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Helmholtz Zentrum für Infektionsforschung Repository > Dept. Immunocontrol (IMMK) > publications of the department of immunocontrol (IMMK) > TCR-mediated Erk activation does not depend on Sos and Grb2 in peripheral human T cells.


Please use this identifier to cite or link to this item: http://hdl.handle.net/10033/233572
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Title: TCR-mediated Erk activation does not depend on Sos and Grb2 in peripheral human T cells.
Authors: Warnecke, Nicole
Poltorak, Mateusz
Kowtharapu, Bhavani S
Arndt, Boerge
Stone, James C
Schraven, Burkhart
Simeoni, Luca
Affiliation: Institute of Molecular and Clinical Immunology, Otto-von-Guericke University, Leipziger Strasse 44, Magdeburg 39120, Germany.
Citation: TCR-mediated Erk activation does not depend on Sos and Grb2 in peripheral human T cells. 2012, 13 (4):386-91 EMBO Rep.
Journal: EMBO reports
Issue Date: Apr-2012
URI: http://hdl.handle.net/10033/233572
DOI: 10.1038/embor.2012.17
PubMed ID: 22344067
Abstract: Sos proteins are ubiquitously expressed activators of Ras. Lymphoid cells also express RasGRP1, another Ras activator. Sos and RasGRP1 are thought to cooperatively control full Ras activation upon T-cell receptor triggering. Using RNA interference, we evaluated whether this mechanism operates in primary human T cells. We found that T-cell antigen receptor (TCR)-mediated Erk activation requires RasGRP1, but not Grb2/Sos. Conversely, Grb2/Sos—but not RasGRP1—are required for IL2-mediated Erk activation. Thus, RasGRP1 and Grb2/Sos are insulators of signals that lead to Ras activation induced by different stimuli, rather than cooperating downstream of the TCR.
Type: Article
Language: en
ISSN: 1469-3178
Appears in Collections: publications of the department of immunocontrol (IMMK)

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