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以W/Fu C58(NT)D作为融合亲本分离大鼠/大鼠T细胞杂交瘤。

Isolation of rat/rat T cell hybrids using W/Fu C58(NT)D as fusion partner.

作者信息

Curling E, Slade C, Hutchinson I, Morris P

机构信息

Nuffield Department of Surgery, University of Oxford, U.K.

出版信息

J Immunol Methods. 1988 Apr 6;108(1-2):171-8. doi: 10.1016/0022-1759(88)90416-4.

Abstract

Functional rat/rat T cell hybrids were isolated for the first time by the fusion of spleen cells from rats tolerized to the hapten TNP to a HAT-sensitive rat thymoma (C58(NT)D). 11 fusions using different protocols were attempted to assess the optimal conditions for high hybridization frequency of the desired specificity. Interestingly, the cell density requirement of the non-transformed fusion partner took precedence over that of the C58 cell line, i.e., rat cells needed to be at high density after fusion, but others have reported that mouse cells prefer a much lower density even when the same line (C58) is used. Six fusions yielded hybridomas with between 3% and 70% of wells containing hybrids after three weeks of culture, depending on the protocol used. Phenotypically, all of the hybrids and clones tested expressed the W3/25 (rat CD4) antigen, but no OX-8 (rat CD8) or immunoglobulin molecules. A minority of hybrids were found to secrete factors able to suppress (a) proliferation, (b) antibody production, and (c) cells bearing IL-2 receptors, but none appeared to suppress the production of IL-2 itself. In contrast to non-transformed rat T cell lines, the T hybrids isolated were easy to grow to high densities, clone and freeze without the need to add exogenous antigen or lymphokines to the cultures at any stage.

摘要

通过将对半抗原TNP耐受的大鼠脾细胞与对HAT敏感的大鼠胸腺瘤(C58(NT)D)融合,首次分离出了功能性大鼠/大鼠T细胞杂交瘤。尝试了11次使用不同方案的融合,以评估获得所需特异性高杂交频率的最佳条件。有趣的是,未转化融合伙伴的细胞密度要求优先于C58细胞系,即融合后大鼠细胞需要处于高密度,但其他人报告说,即使使用相同的细胞系(C58),小鼠细胞更喜欢低得多的密度。根据所使用的方案,6次融合产生了杂交瘤,培养三周后,3%至70%的孔中含有杂交瘤。从表型上看,所有测试的杂交瘤和克隆都表达W3/25(大鼠CD4)抗原,但不表达OX-8(大鼠CD8)或免疫球蛋白分子。发现少数杂交瘤分泌能够抑制(a)增殖、(b)抗体产生和(c)携带IL-2受体的细胞的因子,但似乎没有一个能抑制IL-2本身的产生。与未转化的大鼠T细胞系不同,分离出的T杂交瘤易于生长到高密度、克隆和冷冻,在任何阶段都无需向培养物中添加外源性抗原或淋巴因子。

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