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内耳毛细胞成熟和存活而非命运决定过程中对Brn-3c的需求

Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells.

作者信息

Xiang M, Gao W Q, Hasson T, Shin J J

机构信息

Center for Advanced Biotechnology and Medicine, Department of Pediatrics, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

出版信息

Development. 1998 Oct;125(20):3935-46. doi: 10.1242/dev.125.20.3935.

Abstract

Mutations in the POU domain gene Brn-3c causes hearing impairment in both the human and mouse as a result of inner ear hair cell loss. We show here that during murine embryogenesis, Brn-3c is expressed in postmitotic cells committed to hair cell phenotype but not in mitotic progenitors in the inner ear sensory epithelium. In developing auditory and vestibular sensory epithelia of Brn-3c-/- mice, hair cells are found to be generated and undergo initial differentiation as indicated by their morphology, laminar position and expression of hair cell markers, including myosins VI and VIIa, calretinin and parvalbumin. However, a small number of hair cells are anomalously retained in the supporting cell layer in the vestibular sensory epithelia. Furthermore, the initially differentiated hair cells fail to form stereociliary bundles and degenerate by apoptosis in the Brn-3c-/- mice. These data indicate a crucial role for Brn-3c in maturation, survival and migration of hair cells, but not in proliferation or commitment of hair cell progenitors.

摘要

POU结构域基因Brn-3c的突变会导致人和小鼠因内耳毛细胞丢失而出现听力障碍。我们在此表明,在小鼠胚胎发育过程中,Brn-3c在已确定为毛细胞表型的有丝分裂后细胞中表达,但在内耳感觉上皮的有丝分裂祖细胞中不表达。在Brn-3c基因敲除小鼠发育中的听觉和前庭感觉上皮中,发现毛细胞能够生成并经历初始分化,这可通过它们的形态、层状位置以及毛细胞标志物(包括肌球蛋白VI和VIIa、钙视网膜蛋白和小白蛋白)的表达来表明。然而,少数毛细胞异常地保留在前庭感觉上皮的支持细胞层中。此外,在Brn-3c基因敲除小鼠中,最初分化的毛细胞无法形成静纤毛束,并通过凋亡而退化。这些数据表明Brn-3c在毛细胞的成熟、存活和迁移中起关键作用,但在毛细胞祖细胞的增殖或分化中不起作用。

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