Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/93328
Type: Artigo de periódico
Title: Cd4+ T Cells Downregulate Bcl-2 In Germinal Centers
Author: Schenka A.A.
Muller S.
Fournie J.-J.
Capila F.
Vassallo J.
Delsol G.
Valitutti S.
Brousset P.
Abstract: Germinal centers (GCs) are the main site of T cell-dependent antibody responses. Upon antigen challenge, GCs comprise mostly B cells undergoing proliferation, somatic hypermutation and antigen-affinity selection. GC B cells down-modulate the expression of Bcl-2 protein and are highly sensitive to apoptosis to eliminate autoreactive or low-affinity cells. Bcl-2 is still expressed in a few GC cells, whose identity remains unclear. To address this issue, we examined by confocal microscopy the expression of Bcl-2 by different GC lymphocyte subsets in hyperplastic tonsils. We found that the vast majority of Bcl-2+ GC cells are T lymphocytes. Conversely, while in the mantle zone and in the interfollicular areas T cells are almost exclusively Bcl-2 +, in the GC, most T lymphocytes are Bcl-2-. In addition, most of the CD4+ GC T cells are Bcl-2-, while nearly 100% of the CD8+ GC T cells are Bcl-2+. The Bcl-2 downregulation by both B and CD4+ T GC cells supports the concept that these two subsets may undergo a selection process in this microenvironment. © 2005 Springer Science+Business Media, Inc.
Editor: 
Rights: fechado
Identifier DOI: 10.1007/s10875-005-4084-4
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-21244476769&partnerID=40&md5=ff05c562802f4259a232b721c23dec4c
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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