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- W2089660432 abstract "Abstract The neural cell adhesion molecule (NCAM) plays a key role in neural development, regeneration and synaptic plasticity. This study describes a novel function of NCAM140 in stimulating integrin‐dependent cell migration. Expression of NCAM140 in rat B35 neuroblastoma cells resulted in increased migration toward the extracellular matrix proteins fibronectin, collagen IV, vitronectin, and laminin. NCAM‐potentiated cell migration toward fibronectin was dependent on β1 integrins and required extracellular‐regulated kinase (ERK)1/2 mitogen‐activated protein kinase (MAPK) activity. NCAM140 in B35 neuroblastoma cells was subject to ectodomain cleavage resulting in a 115 kDa soluble fragment released into the media and a 30 kDa cytoplasmic domain fragment remaining in the cell membrane. NCAM140 ectodomain cleavage was stimulated by the tyrosine phosphatase inhibitor pervanadate and inhibited by the broad spectrum metalloprotease inhibitor GM6001, characteristic of a metalloprotease. Moreover, treatment of NCAM140‐B35 cells with GM6001 reduced NCAM140‐stimulated cell migration toward fibronectin and increased cellular attachment to fibronectin to a small but significant extent. These results suggested that metalloprotease‐induced cleavage of NCAM140 from the membrane promotes integrin‐ and ERK1/2‐dependent cell migration to extracellular matrix proteins." @default.
- W2089660432 created "2016-06-24" @default.
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- W2089660432 date "2005-11-08" @default.
- W2089660432 modified "2023-10-17" @default.
- W2089660432 title "NCAM140 stimulates integrin‐dependent cell migration by ectodomain shedding" @default.
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- W2089660432 doi "https://doi.org/10.1111/j.1471-4159.2005.03475.x" @default.
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