期刊论文详细信息
BMC Nephrology
Effects of chemokines on proliferation and apoptosis of human mesangial cells
Bernhard Banas1  Monika Merkle1  Holger Schmid1  Markus Wörnle1 
[1] Medical Policlinic, Ludwig-Maximilians-University, Munich, Germany
关键词: chemokine receptor;    chemokine;    apoptosis;    proliferation;    Mesangial cell;   
Others  :  1083439
DOI  :  10.1186/1471-2369-5-8
 received in 2004-01-11, accepted in 2004-07-20,  发布年份 2004
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【 摘 要 】

Background

Proliferation and apoptosis of mesangial cells (MC) are important mechanisms during nephrogenesis, for the maintenance of glomerular homeostasis as well as in renal disease and glomerular regeneration. Expression of chemokines and chemokine receptors by intrinsic renal cells, e.g. SLC/CCL21 on podocytes and CCR7 on MC is suggested to play a pivotal role during these processes. Therefore the effect of selected chemokines on MC proliferation and apoptosis was studied.

Methods

Proliferation assays, cell death assays including cell cycle analysis, hoechst stain and measurement of caspase-3 activity were performed.

Results

A dose-dependent, mesangioproliferative effect of the chemokine SLC/CCL21, which is constitutively expressed on human podocytes was seen via activation of the chemokine receptor CCR7, which is constitutively expressed on MC. In addition, in cultured MC SLC/CCL21 had a protective effect on cell survival in Fas-mediated apoptosis. The CXCR3 ligands IP-10/CXCL10 and Mig/CXCL9 revealed a proproliferative effect but did not influence apoptosis of MC. Both the CCR1 ligand RANTES/CCL5 and the amino-terminally modified RANTES analogue Met-RANTES which blocks CCR1 signalling had no effect on proliferation and apoptosis.

Conclusions

The different effects of chemokines and their respective receptors on proliferation and apoptosis of MC suggest highly regulated, novel biological functions of chemokine/chemokine receptor pairs in processes involved in renal inflammation, regeneration and glomerular homeostasis.

【 授权许可】

   
2004 Wörnle et al; licensee BioMed Central Ltd.

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