Inducing of epithelial mesenchymal transition of HK-2 cells by connective tissue growth factor in vitro.
- Author:
Zhao DING
1
;
Zhi-shui CHEN
;
Xi-lin CHEN
;
Hui GUO
;
Nian-qiao GONG
Author Information
- Publication Type:Journal Article
- MeSH: Actins; metabolism; Cadherins; metabolism; Cell Line; Cell Movement; drug effects; Connective Tissue Growth Factor; pharmacology; Epithelial Cells; cytology; metabolism; Epithelial-Mesenchymal Transition; drug effects; Humans; Kidney Tubules, Proximal; cytology; Mesoderm; cytology; Mitogen-Activated Protein Kinase 1; metabolism; Random Allocation; Signal Transduction; Vimentin; metabolism
- From: Chinese Journal of Pathology 2009;38(7):462-465
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the role of connective tissue growth factor (CTGF) in epithelial mesenchymal transition of HK-2 cells in vitro.
METHODSHK-2 cells were randomly divided into two groups: (1) control group including cells cultured in DMEM medium supplemented with 10% fetal bovine serum only; and (2) experimental group including cells cultured in DMEM medium supplemented with 10% fetal bovine serum and recombinant CTGF at a final concentration of 5 microg/L. The cells were collected at 72 h time points. Direct immunofluorescence staining and immunohistochemistry were used to evaluate the E-cadherin, Vimentin, alpha-SMA and ERK2 in cells. Western-blotting was used to detect the E-cadherin, Vimentin and ERK2 protein expression. Boyden Chamber was used to detect the migration of tubular endothelium at 1 d, 3 d and 5 d.
RESULTSThere were less E-cadherin but more Vimentin expressed in cells of the experimental group. The presence of alpha-SMA was detected at 48 h with peak at 72 h in the cells of the experimental group. On the first day, the cellular migration in the two groups showed no difference. However, after 3 days, the transformed cells migrated surpassed the control group with peak at the 5th day [(45.0+/-1.1):(14.0+/-1.2), P<0.05)].
CONCLUSIONConnective tissue growth factor induces mesenchymal transformation of HK-2 cells, in which the ERK2 signaling pathway may play an important role.