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Activated Ras signals differentiation and expansion of CD4+8+ thymocytes.

机译:激活的Ras信号指示CD4 + 8 +胸腺细胞的分化和扩增。

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摘要

We describe a novel approach to assay the ability of particular gene products to signal transitions in lymphocyte differentiation in vivo. The method involves transfection of test expression constructs into RAG-1-deficient embryonic stem cells, which are subsequently assayed by the RAG-2-deficient blastocyst complementation approach. We have used this method to demonstrate that expression of activated Ras in CD4-8- (double negative, DN) prothymocytes in vivo induces their differentiation into small CD4+8+ (double positive, DP) cortical thymocytes with accompanying expansion to normal thymocyte numbers. However, activated Ras expression in DP cells does not cause proliferation or maturation to CD4+8- or CD4-8+ (single positive) thymocytes. Therefore, signaling through Ras is sufficient for promoting differentiation of DN to DP cells, but further differentiation requires the activity of additional signaling pathways.
机译:我们描述了一种新颖的方法来分析特定基因产物在体内淋巴细胞分化中信号转变的能力。该方法涉及将测试表达构建体转染至RAG-1缺陷型胚胎干细胞中,随后通过RAG-2缺陷型胚泡互补方法对其进行分析。我们已经使用这种方法来证明激活的Ras在体内CD4-8-(双阴性,DN)前胸腺细胞中的表达诱导其分化为小的CD4 + 8 +(双阳性,DP)皮层胸腺细胞,并伴随着正常胸腺细胞数量的增加。但是,激活的Ras表达在DP细胞中不会引起CD4 + 8-或CD4-8 +(单阳性)胸腺细胞增殖或成熟。因此,通过Ras进行信号传导足以促进DN向DP细胞的分化,但进一步的分化则需要其他信号通路的活性。

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