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EphA4 缺陷型小鼠中观察到的胸腺细胞发育改变伴随着胸腺上皮细胞和细胞外基质组织的变化。

Altered thymocyte development observed in EphA4-deficient mice courses with changes in both thymic epithelial and extracellular matrix organization.

机构信息

Department of Cell Biology, Faculty of Biology, Complutense University of Madrid, 28040, Madrid, Spain.

Health Research Institute, Hospital 12 de Octubre (imas12), 28041, Madrid, Spain.

出版信息

Cell Mol Life Sci. 2022 Nov 5;79(11):583. doi: 10.1007/s00018-022-04610-w.

Abstract

Eph receptors and their ligands, Ephrins, are involved in the thymocyte-thymic epithelial cell (TEC) interactions, key for the functional maturation of both thymocytes and thymic epithelium. Several years ago, we reported that the lack of EphA4, a Eph of the subfamily A, coursed with reduced proportions of double positive (DP) thymocytes apparently due to an altered thymic epithelial stroma [Munoz et al. in J Immunol 177:804-813, 2006]. In the present study, we reevaluate the lymphoid, epithelial, and extracellular matrix (ECM) phenotype of EphA4 mice grouped into three categories with respect to their proportions of DP thymocytes. Our results demonstrate a profound hypocellularity, specific alterations of T cell differentiation that affected not only DP thymocytes, but also double negative and single positive T cell subsets, as well as the proportions of positively and negatively selected thymocytes. In correlation, thymic histological organization changed markedly, especially in the cortex, as well as the proportions of both Ly51UEA-1 cortical TECs and Ly51UEA-1 medullary TECs. The alterations observed in the expression of ECM components (Fibronectin, Laminin, Collagen IV), integrin receptors (VLA-4, VLA-6), chemokines (CXCL12, CCL25, CCL21) and their receptors (CXCR4, CCR7, CCR9) and in vitro transwell assays on the capacity of migration of WT and mutant thymocytes suggest that the lack of EphA4 alters T-cell differentiation by presumably affecting cell adhesion between TECs and T-TEC interactions rather than by thymocyte migration.

摘要

Eph 受体及其配体 Ephrins 参与了胸腺细胞与胸腺上皮细胞(TEC)的相互作用,这对于胸腺细胞和胸腺上皮细胞的功能成熟都至关重要。几年前,我们报道了 EphA4(Eph 亚家族 A 的一种受体)缺失会导致双阳性(DP)胸腺细胞比例降低,这显然是由于胸腺上皮细胞基质发生了改变[Munoz 等人在《免疫学杂志》(J Immunol)177:804-813, 2006 年]。在本研究中,我们根据 DP 胸腺细胞的比例,将 EphA4 小鼠重新分为三组,评估了它们的淋巴细胞、上皮细胞和细胞外基质(ECM)表型。我们的结果表明,这些小鼠的组织细胞明显减少,T 细胞分化也出现了特异性改变,不仅影响 DP 胸腺细胞,还影响双阴性和单阳性 T 细胞亚群,以及阳性和阴性选择的胸腺细胞比例。相应地,胸腺组织学结构也发生了显著变化,尤其是皮质,还有 Ly51UEA-1 皮质 TEC 和 Ly51UEA-1 髓质 TEC 的比例也发生了变化。EphA4 缺失导致 ECM 成分(纤连蛋白、层粘连蛋白、IV 型胶原)、整合素受体(VLA-4、VLA-6)、趋化因子(CXCL12、CCL25、CCL21)及其受体(CXCR4、CCR7、CCR9)的表达以及 WT 和突变型胸腺细胞体外迁移能力的 Transwell 实验发生变化,这表明 EphA4 缺失通过影响 TEC 之间的细胞黏附以及 T-TEC 相互作用,从而改变 T 细胞分化,而不是通过胸腺细胞迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77f4/9637064/be1491ec3a2f/18_2022_4610_Fig1_HTML.jpg

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