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Maternal Microchimerism Leads to the Presence of Interleukin-2 in Interleukin-2 Knock out Mice: Implications for the Role of Interleukin-2 in Thymic Function

机译:母体微嵌合体导致白细胞介素2敲除小鼠中白细胞介素2的存在:白细胞介素2在胸腺功能中的作用的暗示。

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摘要

The role of interleukin-2 (IL-2) in thymic development is uncertain. Not surprisingly, IL-2 knockout (KO) mice have been used to address this question. However, as we report here, such mice are chimeric, containing both IL-2 KO cells and IL-2-expressing cells transferred in utero from their heterozygous mothers. These cells produce IL-2 in amounts detectable by conventional means, and their presence in lymphoid tissues confounds efforts to define the true IL-2 KO phenotype. To minimize the amount of IL-2 available to the thymus, we subjected recombinase activating gene-1 KO mice to bone marrow transplantation using IL-2 KO donors, and then followed the reconstitution of the thymus. The thymuses of these mice became increasingly aberrant over time, including abnormalities in both stromal cells and thymocytes. These results demonstrate that IL-2 is critical to several aspects of thymic function, a finding previously obscured by the presence of IL-2 in IL-2 KO mice.
机译:白细胞介素2(IL-2)在胸腺发育中的作用尚不确定。毫不奇怪,IL-2基因敲除(KO)小鼠已被用来解决这个问题。但是,正如我们在此报告的那样,此类小鼠是嵌合的,既包含从其杂合子母亲的子宫内转移而来的IL-2 KO细胞和IL-2表达细胞。这些细胞产生的IL-2的量可通过常规方法检测到,并且它们在淋巴组织中的存在使定义真正的IL-2 KO表型的努力变得混乱。为了使可用于胸腺的IL-2的量最小化,我们使用IL-2 KO供体对重组酶激活基因1 KO小鼠进行了骨髓移植,然后进行了胸腺的重建。随着时间的推移,这些小鼠的胸腺变得越来越异常,包括基质细胞和胸腺细胞的异常。这些结果表明,IL-2对于胸腺功能的多个方面至关重要,这一发现先前因IL-2 KO小鼠中IL-2的存在而被掩盖。

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