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Prdx1 (peroxiredoxin 1) deficiency reduces cholesterol efflux via impaired macrophage lipophagic flux

Title
Prdx1 (peroxiredoxin 1) deficiency reduces cholesterol efflux via impaired macrophage lipophagic flux
Authors
Jeong, Se-JinKim, SinaiPark, Jong-GilJung, In-hyukLee, Mi-NiJeon, SejinKweon, Hyae YonYu, Dae-YeulLee, Sang-HakJang, YangsooKang, Sang WonHan, Ki-HwanMiller, Yury I.Park, Young MiCheong, CheolhoChoi, Jae-HoonOh, Goo Taeg
Ewha Authors
오구택한기환박영미이미니
SCOPUS Author ID
오구택scopus; 한기환scopus; 박영미scopus; 이미니scopusscopus
Issue Date
2018
Journal Title
AUTOPHAGY
ISSN
1554-8627JCR Link1554-8635JCR Link
Citation
vol. 14, no. 1, pp. 120 - 133
Keywords
atherosclerosislipophagymacrophageoxidative stressperoxiredoxin 1
Publisher
TAYLOR & FRANCIS INC
Indexed
SCIE; SCOPUS WOS scopus
Abstract
Oxidative stress activates macroautophagy/autophagy and contributes to atherogenesis via lipophagic flux, a form of lipid removal by autophagy. However, it is not known exactly how endogenous antioxidant enzymes are involved in lipophagic flux. Here, we demonstrate that the antioxidant PRDX1 (peroxiredoxin 1) has a crucial role in the maintenance of lipophagic flux in macrophages. PRDX1 is more highly expressed than other antioxidant enzymes in monocytes and macrophages. We determined that Prdx1 deficiency induced excessive oxidative stress and impaired maintenance of autophagic flux in macrophages. Prdx1-deficient macrophages had higher intracellular cholesterol mass and lower cholesterol efflux compared with wild type. This perturbation in cholesterol homeostasis was due to impaired lipophagic cholesterol hydrolysis caused by excessive oxidative stress, resulting in the inhibition of free cholesterol formation and the reduction of NR1H3 (nuclear receptor subfamily 1, group H, member 3) activity. Notably, impairment of both lipophagic flux and cholesterol efflux was restored by the 2-Cys PRDX-mimics ebselen and gliotoxin. Consistent with this observation, apoe (-/-) mice transplanted with bone marrow from prdx1(-/-)apoe(-/-) mice had increased plaque formation compared with apoe(-/-) BM-transplanted recipients. This study reveals that PRDX1 is crucial to regulating lipophagic flux and maintaining macrophage cholesterol homeostasis against oxidative stress. We suggest that PRDX1-dependent control of oxidative stress may provide a strategy for treating atherosclerosis and autophagy-related human diseases.
DOI
10.1080/15548627.2017.1327942
Appears in Collections:
자연과학대학 > 생명과학전공 > Journal papers
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