| Literature DB >> 30100066 |
Myoung Sup Shim1, Keun-Young Kim2, Mark Noh1, Ji Yoon Ko1, Sangphil Ahn1, Michelle A An1, Takeshi Iwata3, Guy A Perkins2, Robert N Weinreb1, Won-Kyu Ju4.
Abstract
Optineurin (OPTN) mutations are linked to glaucoma pathology and E50K mutation shows massive cell death in photoreceptor cells and retinal ganglion cells. However, little is known about E50K-mediated mitochondrial dysfunction in photoreceptor cell degeneration. We here show that overexpression of E50K expression triggered BDNF deficiency, leading to Bax activation in RGC-5 cells. BDNF deficiency induced mitochondrial dysfunction by decreasing mitochondrial maximal respiration and reducing intracellular ATP level in RGC-5 cells. However, BDNF deficiency did not alter mitochondrial dynamics. Also, BDNF deficiency resulted in LC3-mediated mitophagosome formation in RGC-5 cells. These results strongly suggest that E50K-mediated BDNF deficiency plays a critical role in compromised mitochondrial function in glaucomatous photoreceptor cell degeneration.Entities:
Keywords: BDNF; E50K mutation; Glaucoma; Mitochondrial dysfunction; Optineurin; RGC-5 cell
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Year: 2018 PMID: 30100066 PMCID: PMC6133749 DOI: 10.1016/j.bbrc.2018.08.025
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575