作者: DJ Veis , Ch L Sentman , EA Bach , SJ Korsmeyer , None
DOI:
关键词: T lymphocyte 、 Lymph node 、 Spleen 、 Antibody 、 Population 、 Flow cytometry 、 Immunology 、 Thymocyte 、 Biology 、 CD8 、 Molecular biology
摘要: Bcl-2, a proto-oncogene that can block apoptosis, was found to be expressed throughout the thymic medulla, but in only scattered cells cortex. In order determine precise distribution of Bcl-2 protein during thymocyte development, we utilized mAb specific for either mouse or human Bcl-2. Thymocyte subpopulations were assessed using three-color flow cytometry and saponin-permeabilization method. Staining adult thymocytes comparable, with 20 35% expressing nearly all CD4+ CD8+, CD3hi cells, 5 10% CD4+8+ cells. The CD4-8- population more variable, 25 40% 65 80% murine sorted very immature Pgp-1+/IL-2R alpha- subset had high percentage Bcl-2+ expression also examined fetal development. At day 15.5 16.5, 60 70% total By 17.5, overall fell levels 30%. present peripheral T from lymph node, spleen, blood at uniformly levels. vitro stimulation anti-CD3 anti-TCR antibodies increased cultures, could not induce even addition variety cytokines. These data suggest early double negative express lose differentiation positive stage. Thymocytes regain selection single state retain periphery.