首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Antigen-specific suppression in genetic responder mice to L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT). Characterization of conventional and hybridoma-derived factors produced by suppressor T cells from mice injected as neonates with syngeneic GAT macrophages
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Antigen-specific suppression in genetic responder mice to L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT). Characterization of conventional and hybridoma-derived factors produced by suppressor T cells from mice injected as neonates with syngeneic GAT macrophages

机译:在遗传应答小鼠中对L-谷氨酸60-L-丙氨酸30-L-酪氨酸10(GAT)的抗原特异性抑制。常规和杂交瘤来源的因子的表征这些因子是由新生小鼠经同源GAT巨噬细胞注射后产生的抑制性T细胞产生的

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摘要

Spleen cells from C57BL/10 mice injected with syngeneic B10 L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT)-pulsed macrophages (GAT-M phi) within 18 h of birth were unable to respond to soluble GAT, GAT- methylated bovine serum albumin, or B10 GAT-M phi as adults. Spleen cells from these neonatally treated mice responded at control levels to GAT presented in allogeneic M phi and to sheep erythrocytes. Partially purified T cells from these neonatally treated mice suppressed responses by syngeneic virgin, but not primed, spleen cells in an antigen-specific manner and acted during the early phases of the response. These responder GAT-specific suppressor T cells (GAT-TSR) were sensitive to anti-Thy-1 + C and 500-rad irradiation and have the phenotype Ly-1-2+, I-J+; GAT-TSR cells can only suppress responses by spleen cells syngeneic with the GAT-TSR cells at the I-J subregion of H- 2. Restimulation of these Ts cells with syngeneic GAT-M phi induces an antigen-specific suppressor factor within the supernatant fluid. The factor, GAT-TsFR, is a glycoprotein with a molecular weight between 48,000 and 63,000, as determined by gel filtration chromatography using isotonic buffers; it bears serologically detectable determinants encoded by the I-J subregion of the H-2 complex, has an antigen-binding site for GAT and L-glutamic acid50-L-tyrosine50, and shares idiotypic determinants with anti-GAT antibodies. The presence of GAT-TsFR in the first 36 h of in vitro culture is required for significant suppression. Furthermore, only responses by spleen cell syngeneic with the cells producing GAT-TsFR at the I-J subregion are suppressed. The fusion of GAT-TsFR-producing cells with BW5147 resulted in generation of two hybridomas with properties and characteristics identical to those of the conventional GAT-TsFR with one exception: conventional and hybridoma 372.D6.5 GAT-TsFR only suppress responses by spleen cells of the I-Jb haplotype, whereas suppression mediated by the second hybridoma GAT-TsFR (372.B3.5) is genetically unrestricted. These hybridoma GAT-TsFR are compared with nonresponder GAT-Ts factor (GAT- TsF) and these responder and nonresponder GAT-TsF are considered in the context of suppressor pathways.
机译:出生后18小时内注射同基因B10 L-谷氨酸60-L-丙氨酸30-L-酪氨酸10(GAT)脉冲巨噬细胞(GAT-M phi)的C57BL / 10小鼠的脾细胞无法对可溶性GAT,GAT-甲基化的牛血清白蛋白或成年的B10 GAT-M phi。这些新生小鼠的脾细胞在控制水平上对同种异体M phi中的GAT和绵羊红细胞有反应。这些新生小鼠的部分纯化的T细胞以抗原特异性方式抑制了同基因初生脾脏细胞的反应,但未引发这些脾细胞,并在反应的早期起作用。这些响应者GAT特异性抑制性T细胞(GAT-TSR)对抗Thy-1 + C和500-rad辐射敏感,并具有Ly-1-2 +,I-J +表型。 GAT-TSR细胞只能抑制与H-2的I-J子区域的GAT-TSR细胞同质的脾细胞的应答。用同源GAT-M phi对这些Ts细胞进行再刺激会在上清液中诱导抗原特异性抑制因子。因子GAT-TsFR是一种糖蛋白,分子量介于48,000至63,000之间,通过等渗缓冲液的凝胶过滤色谱法测定;它具有由H-2复合物的I-J子区域编码的可通过血清学检测的决定簇,具有GAT和L-谷氨酸50-L-酪氨酸50的抗原结合位点,并与抗GAT抗体共享独特型决定簇。显着抑制需要在体外​​培养的前36小时内存在GAT-TsFR。此外,仅抑制了与在I-J子区域产生GAT-TsFR的细胞同质的脾细胞的应答。产生GAT-TsFR的细胞与BW5147融合,产生了两个杂交瘤,其性质和特征与常规GAT-TsFR相同,但有一个例外:常规和杂交瘤372.D6.5 GAT-TsFR仅抑制脾脏的应答I-Jb单倍型细胞,而第二种杂交瘤GAT-TsFR(372.B3.5)介导的抑制作用在遗传上不受限制。将这些杂交瘤GAT-TsFR与无应答GAT-TsF因子(GAT-TsF)进行比较,并在抑制途径中考虑这些有应答和无应答GAT-TsF。

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