Pearson Alex L, Colville-Nash Paul, Kwan Jonathan T C, Dockrell Mark E C
South West Thames Institute for Renal Research, St. Helier Hospital, Carshalton, Surrey - UK.
J Nephrol. 2008 Nov-Dec;21(6):887-93.
Proximal tubule epithelial cells (PTECs) release proinflammatory and profibrogenic mediators when exposed to serum albumin that may contribute to progression of kidney disease. Interleukin 6 (IL-6) may influence renal fibrosis by modulating transforming growth factor beta1 (TGFbeta1) signalling. PTECs have been demonstrated to produce IL-6 in response to albumin treatment, but the mechanism has not been investigated. We hypothesized that albumin would induce release of IL-6 from PTECs, which would be sensitive to inhibition of PI3K, ERK1,2, p38 MAPK and NFkB.
Primary human PTECs were exposed to albumin (0.75-150 micronM) for 8 and 24 hours. IL-6 release was determined using enzyme-linked immunosorbent assay (ELISA). The effects of LY294002 (10 micronM), NH4Cl (10 mM), pyrrolidine dithiocarbamate (PDTC) (20 micronM), CAPE (17.5 micronM), PD098059 (20 micronM), SB202190 (5 micronM) and MG132 (10 micronM) on albumin-mediated IL-6 release were studied.
Albumin caused a significant time- and concentration-dependent increase in IL-6 release by PTECs. LY294002, NH4Cl, CAPE, PD098059 and SB202190 all reduced albumin-mediated IL-6 release, but neither PDTC nor MG132 had any effect.
These data demonstrate that albumin induces IL-6 release by primary human PTECs, and support a role for endocytosis, p38 MAPK, ERK1,2 and in this process.
近端肾小管上皮细胞(PTECs)在暴露于血清白蛋白时会释放促炎和促纤维化介质,这可能有助于肾脏疾病的进展。白细胞介素6(IL-6)可能通过调节转化生长因子β1(TGFβ1)信号通路影响肾纤维化。已证明PTECs在白蛋白处理后会产生IL-6,但该机制尚未得到研究。我们假设白蛋白会诱导PTECs释放IL-6,而IL-6对PI3K、ERK1、2、p38 MAPK和NFkB的抑制敏感。
将原代人PTECs暴露于白蛋白(0.75 - 150 μM)8小时和24小时。使用酶联免疫吸附测定(ELISA)测定IL-6的释放。研究了LY294002(10 μM)、NH4Cl(10 mM)、吡咯烷二硫代氨基甲酸盐(PDTC)(20 μM)、咖啡酸苯乙酯(CAPE)(17.5 μM)、PD098059(20 μM)、SB202190(5 μM)和MG132(10 μM)对白蛋白介导的IL-6释放的影响。
白蛋白导致PTECs释放IL-6出现显著的时间和浓度依赖性增加。LY294002、NH4Cl、CAPE、PD098059和SB202190均降低了白蛋白介导的IL-6释放,但PDTC和MG132均无任何作用。
这些数据表明白蛋白诱导原代人PTECs释放IL-6,并支持内吞作用、p38 MAPK、ERK1、2在此过程中的作用。