Effects of nitric oxide on apoptosis and voltage-gated calcium channels in human cardiac myofibroblasts
DC Field | Value | Language |
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dc.contributor.author | Bae, Hyemi | - |
dc.contributor.author | Kim, Taeho | - |
dc.contributor.author | Lim, Inja | - |
dc.date.available | 2020-04-03T00:56:13Z | - |
dc.date.issued | 2020-01 | - |
dc.identifier.issn | 0305-1870 | - |
dc.identifier.issn | 1440-1681 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/37879 | - |
dc.description.abstract | We characterised the voltage-gated Ca2+ channels (VGCCs) in human cardiac fibroblasts (HCFs) and myofibroblasts (HCMFs) and investigated the effects of nitric oxide (NO) on apoptosis and on these channels. Western blotting and immunofluorescence analyses show that α-smooth muscle actin (a myofibroblast marker) was markedly expressed in passage (P) 12-15 but not in P4 HCF cells, whereas calponin (a fibroblast marker) was expressed only in P4 cells. CaV1.2 (L-type) and CaV3.3 (T-type) of VGCCs were highly expressed in P12-15 cells, but only weak CaV2.3 (R-type) expression was identified in P4 cells using reverse transcription-polymerase chain reaction analysis. S-Nitroso-N-acetylpenicillamine (SNAP, an NO donor) decreased cell viability of HCMFs in a dose-dependent manner and induced apoptotic changes, and nifedipine (an L-type Ca2+ channel blocker) prevented apoptosis as shown with immunofluorescence staining and flow cytometry. Whole-cell mode patch-clamp recordings demonstrate the presence of L-type Ca2+ (IC a,L) and T-type Ca2+ (IC a,T) currents in HCMFs. SNAP inhibited IC a,L of HCMFs, but pre-treatment with ODQ (a guanylate cyclase inhibitor) or KT5823 (a PKG inhibitor) prevented it. Pre-treating cells with KT5720 (a PKA inhibitor) or SQ22536 (an adenylate cyclase inhibitor) blocked SNAP-induced inhibition of IC a,L. 8-Bromo-cyclic GMP or 8-bromo-cyclic AMP also inhibited IC a,L. However, pre-treatment with N-ethylmaleimide (a thiol-alkylating reagent) did not block the SNAP effect, nor did DL-dithiothreitol (a reducing agent) reverse it. These data suggest that high concentrations of NO injure HCMFs and inhibit IC a,L through the PKG and PKA signalling pathways but not through the S-nitrosylation pathway. © 2019 John Wiley & Sons Australia, Ltd | - |
dc.format.extent | 11 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Blackwell Publishing | - |
dc.title | Effects of nitric oxide on apoptosis and voltage-gated calcium channels in human cardiac myofibroblasts | - |
dc.type | Article | - |
dc.identifier.doi | 10.1111/1440-1681.13178 | - |
dc.identifier.bibliographicCitation | Clinical and Experimental Pharmacology and Physiology, v.47, no.1, pp 16 - 26 | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000585170800003 | - |
dc.identifier.scopusid | 2-s2.0-85074476275 | - |
dc.citation.endPage | 26 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 16 | - |
dc.citation.title | Clinical and Experimental Pharmacology and Physiology | - |
dc.citation.volume | 47 | - |
dc.type.docType | Article | - |
dc.publisher.location | 미국 | - |
dc.subject.keywordAuthor | apoptosis | - |
dc.subject.keywordAuthor | human cardiac myofibroblasts | - |
dc.subject.keywordAuthor | L-type Ca2+ channels | - |
dc.subject.keywordAuthor | nitric oxide | - |
dc.subject.keywordAuthor | protein kinases | - |
dc.subject.keywordAuthor | S-nitrosylation | - |
dc.subject.keywordPlus | SMOOTH-MUSCLE-CELLS | - |
dc.subject.keywordPlus | S-NITROSYLATION | - |
dc.subject.keywordPlus | CA2+ CURRENT | - |
dc.subject.keywordPlus | CROSS-TALK | - |
dc.subject.keywordPlus | CGMP | - |
dc.subject.keywordPlus | MECHANISM | - |
dc.subject.keywordPlus | DIFFERENTIATION | - |
dc.subject.keywordPlus | CARDIOMYOCYTES | - |
dc.subject.keywordPlus | FIBROBLASTS | - |
dc.subject.keywordPlus | INCREASES | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Physiology | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Physiology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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