A model for lymphatic regeneration in tissue repair of the intestinal muscle coat.

Hiroshi Shimoda, Seiji Kato
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引用次数: 15

Abstract

The gastrointestinal lymphatic system, which comprises a network of thin-walled vessels, is essential for the regulation of tissue fluid volume, immune function, and transport of fatty nutrients. The identification of specific lymphatic endothelial markers has facilitated analyses of lymphatic organization and lymphangiogenesis during individual development and tissue repair. The intestinal muscle coat producing motor activity develops a dense maze-like lymphatic network by vascular sprouting consisting of thin lymphatic endothelial projections and splitting of the vessels. The lymphatic regeneration in the tissue repair of the intestinal muscle coat is essentially attributable to sprouting from preexisting lymphatics, and it progresses vigorously with vascular maturation. The regrowing lymphatic endothelial cells exhibit structural changes indicating a high migratory potential and a close association with regenerating stromal cells. The upregulation of VEGF-C, a specific lymphangiogenic molecule, in a subpopulation of the stromal cells probably contributes to lymphatic regeneration by activating its receptor, VEGFR-3, on the regrowing lymphatic endothelial cells.

肠肌被组织修复中淋巴再生模型的建立。
胃肠道淋巴系统由薄壁血管网络组成,对组织液体体积的调节、免疫功能和脂肪营养物质的运输至关重要。特异性淋巴内皮标志物的鉴定有助于分析个体发育和组织修复过程中的淋巴组织和淋巴管生成。产生运动活动的肠肌被膜通过细小的淋巴内皮突起和血管的分裂形成密集的迷宫状淋巴网络。肠肌被组织修复中的淋巴再生本质上是由原有淋巴萌发而来,并随着血管的成熟而蓬勃发展。再生的淋巴内皮细胞表现出结构变化,表明其具有高迁移潜力,并与再生的基质细胞密切相关。在基质细胞亚群中,VEGF-C(一种特殊的淋巴管生成分子)的上调可能通过激活再生淋巴内皮细胞上的受体VEGFR-3来促进淋巴再生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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