Histone H4 is cleaved by granzyme A during staurosporine-induced cell death in B-lymphoid Raji cells
DC Field | Value | Language |
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dc.contributor.author | Lee, Phil Young | - |
dc.contributor.author | Park, Byoung Chul | - |
dc.contributor.author | Chi, Seung Wook | - |
dc.contributor.author | Bae, Kwang-Hee | - |
dc.contributor.author | Kim, Sunhong | - |
dc.contributor.author | Cho, Sayeon | - |
dc.contributor.author | Kang, Seongman | - |
dc.contributor.author | Kim, Jeong-Hoon | - |
dc.contributor.author | Park, Sung Goo | - |
dc.date.accessioned | 2021-09-03T18:03:13Z | - |
dc.date.available | 2021-09-03T18:03:13Z | - |
dc.date.created | 2021-06-16 | - |
dc.date.issued | 2016-10-31 | - |
dc.identifier.issn | 1976-6696 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/87134 | - |
dc.description.abstract | Granzyme A (GzmA) was first identified as a cytotoxic T lymphocyte protease protein with limited tissue expression. A number of cellular proteins are known to be cleaved by GzmA, and its function is to induce apoptosis. Histones H1, H2B, and H3 were identified as GzmA substrates during apoptotic cell death. Here, we demonstrated that histone H4 was cleaved by GzmA during staurosporine-induced cell death; however, in the presence of caspase inhibitors, staurosporine-treated Raji cells underwent necroptosis instead of apoptosis. Furthermore, histone H4 cleavage was blocked by the GzmA inhibitor nafamostat mesylate and by GzmA knockdown using siRNA. These results suggest that histone H4 is a novel substrate for GzmA in staurosporine-induced cells. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY | - |
dc.subject | CASPASE INHIBITORS | - |
dc.subject | APOPTOSIS | - |
dc.subject | NUCLEOSOME | - |
dc.subject | TARGET | - |
dc.title | Histone H4 is cleaved by granzyme A during staurosporine-induced cell death in B-lymphoid Raji cells | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kang, Seongman | - |
dc.identifier.doi | 10.5483/BMBRep.2016.49.10.105 | - |
dc.identifier.scopusid | 2-s2.0-84996563626 | - |
dc.identifier.wosid | 000386570900007 | - |
dc.identifier.bibliographicCitation | BMB REPORTS, v.49, no.10, pp.560 - 565 | - |
dc.relation.isPartOf | BMB REPORTS | - |
dc.citation.title | BMB REPORTS | - |
dc.citation.volume | 49 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 560 | - |
dc.citation.endPage | 565 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.identifier.kciid | ART002159391 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.subject.keywordPlus | CASPASE INHIBITORS | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | NUCLEOSOME | - |
dc.subject.keywordPlus | TARGET | - |
dc.subject.keywordAuthor | Caspase-independent cell death | - |
dc.subject.keywordAuthor | Granzyme A | - |
dc.subject.keywordAuthor | Histone H4 | - |
dc.subject.keywordAuthor | Raji cell | - |
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