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诱导性T细胞克隆中新基因程序的顺序表达。

Sequential expression of new gene programs in inducer T-cell clones.

作者信息

Freeman G J, Clayberger C, DeKruyff R, Rosenblum D S, Cantor H

出版信息

Proc Natl Acad Sci U S A. 1983 Jul;80(13):4094-8. doi: 10.1073/pnas.80.13.4094.

Abstract

We have prepared a cDNA probe that detects genes that are rapidly and abundantly expressed after exposure of inducer T-lymphocyte clones to antigen or mitogen. All inducer cells tested express a characteristic set of new mRNA, and these mRNAs are not expressed after activation of other lymphocytes. This initial burst of mRNA synthesis is paralleled by synthesis and secretion of a family of polypeptides that mediate inducer cell activity, including T- and B-cell growth factors, interferon, and molecules that bind to antigen. Expression of this initial genetic program precedes mitosis and is replaced within 74 hr by a different genetic program, which may control further cell division. The action of these sequential sets of genetic programs defines two stages of the cell's differentiation and accounts for altered expression of the cell's immunological functions.

摘要

我们制备了一种cDNA探针,它能检测诱导性T淋巴细胞克隆暴露于抗原或有丝分裂原后迅速大量表达的基因。所有测试的诱导细胞都表达一组特征性的新mRNA,而这些mRNA在其他淋巴细胞激活后不表达。mRNA合成的这一初始爆发与介导诱导细胞活性的一族多肽的合成和分泌同时发生,这些多肽包括T细胞和B细胞生长因子、干扰素以及与抗原结合的分子。这一初始遗传程序的表达先于有丝分裂,并在74小时内被另一种不同的遗传程序所取代,后者可能控制进一步的细胞分裂。这些相继的遗传程序的作用定义了细胞分化的两个阶段,并解释了细胞免疫功能表达的改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ec/394207/6384d40cde1c/pnas00639-0226-a.jpg

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