首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-β receptor-IgG1 fusion protein
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Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-β receptor-IgG1 fusion protein

机译:脾脏结构破坏,但表达可溶性淋巴毒素-β受体-IgG1融合蛋白的小鼠正常淋巴结发育

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摘要

Early in ontogeny, the secondary lymphoid organs become populated with numerous cells of mesodermal origin which forms both the lymphoid and stromal elements. The critical receptor/ligand interactions necessary for lym- phoid organogenesis to occur are for the most part unknown. Although lymphotoxin-α (LTα) has been shown to be required for normal lymph node, Peyer's patch, and splenic develop- ment, it is unclear if soluble LTα3, and/or cell-bound lym- photoxin-αβ (LTαβ) mediate these developmental events.
机译:在个体发育的早期,次级淋巴器官被大量中胚层来源的细胞所占据,这些细胞同时形成淋巴和基质成分。淋巴器官发生所必需的关键受体/配体相互作用在很大程度上是未知的。尽管已证明正常的淋巴结,淋巴集结和脾脏发育需要淋巴毒素-α(LTα),但尚不清楚可溶性LTα3和/或细胞结合的淋巴-光毒素-αβ(LTαβ)是否介导这些作用。发展事件。

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