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II类抗原阴性患者和突变B细胞系代表至少三种,可能四种由互补分析定义的不同遗传缺陷。

Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis.

作者信息

Bénichou B, Strominger J L

机构信息

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, MA 02138.

出版信息

Proc Natl Acad Sci U S A. 1991 May 15;88(10):4285-8. doi: 10.1073/pnas.88.10.4285.

Abstract

Expression of class II major histocompatibility complex antigens in defective B-lymphoblastoid cell lines from patients with class II antigen deficiency and from in vitro mutants generated with the same phenotype was studied. By heterogenetic fusion experiments, at least three, and probably four, complementation groups were defined. Furthermore, clone 13 (a DR-, DP-, but DQ+ cell line) appeared to belong to the RJ2.2.5 complementation group, for which all other members are DR-, DP-, and also DQ-. Thus, it is hypothesized that the cell lines of this group lack the activity of a gene that can differentially regulate the DR/DP and the DQ promoters.

摘要

研究了来自II类抗原缺陷患者的缺陷性B淋巴母细胞系以及具有相同表型的体外突变体中II类主要组织相容性复合体抗原的表达。通过异种融合实验,确定了至少三个,可能是四个互补群。此外,克隆13(一种DR -、DP - 但DQ + 的细胞系)似乎属于RJ2.2.5互补群,该互补群的所有其他成员均为DR -、DP - 且DQ -。因此,推测该组细胞系缺乏一个能够差异调节DR/DP和DQ启动子的基因的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/51643/7928d14c9b70/pnas01060-0237-a.jpg

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