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在对胸腺白血病抗体和豚鼠补体具有抗性的小鼠白血病细胞表面膜上检测胸腺白血病抗原。

Detection of thymus leukemia antigens on the surface membranes of murine leukemia cells resistant to thymus leukemia antibodies and guinea pig complement.

作者信息

Liang W, Cohen E P

出版信息

J Natl Cancer Inst. 1977 Apr;58(4):1079-86. doi: 10.1093/jnci/58.4.1079.

Abstract

The thymus leukemia (TL) antigens of ASL-1 murine leukemia reversibly disappeared from the membranes of cells exposed to TL antisera; the cells acquired resistance to fresh TL antiserum and complement (antigenic modulation). Three independent methods, however, indicated that the acquisition of complement resistance preceded the complete disappearance of TL antigens from the cell surface. Modulated cells reduced known titers of TL antisera by absorption; they stained positively in immunofluorescence studies involving TL antibodies and fluorescence-labeled rabbit anti-mouse immunoglobulin. TL antigens labeled previously with 125I were recovered by immunoprecipitation from cellular extracts prepared with nonionic detergent. Continued exposure of the cells to TL antiserum led to virtually complete disappearance of the antigens. Similar results were obtained for RADA-1 cells, another murine leukemia that forms TL antigens, although in this instance the cells were resistant to the cytolytic effects of TL antisera and guinea pig complement (GPC) without prior exposure to TL antibodies. The density of TL antigens remaining on the surface of different TL(+) cell types failed to correlate with resistance to TL antibodies and GPC. Cells from F, hybrids of TL(+) and TL(-) mouse strains formed TL antigens and were susceptible to TL antibodies and GPC even though the density of TL antigens formed by the susceptible cells was less than the density of TL antigens formed by modulated cells. Stable somatic hybrids of RADA-1 cells and TL(-) cells formed TL antigens at lower density than did RADA-1 cells and lysed in the presence of aliquots of the TL antisera and GPC used in previous tests.

摘要

ASL-1小鼠白血病的胸腺白血病(TL)抗原在暴露于TL抗血清的细胞表面膜上可逆性消失;细胞获得了对新鲜TL抗血清和补体的抗性(抗原调制)。然而,三种独立的方法表明,补体抗性的获得先于TL抗原从细胞表面完全消失。经调制的细胞通过吸收降低了已知效价的TL抗血清;在涉及TL抗体和荧光标记的兔抗小鼠免疫球蛋白的免疫荧光研究中,它们呈阳性染色。先前用125I标记的TL抗原通过免疫沉淀从用非离子去污剂制备的细胞提取物中回收。细胞持续暴露于TL抗血清导致抗原几乎完全消失。对于另一种形成TL抗原的小鼠白血病RADA-1细胞也获得了类似的结果,尽管在这种情况下,细胞在未事先暴露于TL抗体的情况下对TL抗血清和豚鼠补体(GPC)的溶细胞作用具有抗性。不同TL(+)细胞类型表面残留的TL抗原密度与对TL抗体和GPC的抗性无关。来自TL(+)和TL(-)小鼠品系的F1杂种细胞形成TL抗原,并且易受TL抗体和GPC的影响,尽管易感细胞形成的TL抗原密度低于经调制细胞形成的TL抗原密度。RADA-1细胞与TL(-)细胞的稳定体细胞杂种形成的TL抗原密度低于RADA-1细胞,并且在先前试验中使用的TL抗血清和GPC的等分试样存在下裂解。

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