T细胞纤维连接蛋白:一种意想不到的炎症淋巴因子。

Lymphokine research Pub Date : 1990-01-01
H P Godfrey
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引用次数: 0

摘要

T细胞纤维连接蛋白(FN)是抗原和丝裂原激活人、鼠和豚鼠T淋巴细胞的产物。操作和功能上,T细胞FN是一种与迟发性超敏反应相关的淋巴因子。T细胞FN在飞摩尔浓度下可凝集单核吞噬细胞,并通过模型细胞外基质转移单核细胞和中性粒细胞,其活性是其他FN的1.1 × 10(4)至2.3 × 10(6)倍。它不作用于外周血淋巴细胞。T细胞FN介导的巨噬细胞凝集需要细胞代谢,依赖于多种类型的细胞表面蛋白受体与FN明胶和细胞结合结构域之间的相互作用。相反,由T细胞FN介导的人工基质介导的细胞移位是一个生物物理过程,依赖于应答细胞上的表面硫酸肝素与FN氨基末端肝素结合和明胶结合结构域之间的相互作用。克隆小鼠T细胞系产生FN的能力与其转移迟发性超敏反应的能力之间的相关性表明,T细胞FN的分泌可能是这些反应启动的重要因素。T细胞FN的双重活性可以增强吞噬效应细胞的内流,并在T细胞活化的组织部位保留单核细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T cell fibronectin: an unexpected inflammatory lymphokine.

T cell fibronectin (FN) is a product of antigen and mitogen activated human, murine and guinea pig T lymphocytes. Operationally and functionally, T cell FN is a lymphokine associated with delayed hypersensitivity. T cell FN acts at femtomolar concentrations to agglutinate mononuclear phagocytes and translocate monocytes and neutrophils through model extracellular matrices, and is 1.1 x 10(4) to 2.3 x 10(6) times more potent than other FN for these activities. It does not act on peripheral blood lymphocytes. Macrophage agglutination mediated by T cell FN requires cellular metabolism and depends on interactions between multiple classes of cell surface protein receptors and FN gelatin- and cell-binding domains. In contrast, translocation of cells through artificial matrices mediated by T cell FN is a biophysical process dependent on interactions between surface heparan sulfates on responding cells and FN amino-terminal heparin-binding and gelatin-binding domains. The correlation between the ability of cloned murine T cell lines to produce FN and their ability to transfer delayed hypersensitivity reactions suggests that secretion of T cell FN may be an important element in the initiation of these responses. The double activity of T cell FN could allow it to enhance influx of phagocytic effector cells and retain monocytes at tissue sites of T cell activation.

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