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IL7-hCD25和IL7-Cre BAC转基因小鼠品系:用于分析表达IL-7细胞的新工具。

IL7-hCD25 and IL7-Cre BAC transgenic mouse lines: new tools for analysis of IL-7 expressing cells.

作者信息

Repass John F, Laurent Micheline N, Carter Carla, Reizis Boris, Bedford Mark T, Cardenas Kim, Narang Priyanka, Coles Mark, Richie Ellen R

机构信息

Department of Carcinogenesis, University of Texas MD Anderson Cancer Center, Science Park Research Division, Smithville, Texas 78957, USA.

出版信息

Genesis. 2009 Apr;47(4):281-7. doi: 10.1002/dvg.20497.

Abstract

IL-7 is a cytokine that is required for T-cell development and homeostasis as well as for lymph node organogenesis. Despite the importance of IL-7 in the immune system and its potential therapeutic relevance, questions remain regarding the sites of IL-7 synthesis, specific cell types involved and molecular mechanisms regulating IL-7 expression. To address these issues, we generated two bacterial artificial chromosome (BAC) transgenic mouse lines in which IL-7 regulatory elements drive expression of either Cre recombinase or a human CD25 (hCD25) cell surface reporter molecule. Expression of the IL-7.hCD25 BAC transgene, detected by reactivity with anti-hCD25 antibody, mimicked endogenous IL-7 expression. Fetal and adult tissues from crosses between IL-7.Cre transgenic mice and Rosa26R or R26-EYFP reporters demonstrated X-gal or YFP staining in tissues known to express endogenous IL-7 at some stage during development. These transgenic lines provide novel genetic tools to identify IL-7 producing cells in various tissues and to manipulate gene expression selectively in IL-7 expressing cells.

摘要

白细胞介素-7(IL-7)是一种细胞因子,对于T细胞的发育、稳态维持以及淋巴结器官发生而言必不可少。尽管IL-7在免疫系统中具有重要作用及其潜在的治疗意义,但关于IL-7的合成位点、所涉及的特定细胞类型以及调节IL-7表达的分子机制等问题依然存在。为了解决这些问题,我们构建了两种细菌人工染色体(BAC)转基因小鼠品系,其中IL-7调控元件驱动Cre重组酶或人CD25(hCD25)细胞表面报告分子的表达。通过与抗hCD25抗体反应检测到的IL-7.hCD25 BAC转基因的表达,模拟了内源性IL-7的表达。来自IL-7.Cre转基因小鼠与Rosa26R或R26-EYFP报告基因杂交的胎儿和成年组织,在已知在发育的某个阶段表达内源性IL-7的组织中显示出X-gal或YFP染色。这些转基因品系提供了新的遗传工具,用于鉴定各种组织中产生IL-7的细胞,并在表达IL-7的细胞中选择性地操纵基因表达。

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