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由类暗蛋白维持的顶端细胞扩张为角膜晶状体形态发生建立了一个支架。

Apical cell expansion maintained by Dusky-like establishes a scaffold for corneal lens morphogenesis.

作者信息

Ghosh Neha, Treisman Jessica E

出版信息

bioRxiv. 2024 Jan 19:2024.01.17.575959. doi: 10.1101/2024.01.17.575959.

Abstract

The biconvex shape of the corneal lens, which enables it to focus light onto the retina, arises by organized assembly of chitin and other apical extracellular matrix components. We show here that the Zona Pellucida domain-containing protein Dusky-like is essential for normal corneal lens morphogenesis. Dusky-like transiently localizes to the expanded apical surfaces of the corneal lens-secreting cells, and in its absence, these cells undergo apical constriction and apicobasal contraction. Dusky-like also controls the arrangement of two other Zona Pellucida-domain proteins, Dumpy and Piopio, external to the developing corneal lens. Loss of either or delays chitin accumulation and disrupts the outer surface of the corneal lens. Artificially inducing apical constriction with constitutively active Myosin light chain kinase is sufficient to similarly alter chitin deposition and corneal lens morphology. These results demonstrate the importance of cell shape for the morphogenesis of overlying apical extracellular matrix structures.

摘要

角膜晶状体的双凸形状使其能够将光线聚焦到视网膜上,它是由几丁质和其他顶端细胞外基质成分有序组装而成的。我们在此表明,含透明带结构域蛋白类灰暗蛋白对于正常角膜晶状体形态发生至关重要。类灰暗蛋白短暂定位于角膜晶状体分泌细胞扩大的顶端表面,在其缺失时,这些细胞会发生顶端收缩和顶-基收缩。类灰暗蛋白还控制发育中的角膜晶状体外部另外两种透明带结构域蛋白,矮胖蛋白和皮皮奥蛋白的排列。缺失其中任何一种都会延迟几丁质积累并破坏角膜晶状体的外表面。用组成型活性肌球蛋白轻链激酶人工诱导顶端收缩足以类似地改变几丁质沉积和角膜晶状体形态。这些结果证明了细胞形状对于覆盖其上的顶端细胞外基质结构形态发生的重要性。

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