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人恶性黑色素瘤细胞系上常见急性淋巴细胞白血病抗原(CALLA)的表达

Expression of common acute lymphoblastic leukemia antigen (CALLA) on human malignant melanoma cell lines.

作者信息

Carrel S, Schmidt-Kessen A, Mach J P, Heumann D, Girardet C

出版信息

J Immunol. 1983 May;130(5):2456-60.

PMID:6339629
Abstract

Fifteen human melanoma cells lines were tested by an antibody-binding radioimmunoassay using a monoclonal antibody (A12) directed against the common acute lymphoblastic leukemia antigen (CALLA). Cells from six melanoma lines were found to react with this antibody. The level of antigen and the percentage of positive cells in these six melanoma lines showed wide variation, as demonstrated by analysis in the fluorescence-activated cell sorter (FACS). Immunoprecipitation of solubilized 125I-labeled membrane proteins from CALLA positive melanoma cells with A12 monoclonal antibody revealed a major polypeptide chain with an apparent m.w. of 100,000 daltons, characteristic for CALLA as determined on SDS-polyacrylamide gel electrophoresis. The expression of CALLA on MP-6 melanoma cells was modulated when the cells were cultured in the presence of A12 antibody. Reexpression of CALLA on these cells occurred within 5 days after transfer of the modulated cells into medium devoid of monoclonal antibody.

摘要

利用一种针对常见急性淋巴细胞白血病抗原(CALLA)的单克隆抗体(A12),通过抗体结合放射免疫测定法对15个人类黑色素瘤细胞系进行了检测。发现来自6个黑色素瘤细胞系的细胞与该抗体发生反应。通过荧光激活细胞分选仪(FACS)分析表明,这6个黑色素瘤细胞系中的抗原水平和阳性细胞百分比显示出很大差异。用A12单克隆抗体对CALLA阳性黑色素瘤细胞中溶解的125I标记膜蛋白进行免疫沉淀,揭示了一条主要的多肽链,其表观分子量为100,000道尔顿,这是SDS-聚丙烯酰胺凝胶电泳测定的CALLA的特征。当MP-6黑色素瘤细胞在A12抗体存在下培养时,CALLA在这些细胞上的表达受到调节。将受调节的细胞转移到不含单克隆抗体的培养基中后,这些细胞在5天内重新表达了CALLA。

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