Suppression of the lipopolysaccharide-induced expression of MARCKS-related protein (MRP) affects transmigration in activated RAW264.7 cells

被引：16

作者：

Chun, Kwang-Rok ^{[1
]}

Bae, Eun Mi ^{[1
]}

Kim, Jae-Kwan ^{[1
]}

Suk, Kyoungho ^{[2
]}

Lee, Won-Ha ^{[1
]}

机构：

[1] Kyungpook Natl Univ, Sch Life Sci & Biotechnol, Dept Genet Engn, Taegu 702701, South Korea

[2] Kyungpook Natl Univ, Sch Med, Dept Pharmacol, Taegu 702701, South Korea

来源：

CELLULAR IMMUNOLOGY | 2009年 / 256卷 / 1-2期

关键词：

Macrophage; MARCKS; PKC; Transmigration; Inflammation; shRNA; C-KINASE-SUBSTRATE; INFLAMMATORY ACTIVATION; FIBRONECTIN; MACMARCKS; PHOSPHORYLATION; FAMILY; PHAGOCYTOSIS; MIGRATION; DYNAMITIN; BINDING;

D O I：

10.1016/j.cellimm.2009.01.011

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

The molecular action mechanism of MRP, one of the protein kinase C (PKC) substrates, has been under intense investigation, but reports on its role in macrophage function remain controversial. The treatment of macrophage cell lines with bacterial lipopolysaccharide (LPS) induced a high level of MRP expression suggesting that MRP plays a role in the function of activated macrophages. In order to investigate the role of MRP in activated RAW264.7 cells, we stably transfected MRP-specific shRNA expression constructs and tested for alterations in macrophage-related functions. The down-regulation of MRP expression resulted in a marked reduction in chemotaxis toward MCP-1 or extracellular matrix proteins. Furthermore, pharmacological inhibitors of PKC significantly inhibited the chemotaxis in RAW264.7 cells. These data reveals the pivotal role of MRP in the transmigration of activated RAW264.7 cells. (C) 2009 Elsevier Inc. All rights reserved.

引用

页码：92 / 98

页数：7

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