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Title: Cytochrome P450-2C11 mRNA is not expressed in endothelial cells dissected from rat renal arterioles.
Author(s): Heil, S.G. (271432624)
Vriese, A.S. de
Kluijtmans, L.A.J. (168872579)
Dijkman, H.
Strien, D. van
Akkers, R.
Blom, H.J. (073808628)
Publication year: 2005
Document type: Article / Letter to editor
Journal: Nephron Physiology
ISSN: 1660-8151
Volume: vol. 99
Issue: iss. 2
Start page: p. 43
End page: p. 49
Abstract: BACKGROUND: Cytochrome P450 (CYP) isoenzymes (CYP2C and CYP2J) are involved in the production of epoxyeicosatrienoic acids, which are postulated as endothelium-derived hyperpolarizing factors (EDHFs). We hypothesized that if CYP2C11 is involved in the EDHF-mediated responses, its mRNA should be expressed in endothelial cells. We, therefore, examined the mRNA expression of CYP2C11 in endothelial cells of renal arterioles. METHODS: Laser microdissection was applied to isolate endothelial cells from the renal arterioles of 4 male and 4 female Wistar rats. As a positive control of CYP2C11 expression, hepatocytes were also dissected from these rats. RNA was isolated and real-time quantitative polymerase chain reaction (Q-PCR) analysis was applied. RESULTS: Q-PCR analysis showed that CYP2C11 mRNA was not expressed in laser microdissected endothelial cells of renal arterioles of male and female rats. CYP2C11 mRNA expression was highly abundant in hepatocytes dissected from male livers, but in female livers hardly any CYP2C11 mRNA was detected. CONCLUSION: We have shown that endothelial cells can be dissected from small renal arterioles by laser microdissection to study the mRNA expression of specific genes by Q-PCR. Using this novel tool, we demonstrated that the CYP2C11 mRNA was not expressed in the endothelial cells of renal arterioles. Therefore, we speculate that CYP2C11 does not contribute to the EDHF-mediated responses in renal arterioles.
Subject: Molecular Animal Physiology
UMCN 2.2: Vascular medicine and diabetes
UMCN 5.4: Renal disorders
Organization: Paediatrics
UMCN Extern
Ecogenomics
Organization (former): Molecular Animal Physiology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/32376

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