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dc.contributor.author Kapuy, Orsolya
dc.contributor.author Márton, Margita
dc.contributor.author Bánhegyi, Gábor
dc.contributor.author Vinod, PK
dc.date.accessioned 2020-09-18T08:24:29Z
dc.date.available 2020-09-18T08:24:29Z
dc.date.issued 2020
dc.identifier.citation journalVolume=594;journalIssueNumber=6;journalTitle=FEBS LETTERS;pagerange=1112-1123;journalAbbreviatedTitle=FEBS LETTERS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8177
dc.identifier.uri doi:10.1002/1873-3468.13689
dc.description.abstract Scientific results have revealed that autophagy is able to promote cell survival in response to endoplasmic reticulum (ER) stress while drastic events result in apoptotic cell death. Here, we analyse the important crosstalk of life-and-death decisions from a systems biological perspective by studying the regulatory modules of the unfolded protein response (UPR). While a double negative loop between autophagy and apoptosis inducers is crucial for the switch-like characteristic of the stress response mechanism, a positive feedback loop between ER stress sensors is also essential. Corresponding to experimental data, here, we show the dynamical significance of Gadd34-CHOP connections inside the PERK branch of the UPR. The multiple system-level feedback loops seem to be crucial for managing a robust life-and-death decision depending on the level and durability of cellular stress.
dc.relation.ispartof urn:issn:0014-5793
dc.title Multiple system-level feedback loops control life-and-death decisions in endoplasmic reticulum stress
dc.type Journal Article
dc.date.updated 2020-02-03T08:59:46Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 30939096
dc.identifier.wos 000502104500001
dc.identifier.pubmed 31769869
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.department SE/AOK/I/BMBI/MBT/MTA-SE Pathobiokémiai Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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