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人淋巴内皮细胞上连接黏附分子的表达

Expression of junctional adhesion molecules on the human lymphatic endothelium.

作者信息

Ueki Takeshi, Iwasawa Kana, Ishikawa Hiroyuki, Sawa Yoshihiko

机构信息

Department of Oral Growth and Development, Fukuoka Dental College, 2-15-1 Tamura, Sawara-Ku, Fukuoka, 814-0193, Japan.

出版信息

Microvasc Res. 2008 Mar;75(2):269-78. doi: 10.1016/j.mvr.2007.07.005. Epub 2007 Aug 3.

DOI:10.1016/j.mvr.2007.07.005
PMID:17822725
Abstract

Human lymphatic vessels express several leukocyte adhesion molecules. The study here investigated the expression of three junctional adhesion molecules (JAM) which are a newly reported glycoprotein family of adhesion molecules on human lymphatic endothelium. In this study, JAM-1 and JAM-3 but not JAM-2 were detected in cultured human neonatal dermal lymphatic endothelial cells (LEC) at the gene and protein levels by microarray, RT-PCR, real-time PCR, and immunohistochemical analysis. The JAM-1 and JAM-3 expression was not altered in the TNF-alpha-treated LEC or in the untreated cells. In human tissue, the expression of JAM-1, and the expression of JAM-1, JAM-2, and JAM-3 were observed in collecting lymphatic vessels of uninflamed small intestine, and in initial lymphatics of inflamed tongue and uninflamed gingival tissue. It is thought that JAM-2 mRNA could be produced in mature vascular endothelium but not in cultured cells, and that human intestinal and oral lymphatic vessels usually express JAM-1, JAM-2, and JAM-3. There were initial lymphatics simultaneously expressing JAM-1, JAM-2, and JAM-3 in the mucosal connective tissue papillae of gingival tissue. The three JAM expressions on the lymphatic endothelium may contribute to both seal the cell-cell contact at interendothelial junctions and also allow lymphocytes to transmigrate into lymphatic vessels from tissue, independent of inflammatory cytokines.

摘要

人类淋巴管表达多种白细胞粘附分子。本研究调查了三种连接粘附分子(JAM)的表达情况,这是一类新报道的存在于人类淋巴内皮上的粘附分子糖蛋白家族。在本研究中,通过微阵列、逆转录聚合酶链反应(RT-PCR)、实时定量聚合酶链反应(real-time PCR)和免疫组织化学分析,在培养的人新生儿真皮淋巴管内皮细胞(LEC)中从基因和蛋白质水平检测到了JAM-1和JAM-3,但未检测到JAM-2。在经肿瘤坏死因子-α(TNF-α)处理的LEC或未处理的细胞中,JAM-1和JAM-3的表达未发生改变。在人体组织中,在未发炎的小肠集合淋巴管以及发炎的舌部和未发炎的牙龈组织的初始淋巴管中观察到了JAM-1的表达,以及JAM-1、JAM-2和JAM-3的表达。据认为,JAM-2 mRNA可能在成熟血管内皮中产生,但在培养细胞中不产生,并且人类肠道和口腔淋巴管通常表达JAM-1、JAM-2和JAM-3。在牙龈组织的黏膜结缔组织乳头中有同时表达JAM-1、JAM-2和JAM-3的初始淋巴管。淋巴管内皮上这三种JAM的表达可能有助于封闭内皮细胞间连接的细胞-细胞接触,也能使淋巴细胞从组织迁移至淋巴管,且不依赖于炎性细胞因子。

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