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Thymic Microenvironment and Lymphoid Responses toSublethal Irradiation

机译:胸腺微环境和淋巴对亚致死辐射的反应。

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Sublethal irradiation of the murine thymus has been a useful tool for depleting the thymusof dividing immature thymocyte subsets, to sequence thymocyte differentiation eventsoccurring from radiation-resistant precursors. This massive reduction in thymocytes alsorepresents a model in which the bidirectional interplay between the thymic stromal cellsand lymphocytes can be investigated. The purpose of this study was thus twofold: toprecisely map the initiation of thymopoiesis as a prelude to assessing the effects of injectedmAb to novel thymic antigens; and to use a panel of mAbs to determine the alterations inthe thymic stroma during the T-cell depletion and reconstitution phases. The strikingfinding from this study was that following T-cell depletion, there was a marked upregulationof specific stromal antigens, which retracted with the reappearance of T cells. Thus,following sublethal irradiation, there are modifications in the thymic microenvironment thatmay be necessary to support renewed thymopoiesis and the complete restoration of thethymus involved the synchronous development of both the stromal and lymphocyticcomponents.
机译:鼠胸腺的亚致死辐射一直是一种有用的工具,可用于耗尽分裂的未成熟胸腺细胞亚群的胸腺,以对由抗辐射前体引起的胸腺细胞分化事件进行测序。胸腺细胞的这种大量减少也代表了一个模型,其中可以研究胸腺基质细胞和淋巴细胞之间的双向相互作用。因此,本研究的目的是双重的:准确绘制胸腺生成的起始图谱,以此作为评估注射的mAb对新型胸腺抗原作用的序幕;并使用一组单克隆抗体确定T细胞耗竭和重建阶段胸腺基质的变化。这项研究的惊人发现是,T细胞耗竭后,特定的基质抗原显着上调,随着T细胞的出现而缩回。因此,在致死性照射之后,胸腺微环境可能需要进行修饰,以支持新的胸腺生成,胸腺的完全恢复涉及基质和淋巴细胞成分的同步发展。

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