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补体蛋白D的肾脏滤过与分解代谢。

Renal filtration and catabolism of complement protein D.

作者信息

Volanakis J E, Barnum S R, Giddens M, Galla J H

出版信息

N Engl J Med. 1985 Feb 14;312(7):395-9. doi: 10.1056/NEJM198502143120702.

Abstract

Complement protein D, a serine protease participating in the formation of the C3 convertase of the alternative complement pathway, has the lowest molecular weight (23,750) and serum concentration of all complement proteins. In normal serum, D is the rate-limiting protease of the alternative pathway of complement activation. We report that the serum concentrations of D in 20 patients with chronic renal failure (mean +/- S.D., 0.42 +/- 0.28 mg per deciliter) and in 16 patients on long-term dialysis (1.53 +/- 0.39 mg per deciliter) were significantly higher (P less than 0.001) than in 22 healthy adults (0.18 +/- 0.04 mg per deciliter). In chronic renal failure the serum concentration of D correlated with that of creatinine (r = 0.75, P less than 0.001). The serum concentrations of D found in patients with renal failure reached and in some cases exceeded those at which the protease is no longer rate-limiting. Thus, enhanced activity of the alternative pathway of complement should be expected in patients with advanced renal failure. Urinary D was undetectable (less than 0.2 micrograms per deciliter) in 17 normal adults and either undetectable or below the concentration expected from the degree of proteinuria in 10 patients with nephrotic syndrome. However, in a patient with Fanconi's syndrome the urinary concentration of D (1.3 mg per deciliter) was an order of magnitude higher than the serum concentration, representing 0.5 per cent of the total protein. The urinary D in this patient had normal hemolytic activity, antigenicity, and size. These results indicate that D is filtered through the glomerular membrane and is probably catabolized in the proximal renal tubules.

摘要

补体蛋白D是一种参与替代补体途径C3转化酶形成的丝氨酸蛋白酶,在所有补体蛋白中分子量最低(23,750)且血清浓度最低。在正常血清中,D是补体激活替代途径的限速蛋白酶。我们报告,20例慢性肾衰竭患者(均值±标准差,0.42±0.28毫克/分升)和16例长期透析患者(1.53±0.39毫克/分升)的血清D浓度显著高于22例健康成年人(0.18±0.04毫克/分升)(P<0.001)。在慢性肾衰竭中,D的血清浓度与肌酐浓度相关(r = 0.75,P<0.001)。肾衰竭患者中发现的D血清浓度达到且在某些情况下超过了该蛋白酶不再是限速酶时的浓度。因此,预计晚期肾衰竭患者的补体替代途径活性增强。17例正常成年人尿中未检测到D(<0.2微克/分升),10例肾病综合征患者中要么未检测到D,要么其浓度低于根据蛋白尿程度预期的浓度。然而,在一名范科尼综合征患者中,尿中D的浓度(1.3毫克/分升)比血清浓度高一个数量级,占总蛋白的0.5%。该患者尿中的D具有正常的溶血活性、抗原性和大小。这些结果表明,D可通过肾小球滤过膜滤过,可能在近端肾小管中被分解代谢。

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