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A requirement for the Rho-family GTP exchange factor Vav in positive and negative selection of thymocytes

  • Martin Turner
    ,
  • P. Joseph Mee
    ,
  • Alice E. Walters
    ,
  • Marian E. Quinn
    ,
  • Andrew L. Mellor
    ,
  • Rose Zamoyska
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

The T cell repertoire is shaped by positive and negative selection of thymocytes that express low levels of T cell receptor (TCR) and both CD4 and CD8. TCR-mediated signals that determine these selection processes are only partly understood. Vav, a GDP-GTP exchange factor for Rho-family proteins, is tyrosine phosphorylated following TCR stimulation, suggesting that it may transduce TCR signals. We now demonstrate that mice lacking Vav are viable and display a profound defect in the positive selection of both class I- and class II-restricted T cells. In contrast, Vav is not essential far negative selection, though in its absence negative selection is much less effective. Vav may influence the efficiency of TCR-induced selection events by regulating the intracellular calcium flux of thymocytes.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 451-460 (10 pages)

Journal (Volume, Issue Number)

Immunity (Volume 7, Issue 4)

Publication milestones

  • Published - 10/1997

Publication status

Published - 10/1997

ISSN

1074-7613

Publication IDs

  • Scopus: 0030719389
  • PubMed: 9354466

Publication metrics

Metrics

SciVal
FWCI
7.94
SciVal
Author count
7
SciVal
citations
247
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
48
Citation count
245

Funding Details

Correspondence should be addressed to V.L.J.T. (v-tybule@nimr. mrc.ac.uk). We thank C. Atkins for flow cytometric analysis, R. Szydto for statistical analysis, and Dimitris Kioussis, Patrick Costello, Owen Williams, and Tomasz Żal for advice and discussions. The work described here was supported by the Medical Research Council and in part by a grant from the Leukemia Research Fund (to V.L.J.T.).
FundersFunding numbers
LRF
-
MRC
-