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Merck

Diurnal Rhythms Spatially and Temporally Organize Autophagy.

Cell reports (2019-02-14)
Mikhail Ryzhikov, Anna Ehlers, Deborah Steinberg, Wenfang Xie, Eitan Oberlander, Samuel Brown, Petra E Gilmore, Reid R Townsend, William S Lane, Tamas Dolinay, Kiichi Nakahira, Augustine M K Choi, Jeffrey A Haspel
摘要

Circadian rhythms are a hallmark of physiology, but how such daily rhythms organize cellular catabolism is poorly understood. Here, we used proteomics to map daily oscillations in autophagic flux in mouse liver and related these rhythms to proteasome activity. We also explored how systemic inflammation affects the temporal structure of autophagy. Our data identified a globally harmonized rhythm for basal macroautophagy, chaperone-mediated autophagy, and proteasomal activity, which concentrates liver proteolysis during the daytime. Basal autophagy rhythms could be resolved into two antiphase clusters that were distinguished by the subcellular location of targeted proteins. Inflammation induced by lipopolysaccharide reprogrammed autophagic flux away from a temporal pattern that favors cytosolic targets and toward the turnover of mitochondrial targets. Our data detail how daily biological rhythms connect the temporal, spatial, and metabolic aspects of protein catabolism.

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亮肽素, microbial, ≥90% (HPLC)
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氯喹 二磷酸盐, powder or crystals, 98.5-101.0% (EP)
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SIGMAFAST蛋白酶抑制剂片剂, For General Use
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Z-Leu-Leu-Leu-al, ≥90% (HPLC)
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抗p62/SQSTM1 兔抗, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution