Apoptosis and proliferation of cultured mesangial cells isolated from kidneys of rosiglitazone-treated pregnant diabetic rats

被引:21
作者
Weissgarten, J [1 ]
Berman, S
Efrati, S
Rapoport, M
Averbukh, Z
Feldman, L
机构
[1] Assaf Harofeh Med Ctr, Div Nephrol, IL-70300 Zerifin, Israel
[2] Assaf Harofeh Med Ctr, Dept Internal Med C, IL-70300 Zerifin, Israel
关键词
angiotensin II; apoptosis; diabetes; PPAR; pregnancy; proliferation;
D O I
10.1093/ndt/gfk084
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. The peroxisome proliferator activating nuclear receptors (PPAR) are activated in the context of inflammation, diabetes or normal pregnancy. Renal mesangial cells express PPAR-gamma which upon activation are capable of exerting anti-inflammatory effects. We investigated the effect of in vivo treatment by rosiglitazone on angiotensin II (A-II) stimulated manifestations of inflammation in cultured renal mesangial cells, such as proliferation, apoptosis, TGF-beta 1 production and nuclear factor kappa B (NF-kappa B) activation, in the situation of pregnancies, complicated or not with diabetes. Methods. Mesangial cells were isolated from the following groups, receiving or not 5 mg/kg rosiglitazone for 20 days: normal controls, normal pregnant rats, those with streptozotocine induced diabetes and pregnant diabetic rats. Proliferation was assessed by H-3-thymidine incorporation. Apoptosis was evaluated by TUNEL assay. AT-1/AT-2 receptor density was assessed by I-125-AT-2 labelling, TGF-beta and NF-kappa B by specific ELISAs. Results. Rosiglitazone pretreatment resulted in significantly decreased proliferation, apoptosis and reduced responsiveness to A-II stimulation in cultures from controls, pregnant rats and non-pregnant diabetic animals. In the pregnant diabetic group which received rosiglitazone prior to sacrifice, responsiveness to A-II was completely blunted. Moderate attenuation of TGF-beta synthesis and significant decrease in the levels of NF-kappa B in mesangial cell nuclei were observed in all rosiglitazone treated groups. Conclusions. PPAR-gamma activation by rosiglitazone resulted in decreased manifestation of inflammatory hallmarks, including inhibition of mesangial cell proliferation, downregulation of apoptosis and blunted responsiveness to A-II. These anti-inflammatory renoprotective effects were maximally expressed in cultures from pregnant diabetic animals. The therapeutic relevance of these observations is a matter of further investigations.
引用
收藏
页码:1198 / 1204
页数:7
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