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Selective autophagy bears bone
DOI:10.15252/embj.2020105965.png)
摘要
En 中文
The endoplasmic reticulum (ER) is a dynamic intracellular network responsible for folding and maturation of organellar and secreted proteins. Selective autophagy of ER (ER-phagy) is emerging as an essential process that maintains proteostasis in the ER and is regulated by growth conditions. In this issue, Cinque et al (2020) show that fibroblast growth factor 18 (FGF18) specifically activates ER-phagy through a TFEB/TFE-dependent transcriptional regulation of the ER-phagy receptor Fam134b, a process essential for bone ossification and skeletal development.
Keyword:
ER-PHAGY
GROWTH
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期刊
IF:
8.3
论文数:
1.3W
被引数:
6.3W
机构
引用论文
ER-Phagy: Quality Control and Turnover of Endoplasmic ReticulumER-吞噬: 内质网的质量控制和周转
TRENDS IN CELL BIOLOGY
IF18.1
MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134BMiT/TFE因子通过FAM134B的转录调控来控制吞噬
EMBO JOURNAL
IF8.3
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