Impact of Social Confrontation on Rat CD4 T Cells Bearing Different CD45R Isoforms |
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Authors: | Volker Stefanski George F. Solomon Arthur S. Kling John Thomas Susan Plaeger |
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Affiliation: | aNorman Cousins Program in Psychoneuroimmunology, School of Medicine, UCLA, Los Angeles, California, 90095;bDepartment of Psychiatry, VA Medical Center, Sepulveda, California, 91343;cClinical Immunology, Department of Pediatrics, School of Medicine, University of California, Los Angeles, California, 90095 |
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Abstract: | The impact of social defeat on lymphocyte subpopulations and T helper subsets was investigated in Long Evans rats. CD4 T helper cell subsets with distinct functional properties and different cytokine profiles can be distinguished by using the mAbs OX-22 (anti-CD45RC) and OX-7 (anti-CD90, Thy1.1). Male intruders were exposed for 2, 6, or 48 h to aggressive resident pairs. All intruders were attacked upon introduction and were defeated as indicated by frequent display of full submissive postures. After 2 and 48 h of confrontation, drastic but differential effects on blood leukocyte numbers, CD4 and CD8a cells, and CD4 subsets were evident. However, after 6 h of confrontation most lymphocyte subset numbers corresponded to baseline levels. Focusing on CD4 subsets after 2 h of confrontation, we demonstrated that only the number of the CD45RC−CD90−subset declines, whereas neither the number of the CD45RC+CD90−subset nor the number of the CD45RC−CD90+subset (recent thymic emigrants) was influenced. Con A stimulation of sorted subsets identified the CD45RC−CD90−as a poor producer of IFN-γ. The data clearly demonstrate that social factors might differentially influence not only T cell subsets but also T helper cell subsets with distinct cytokine profiles in a possibly time-dependent manner. Such a stress-induced shift toward a CD45RC+CD90−-dominated milieu may have important consequences in interpreting results obtained from mitogenic stimulation of blood lymphocytes and cytokine production profiles measured after such a stimulation. In addition, a shift toward a CD45RC+CD90−dominance may modify the type and magnitude of immune response, at least temporarily. |
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