Scientific reports · 2017
Isoform-selective Hsp90 inhibition rescues model of hereditary open-angle glaucoma.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Stothert Andrew R, Suntharalingam Amirthaa, Tang Xiaolan, Crowley Vincent M, Mishra Sanket J, Webster Jack M, Nordhues Bryce A, Huard Dustin J E, Passaglia Christopher L, Lieberman Raquel L, Blagg Brian S J, Blair Laura J, Koren John, Dickey Chad A
Аннотация
The heat shock protein 90 (Hsp90) family of molecular chaperones regulates protein homeostasis, folding, and degradation. The ER-resident Hsp90 isoform, glucose-regulated protein 94 (Grp94), promotes the aggregation of mutant forms of myocilin, a protein associated with primary open-angle glaucoma. While inhibition of Grp94 promotes the degradation of mutant myocilin in vitro, to date no Grp94-selective inhibitors have been investigated in vivo. Here, a Grp94-selective inhibitor facilitated mutant myocilin degradation and rescued phenotypes in a transgenic mouse model of hereditary primary open-angle glaucoma. Ocular toxicities previously associated with pan-Hsp90 inhibitors were not evident with our Grp94-selective inhibitor, 4-Br-BnIm. Our study suggests that selective inhibition of a distinct Hsp90 family member holds translational promise for ocular and other diseases associated with cell stress and protein misfolding.