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小鼠畸胎瘤细胞系上的H-2 I类抗原表达

H-2 class I antigen expression on mouse teratocarcinoma cell lines.

作者信息

Démant P, Oudshoorn-Snoek M

出版信息

Immunogenetics. 1985;22(6):543-52. doi: 10.1007/BF00430302.

Abstract

Immunity against PCC3 teratocarcinoma cells (129, H-2b) was induced in allogeneic (C3H, H-2k) mice by preimmunization with L cells (C3H, H-2k) expressing cosmid-introduced Kb or Db genes, but not with nontransfected L cells. In addition, the growth of PCC3 cells in sublethally irradiated (C3H X B6-H-2bm1)F1 and (C3H X B6-H-2bm13)F1 mice bearing the Kbm1 and Dbm13 mutations, respectively, was either prevented, stopped, or delayed in comparison with the (C3H X B6)F1 (k X b) mice, which failed to reject the PCC3 cells. The teratocarcinoma line OC15S was exceptional because it reacted specifically with Kb- and Db-specific (but not Ib-specific) alloantisera, and because Kb- and Db-specific antibodies could be absorbed by OC15S cells. The subpopulation of OC15S cells bearing the ECMA-7 antigen characteristic for embryonic carcinoma (EC) cells was isolated by the fluorescence-activated cell sorter and was shown to react specifically with Kb- and Db-specific antisera. These experiments show that teratocarcinoma cells express antigens similar or identical to the K- and D-region products of differentiated cells. The lack of expression of class I antigens is thus neither a condition nor a consequence of the pluripotentiality of the EC cells. The exact nature of the major histocompatibility complex antigens on EC cells has yet to be established using the methods of molecular biology and biochemistry.

摘要

通过用表达黏粒导入的Kb或Db基因的L细胞(C3H,H-2k)进行预免疫,在同种异体(C3H,H-2k)小鼠中诱导了对PCC3畸胎瘤细胞(129,H-2b)的免疫,而未转染的L细胞则不能诱导免疫。此外,与未能排斥PCC3细胞的(C3H×B6)F1(k×b)小鼠相比,分别携带Kbm1和Dbm13突变的亚致死剂量照射的(C3H×B6-H-2bm1)F1和(C3H×B6-H-2bm13)F1小鼠中PCC3细胞的生长被阻止、停止或延迟。畸胎瘤细胞系OC15S是个例外,因为它能与Kb和Db特异性(但不是Ib特异性)同种异体抗血清发生特异性反应,并且Kb和Db特异性抗体可被OC15S细胞吸收。通过荧光激活细胞分选仪分离出具有胚胎癌(EC)细胞特征性的携带ECMA-7抗原的OC15S细胞亚群,并显示其能与Kb和Db特异性抗血清发生特异性反应。这些实验表明,畸胎瘤细胞表达的抗原与分化细胞的K区和D区产物相似或相同。因此,I类抗原的缺乏既不是EC细胞多能性的条件,也不是其结果。EC细胞上主要组织相容性复合体抗原的确切性质仍有待用分子生物学和生物化学方法来确定。

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