Shear stress induces autophagy in Schlemm's canal cells via primary cilia-mediated SMAD2/3 signaling pathway.

Autophagy reports Pub Date : 2023-01-01 Epub Date: 2023-07-20 DOI:10.1080/27694127.2023.2236519
Myoung Sup Shim, Angela Dixon, April Nettesheim, Kristin M Perkumas, W Daniel Stamer, Yang Sun, Paloma B Liton
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Abstract

The Schlemm's canal (SC) is a circular, lymphatic-like vessel located at the limbus of the eye that participates in the regulation of aqueous humor drainage to control intraocular pressure (IOP). Circumferential flow of aqueous humor within the SC lumen generates shear stress, which regulates SC cell behaviour. Using biochemical analysis and real-time live cell imaging techniques, we have investigated the activation of autophagy in SC cells by shear stress. We report, for the first time, the primary cilium (PC)-dependent activation of autophagy in SC cells in response to shear stress. Moreover, we identified PC-dependent shear stress-induced autophagy to be positively regulated by phosphorylation of SMAD2 in its linker and C-terminal regions. Additionally, SMAD2/3 signaling was found to transcriptionally activate LC3B, ATG5 and ATG7 in SC cells. Intriguingly, concomitant to SMAD2-dependent activation of autophagy, we also report here the activation of mTOR pathway, a classical autophagy inhibitor, in SC cells by shear stress. mTOR activation was found to also be dependent on the PC. Moreover, pharmacological inhibition of class I PI3K increased phosphorylation of SMAD2 at the linker and activated autophagy. Together, our data indicates an interplay between PI3K and SMAD2/3 signaling pathways in the regulation of PC-dependent shear stress-induced autophagy in SC cells.

剪切应力通过初级纤毛介导的 SMAD2/3 信号通路诱导 Schlemm 管细胞自噬。
施莱姆管(Schlemm's canal,SC)是位于眼球边缘的环形淋巴管,参与调节房水的排出,从而控制眼压(IOP)。房水在 SC 管腔内的环流会产生剪切应力,从而调节 SC 细胞的行为。我们利用生化分析和实时活细胞成像技术,研究了剪切应力对 SC 细胞自噬的激活作用。我们首次报道了原生纤毛(PC)在剪切应力作用下对 SC 细胞自噬的依赖性激活。此外,我们还发现PC依赖的剪切应力诱导的自噬受SMAD2在其连接区和C端区域的磷酸化的正向调节。此外,我们还发现 SMAD2/3 信号可转录激活 SC 细胞中的 LC3B、ATG5 和 ATG7。耐人寻味的是,在SMAD2依赖性激活自噬的同时,我们还报道了剪切应力激活了SC细胞中的mTOR通路(一种经典的自噬抑制剂)。此外,对 I 类 PI3K 的药理抑制增加了 SMAD2 在链接处的磷酸化并激活了自噬。总之,我们的数据表明,PI3K 和 SMAD2/3 信号通路在调节 PC 依赖性剪切应力诱导的 SC 细胞自噬过程中相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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