The Changes of P-glycoprotein Activity by Interferon-gamma and Tumor Necrosis Factor-alpha in Primary and Immortalized Human Brain Microvascular Endothelial Cells
DC Field | Value | Language |
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dc.contributor.author | Lee, Na-Young | - |
dc.contributor.author | Rieckmann, Peter | - |
dc.contributor.author | Kang, Young-Sook | - |
dc.date.available | 2021-02-22T12:46:22Z | - |
dc.date.issued | 2012-05 | - |
dc.identifier.issn | 1976-9148 | - |
dc.identifier.issn | 2005-4483 | - |
dc.identifier.uri | https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11900 | - |
dc.description.abstract | The purpose of this study was to investigate the modification of expression and functionality of the drug transporter P-glycoprotein (P-gp) by tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) at the blood-brain barrier (BBB). We used immortalized human brain microvessel endothelial cells (iHBMEC) and primary human brain microvessel endothelial cells (pHBMEC) as in vitro BBB model. To investigate the change of p-gp expression, we carried out real time PCR analysis and Western blotting. To test the change of p-gp activity, we performed rhodamin123 (Rh123) accumulation study in the cells. In results of real time PCR analysis, the P-gp mRNA expression was increased by TNF-alpha or IFN-gamma treatment for 24 hr in both cell types. However, 48 hr treatment of TNF-alpha or IFN-gamma did not affect P-gp mRNA expression. In addition, co-treatment of TNF-alpha and IFN-gamma markedly increased the P-gp mRNA expression in both cells. TNF-alpha or IFN-gamma did not influence P-gp protein expression whatever the concentration of cytokines or duration of treatment in both cells. However, P-gp expression was increased after treatments of both cytokines together in iHBMEC cells only compared with untreated control. Furthermore, in both cell lines, TNF-alpha or IFN-gamma induced significant decrease of P-gp activity for 24 hr treatment. And, both cytokines combination treatment also decreased significantly P-gp activity. These results suggest that P-gp expression and function at the BBB is modulated by TNF-alpha or/and IFN-gamma. Therefore, the distribution of P-gp depending drugs in the central nervous system can be modulated by neurological inflammatory diseases. | - |
dc.format.extent | 6 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | KOREAN SOC APPLIED PHARMACOLOGY | - |
dc.title | The Changes of P-glycoprotein Activity by Interferon-gamma and Tumor Necrosis Factor-alpha in Primary and Immortalized Human Brain Microvascular Endothelial Cells | - |
dc.type | Article | - |
dc.publisher.location | 대한민국 | - |
dc.identifier.doi | 10.4062/biomolther.2012.20.3.293 | - |
dc.identifier.scopusid | 2-s2.0-84862666365 | - |
dc.identifier.wosid | 000305847500007 | - |
dc.identifier.bibliographicCitation | BIOMOLECULES & THERAPEUTICS, v.20, no.3, pp 293 - 298 | - |
dc.citation.title | BIOMOLECULES & THERAPEUTICS | - |
dc.citation.volume | 20 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 293 | - |
dc.citation.endPage | 298 | - |
dc.type.docType | Article | - |
dc.identifier.kciid | ART001663773 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.subject.keywordPlus | KAPPA-B | - |
dc.subject.keywordPlus | BARRIER | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | TRANSPORT | - |
dc.subject.keywordPlus | ADHESION | - |
dc.subject.keywordPlus | DRUGS | - |
dc.subject.keywordPlus | MODULATION | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordPlus | CYTOKINES | - |
dc.subject.keywordPlus | LINE | - |
dc.subject.keywordAuthor | TNF-alpha | - |
dc.subject.keywordAuthor | IFN-gamma | - |
dc.subject.keywordAuthor | P-glycoprotein | - |
dc.subject.keywordAuthor | Human brain microvascular endothelial cell | - |
dc.subject.keywordAuthor | Blood-brain barrier | - |
dc.subject.keywordAuthor | Efflux transport | - |
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