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Role of two adaptor molecules SLP-76 and LAT in the PI3K signaling pathway in activated T cells

Title
Role of two adaptor molecules SLP-76 and LAT in the PI3K signaling pathway in activated T cells
Authors
Shim E.K.Jung S.H.Lee J.R.
Ewha Authors
이종란
SCOPUS Author ID
이종란scopus
Issue Date
2011
Journal Title
Journal of Immunology
ISSN
0022-1767JCR Link
Citation
vol. 186, no. 5, pp. 2926 - 2935
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
Previously, we identified p85, a subunit of PI3K, as one of the molecules that interacts with the N-terminal region of Src homology 2 domain-containing leukocyte protein of 76 kDa (SLP-76).We also demonstrated that tyrosine phosphorylation either at the 113 and/ or 128 position is sufficient for the association of SLP-76 with the Src homology 2 domain near the N terminus of p85. The present study further examines the role of the association of these two molecules on the activation of PI3K signaling cascade. Experiments were done to determine the role of SLP-76, either wild-type, tyrosine mutants, or membrane-targeted forms of various SLP-76 constructs, on the membrane localization and phosphorylation of Akt, which is an event downstream of PI3K activation. Reconstitution studies with these various SLP-76 constructs in a Jurkat variant cell line that lacks SLP-76 or linker for activation of T cells (LAT) show that the activation of PI3K pathway following TCR ligation requires both SLP-76 and LATadaptor proteins. The results suggest that SLP-76 associates with p85 after T cell activation and that LAT recruits this complex to the membrane, leading to Akt activation. Copyright © 2011 by The American Association of Immunologists, Inc.
DOI
10.4049/jimmunol.1001785
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자연과학대학 > 생명과학전공 > Journal papers
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