AI Article Synopsis

  • - The Schlemm's canal (SC) is a vessel in the eye that helps regulate fluid drainage, impacting intraocular pressure; shear stress from fluid flow affects how SC cells behave.
  • - Researchers discovered that shear stress activates autophagy in SC cells through the primary cilium (PC), with an important role played by phosphorylated SMAD2, which also activates certain signaling pathways.
  • - Interestingly, while autophagy is usually inhibited by the mTOR pathway, shear stress activates mTOR in SC cells, indicating a complex relationship between the PI3K and SMAD2/3 pathways in regulating autophagy in response to fluid flow.

Article 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 , and 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448710PMC
http://dx.doi.org/10.1080/27694127.2023.2236519DOI Listing

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