Munechika N
Hokkaido Igaku Zasshi. 1985 Jul;60(4):593-601.
To study adaptive differentiation phenomenon of T lymphocytes, a number of irradiation chimeras constructed from various combinations of marrow cells and recipient mice were prepared, and Ly-1 T cell suppressor inducer factor (Ly-1 TsiF) and Ly-2 T cell suppressor factor (Ly-2 TsF) from these chimeras were analyzed for their ability to inhibit in vitro primary antibody responses to sheep erythrocytes (SRBC) of spleen cells from various strains of mice. AKR mice reconstructed with B10 marrow cells, [B10----AKR] chimeras, were able to produce Ly-1 TsiF and Ly-2 TsF following hyper-immunization with SRBC. The Ly-1 TsiF from [B10----AKR] chimeras suppressed antigen-specifically primary antibody responses to SRBC generated in the spleen cells of the same Igh-Vb haplotype as that of donor strains but not those in the cells of different Igh-V type. The Ly-2 TsF from [B10----AKR] chimeras was also shown to be donor restricted, but in this case restriction molecules were demonstrated to be H-2 products. Furthermore, the Ly-2 TsF from [B10----AKR] chimeras suppressed the responses seen in B10.A (3R) and B10.A (5R) mice but not those in B10.A (4R) mice, indicating that identity between the factor producing cells and target cells was required at the left side from E beta locus of the H-2 for the factor to show suppressive activity and that putative I-Jb was not involved in the suppression. Very similar results were obtained when Ly-1 TsiF and Ly-2 TsF from [B6----BALB/c] and [BALB/c----B6] chimeras were analyzed.(ABSTRACT TRUNCATED AT 250 WORDS)
为研究T淋巴细胞的适应性分化现象,制备了多种由骨髓细胞和受体小鼠不同组合构建的辐射嵌合体,并分析了这些嵌合体中Ly-1 T细胞抑制诱导因子(Ly-1 TsiF)和Ly-2 T细胞抑制因子(Ly-2 TsF)对不同品系小鼠脾细胞体外针对绵羊红细胞(SRBC)的初次抗体反应的抑制能力。用B10骨髓细胞重建的AKR小鼠,即[B10→AKR]嵌合体,在用SRBC进行超免疫后能够产生Ly-1 TsiF和Ly-2 TsF。[B10→AKR]嵌合体的Ly-1 TsiF抗原特异性地抑制了与供体品系相同Igh-Vb单倍型的脾细胞中产生的针对SRBC的初次抗体反应,但不抑制不同Igh-V类型细胞中的反应。[B10→AKR]嵌合体的Ly-2 TsF也显示为供体限制性,但在这种情况下,限制分子被证明是H-2产物。此外,[B10→AKR]嵌合体的Ly-2 TsF抑制了B10.A(3R)和B10.A(5R)小鼠中的反应,但不抑制B10.A(4R)小鼠中的反应,这表明为使该因子显示抑制活性,在H-2的Eβ基因座左侧,产生因子的细胞与靶细胞之间需要有同一性,并且推测的I-Jb不参与抑制作用。当分析[B6→BALB/c]和[BALB/c→B6]嵌合体的Ly-1 TsiF和Ly-2 TsF时,获得了非常相似的结果。(摘要截短于250字)