Elliott B E, Haskill J S, Axelrad M A
J Exp Med. 1973 Nov 1;138(5):1133-43. doi: 10.1084/jem.138.5.1133.
Rosettes against SRBC were made from normal spleen cells. Although T rosettes tend to dissociate, they could be stabilized with 0.05% sodium azide. A clear separation of nonrosettes, T rosettes, and B rosettes was obtained by subjecting the suspension of splenic rosettes to velocity sedimentation at unit gravity. Each fraction was injected with either normal bone marrow cells or normal thymus cells with antigen into 650-R-irradiated hosts. Direct plaque-forming cells (PFC) were assayed in the spleens 7 days later. Synergism with thymus cells occurred only in the B-rosette fraction; PFC precursors therefore sedimented as B rosettes. Synergism with bone marrow cells occurred only in the nonrosette small lymphocyte fraction; helper cells therefore did not bind detectable numbers of sheep red blood cells (SRBC). Thus T rosettes are not helper cells in the direct PFC response of bone marrow B cells to SRBC.
抗绵羊红细胞(SRBC)玫瑰花结是由正常脾细胞制成的。虽然T玫瑰花结往往会解离,但可以用0.05%叠氮化钠使其稳定。通过使脾玫瑰花结悬液在单位重力下进行速度沉降,可将非玫瑰花结、T玫瑰花结和B玫瑰花结清晰分离。将每个组分与正常骨髓细胞或带有抗原的正常胸腺细胞一起注射到经650伦琴(R)照射的宿主体内。7天后在脾脏中检测直接溶血空斑形成细胞(PFC)。与胸腺细胞的协同作用仅发生在B玫瑰花结组分中;因此PFC前体细胞以B玫瑰花结形式沉降。与骨髓细胞的协同作用仅发生在非玫瑰花结小淋巴细胞组分中;因此辅助细胞不结合可检测数量的绵羊红细胞(SRBC)。因此,在骨髓B细胞对SRBC的直接PFC反应中,T玫瑰花结不是辅助细胞。