Calpain-mediated proteolysis of polycystin-1 C-terminus induces JAK2 and ERK signal alterations
DC Field | Value | Language |
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dc.contributor.author | Kim, Hyunho | - |
dc.contributor.author | Kang, Ah-Young | - |
dc.contributor.author | Ko, Ah-ra | - |
dc.contributor.author | Park, Hayne Cho | - |
dc.contributor.author | So, Insuk | - |
dc.contributor.author | Park, Jong Hoon | - |
dc.contributor.author | Cheong, Hae Il | - |
dc.contributor.author | Hwang, Young-Hwan | - |
dc.contributor.author | Ahn, Curie | - |
dc.date.available | 2021-02-22T12:01:39Z | - |
dc.date.issued | 2014-01 | - |
dc.identifier.issn | 0014-4827 | - |
dc.identifier.issn | 1090-2422 | - |
dc.identifier.uri | https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11020 | - |
dc.description.abstract | Autosomal dominant polycystic kidney disease (ADPKD), a hereditary renal disease caused by mutations in PKD1 (85%) or PKD2 (15%), is characterized by the development of gradually enlarging multiple renal cysts and progressive renal failure. Polycystin-1 (PC1), PKD1 gene product, is an integral membrane glycoprotein which regulates a number of different biological processes including cell proliferation, apoptosis, cell polarity, and tubulogenesis. PC1 is a target of various proteolytic cleavages and proteosomal degradations, but its role in intracellular signaling pathways remains poorly understood. Herein, we demonstrated that PC1 is a novel substrate for mu- and m-calpains, which are calcium-dependent cysteine proteases. Overexpression of PC1 altered both Janus-activated kinase 2 (JAK2) and extracellular signal-regulated kinase (ERK) signals, which were independently regulated by calpain-mediated PC1 degradation. They suggest that the PC1 function on JAK2 and ERK signaling pathways might be regulated by calpains in response to the changes in intracellular calcium concentration. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved. | - |
dc.format.extent | 7 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER INC | - |
dc.title | Calpain-mediated proteolysis of polycystin-1 C-terminus induces JAK2 and ERK signal alterations | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1016/j.yexcr.2013.10.012 | - |
dc.identifier.scopusid | 2-s2.0-84888198672 | - |
dc.identifier.wosid | 000327911900007 | - |
dc.identifier.bibliographicCitation | EXPERIMENTAL CELL RESEARCH, v.320, no.1, pp 62 - 68 | - |
dc.citation.title | EXPERIMENTAL CELL RESEARCH | - |
dc.citation.volume | 320 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 62 | - |
dc.citation.endPage | 68 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Oncology | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalWebOfScienceCategory | Oncology | - |
dc.relation.journalWebOfScienceCategory | Cell Biology | - |
dc.subject.keywordPlus | KIDNEY-DISEASE | - |
dc.subject.keywordPlus | AUTOSOMAL-DOMINANT | - |
dc.subject.keywordPlus | PATHWAY | - |
dc.subject.keywordPlus | PKD1 | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordPlus | GENE | - |
dc.subject.keywordPlus | PHOSPHORYLATION | - |
dc.subject.keywordPlus | INHIBITION | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordPlus | MECHANISMS | - |
dc.subject.keywordAuthor | Polycystic kidney disease | - |
dc.subject.keywordAuthor | Polycystin-1 | - |
dc.subject.keywordAuthor | Calpain | - |
dc.subject.keywordAuthor | PEST | - |
dc.subject.keywordAuthor | Calcium homeostasis | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0014482713004527?via%3Dihub | - |
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