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Publication : Slit3 regulates cell motility through Rac/Cdc42 activation in lipopolysaccharide-stimulated macrophages.

First Author  Tanno T Year  2007
Journal  FEBS Lett Volume  581
Issue  5 Pages  1022-6
PubMed ID  17306799 Mgi Jnum  J:118874
Mgi Id  MGI:3700593 Doi  10.1016/j.febslet.2007.02.001
Citation  Tanno T, et al. (2007) Slit3 regulates cell motility through Rac/Cdc42 activation in lipopolysaccharide-stimulated macrophages. FEBS Lett 581(5):1022-6
abstractText  Three slit genes, slit1 to slit3, have been cloned to date. Slit1 and slit2 act as chemorepellent factors for axon guidance. Slit3 is involved in the formation of the diaphragm and kidney during embryogenesis. However, its molecular function remains unclear. We found that slit3 expression was induced by lipopolysaccharide (LPS)-stimulation in macrophages and that it was localized in the mitochondria and along the plasma membrane. Silencing of slit3 expression by RNA interference reduced cell motility and Rac/Cdc42 activation. These results suggest that slit3 functions as an intracellular signaling molecule for cell motility as part of the LPS-induced signaling cascade.
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