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A glycophospholipid anchor is required for Qa-2-mediated T cell activation

  • P. J. Robinson
    ,
  • M. Millrain
    ,
  • J. Antoniou
    ,
  • E. Simpson
    ,
  • A. L. Mellor
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

A NUMBER of lymphocyte surface proteins are anchored in the cell membrane by glycophosphatidyl inositol (known as GPI) linkages instead of hydrophobic protein domains1,2. Treatment of mouse T lymphocytes with antibodies specific for two such proteins, Thy-1 and Ly-6, are known to induce proliferation3,4. We have found that antibodies specific for Qa-2, a GPI-anchored class I histocompatibility antigen5, can also activate mouse T cells. To determine whether the GPI-anchor is important for this pathway of cell activation, we produced transgenic mice expressing either normal GPI-anchored Qa-2, or Qa-2 molecules with a membrane-spanning protein domain derived from H-2. Our studies show that only lymphocytes from transgenic mice carrying GPI-anchored forms of Qa-2 can be activated in vitro by Qa-2-specific antibodies. We also show that transgenic mouse T cells expressing a GPI-anchored form of H-2Db can be activated by anti-H-2Db antibodies. These results strongly indicate that the GPI-anchor is critical for this pathway of T cell activation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 85-87 (3 pages)

Journal (Volume, Issue Number)

Nature (Volume 342, Issue 6245)

Publication milestones

  • Published - 1989

Publication status

Published - 1989

ISSN

0028-0836

Publication IDs

  • Scopus: 0024449097
  • PubMed: 2530453

Publication metrics

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Scopus
citations
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1

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