[Inducing of epithelial mesenchymal transition of HK-2 cells by connective tissue growth factor in vitro]

Zhonghua Bing Li Xue Za Zhi. 2009 Jul;38(7):462-5.
[Article in Chinese]

Abstract

Objective: To investigate the role of connective tissue growth factor (CTGF) in epithelial mesenchymal transition of HK-2 cells in vitro.

Methods: HK-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.

Results: There 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)].

Conclusion: Connective tissue growth factor induces mesenchymal transformation of HK-2 cells, in which the ERK2 signaling pathway may play an important role.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Cadherins / metabolism*
  • Cell Line
  • Cell Movement / drug effects*
  • Connective Tissue Growth Factor / pharmacology*
  • Epithelial Cells / cytology
  • Epithelial Cells / 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

Substances

  • ACTA2 protein, human
  • Actins
  • Cadherins
  • Vimentin
  • Connective Tissue Growth Factor
  • MAPK1 protein, human
  • Mitogen-Activated Protein Kinase 1