Singh S B, Tevethia S S
Infect Immun. 1973 Jan;7(1):46-52. doi: 10.1128/iai.7.1.46-52.1973.
The ability of hamster lymphoid cells to become cytotoxic in vitro to xenogeneic human cells after stimulation with concanavalin A (ConA) was investigated by using the cell-mediated (51)Cr release test. Cytotoxicity developed by 12 to 16 hr with peak values acquired within 24 hr of stimulation with ConA. The cytotoxicity was found to be mediated by the lymphoid cells themselves rather than by soluble substances. Spleen cells were more efficient than lymph node cells in releasing radioactivity from human cells. The concentration of mitogen was found to be critical in the development of cytotoxicity. ConA concentrations of 12.5 mug or less per culture conferred upon the lymphoid cells the capacity to release (51)Cr from target cells whereas higher concentrations were ineffective and even inhibitory. The cell-mediated cytotoxicity could be reversed by methyl alpha-d-glucopyranoside, but only during the first 8 to 12 hr of stimulation. The lytic reaction did not require the presence of ConA.
通过细胞介导的(51)铬释放试验,研究了仓鼠淋巴细胞在用刀豆球蛋白A(ConA)刺激后在体外对异种人类细胞产生细胞毒性的能力。细胞毒性在12至16小时内发展,在用ConA刺激24小时内达到峰值。发现细胞毒性是由淋巴细胞自身介导的,而不是由可溶性物质介导的。脾细胞在从人类细胞释放放射性方面比淋巴结细胞更有效。发现丝裂原的浓度在细胞毒性的发展中至关重要。每培养物中ConA浓度为12.5微克或更低时,淋巴细胞具有从靶细胞释放(51)铬的能力,而更高的浓度则无效甚至具有抑制作用。细胞介导的细胞毒性可以被α-D-吡喃葡萄糖苷甲基酯逆转,但仅在刺激的前8至12小时内。裂解反应不需要ConA的存在。