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Inhibition of aquaporin-1 expression by RNAi protects against aristolochic acid I-induced apoptosis in human proximal tubular epithelial (HK-2) cells.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2011 Feb 04; Vol. 405 (1), pp. 68-73. Date of Electronic Publication: 2011 Jan 05. - Publication Year :
- 2011
-
Abstract
- The aim of this study was to investigate the protective effect of inhibition of aquaporin-1 (AQP1) expression against aristolochic acid I (AA-I)-induced apoptosis. HK-2 cells impaired by AA-I were used in this study as the cell model of aristolochic acid nephropathy. Apoptosis was studied by different methods, including 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assays, flow cytometry, and caspase 3 activity assays. We compared AA-I-mediated apoptosis in HK-2 cells with or without knockdown of AQP1 expression by RNA interference. MTT assays showed that AA-I inhibited the viability of HK-2 cells in a time- and concentration-dependent manner. Apoptosis was evidenced by the results of the Annexin V/propidium iodide assay and the occurrence of a sub-G1 peak in cell-cycle analysis. The activity of caspase 3 was found to have been increased by AA-I in a concentration-dependent manner. However, AQP1 RNA interference provided protection against injury in cells treated with AA-I (40 μM) for 24 h and attenuated the number of apoptotic cells. These results suggested that AQP1 plays an important role in AA-I-induced apoptosis and that inhibition of AQP1 expression may protect HK-2 cells from AA-I-induced apoptotic damage.<br /> (Copyright © 2011. Published by Elsevier Inc.)
- Subjects :
- Cell Line
Epithelial Cells drug effects
Epithelial Cells pathology
Humans
Kidney Diseases pathology
Kidney Tubules, Proximal pathology
Models, Biological
Apoptosis genetics
Aquaporin 1 genetics
Aristolochic Acids toxicity
Kidney Diseases chemically induced
Kidney Tubules, Proximal drug effects
RNA Interference
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 405
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 21215257
- Full Text :
- https://doi.org/10.1016/j.bbrc.2010.12.128