SKAP1 protein PH domain determines RapL membrane localization and Rap1 protein complex formation for T cell receptor (TCR) activation of LFA-1
- Although essential for T cell function, the identity of the T cell receptor (TCR) “inside-out” pathway for the activation of lymphocyte function-associated antigen 1 (LFA-1) is unclear. SKAP1 (SKAP-55) is the upstream regulator needed for TCR-induced RapL-Rap1 complex formation and LFA-1 activation. In this paper, we show that SKAP1 is needed for RapL binding to membranes in a manner dependent on the PH domain of SKAP1 and the PI3K pathway. A SKAP1 PH domain-inactivating mutation (i.e. R131M) markedly impaired RapL translocation to membranes for Rap1 and LFA-1 binding and the up-regulation of LFA-1-intercellular adhesion molecule 1 (ICAM-1) binding. Further, N-terminal myr-tagged SKAP1 for membrane binding facilitated constitutive RapL membrane and Rap1 binding and effectively substituted for PI3K and TCR ligation in the activation of LFA-1 in T cells.
Author: | Monika RaabORCiD, Xin Smith, Yves MatthessORCiDGND, Klaus StrebhardtORCiDGND, Christopher E. Rudd |
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URN: | urn:nbn:de:hebis:30:3-255436 |
URL: | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191007/ |
DOI: | https://doi.org/10.1074/jbc.M111.222661 |
ISSN: | 0021-9258 |
ISSN: | 1083-351X |
Pubmed Id: | https://pubmed.ncbi.nlm.nih.gov/21669874 |
Parent Title (English): | The journal of biological chemistry |
Publisher: | American Society for Biochemistry and Molecular Biology |
Place of publication: | Bethesda, Md. |
Document Type: | Article |
Language: | English |
Date of Publication (online): | 2011/06/13 |
Date of first Publication: | 2011/06/13 |
Publishing Institution: | Universitätsbibliothek Johann Christian Senckenberg |
Release Date: | 2012/07/16 |
Tag: | Cell Adhesion; Immunology; Inside-out Signaling; Integrin; LFA-1; Lymphocyte; PI3K; Protein Translocation; SKAP1; T Cells |
Volume: | 286 |
Issue: | 34 |
Page Number: | 9 |
First Page: | 29663 |
Last Page: | 29670 |
Note: | © 2011 by The American Society for Biochemistry and Molecular Biology, Inc. |
HeBIS-PPN: | 357829166 |
Institutes: | Medizin / Medizin |
Dewey Decimal Classification: | 5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie |
Sammlungen: | Universitätspublikationen |
Sammlung Biologie / Sondersammelgebiets-Volltexte | |
Licence (German): | Creative Commons - Namensnennung-Nicht kommerziell 3.0 |