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Molecular Networks Orchestrating GALT Development

机译:分子网络协调GALT的发展

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During evolution, the development of secondary lymphoid organs has evolved as a strategy to promote adaptive immune responses at sites of antigen sequestration. Mesenteric lymph nodes (LNs) and Peyer's patches (PPs) are localized in proximity to mucosal surfaces, and their development is coordinated by a series of temporally and spatially regulated molecular events involving the collaboration between hematopoietic, mesenchymal, and, for PPs, epithelial cells. Transcriptional control of cellular differentiation, production of cytokines as well as adhesion molecules are mandatory for organogenesis, recruitment of mature leukocytes, and lymphoid tissue organization. Similar to fetal and neonatal organogenesis, lymphoid tissue neoformation can occur in adult individuals at sites of chronic stimulation via cytokines and TNF-family member molecules. These molecules represent new therapeutic targets to manipulate the microenvironment during autoimmune diseases.
机译:在进化过程中,次级淋巴器官的发育已发展为在抗原螯合位点促进适应性免疫应答的策略。肠系膜淋巴结(LNs)和Peyer斑块(PPs)定位在粘膜表面附近,它们的发育由一系列时空调节的分子事件协调,这些事件涉及造血,间质以及PPs上皮细胞之间的协作。细胞分化的转录控制,细胞因子的产生以及粘附分子对于器官发生,成熟白细胞募集和淋巴组织的组织是必不可少的。与胎儿和新生儿器官发生相似,成年个体可通过细胞因子和TNF家族成员分子在慢性刺激部位发生淋巴组织新形成。这些分子代表了在自身免疫性疾病中操纵微环境的新治疗靶标。

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