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次要组织相容性抗原在小鼠胚胎癌细胞及其早期分化衍生物上受到发育调控。

Minor histocompatibility antigens are developmentally regulated on murine embryonal carcinoma cells and their early differentiated derivatives.

作者信息

Avner P, Simmler M C

出版信息

Cell Differ. 1985 Aug;17(2):115-23. doi: 10.1016/0045-6039(85)90477-4.

Abstract

Differences in the expression of minor histocompatibility (Hm) alloantigens on two mouse embryonal carcinoma (EC) cell lines and the PYS-2 and T.D.M.-1 differentiated derivatives have been demonstrated by their ability to elicit a cytolytic T lymphocyte response. Experiments involving the use of various responder-target strain combinations and recombinant inbred mice strains have shown that: (1) there are major differences in Hm expression on EC cells compared with differentiated derivatives whose Hm expression appears more like that of adult splenocytes; (2) although both EC cell lines show reduced Hm immunogenicity compared with adult splenocytes, major differences in the expression and possible presentation of Hm between the F9 and PCC3 EC cell lines can be detected by in vivo priming and by in vitro cold competition target experiments. These observations are discussed in relation to the differences in allograft rejection patterns observed with PCC3 and F9 and to possible differences in developmental staging of these cell lines.

摘要

通过两种小鼠胚胎癌(EC)细胞系以及PYS - 2和T.D.M.-1分化衍生物引发细胞毒性T淋巴细胞反应的能力,已证明它们在次要组织相容性(Hm)同种异体抗原表达上存在差异。涉及使用各种应答者 - 靶标品系组合和重组近交小鼠品系的实验表明:(1)与分化衍生物相比,EC细胞上的Hm表达存在主要差异,分化衍生物的Hm表达更类似于成年脾细胞;(2)尽管与成年脾细胞相比,两种EC细胞系均显示出Hm免疫原性降低,但通过体内致敏和体外冷竞争靶标实验,可以检测到F9和PCC3 EC细胞系之间Hm表达和可能呈递方面的主要差异。结合PCC3和F9观察到的同种异体移植排斥模式差异以及这些细胞系发育阶段可能存在的差异,对这些观察结果进行了讨论。

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