Focal Adhesion Kinases in Adhesion Structures and Disease
Author(s) -
Pierre P. Eleniste,
Angela Bruzzaniti
Publication year - 2012
Publication title -
journal of signal transduction
Language(s) - English
Resource type - Journals
eISSN - 2090-1739
pISSN - 2090-1747
DOI - 10.1155/2012/296450
Subject(s) - podosome , invadopodia , focal adhesion , paxillin , microbiology and biotechnology , proto oncogene tyrosine protein kinase src , ptk2 , extracellular matrix , integrin , tyrosine kinase , cell adhesion , adhesion , kinase , receptor tyrosine kinase , medicine , biology , signal transduction , cell , chemistry , cytoskeleton , biochemistry , protein kinase a , mitogen activated protein kinase kinase , organic chemistry , cancer , cancer cell
Cell adhesion to the extracellular matrix (ECM) is essential for cell migration, proliferation, and embryonic development. Cells can contact the ECM through a wide range of matrix contact structures such as focal adhesions, podosomes, and invadopodia. Although they are different in structural design and basic function, they share common remodeling proteins such as integrins, talin, paxillin, and the tyrosine kinases FAK, Pyk2, and Src. In this paper, we compare and contrast the basic organization and role of focal adhesions, podosomes, and invadopodia in different cells. In addition, we discuss the role of the tyrosine kinases, FAK, Pyk2, and Src, which are critical for the function of the different adhesion structures. Finally, we discuss the essential role of these tyrosine kinases from the perspective of human diseases.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom