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细胞外基质蛋白可调节促红细胞生成素对培养大鼠肾小球足细胞的保护作用。

The protective effects of erythropoietin on rat glomerular podocytes in culture are modulated by extracellular matrix proteins.

机构信息

Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.

出版信息

Kidney Blood Press Res. 2013;38(1):142-55. doi: 10.1159/000355762. Epub 2014 Mar 15.

Abstract

BACKGROUND/AIMS: Podocytes are typically cultured on collagen I; however, collagen I is absent from healthy glomerular basement membranes. Erythropoietin (EPO) is thought to protect podocytes in vivo. Here, we studied how various types of extracellular matrix (ECM) proteins and EPO affect podocytes in culture.

METHODS

Primary rat podocytes were replated on collagen I, collagen IV, whole ECM extract, laminin, or bare plastic. Cellular adhesion (8 hours after plating), proliferation (5 days, 10 % serum), and resistance to serum deprivation (3 days, 0.5 % serum) were assessed. BrdU incorporation and expression of podocyte-specific markers were employed as measures of cellular proliferation and differentiation, respectively. qPCR was used to verify expression of EPO receptor in cultured podocytes.

RESULTS

Cellular adhesion was similar on all ECM proteins and unaffected by EPO. Proliferation was accelerated by laminin and the ECM extract, but the final cell density was similar on all ECM surfaces. Collagen IV supported the serum-deprived cells better than the other ECM proteins. EPO (2-20 ng/ml) improved viability of serum-deprived podocytes on collagen I, collagen IV, and ECM, but not on laminin or bare plastic. The cells expressed mRNA for EPO receptor.

CONCLUSION

The physiological ECM proteins are more supportive of primary podocytic cultures compared with collagen I. The protective effects of EPO during serum deprivation are modulated by the cultivation surface.

摘要

背景/目的:足细胞通常在胶原蛋白 I 上培养;然而,胶原蛋白 I 在健康的肾小球基底膜中不存在。促红细胞生成素(EPO)被认为在体内保护足细胞。在这里,我们研究了各种细胞外基质(ECM)蛋白和 EPO 如何影响培养中的足细胞。

方法

原代大鼠足细胞在胶原蛋白 I、胶原蛋白 IV、全 ECM 提取物、层粘连蛋白或裸塑料上再铺板。评估细胞黏附(铺板后 8 小时)、增殖(5 天,10%血清)和抵抗血清剥夺(3 天,0.5%血清)。BrdU 掺入和足细胞特异性标志物的表达分别作为细胞增殖和分化的指标。qPCR 用于验证培养的足细胞中 EPO 受体的表达。

结果

细胞黏附在所有 ECM 蛋白上相似,不受 EPO 影响。层粘连蛋白和 ECM 提取物加速了细胞增殖,但在所有 ECM 表面上的最终细胞密度相似。胶原蛋白 IV 比其他 ECM 蛋白更能支持血清剥夺的细胞。EPO(2-20 ng/ml)在胶原蛋白 I、胶原蛋白 IV 和 ECM 上提高了血清剥夺的足细胞的存活率,但在层粘连蛋白或裸塑料上没有。细胞表达 EPO 受体的 mRNA。

结论

与胶原蛋白 I 相比,生理 ECM 蛋白更能支持原代足细胞培养。EPO 在血清剥夺期间的保护作用受到培养表面的调节。

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