| Literature DB >> 33440163 |
Ji Pang1, Liang Le2, Yi Zhou3, Renjun Tu2, Qiang Hou4, Dai Tsuchiya2, Nancy Thomas2, Yongfu Wang2, Zulin Yu2, Richard Alexander2, Marina Thexton2, Brandy Lewis2, Timothy Corbin2, Michael Durnin2, Hua Li2, Ruth Ashery-Padan5, Deyue Yan6, Ting Xie7.
Abstract
Anterior segment dysgenesis is often associated with cornea diseases, cataracts, and glaucoma. In the anterior segment, the ciliary body (CB) containing inner and outer ciliary epithelia (ICE and OCE) secretes aqueous humor that maintains intraocular pressure (IOP). However, CB development and function remain poorly understood. Here, this study shows that NOTCH signaling in the CB maintains the vitreous, IOP, and eye structures by regulating CB morphogenesis, aqueous humor secretion, and vitreous protein expression. Notch2 and Notch3 function via RBPJ in the CB to control ICE-OCE adhesion, CB morphogenesis, aqueous humor secretion, and protein expression, thus maintaining IOP and eye structures. Mechanistically, NOTCH signaling transcriptionally controls Nectin1 expression in the OCE to promote cell adhesion for driving CB morphogenesis and to directly stabilize Cx43 for controlling aqueous humor secretion. Finally, NOTCH signaling directly controls vitreous protein secretion in the ICE. Therefore, this study provides important insight into CB functions and involvement in eye diseases.Entities:
Keywords: Cx43; IOP; NOTCH signaling; Nectin1; anterior segment; aqueous humor; ciliary body; eye degeneration; morphogenesis; secretion; viteous
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Year: 2021 PMID: 33440163 PMCID: PMC8422303 DOI: 10.1016/j.celrep.2020.108603
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423