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Publication : Wip1-dependent regulation of autophagy, obesity, and atherosclerosis.

First Author  Le Guezennec X Year  2012
Journal  Cell Metab Volume  16
Issue  1 Pages  68-80
PubMed ID  22768840 Mgi Jnum  J:187401
Mgi Id  MGI:5436360 Doi  10.1016/j.cmet.2012.06.003
Citation  Le Guezennec X, et al. (2012) Wip1-dependent regulation of autophagy, obesity, and atherosclerosis. Cell Metab 16(1):68-80
abstractText  Obesity and atherosclerosis-related diseases account for over one-third of deaths in the western world. Controlling these conditions remains a major challenge due to an incomplete understanding of the molecular pathways involved. Here, we show that Wip1 phosphatase, a known negative regulator of Atm-dependent signaling, plays a major role in controlling fat accumulation and atherosclerosis in mice; specifically, Wip1 deficiency prevents both conditions. In the course of atherosclerosis, deletion of Wip1 results in suppression of macrophage conversion into foam cells, thus preventing the formation of atherosclerotic plaques. This process appears to be independent of p53 but rely on a noncanonical Atm-mTOR signaling pathway and on selective autophagy in regulation of cholesterol efflux. We propose that the Wip1-dependent control of autophagy and cholesterol efflux may provide avenues for treating obesity and atherosclerosis.
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