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Item Type: | Article |
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Title: | Transient receptor potential vanilloid 4 channel deficiency aggravates tubular damage after acute renal ischaemia reperfusion |
Creators Name: | Mannaa, M., Markó, L., Balogh, A., Vigolo, E., N'diaye, G., Kaßmann, M., Michalick, L., Weichelt, U., Schmidt-Ott, K.M., Liedtke, W.B., Huang, Y., Müller, D.N., Kuebler, W.M. and Gollasch, M. |
Abstract: | Transient receptor potential vanilloid 4 (TRPV4) cation channels are functional in all renal vascular segments and mediate endothelium-dependent vasorelaxation. Moreover, they are expressed in distinct parts of the tubular system and activated by cell swelling. Ischaemia/reperfusion injury (IRI) is characterized by tubular injury and endothelial dysfunction. Therefore, we hypothesised a putative organ protective role of TRPV4 in acute renal IRI. IRI was induced in TRPV4 deficient (Trpv4 KO) and wild-type (WT) control mice by clipping the left renal pedicle after right-sided nephrectomy. Serum creatinine level was higher in Trpv4 KO mice 6 and 24 hours after ischaemia compared to WT mice. Detailed histological analysis revealed that IRI caused aggravated renal tubular damage in Trpv4 KO mice, especially in the renal cortex. Immunohistological and functional assessment confirmed TRPV4 expression in proximal tubular cells. Furthermore, the tubular damage could be attributed to enhanced necrosis rather than apoptosis. Surprisingly, the percentage of infiltrating granulocytes and macrophages were comparable in IRI-damaged kidneys of Trpv4 KO and WT mice. The present results suggest a renoprotective role of TRPV4 during acute renal IRI. Further studies using cell-specific TRPV4 deficient mice are needed to clarify cellular mechanisms of TRPV4 in IRI. |
Keywords: | Acute Kidney Injury, Animal Disease Models, Apoptosis, Ischemia, Kidney, Kidney Tubules, Knockout Mice, Reperfusion, Reperfusion Injury, TRPV Cation Channels, Animals, Mice |
Source: | Scientific Reports |
ISSN: | 2045-2322 |
Publisher: | Nature Publishing Group |
Volume: | 8 |
Number: | 1 |
Page Range: | 4878 |
Date: | 20 March 2018 |
Official Publication: | https://doi.org/10.1038/s41598-018-23165-0 |
PubMed: | View item in PubMed |
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