Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2000;21(2-3):83-8.
doi: 10.1385/IR:21:2-3:83.

Molecular signaling mechanisms of cell migration and invasion

Affiliations
Review

Molecular signaling mechanisms of cell migration and invasion

D G Stupack et al. Immunol Res. 2000.

Abstract

The ability of immune cells to migrate and invade the extracellular matrix (ECM) is a central process involved in immunologic surveillance as well as inflammation. We have shown that interaction of cells with adhesive proteins or growth factors (chemokines) present in the ECM control cell migration/invasion through activation of mitogen-activated protein kinases ERK1 and ERK2 and molecular coupling of the adapter proteins p130CAS and c-CrkII. During cell migration, ERK and CAS/Crk coupling operate as distinct signaling pathways that facilitate actin-myosin motor assembly and actin membrane ruffles, respectively. Furthermore, activation of these signaling pathways protects cells from apoptosis during invasion of the ECM, which is necessary as migratory cells colonize foreign sites in the body.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Cell Biol. 1999 Sep 6;146(5):1107-16 - PubMed
    1. Nature. 1992 Apr 2;356(6368):397-400 - PubMed
    1. J Cell Biol. 1998 Feb 23;140(4):961-72 - PubMed
    1. J Cell Physiol. 1998 Dec;177(4):535-52 - PubMed
    1. J Exp Biol. 1996 Apr;199(Pt 4):741-7 - PubMed

LinkOut - more resources