Integrin regulation of cell signalling and motility

RL Juliano, P Reddig, S Alahari, M Edin… - Biochemical Society …, 2004 - portlandpress.com
RL Juliano, P Reddig, S Alahari, M Edin, A Howe, A Aplin
Biochemical Society Transactions, 2004portlandpress.com
Integrins clearly play a key role in regulating both mitogenic signalling and cell migration.
Thus integrins modulate the efficiency of the Erk (extracellular-signal-regulated kinase)/MAP
kinase (mitogen-activated protein kinase) pathway, acting at several distinct levels. We have
shown that both cAMP-dependent protein kinase and PAKs (p21-activated kinases) play a
role in integrin regulation of the Erk pathway, acting primarily at the level of Raf-1. Integrins
and PAKs also play a role in the control of cell migration. Thus we have discovered a novel …
Integrins clearly play a key role in regulating both mitogenic signalling and cell migration. Thus integrins modulate the efficiency of the Erk (extracellular-signal-regulated kinase)/MAP kinase (mitogen-activated protein kinase) pathway, acting at several distinct levels. We have shown that both cAMP-dependent protein kinase and PAKs (p21-activated kinases) play a role in integrin regulation of the Erk pathway, acting primarily at the level of Raf-1. Integrins and PAKs also play a role in the control of cell migration. Thus we have discovered a novel protein that links the α5β1 integrin to migration controlled by Rho-family GTPases. This protein, termed Nischarin, is a large cytosolic macromolecule that is not related to well-known protein families. The N-terminus of Nischarin interacts with a short segment of the cytoplasmic domain of the α5 integrin subunit. Overexpression of Nischarin alters actin organization and inhibits Rac-driven cell migration and tumour cell invasion. Use of effector domain mutants of Rac suggest that Nischarin acts downstream of Rac, probably at the level of PAK-family kinases. These studies emphasize the intricate connection between integrins and Rho-family GTPases and their effectors in controlling both mitogenesis and migration.
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