LOW-MOLECULAR-WEIGHT HEPARINS AND TRIAMCINOLONE ACETONIDE INHIBIT PROLIFERATION AND MCP-1 EXPRESSION AND SECRETION IN RAT GLOMERULAR MESANGIAL CELLS BY NF-kappa B

Wu Xiao-Chuan, Yi Zhu-Wen, Xiao Jian-Wu, He Xiao-Jie

Laboratory of Pediatric Nephrology, The Second Hospital of Xiang Ya School of Medicine, Central South University, Changsha, China

 

Objective: In order to investigate the mechanism that Low-Molecular-Weight Heparins (LMWH) and Triamcinolone Acetonide (TA) inhibit proliferation of glomerular mesangial cells (GMCs).

Methods: Rat GMCs line was cultured in vitro, Lipopolysaccharide (LPS), LPS and LMWH, LPS and TA were added into the culture medium, named as LPS group, LMWH group, TA group, respectively. GMCs cultured without any drugs served as control group, named as GMCs group. GMCs proliferative rate was detected by MTT, MCP-1 concentration was determined by ELISA, MCP-1 and NF-kappa B expression were checked by immunohistochemistry.

Results: Both in LMWH group and TA group, the GMCs proliferative rate were obviously lower than that either in LPS group or in GMCs group (p<0.01). The MCP-1 expression of GMCs in LMWH group was obviously lower than that in any of the other groups (p<0.01). The MCP-1 expression of GMCs both in TA group and GMCs group were obviously lower than that in LPS group (p<0.01), while it had no difference between in these two groups (p>0.05). Contrast to LPS group, the MCP-1 concentration in culture supernatant were significantly lower both in LMWH group and TA group (p<0.01), while it had no difference compared with that in GMCs group (p>0.05). The NF-kappa B expression in GMCs both in LMWH group and TA group were significantly lower than that in LPS group (p<0.01), while in LPS group, it was obviously higher than that in GMCs group (p<0.01), however, in LMWH group, TA group and GMCs group, it had no significant difference between any two of them (p>0.05).

Conclusions: It suggests that LMWH and TA can obviously inhibit proliferation of GMCs, downregulate the abnormal expression and secretion of MCP-1, inhibit activation of NF-kappa B, but it has no effect on the normal activation of NF-kappa B. Perhaps, LMWH and TA inhibit proliferation of GMCs and MCP-1 expression in GMCs via reducing activation of NF-kappa B.

 
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