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趋化因子SLC/CCL21与其受体CCR7的结合增强了人系膜细胞的黏附特性。

Binding of the chemokine SLC/CCL21 to its receptor CCR7 increases adhesive properties of human mesangial cells.

作者信息

Banas Bernhard, Wörnle Markus, Merkle Monika, Gonzalez-Rubio Mercedes, Schmid Holger, Kretzler Matthias, Pietrzyk Miriam C, Fink Monika, Perez de Lema Guillermo, Schlöndorff Detlef

机构信息

Nephrologisches Zentrum, Medizinische Poliklinik, Ludwig-Maximilians-Universität München, Germany.

出版信息

Kidney Int. 2004 Dec;66(6):2256-63. doi: 10.1111/j.1523-1755.2004.66037.x.

Abstract

BACKGROUND

Adherence of human mesangial cells to the surrounding matrix contributes to glomerular homeostasis and is important for the maintenance of glomerular architecture and function in normal adult human kidney. The expression of chemokines and corresponding chemokine receptors on adjacent intrinsic renal cells indicates a novel chemokine/chemokine receptor function on nonimmune cells important for glomerular homeostasis. A constitutive expression of the chemokine SLC/CCL21 on human podocytes and of its corresponding receptor CCR7 on mesangial cells was shown before. SLC/CCL21 has a positive effect on proliferation and migration of mesangial cells and leads to increased cell survival in Fas-induced apoptosis. In leukocytes chemokines mediate integrin-dependent firm adhesion. Therefore, we examined the influence of chemokine receptor CCR7 activation by SLC/CCL21 on adhesive properties of human mesangial cells to matrix molecules.

METHODS

Adhesion assays, mechanical detachment assays, and evaluation of integrin activation by integrin-linked kinase activity were performed. Changes in the cytoskeletal F-actin were illustrated by phalloidin immunofluorescence staining.

RESULTS

SLC/CCL21 stimulation enhanced adhesiveness to fibronectin in a time- and concentration-dependent manner. SLC/CCL21 also increased the firmness of mesangial cells adhesion as judged by detachment assays. Furthermore activation of integrin-linked kinase occurred with SLC/CCL21 addition to mesangial cells, resulting in increased phosphorylation of glycogen synthase kinase-3 (GSK-3) and protein kinase B (PKB/Akt). Exposure of mesangial cells to SLC/CCL21 also resulted in F-actin rearrangements with membrane ruffling and extensions leading to bridging between mesangial cells.

CONCLUSION

Activation of CCR7 on mesangial cells by SLC/CCL21 enhances the degree and firmness of cell adhesion and increases cell spreading and the formation of cell-cell contacts. This includes integrin-linked kinase activation and F-actin rearrangements. Thus, local chemokine generation and chemokine receptor expression on mesangial cells may play an important role in the maintenance of glomerular homeostasis and in local remodeling processes.

摘要

背景

人系膜细胞与周围基质的黏附有助于肾小球内环境稳定,对维持正常成人肾脏的肾小球结构和功能至关重要。相邻肾固有细胞上趋化因子及其相应趋化因子受体的表达表明非免疫细胞上一种新型趋化因子/趋化因子受体功能对肾小球内环境稳定很重要。之前已显示趋化因子SLC/CCL21在人足细胞上组成性表达,其相应受体CCR7在系膜细胞上组成性表达。SLC/CCL21对系膜细胞的增殖和迁移有积极作用,并导致Fas诱导的凋亡中细胞存活率增加。在白细胞中,趋化因子介导整合素依赖性牢固黏附。因此,我们研究了SLC/CCL21激活趋化因子受体CCR7对人系膜细胞与基质分子黏附特性的影响。

方法

进行了黏附试验、机械分离试验以及通过整合素连接激酶活性评估整合素激活情况。用鬼笔环肽免疫荧光染色说明细胞骨架F-肌动蛋白的变化。

结果

SLC/CCL21刺激以时间和浓度依赖性方式增强了对纤连蛋白的黏附性。根据分离试验判断,SLC/CCL21还增加了系膜细胞黏附的牢固性。此外,向系膜细胞中添加SLC/CCL21会激活整合素连接激酶,导致糖原合酶激酶-3(GSK-3)和蛋白激酶B(PKB/Akt)的磷酸化增加。系膜细胞暴露于SLC/CCL21还会导致F-肌动蛋白重排,出现膜皱褶和延伸,导致系膜细胞之间形成桥接。

结论

SLC/CCL21激活系膜细胞上的CCR7可增强细胞黏附的程度和牢固性,并增加细胞铺展和细胞间接触的形成。这包括整合素连接激酶激活和F-肌动蛋白重排。因此,系膜细胞上局部趋化因子的产生和趋化因子受体的表达可能在维持肾小球内环境稳定和局部重塑过程中起重要作用。

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