Mechanosensitive TRPV4 Channel is Involved in Fibrotic Transdifferentiation of Retinal Pigment Epithelial Cells
Abstract
Sustained presence of myofibroblasts during wound healing can cause fibrosis. Within the eye, transdifferentiation of retinal pigment epithelial (RPE) cells to myofibroblasts have been implicated as a key event leading to fibrotic scarring of the retina. While TGF‐beta signaling has been shown to play key roles in this process, inhibition of this pathway can result in undesirable side‐effects by preventing physiological function of this multifaceted cytokine. Therefore, identification of other pathways/molecules that could potentially be targeted to prevent fibrotic scarring is warranted. In this study, roles of mechanosensitive channel TRPV4, which has been implicated to play roles in several fibrotic diseases, and its downstream effector MLCK in myofibroblast transdifferentiation of RPE cells as well as matrix contraction, a key phenomenon of retinal scarring, were examined.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Apr 01, 2018
- Source ID
- 10.1096/fasebj.2018.32.1_supplement.414.9
Entities
People
- Kevin McDonald
- Shigeo Tamiya
- Shunichiro Ueda
Organizations
- United States Department of Defense
- University of Louisville