A glycophospholipid anchor is required for Qa-2-mediated T cell activation
- P. J. Robinson,
- M. Millrain,
- J. Antoniou,
- E. Simpson,
- A. L. Mellor
- MRC Clinical Research Centre,
- ,
- Medical Research Council
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
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
ISSN
0028-0836Publication IDs
- Scopus: 0024449097
- PubMed: 2530453
