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Comparison of peptides bound to spleen and thymus class II

  • Philippa Marrack(corresponding author)
    ,
  • Leszek Ignatowicz
    ,
  • John W. Kappler
    ,
  • Joel Boymel
    ,
  • John H. Freed
*Corresponding author for this work
  • University of Colorado Anschutz Medical Campus
    ,
  • Howard Hughes Medical Institute
    ,
  • National Jewish Medical and Research Center
Scholary Output:
Contribution to journal
Review article
Peer-review

Abstract

In the past we and others have suggested that positive selection of developing thymocytes may depend upon interaction between the αβ receptors on these cells and major histocompatibility complex (MHC) proteins bound to peptides found uniquely in the selecting tissue, thymus cortical epithelium. To test this hypothesis, peptides were isolated from MHC class II proteins of spleen, thymus cortical plus medullary epithelium, or thymus cortical epithelium alone. The results showed that the major peptides bound to class II on thymus cortical epithelium were also associated with spleen class II. Some peptides could only be detected in isolates from spleen, probably because of differences in the distribution or uptake of the donor proteins between spleen and thymus. Thus, although we found some tissue-specific distribution of self-peptides, our data suggest that there are no fundamental differences among these tissues in the occupancy of class II MHC by self-peptides. These results limit hypotheses which depend on a specialized mechanism of peptide generation and/or MHC class II loading to account for the positive selection of T cells on thymic cortical epithelium.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2173-2183 (11 pages)

Journal (Volume, Issue Number)

Journal of Experimental Medicine (Volume 178, Issue 6)

Publication milestones

  • Published - 12/01/1993

Publication status

Published - 12/01/1993

ISSN

0022-1007

Publication IDs

  • Scopus: 0027448853
  • PubMed: 8245790

Publication metrics

Metrics

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

PlumX

Citation count
175
Captures
23

Funding Details

FundersFunding numbers
NIH
-
NIAID
R01AI018785, R56AI017134, P01AI022295