Lumican Inhibits Cell Migration Through Alpha 2 Beta 1 Integrin
EXPERIMENTAL CELL RESEARCH(2010)
摘要
Lumican, an extracellular matrix protein of the small leucine-rich proteoglycan family, has been shown to impede melanoma progression by inhibiting cell migration. In the present study, we show that lumican targets alpha 2 beta 1 integrin thereby inhibiting cell migration. A375 melanoma cells were transfected with siRNA directed against the alpha 2 integrin subunit. Compared to A375 control cells, the anti-migratory effect of lumican was abrogated on transfected A375 cells. Moreover, lumican inhibited the chemotactic migration of Chinese hamster ovary (CHO) cells stably transfected with a2 integrin subunit (CHO-A2) but not that of wild-type CHO cells (CHO-WT) lacking this subunit. In contrast to CHO-WT cells, we observed in time-lapse microscopy a decrease of CHO-A2 cell migration speed in presence of lumican. Focal adhesion kinase phosphorylated at tyrosine-397 (pFAK) and total FAR were analysed in CHO-WT and CHO-A2 cells. A significant decrease of the ratio pFAK/FAK was shown in presence of recombinant human lumican. Using solid phase assays, a direct binding between lumican and the alpha 2 beta 1 integrin was demonstrated. This interaction did not involve the glycan moiety of lumican and was cation independent. Lumican was also able to bind the activated I domain of the alpha 2 integrin subunit with a K-d >= 200 nM. In conclusion, we demonstrated for the first time that the inhibition of cell migration by lumican depends on a direct binding between the core protein of lumican and the alpha 2 beta 1 integrin. (C) 2010 Elsevier Inc. All rights reserved.
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关键词
Lumican, SLRP, Cell migration, alpha 2 beta 1 integrin, alpha I domain
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