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PMID: 2307834 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Antigen presentation by resting B cells. Effectiveness at inducing T cell proliferation is determined by costimulatory signals, not T cell receptor occupancy.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 144 ·No. 5 ·1990-03-01 ·Pages 1585-90

Jenkins MK, Burrell E, Ashwell JD

Abstract

Resting B cells stimulated the proliferation of two T cell clones much less efficiently than T cell-depleted low-density APC. In contrast, low-density cells and resting B cells stimulated the clones to produce similar levels of inositol phosphates, a rapid biochemical event dependent only on occupancy of the TCR. The inefficient stimulation of T cell proliferation by resting B cell APC was dramatically improved by the addition of allogeneic low-density accessory cells incapable of being recognized by the TCR on the responding T cells. The results are most consistent with a model where low-density and resting B cell APC display similar amounts of Ag/Ia molecule complexes capable of being recognized by the TCR on the responding T cells but differ in the provision of costimulatory signals that, together with TCR occupancy, are required for IL-2 production.

MeSH Terms
Animals Antigen-Presenting Cells/immunology B-Lymphocytes/immunology Inositol Phosphates/metabolism Interleukin-1/pharmacology Interleukin-6/pharmacology Lymphocyte Activation/drug effects Lymphocyte Cooperation/drug effects Lymphokines/metabolism Mice Mice, Inbred Strains Receptors, Antigen, T-Cell/physiology T-Lymphocytes/immunology
Chemicals
Inositol Phosphates Interleukin-1 Interleukin-6 Lymphokines Receptors, Antigen, T-Cell
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jenkins M K
Department of Microbiology, University of Minnesota Medical School, Minneapolis 55455.
Burrell E
Ashwell J D
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1990-03-01
Pages
1585-90
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI-27998 · United States
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