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首页> 外文期刊>The journal of immunology >Cutting Edge: Ectopic Expression of the Chemokine TCA4/SLC Is Sufficient to Trigger Lymphoid Neogenesis
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Cutting Edge: Ectopic Expression of the Chemokine TCA4/SLC Is Sufficient to Trigger Lymphoid Neogenesis

机译:前沿:趋化因子TCA4 / SLC的异位表达足以触发淋巴新生

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To test whether accumulation of naive lymphocytes is sufficient to trigger lymphoid development, we generated mice with islet expression of the chemokine TCA4/SLC. This chemokine is specific for naive lymphocytes and mature dendritic cells (DC) which express the CCR7 receptor. Islets initially developed accumulations of T cells with DC, with scattered B cells at the perimeter. These infiltrates consolidated into organized lymphoid tissue, with high endothelial venules and stromal reticulum. Infiltrate lymphocytes showed a naive CD44low CD25? CD69? phenotype, though half were CD62L negative. When backcrossed to RAG-1 knockout, DC were not recruited. Interestingly, islet lymphoid tissue developed in backcrosses to Ikaros knockout mice despite the absence of normal peripheral nodes. Our results indicate that TCA4/SLC can induce the development and organization of lymphoid tissue through diffential recruitment of T and B lymphocytes and secondary effects on stromal cell development.
机译:为了测试幼稚淋巴细胞的积累是否足以触发淋巴样发育,我们生成了具有胰岛趋化因子TCA4 / SLC表达的小鼠。这种趋化因子特异于表达CCR7受体的幼稚淋巴细胞和成熟树突状细胞(DC)。胰岛最初形成T细胞与DC的积累,周围散布着B细胞。这些浸润巩固形成有组织的淋巴组织,并具有高内皮微静脉和间质网。浸润淋巴细胞显示幼稚的CD44low CD25? CD69?表型,尽管一半是CD62L阴性。当回交至RAG-1基因敲除时,DC未募集。有趣的是,尽管缺乏正常的外周淋巴结,胰岛淋巴样组织仍与伊卡罗斯基因敲除小鼠回交。我们的结果表明,TCA4 / SLC可以通过T和B淋巴细胞的差异募集以及对基质细胞发育的继发效应来诱导淋巴组织的发育和组织。

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