Linked Life Data

12615084

Source:http://linkedlifedata.com/resource/pubmed/id/12615084

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-3-4
pubmed:abstractText
Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase which in non-neuronal cells is localized to focal adhesions, where it participates to adhesion-dependent intracellular signalling. FAK is highly expressed in the central nervous system both during development and in the adult. FAK(+), a splice isoform of FAK selectively enriched in neurons, contains a three-amino acid insertion in the carboxy-terminal sequence responsible for the localization of FAK to focal adhesions. Enhanced green fluorescent protein-tagged constructs were used to study the targeting of FAK and FAK(+) in neuronal and non-neuronal cells of the central nervous system. In transfected non-neuronal cells, both fusion proteins colocalized with vinculin in focal contacts. When expressed in hippocampal neurons in culture, both chimeras were locally concentrated in the growth cone, where they overlapped with F-actin enrichments but not with vinculin. In the growth cone of living neurons, the FAK(+) chimera showed a dynamic relocalization to membrane ruffles and to the tips of the membrane protrusions induced by cytochalasin D treatment, indicating a dependence of FAK distribution on F-actin organization. Since virtually identical patterns of distribution were found for FAK and FAK(+) chimeras, it follows that the additional insertion in FAK(+) is not responsible for the localization of the kinase. Finally, we showed that the carboxy-terminal domain of both FAK and FAK(+) is sufficient to mediate the localization of the proteins to focal adhesions in non-neuronal cells and to maintain their correct intracellular targeting in neurons.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0736-5748
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
83-93
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12615084-Animals, pubmed-meshheading:12615084-Central Nervous System, pubmed-meshheading:12615084-Chick Embryo, pubmed-meshheading:12615084-DNA, Recombinant, pubmed-meshheading:12615084-Fibroblasts, pubmed-meshheading:12615084-Focal Adhesion Kinase 1, pubmed-meshheading:12615084-Focal Adhesion Protein-Tyrosine Kinases, pubmed-meshheading:12615084-Green Fluorescent Proteins, pubmed-meshheading:12615084-Intracellular Membranes, pubmed-meshheading:12615084-Isoenzymes, pubmed-meshheading:12615084-Luminescent Proteins, pubmed-meshheading:12615084-Neurons, pubmed-meshheading:12615084-Protein Structure, Tertiary, pubmed-meshheading:12615084-Protein-Tyrosine Kinases, pubmed-meshheading:12615084-Rats, pubmed-meshheading:12615084-Rats, Sprague-Dawley, pubmed-meshheading:12615084-Recombinant Fusion Proteins, pubmed-meshheading:12615084-Tissue Distribution
pubmed:year
2003
pubmed:articleTitle
Localization of focal adhesion kinase isoforms in cells of the central nervous system.
pubmed:affiliation
Department of Neuroscience, S. Raffaele Scientific Institute and Vita-Salute University, Milano, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't