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人尿激酶型纤溶酶原激活剂氨基末端片段与U937单核细胞上特定受体的分化增强结合。

Differentiation-enhanced binding of the amino-terminal fragment of human urokinase plasminogen activator to a specific receptor on U937 monocytes.

作者信息

Stoppelli M P, Corti A, Soffientini A, Cassani G, Blasi F, Assoian R K

出版信息

Proc Natl Acad Sci U S A. 1985 Aug;82(15):4939-43. doi: 10.1073/pnas.82.15.4939.

Abstract

The purified amino-terminal fragment (ATF) of human urokinase plasminogen activator (residues 1-135), which is not required for activation of plasminogen, binds with high affinity to specific plasma membrane receptors on U937 monocytes. Intact urokinase efficiently competes for 125I-labeled ATF binding; 50% competition occurs with 1 nM urokinase. A large part of receptor-bound urokinase remains on the cell surface for at least 2 hr at 37 degrees C. Differentiation of U937 monocytes into macrophage-like cells specifically increases ATF binding 10- to 20-fold. These results suggest an important role for urokinase in monocyte/macrophage biology: the native enzyme binds to the cells with the amino-terminal domain; the catalytic, carboxyl-terminal domain remains exposed on the cell surface to stimulate localized proteolysis and facilitate cell migration.

摘要

人尿激酶型纤溶酶原激活剂的纯化氨基末端片段(ATF,第1至135位氨基酸残基),其对于纤溶酶原的激活并非必需,它能以高亲和力与U937单核细胞上的特定质膜受体结合。完整的尿激酶能有效竞争125I标记的ATF结合;1 nM尿激酶即可产生50%的竞争。在37℃下,很大一部分与受体结合的尿激酶至少在细胞表面留存2小时。U937单核细胞分化为巨噬细胞样细胞会使ATF结合特异性增加10至20倍。这些结果表明尿激酶在单核细胞/巨噬细胞生物学中具有重要作用:天然酶通过氨基末端结构域与细胞结合;催化性的羧基末端结构域则暴露在细胞表面以刺激局部蛋白水解并促进细胞迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27bb/390473/79db1f3eb02f/pnas00355-0085-a.jpg

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