Gutensohn W, Resta R, Misumi Y, Ikehara Y, Thompson L F
Institute of Anthropology and Human Genetics, University of Munich, Germany.
Cell Immunol. 1995 Apr 1;161(2):213-7. doi: 10.1006/cimm.1995.1029.
It had previously been shown that CD73 (ecto-5'-nucleotidase) expressed on 30% of normal human peripheral T-lymphocytes can mediate costimulatory signals in T cell activation. To check for a possible contribution of the catalytic property of CD73 to this function transfected cell lines were created. Using site-directed mutagenesis on human CD73 cDNA the codons of His92 and His194 were exchanged for alanine codons. Wild type and mutant cDNAs were cloned into an expression vector and stably expressed in the T cell line Jurkat. Surface expression as quantitated by immunofluorescence with anti CD73 mAbs was comparable in wild type and mutant transfectant clones, whereas in contrast to the wild type both His to Ala mutants completely lacked enzymatic activity. The Jurkat transfectants were stimulated with a combination of soluble anti-CD73 mAb and PMA and their response was quantitated by IL-2 production. The responses of different clones of wild type and mutant transfectants varied within a wide range; however, the ranges of wild type and mutants overlap. It is concluded that in order to transmit costimulatory signals CD73 does not require its catalytic activity.
先前的研究表明,在30%的正常人外周血T淋巴细胞上表达的CD73(胞外5'-核苷酸酶)可在T细胞活化过程中介导共刺激信号。为了检测CD73的催化特性对该功能的可能贡献,构建了转染细胞系。利用人CD73 cDNA的定点诱变技术,将His92和His194的密码子替换为丙氨酸密码子。将野生型和突变型cDNA克隆到表达载体中,并在T细胞系Jurkat中稳定表达。通过用抗CD73单克隆抗体进行免疫荧光定量检测,野生型和突变型转染克隆的表面表达相当,然而,与野生型相比,两个His突变为Ala的突变体完全缺乏酶活性。用可溶性抗CD73单克隆抗体和PMA联合刺激Jurkat转染细胞,并通过IL-2产生来定量其反应。野生型和突变型转染细胞不同克隆的反应在很宽的范围内变化;然而,野生型和突变体的范围有重叠。得出的结论是,为了传递共刺激信号,CD73不需要其催化活性。