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FAM134B-mediated ER-phagy regulates ER-mitochondria interaction through MAMs

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成果类型:
期刊论文
作者:
Wei Chen;Xueqian Ouyang;Linxi Chen;Lanfang Li
通讯作者:
Chen, L.;Li, L.
作者机构:
[Ouyang X.; Chen L.; Chen W.; Li L.] Institute of Pharmacy and Pharmacology, Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, 421001, China
通讯机构:
[Chen, L.; Li, L.] I
Institute of Pharmacy and Pharmacology, China
语种:
英文
期刊:
生物化学与生物物理学报
ISSN:
1672-9145
年:
2022
卷:
54
期:
3
页码:
412-414
基金类别:
This work was supported by the grants from the National Natural Science Foundation of China (No. 81970431) and the Hunan Provincial Natural Science Foundation of China (No. 2020JJ4079).
机构署名:
本校为第一机构
院系归属:
药学与生物科学学院
摘要:
Endoplasmic reticulum(ER)is the largest organelle in eukaryotic cells, which can participate in the maintenance of calcium(Ca~(2+))homeostasis, protein synthesis and organelle communication[1]. Endoplasmic reticulum autophagy(ER-phagy)is a cellular quality control pathway mediated by autophagy receptors. ER-phagy involves the engulfing of excess or misfolded proteins and superfluous ER membrane to form autophagosomes which are degraded by lysosome[1]. ER-phagy occurs under normal conditions and is enhanced during starvation. At present, the receptors of ER-phagy in mammalian cells include fami...

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