Wolthuis A, Boes A, Rodemann H P, Grond J
Department of Pathology, University of Groningen, The Netherlands.
Kidney Int. 1992 Jan;41(1):124-31. doi: 10.1038/ki.1992.16.
Mesangial cell (MC) proliferation and extracellular matrix (ECM) formation are hallmarks of chronic glomerular disease. The present in vitro study examined the effects of the vasoactive agents angiotensin II (Ang II), arginine vasopressin (AVP), and serotonin (5-HT) on growth and protein biosynthesis of cultured rat MCs after 72 hours of incubation. AVP and 5-HT (10(-6) M) significantly increased DNA synthesis and growth of quiescent subconfluent MCs to levels of 25 and 45%, respectively, of the optimal stimulatory effect of 10% fetal calf serum (FCS) (both P less than 0.001). The mitogenic effect of Ang II was 10% of the 10% FCS effect (P less than 0.01). ECM production was studied by ELISA assay for fibronectin (FN) secreted into the culture medium (SeFN) and cell-associated FN, that is, intra- and pericellular FN (CaFN). In all incubations, highly significant negative linear relationships were found between the numbers of MCs per well and quantities of both SeFN and CaFN after normalization of the data by logarithmic transformation (SeFN: r values greater than -0.9705; CaFN: r greater than -0.9620; P less than 0.001). Thus, increasing cell densities progressively suppressed ECM formation by MCs. The ECM production was found to be independent of growth activity. AVP significantly increased SeFN (P less than 0.05) and decreased CaFN (P less than 0.001) in subconfluent cultures; Ang II and 5-HT had no effect. Metabolic labeling with 35S-methionine (18 hr, 200 microCi/ml medium) and 2-D electrophoresis of MC lysates resulted in resolution of greater than 500 different radiolabeled intracellular proteins in molecular weight from 110 to 20 Kd over an isoelectric interval of 5.0 to 7.0.(ABSTRACT TRUNCATED AT 250 WORDS)
系膜细胞(MC)增殖和细胞外基质(ECM)形成是慢性肾小球疾病的标志。本体外研究检测了血管活性物质血管紧张素II(Ang II)、精氨酸加压素(AVP)和5-羟色胺(5-HT)在培养72小时后对培养的大鼠MC生长和蛋白质生物合成的影响。AVP和5-HT(10⁻⁶ M)显著增加静止亚汇合MC的DNA合成和生长,分别达到10%胎牛血清(FCS)最佳刺激作用水平的25%和45%(P均小于0.001)。Ang II的促有丝分裂作用为10% FCS作用的10%(P小于0.01)。通过ELISA法检测分泌到培养基中的纤连蛋白(FN)(SeFN)和细胞相关FN(即细胞内和细胞周围FN,CaFN)来研究ECM产生。在所有培养中,经对数转换对数据进行归一化后,发现每孔MC数量与SeFN和CaFN数量之间均存在高度显著的负线性关系(SeFN:r值大于-0.9705;CaFN:r大于-0.9620;P小于0.001)。因此,细胞密度增加逐渐抑制MC的ECM形成。发现ECM产生与生长活性无关。在亚汇合培养中,AVP显著增加SeFN(P小于0.05)并降低CaFN(P小于0.001);Ang II和5-HT无作用。用³⁵S-蛋氨酸(18小时,200 μCi/ml培养基)进行代谢标记并对MC裂解物进行二维电泳,在分子量110至20 Kd、等电区间5.0至7.0范围内分辨出500多种不同的放射性标记细胞内蛋白质。(摘要截短于250字)