Effects of 2,3,7,8-tetrachlorodibenzo- p-dioxin(TCDD) on Glomerular Mesangial and Tubular Epithelial Cell Activation.
- Author:
Eun Na KIM
1
;
Mi Ra YU
;
Hyun Jin LIM
;
Eui Won HWANG
;
Hun Joo HA
;
Hi Bahl LEE
Author Information
1. Department of Internal and Hyonam Kidney Laboratory, College of Medicine, Soon Chun Hyang University, Seoul, Korea. hblee@seoul.com
- Publication Type:Original Article
- Keywords:
Tetrachlorodibenzo-p-dioxin;
Cell viability;
Proliferation;
Mesangial cell;
Tubular epithelial cell
- MeSH:
Animals;
Blotting, Western;
Cell Survival;
Culture Media, Serum-Free;
Epithelial Cells*;
Fibronectins;
Fibrosis;
Hydrocarbons, Aromatic;
Lactic Acid;
LLC-PK1 Cells;
Madin Darby Canine Kidney Cells;
Mesangial Cells;
Swine;
Tetrachlorodibenzodioxin
- From:Korean Journal of Nephrology
2002;21(1):12-19
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), a prototype compound of polyhalogenated aromatic hydrocarbons, produces diverse biologic effects. Although nephrotoxicity of aromatic hydrocarbons such as benzo[a]pyrene(BP) is well known, little is known about the effects of TCDD on renal function. Thus, the present study examined the effects of TCDD on cell viability, proliferation, and extracellular matrix(ECM) synthesis by glomerular mesangial cells, LLC-PK1 cells representing proximal tubular epithelial cells, and MDCK cells representing distal epithelial cells and compared with the effects of BP. METHODS: Quiescent cells were incubated with serum free media containing different concentrations of TCDD(1-100 nM) and BP(3 and 30 micro M) for 24- 96 hours. Cell viability and proliferation were assessed by lactate dehydrogenase(LDH) release and [3H]-thymidine incorporation, respectively. Secreted fibronectin was measured by Western blot analysis. RESULTS: When cells were continuously exposed to TCDD, LDH release significantly increased in MMC, LLC-PK1, and MDCK in a dose- and a time- dependent manner. [3H]-Thymidine incorporation was increased in MMC and LLC-PK1 but decreased in MDCK by TCDD. Contrary to TCDD, 30 micro BP significantly inhibited [3H]-thymidine incorporation in MMC and MDCK but not in LLC-PK1. Both TCDD and BP increased fibronectin secretion by MMC, LLC-PK1, and MDCK cells, suggesting that TCDD and BP may cause renal fibrosis leading to loss of renal function. CONCLUSION: These data provide experimental evidence that TCDD can alter cell viability and proliferation and increase ECM synthesis by renal cells which may lead to renal injury.
