| Literature DB >> 28687980 |
Philipp Rohne1, Steven Wolf2,3, Carolin Dörr2, Julia Ringen2, Andrew Holtz2, René Gollan4, Benjamin Renner2, Hans Prochnow2,5, Markus Baiersdörfer2, Claudia Koch-Brandt2.
Abstract
Necrosis is a form of cell death that is detrimental to the affected tissue because the cell ruptures and releases its content (reactive oxygen species among others) into the extracellular space. Clusterin (CLU), a cytoprotective extracellular chaperone has been shown to be upregulated in the face of necrosis. We here show that in addition to CLU upregulation, necrotic cell lysates induce JNK/SAPK signaling, the IRE1α branch of the unfolded protein response (UPR), the MAPK/ERK1/2, and the mTOR signaling pathways and results in an enhanced proliferation of the vital surrounding cells. We name this novel response mechanism: Necrosis-induced Proliferation (NiP).Entities:
Keywords: Clusterin; ERK; IRE1a; Necrosis; UPR; mTOR
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Year: 2017 PMID: 28687980 PMCID: PMC5741583 DOI: 10.1007/s12192-017-0825-6
Source DB: PubMed Journal: Cell Stress Chaperones ISSN: 1355-8145 Impact factor: 3.667