Immune cell recruitment to inflammatory loci is impaired in mice deficient in basement membrane protein laminin α4

被引:45
作者
Kenne, Ellinor [1 ]
Soehnlein, Oliver [1 ]
Genove, Guillem [2 ]
Rotzius, Pierre [1 ]
Eriksson, Einar E. [1 ]
Lindbom, Lennart [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, S-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
inflammation; leukocyte recruitment; ENDOTHELIAL BARRIER FUNCTION; NEUTROPHIL MIGRATION; EXTRAVASCULAR TISSUE; ADHESION; PERMEABILITY; CHAIN; ALPHA-4-BETA-1-GAMMA-1; TRANSMIGRATION; EXTRAVASATION; EXPRESSION;
D O I
10.1189/jlb.0110043
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
For leukocytes to penetrate the vessel wall, they need to interact sequentially with the endothelial lining and the perivascular BM. The matrix protein laminin-411 is a major constituent of the vascular BM. The laminin alpha 4 chain is a component of laminin-411 and has structural and signaling functions. Here, we addressed the role of BM laminin alpha 4 in leukocyte recruitment to inflammatory loci. We used several recruitment models in Lam4-/- and WT mice to determine whether lack of laminin-411 in the perivascular BM influences extravasation of inflammatory cells. Recruitment of all major leukocyte subsets (neutrophils, monocytes, and lymphocytes) was reduced in Lam4-/- mice compared with WT. With the use of intravital microscopy, we concluded that this decrease was a result of impaired diapedesis through the vessel wall, as neither leukocyte adhesion to the endothelial lining nor migration in extravascular tissue was hampered in Lam4-/- mice. Collectively, our data suggest a reduced ability of immune cells to penetrate the vessel wall in mice deficient in laminin alpha 4. J. Leukoc. Biol. 88: 523-528; 2010.
引用
收藏
页码:523 / 528
页数:6
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