M D, Lysakowski A, Fashena D S, Naeger R A
Fay and Carl Simons Center for Biology of Hearing and Deafness, Central Institute for the Deaf, 4560 Clayton Road, St. Louis, MO 63110, USA.
Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11722-9. doi: 10.1073/pnas.97.22.11722.
Hair cells in many nonmammalian vertebrates are regenerated by the mitotic division of supporting cell progenitors and the differentiation of the resulting progeny into new hair cells and supporting cells. Recent studies have shown that nonmitotic hair cell recovery after aminoglycoside-induced damage can also occur in the vestibular organs. Using hair cell and supporting cell immunocytochemical markers, we have used confocal and electron microscopy to examine the fate of damaged hair cells and the origin of immature hair cells after gentamicin treatment in mitotically blocked cultures of the bullfrog saccule. Extruding and fragmenting hair cells, which undergo apoptotic cell death, are replaced by scar formations. After losing their bundles, sublethally damaged hair cells remain in the sensory epithelium for prolonged periods, acquiring supporting cell-like morphology and immunoreactivity. These modes of damage appear to be mutually exclusive, implying that sublethally damaged hair cells repair their bundles. Transitional cells, coexpressing hair cell and supporting cell markers, are seen near scar formations created by the expansion of neighboring supporting cells. Most of these cells have morphology and immunoreactivity similar to that of sublethally damaged hair cells. Ultrastructural analysis also reveals that most immature hair cells had autophagic vacuoles, implying that they originated from damaged hair cells rather than supporting cells. Some transitional cells are supporting cells participating in scar formations. Supporting cells also decrease in number during hair cell recovery, supporting the conclusion that some supporting cells undergo phenotypic conversion into hair cells without an intervening mitotic event.
许多非哺乳类脊椎动物的毛细胞可通过支持细胞祖细胞的有丝分裂以及由此产生的子代细胞分化为新的毛细胞和支持细胞来实现再生。最近的研究表明,氨基糖苷类药物诱导损伤后非有丝分裂的毛细胞恢复也可发生在前庭器官中。利用毛细胞和支持细胞免疫细胞化学标记物,我们通过共聚焦显微镜和电子显微镜,研究了牛蛙球囊有丝分裂阻断培养物经庆大霉素处理后受损毛细胞的命运以及未成熟毛细胞的起源。经历凋亡性细胞死亡的挤压和碎片化毛细胞会被瘢痕组织替代。亚致死性损伤的毛细胞在失去其纤毛束后,会在感觉上皮中长期留存,获得类似支持细胞的形态和免疫反应性。这些损伤模式似乎相互排斥,这意味着亚致死性损伤的毛细胞会修复其纤毛束。在由邻近支持细胞扩张形成的瘢痕组织附近可见同时表达毛细胞和支持细胞标记物的过渡细胞。这些细胞中的大多数具有与亚致死性损伤毛细胞相似的形态和免疫反应性。超微结构分析还显示,大多数未成熟毛细胞具有自噬空泡,这意味着它们起源于受损毛细胞而非支持细胞。一些过渡细胞是参与瘢痕形成的支持细胞。在毛细胞恢复过程中支持细胞数量也会减少,这支持了一些支持细胞在没有中间有丝分裂事件的情况下发生表型转化为毛细胞的结论。