The JI PBL Intereron Source
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Molina, I. J.
Right arrow Articles by Huber, B. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Molina, I. J.
Right arrow Articles by Huber, B. T.

The Journal of Immunology, Vol 143, Issue 1 39-44, Copyright © 1989 by American Association of Immunologists


ARTICLES

Macrophages and T cells do not express Mlsa determinants

IJ Molina, NA Cannon, R Hyman and BT Huber
Department of Pathology, Tufts University School of Medicine, Boston, MA 02111.

In order to test the tissue distribution of Mlsa determinants, we have generated highly purified stimulator cell populations. First, Mlsa expression in bone marrow derived macrophages (M phi) of Mlsa genotype was tested in primary MLR and on Mlsa-specific T cell hybridomas (THy). Second, a similar experimental approach was used to analyze thioglycolate, peptone or Con A elicited peritoneal M phi. In all cases, these M phi cell populations were able to generate an excellent alloresponse, whereas no functional Mlsa determinants could be detected. Third, to further investigate whether the expression of Mlsa is lymphocyte specific, but dependent on expression of class II molecules, we have transfected I-Ek alpha and beta cDNA into a panel of thymomas of Mlsa genotype. Although we achieved a high level of surface I-Ek expression in all of these T cell tumors, none of them was able to trigger the Mlsa-specific THy. These results strongly suggest that Mlsa expression is limited to B cells. It is likely that Mlsa is a tissue- specific self-peptide that associates with class II molecules.


This article has been cited by other articles:


Home page
J. Immunol.Home page
S. Vacheron, S. A. Luther, and H. Acha-Orbea
Preferential Infection of Immature Dendritic Cells and B Cells by Mouse Mammary Tumor Virus
J. Immunol., April 1, 2002; 168(7): 3470 - 3476.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
P. P. L. Chiu, A. M. Jevnikar, and J. S. Danska
Genetic Control of T and B Lymphocyte Activation in Nonobese Diabetic Mice
J. Immunol., December 15, 2001; 167(12): 7169 - 7179.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
Webb SR and J Sprent
Induction of neonatal tolerance to Mlsa antigens by CD8+ T cells
Science, June 29, 1990; 248(4963): 1643 - 1646.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1989 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1989 by The American Association of Immunologists, Inc. All rights reserved.