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纤连蛋白在暴露于等离子体的材料表面的沉积:定量及生物学研究。

Deposition of fibronectin on material surfaces exposed to plasma: quantitative and biological studies.

作者信息

Grinnell F, Phan T V

出版信息

J Cell Physiol. 1983 Sep;116(3):289-96. doi: 10.1002/jcp.1041160305.

Abstract

Experiments were carried out to characterize plasma fibronectin deposition onto material surfaces exposed to plasma solutions. Under nonclotting conditions, the amount of fibronectin adsorption on the surfaces, determined by an indirect radioactive antibody assay, was maximal at low plasma concentrations (0.1%). At higher concentrations of plasma, other plasma proteins appeared to compete with and inhibit adsorption of fibronectin. Biological activity (fibronectin-promoted cell spreading) was also greatest at low plasma concentrations and decreased as the plasma concentration was raised. When surfaces were exposed to plasma under clotting conditions (i.e., addition of Ca2+ and thrombin), fibronectin deposition on the surfaces and biological activity remained constant or increased as the plasma concentration was raised. Based on indirect immunofluorescent antibody assays, the fibronectin deposited from clotting plasma appeared to be in a punctate distribution over the entire material surface and occasionally was associated with discrete fibrillar structures. The increased deposition of fibronectin from clotting plasma compared to nonclotting plasma (approximately a 10-fold difference with 10% plasma) was partially a result of covalent crosslinking of fibronectin to fibrin based upon studies with putrescine added to inhibit crosslinking during clotting. On the other hand, the increase in biological activity that occurred if the surfaces were exposed to clotting plasma was completely inhibited by putrescine, indicating that fibronectin had to be crosslinked to fibrin to have biological activity under these conditions. Finally, fibronectin deposition also occurred on surfaces exposed to whole blood and was markedly enhanced when clotting occurred.

摘要

开展实验以表征血浆纤连蛋白在暴露于血浆溶液的材料表面上的沉积情况。在非凝血条件下,通过间接放射性抗体测定法确定的表面纤连蛋白吸附量在低血浆浓度(0.1%)时最大。在较高血浆浓度下,其他血浆蛋白似乎会竞争并抑制纤连蛋白的吸附。生物活性(纤连蛋白促进的细胞铺展)在低血浆浓度时也最大,并随着血浆浓度升高而降低。当表面在凝血条件下(即添加Ca2+和凝血酶)暴露于血浆时,随着血浆浓度升高,表面纤连蛋白沉积和生物活性保持恒定或增加。基于间接免疫荧光抗体测定,从凝血血浆中沉积的纤连蛋白似乎在整个材料表面呈点状分布,偶尔与离散的纤维状结构相关。与非凝血血浆相比,凝血血浆中纤连蛋白沉积增加(10%血浆时约有10倍差异),部分是由于在凝血过程中添加腐胺以抑制交联的研究表明纤连蛋白与纤维蛋白发生了共价交联。另一方面,如果表面暴露于凝血血浆中发生的生物活性增加被腐胺完全抑制,这表明在这些条件下纤连蛋白必须与纤维蛋白交联才能具有生物活性。最后,纤连蛋白沉积也发生在暴露于全血的表面上,并且在发生凝血时会显著增强。

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