Owen F L
J Immunol. 1980 Mar;124(3):1411-7.
The product of a new genetic locus closely linked to Igh-1 in the mouse has previously been shown to be expressed on T cells by using an in vitro fluorescent antibody assay. In vivo studies reported here show the determinant coded for by that locus is expressed in unimmunized animals on the precursor for a suppressor T cell regulating a primary response to SRBC. Antisera raised in allotype congenic animals by immunization with suppressor T cells (Ts) for the ARS.CRI stimulate Lyt2+3+ suppressor cells for unrelated antigens. The suppressive effects of the serum can be absorbed with T cells but not with B cells. Suppression of an IgM PFC response in allotype congenic animals confirms close linkage of the marker to Igh-1 but not to H-2. This determinant is expressed on Ts cells for many antigens and may represent a heavy chain linked "constant" portion of the antigen-specific receptor.
先前通过体外荧光抗体测定法已表明,与小鼠Igh-1紧密连锁的一个新基因座的产物在T细胞上表达。本文报道的体内研究表明,该基因座编码的决定簇在未免疫动物中表达于调节对SRBC初次反应的抑制性T细胞的前体上。通过用针对ARS.CRI的抑制性T细胞(Ts)免疫同种异型近交系动物产生的抗血清,可刺激针对无关抗原的Lyt2+3+抑制性细胞。血清的抑制作用可被T细胞吸收,但不能被B细胞吸收。在同种异型近交系动物中对IgM PFC反应的抑制证实了该标记与Igh-1紧密连锁,但与H-2不连锁。该决定簇在针对多种抗原的Ts细胞上表达,可能代表抗原特异性受体的重链连接的“恒定”部分。