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Expression of mucosal chemokines TECK/CCL25 and MEC/CCL28 during fetal development of the ovine mucosal immune system

机译:胎儿黏膜免疫系统发育过程中黏膜趋化因子TECK / CCL25和MEC / CCL28的表达

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摘要

CCL25/TECK and CCL28/MEC are CC chemokines primarily expressed in thymic dendritic cells and mucosal epithelial cells. The cognate receptors of CCL25 and CCL28, CCR9 and CCR10, respectively, are mainly expressed on T and B lymphocytes. In human, mouse and pig, CCL25 and CCL28 play a key role in the segregation and the compartmentalization of the mucosal immune system through recruitment of immune cells to specific locations. However, little is known about their role in the ontogeny of the mucosal immune system during fetal development. In the present paper, we report the cloning and the sequencing of ovine CCL25, CCL28, CCR9 and CCR10 and the subsequent assessment of their mRNA expression by q-polymerase chain reaction in several tissues, including thymus, gut-associated lymphoid tissue and mammary gland, from young and adult sheep and in the fetal lamb during the development of the immune system. CCL25 mRNA was highly expressed in thymus and gut while CCL28 mRNA was more expressed in large intestine, trachea, tonsils and mammary gland, especially at the end of gestation. These results are consistent with observations in other species suggesting similar roles for these chemokines in sheep. In fetuses, mRNA of CCL25, CCL28 and their receptors are expressed early in the thymus and mucosal tissues, including the small intestine and the nasal mucosa. Furthermore, their expression increased towards the end of gestation. Consequently, we hypothesize that CCL25 and CCL28 play an important role in the lymphocyte colonization of fetal tissues, enabling the development of a functional immune system.
机译:CCL25 / TECK和CCL28 / MEC是主要在胸腺树突状细胞和粘膜上皮细胞中表达的CC趋化因子。 CCL25和CCL28,CCR9和CCR10的同源受体分别主要在T和B淋巴细胞上表达。在人,小鼠和猪中,CCL25和CCL28通过将免疫细胞募集到特定位置,在粘膜免疫系统的分离和分隔中起关键作用。但是,关于它们在胎儿发育过程中在粘膜免疫系统的发育中的作用还知之甚少。在本文中,我们报告了绵羊CCL25,CCL28,CCR9和CCR10的克隆和测序,以及随后通过q-聚合酶链反应在包括胸腺,肠道相关淋巴样组织和乳腺在内的多种组织中对其mRNA表达的评估。 ,来自幼羊和成年绵羊以及在胎儿小羊期间免疫系统的发育。 CCL25 mRNA在胸腺和肠道中高表达,而CCL28 mRNA在大肠,气管,扁桃体和乳腺中表达更高,尤其是在妊娠末期。这些结果与其他物种的观察结果一致,表明这些趋化因子在绵羊中的作用相似。在胎儿中,CCL25,CCL28及其受体的mRNA在胸腺和粘膜组织(包括小肠和鼻粘膜)中早期表达。此外,它们的表达在妊娠快要结束时增加。因此,我们假设CCL25和CCL28在胎儿组织的淋巴细胞定殖中起重要作用,从而能够开发功能性免疫系统。

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