Statins Inhibit the Gliosis of MIO-M1, a Müller Glial Cell Line Induced by TRPV4 Activation

• Published in: International journal of molecular sciences Vol. 23; no. 9; p. 5190
• Main Authors: Jo, Youn Hye, Choi, Go Woon, Kim, Mi-Lyang, Sung, Kyung Rim
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 06-05-2022; MDPI
• Subjects: Apoptosis; Cell activation; Cholesterol; Diabetic retinopathy; Enzyme-linked immunosorbent assay; Enzymes; Ependymoglial Cells - metabolism; Evaluation; Glaucoma; Glaucoma - metabolism; Glial cells; Glial fibrillary acidic protein; Gliosis; Gliosis - metabolism; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology; Mueller cells; Müller gliosis; Nestin; Nestin - metabolism; NF-KappaB Inhibitor alpha - metabolism; NF-κB pathway; NF-κB protein; Nuclear transport; Optic nerve; Phosphorylation; Proteins; Retinal ganglion cells; statin; Statins; TNF-α; Transcription factors; Transient receptor potential proteins; TRPV Cation Channels - metabolism; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-TNF; Tumor necrosis factor-α; Vimentin; Vimentin - metabolism; Western blotting; Müller gliosis; TNF-α; statin; glaucoma; NF-κB pathway
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23095190

We characterized Müller cell gliosis induced by the activation of transient receptor potential vanilloid-type 4 (TRPV4) and assessed whether statins could modulate the gliosis. The human Müller cell line, MIO-M1, was used to analyze the gliosis caused by glaucomatous stimulation. To induce Müller gliosis in MIO-M1 cells, GSK101 was used to activate TRPV4, and Müller gliosis was evaluated by analyzing vimentin, nestin, and glial fibrillary acidic protein (GFAP) expression. The expression level of TNF-α was determined by ELISA. To evaluate the GSK101 activation of the NF-κB pathway, p65 phosphorylation was measured by Western blotting, and the nuclear translocation of p65 and IκBα phosphorylation were assessed by immunostaining. To assess the effect of statins on MIO-M1 gliosis, cells were pretreated for 24 h with statins before GSK101 treatment. Vimentin, nestin, and GFAP expression were upregulated by GSK101, while statins effectively inhibited them. The expression of TNF-α was increased by GSK101. The phosphorylation and nuclear translocation of p65 and IκBα phosphorylation, which occurs prior to p65 activation, were induced. Statins suppressed the GSK101-mediated phosphorylation of IκBα and p65 translocation. Statins can mitigate gliosis in the human Müller cell line. Because TRPV4 activation in Müller cells reflects glaucoma pathophysiology, statins may have the potential to prevent RGC death.