Suppr超能文献

未折叠蛋白反应的细胞内信号传导。

Intracellular signaling by the unfolded protein response.

作者信息

Bernales Sebastián, Papa Feroz R, Walter Peter

机构信息

Howard Hughes Medical Institute, Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143, USA.

出版信息

Annu Rev Cell Dev Biol. 2006;22:487-508. doi: 10.1146/annurev.cellbio.21.122303.120200.

Abstract

The unfolded protein response (UPR) is an intracellular signaling pathway that is activated by the accumulation of unfolded proteins in the endoplasmic reticulum (ER). UPR activation triggers an extensive transcriptional response, which adjusts the ER protein folding capacity according to need. As such, the UPR constitutes a paradigm of an intracellular control mechanism that adjusts organelle abundance in response to environmental or developmental clues. The pathway involves activation of ER unfolded protein sensors that operate in parallel circuitries to transmit information across the ER membrane, activating a set of downstream transcription factors by mechanisms that are unusual yet rudimentarily conserved in all eukaryotes. Recent results shed light on the mechanisms by which unfolded proteins are sensed in the ER and by which the unfolded protein signals are relayed and integrated to reestablish homeostasis in the cell's protein folding capacity or-if this cannot be achieved-commit cells to apoptosis.

摘要

未折叠蛋白反应(UPR)是一种细胞内信号通路,由内质网(ER)中未折叠蛋白的积累激活。UPR激活引发广泛的转录反应,根据需要调节内质网蛋白折叠能力。因此,UPR构成了一种细胞内控制机制的范例,该机制根据环境或发育线索调节细胞器丰度。该通路涉及内质网未折叠蛋白传感器的激活,这些传感器以并行电路运作,通过在所有真核生物中虽不寻常但基本保守的机制跨内质网膜传递信息,激活一组下游转录因子。最近的研究结果揭示了内质网中未折叠蛋白的感知机制,以及未折叠蛋白信号如何被传递和整合,以重建细胞蛋白质折叠能力的稳态,或者——如果无法实现这一点——促使细胞凋亡。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验