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源自结膜上皮细胞的中性粒细胞趋化因子:初步生化特性分析

Neutrophil chemotactic factors derived from conjunctival epithelial cells: preliminary biochemical characterization.

作者信息

Ehlers W H, Fishman J B, Donshik P C, Williams W, Elgebaly S A

机构信息

Surgical Research Center, Division of Ophthalmology, University of Connecticut, School of Medicine, Farmington 06032.

出版信息

CLAO J. 1991 Jan;17(1):65-8.

PMID:2007289
Abstract

We have previously reported on the release of neutrophil chemotactic factors (NCF) from injured conjunctival tissue. The present study was designed to biochemically characterize these conjunctiva-derived chemotactic factors and determine their biological activities. Bulbar conjunctiva was surgically removed from a rabbit eye and incubated with 250 microL of minimal essential medium (MEM) for 6 hours at 37 degrees C in a 5% CO2 atmosphere. Chemotactic activity was assayed using modified Boyden chambers with rabbit peritoneal neutrophils as indicator cells. Following treatment with subtilisin protease for 90 minutes, chemotactic activity of the conjunctival factors was reduced by 74%. Similarly, activity was lost after heating at 56 degrees C for 60 minutes (41% inhibition). Using ultrafiltration techniques, we showed that the majority of the chemotactic activity remained above a 100 kilodalton filter, suggesting the existence of high molecular weight factors. We also showed that the conjunctival factors are not glycoproteins and bind to both anion and cation exchange resins. When 100 microL of conjunctival supernatant was injected in the superior tarsal conjunctiva of rabbits, significant recruitment of neutrophils was evident by 4 hours. Control rabbits injected with MEM did not show neutrophil recruitment. Results of these studies indicate that NCF from traumatized conjunctival tissue are proteins (and not glycoproteins) of high molecular weight, heat labile, exhibit anionic and cationic charges, and are active in vivo.

摘要

我们之前曾报道过受伤结膜组织释放中性粒细胞趋化因子(NCF)的情况。本研究旨在对这些源自结膜的趋化因子进行生化特性分析,并确定其生物活性。从兔眼手术切除球结膜,并在5%二氧化碳气氛中于37℃下与250微升基本培养基(MEM)孵育6小时。使用改良的博伊登小室,以兔腹腔中性粒细胞作为指示细胞来测定趋化活性。用枯草杆菌蛋白酶处理90分钟后,结膜因子的趋化活性降低了74%。同样,在56℃加热60分钟后活性丧失(抑制率41%)。使用超滤技术,我们发现大部分趋化活性保留在100千道尔顿的滤膜之上,表明存在高分子量因子。我们还表明结膜因子不是糖蛋白,并且能与阴离子和阳离子交换树脂结合。当将100微升结膜上清液注射到兔上睑结膜时,4小时后明显可见中性粒细胞大量募集。注射MEM的对照兔未显示中性粒细胞募集。这些研究结果表明,来自创伤结膜组织的NCF是高分子量的蛋白质(而非糖蛋白),对热不稳定,带有阴离子和阳离子电荷,并且在体内具有活性。

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