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Identification and characterization of urokinase receptors in natural killer cells and T‐cell‐derived lymphokine activated killer cells

机译:天然杀伤细胞和T细胞来源的淋巴因子激活的杀伤细胞中尿激酶受体的鉴定和表征

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>Flourescence-activated cell scanning analysis of human blood cells revealed novel urokinase receptors in large granular lymphocytes and a small subset of T-cells (CD3+). Culturing of T-cells with interleukin-2 to generate CD3+ lymphokine-activated killer cells caused a large increase in urokinase binding, suggesting that the urokinase receptor is an activation antigen. The receptor in lymphocytes was similar to that in monocytes with regard to size, affinity and ligand specificity, but did not mediate degration of urokinase-inhibitor complexes. It is suggested that lymphocyte-bound pro-urokinase is activated, e.g. by the human T-cell specific serine proteinase. HuTSP-1, and thereby starts a cascade of plasminogen activation important for extravasation of the cells.
机译:对人血细胞的荧光激活细胞扫描分析显示,大颗粒淋巴细胞和一小部分T细胞(CD3 +)中存在新型尿激酶受体。用白介素2培养T细胞以生成CD3 +淋巴因子激活的杀伤细胞,导致尿激酶结合大大增加,这表明尿激酶受体是一种激活抗原。淋巴细胞的受体在大小,亲和力和配体特异性方面与单核细胞相似,但不介导尿激酶抑制剂复合物的降解。建议淋巴细胞结合的尿激酶原被激活,例如被激活。由人T细胞特异的丝氨酸蛋白酶。 HuTSP-1,从而开始级联的纤溶酶原激活,这对于细胞的渗出很重要。

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