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Protective effect of BMP-7 against aristolochic acid-induced renal tubular epithelial cell injury.
Toxicol Lett. 2010 Oct 20; 198(3):348-57.TL

Abstract

Aristolochic acid nephropathy (AAN) is regarded as a kind of rapidly progressive renal fibrosis caused by the ingestion of herbal remedies containing aristolochic acid (AA). Recent studies showed that bone morphogenetic protein-7 (BMP-7) exerts beneficial effects on acute and chronic kidney injuries induced by different pathological conditions. We examined whether BMP-7 protects human renal tubular epithelial cells (HK-2) against AA-induced injury in vitro. HK-2 cells were cultured with different concentrations of AA and BMP-7 for 48h. Cell viability was determined by Cell Counting Kit-8 assay and lactate dehydrogenase (LDH) release. The apoptosis rate and the activity of caspase 3 protease were also examined. Epithelial-to-mesenchymal transition (EMT) was determined by cell morphology, E-cadherin and α-smooth muscle actin (α-SMA) protein expression, and TGF-β(1) and collagen III secretion. Additionally, the effect of anti-TGF-β1 antibody on AA-induced EMT was assessed. Our results indicated that BMP-7 significantly increased cell proliferation, decreased apoptosis rate and attenuated activation of caspase-3, resulting in the protection of HK-2 cells from AA-induced cytotoxicity. In addition, studies on EMT revealed that BMP-7 could inhibit AA-induced myofibroblast phenotype and restored the epithelial morphology in a dose-dependent manner. It was partially through reducing the activation of a myofibroblast phenotype and production TGF-β1. Treatment with neutralizing anti-TGF-β1 antibody also blocked AA-induced EMT and collagen III secretion. Together, these observations strongly suggest that BMP-7 is a potent inhibitor of AA-induced renal tubular epithelial cell injury and might be a promising agent for aristolochic acid-induced kidney damage.

Authors+Show Affiliations

Institute of Nephrology of Chongqing, Department of Nephrology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20696222

Citation

Wang, Zihua, et al. "Protective Effect of BMP-7 Against Aristolochic Acid-induced Renal Tubular Epithelial Cell Injury." Toxicology Letters, vol. 198, no. 3, 2010, pp. 348-57.
Wang Z, Zhao J, Zhang J, et al. Protective effect of BMP-7 against aristolochic acid-induced renal tubular epithelial cell injury. Toxicol Lett. 2010;198(3):348-57.
Wang, Z., Zhao, J., Zhang, J., Wei, J., Zhang, J., & Huang, Y. (2010). Protective effect of BMP-7 against aristolochic acid-induced renal tubular epithelial cell injury. Toxicology Letters, 198(3), 348-57. https://doi.org/10.1016/j.toxlet.2010.07.018
Wang Z, et al. Protective Effect of BMP-7 Against Aristolochic Acid-induced Renal Tubular Epithelial Cell Injury. Toxicol Lett. 2010 Oct 20;198(3):348-57. PubMed PMID: 20696222.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Protective effect of BMP-7 against aristolochic acid-induced renal tubular epithelial cell injury. AU - Wang,Zihua, AU - Zhao,Jinghong, AU - Zhang,Jing, AU - Wei,Jing, AU - Zhang,Jingbo, AU - Huang,Yunjian, Y1 - 2010/08/07/ PY - 2010/03/26/received PY - 2010/07/05/revised PY - 2010/07/29/accepted PY - 2010/8/11/entrez PY - 2010/8/11/pubmed PY - 2010/10/13/medline SP - 348 EP - 57 JF - Toxicology letters JO - Toxicol Lett VL - 198 IS - 3 N2 - Aristolochic acid nephropathy (AAN) is regarded as a kind of rapidly progressive renal fibrosis caused by the ingestion of herbal remedies containing aristolochic acid (AA). Recent studies showed that bone morphogenetic protein-7 (BMP-7) exerts beneficial effects on acute and chronic kidney injuries induced by different pathological conditions. We examined whether BMP-7 protects human renal tubular epithelial cells (HK-2) against AA-induced injury in vitro. HK-2 cells were cultured with different concentrations of AA and BMP-7 for 48h. Cell viability was determined by Cell Counting Kit-8 assay and lactate dehydrogenase (LDH) release. The apoptosis rate and the activity of caspase 3 protease were also examined. Epithelial-to-mesenchymal transition (EMT) was determined by cell morphology, E-cadherin and α-smooth muscle actin (α-SMA) protein expression, and TGF-β(1) and collagen III secretion. Additionally, the effect of anti-TGF-β1 antibody on AA-induced EMT was assessed. Our results indicated that BMP-7 significantly increased cell proliferation, decreased apoptosis rate and attenuated activation of caspase-3, resulting in the protection of HK-2 cells from AA-induced cytotoxicity. In addition, studies on EMT revealed that BMP-7 could inhibit AA-induced myofibroblast phenotype and restored the epithelial morphology in a dose-dependent manner. It was partially through reducing the activation of a myofibroblast phenotype and production TGF-β1. Treatment with neutralizing anti-TGF-β1 antibody also blocked AA-induced EMT and collagen III secretion. Together, these observations strongly suggest that BMP-7 is a potent inhibitor of AA-induced renal tubular epithelial cell injury and might be a promising agent for aristolochic acid-induced kidney damage. SN - 1879-3169 UR - https://www.unboundmedicine.com/medline/citation/20696222/Protective_effect_of_BMP_7_against_aristolochic_acid_induced_renal_tubular_epithelial_cell_injury_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0378-4274(10)01623-1 DB - PRIME DP - Unbound Medicine ER -