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通过二氢罗丹明123和流式微量细胞荧光测定法诊断慢性肉芽肿病及其遗传方式。

Diagnosis of chronic granulomatous disease and of its mode of inheritance by dihydrorhodamine 123 and flow microcytofluorometry.

作者信息

Roesler J, Hecht M, Freihorst J, Lohmann-Matthes M L, Emmendörffer A

机构信息

Fraunhofer Institute ITA, Department of Immunobiology, Hannover, Federal Republic of Germany.

出版信息

Eur J Pediatr. 1991 Jan;150(3):161-5. doi: 10.1007/BF01963557.

Abstract

Dihydrorhodamine 123 (DHR) attached to membranes of granulocytes (PMN) and monocytes is caused to fluoresce by reactive oxygen intermediates (ROI) indicating the ability of phagocytes to produce these microbicide metabolites in a flow microcytofluorimeter. Whole blood samples from five boys with known chronic granulomatous disease (CGD) and from their mothers (and from one father and one grandmother), were examined following erythrocyte lysis in order to test this new method. An incubation period of 10 min with phorbol-myristate-acetate, followed by another 15 min incubation period with DHR before flow microcytofluorimetric analysis of 5 or 10 x 10(3) phagocytes, was sufficient to obtain the following results. PMN and monocytes from four patients with CGD could clearly not produce any ROI whereas cells from one patient displayed decreased activity in ROI production as compared to cells from a healthy donor. The X-linked mode of inheritance was detected in six carriers by the presence of two different cell populations (one normal ROI-producing and one negative or less active population). All the phagocytes from one mother produced ROI in normal amounts suggesting an autosomal mode of inheritance. All in all, the method presented provides a fast and most simple tool to diagnose CGD, to determine a decrease or total lack of ROI production and to establish the mode of inheritance of the disease.

摘要

附着于粒细胞(PMN)和单核细胞膜上的二氢罗丹明123(DHR)会被活性氧中间体(ROI)激发产生荧光,这表明吞噬细胞能够在流式微细胞荧光计中产生这些杀微生物代谢产物。对五名已知患有慢性肉芽肿病(CGD)的男孩及其母亲(以及一名父亲和一名祖母)的全血样本在红细胞裂解后进行检测,以测试这种新方法。在用佛波醇肉豆蔻酸酯乙酸酯孵育10分钟,然后在对5或10×10³个吞噬细胞进行流式微细胞荧光分析之前再用DHR孵育15分钟,足以获得以下结果。四名CGD患者的PMN和单核细胞显然无法产生任何ROI,而一名患者的细胞与健康供体的细胞相比,ROI产生活性降低。通过存在两种不同的细胞群体(一种正常产生ROI的群体和一种阴性或活性较低的群体),在六名携带者中检测到X连锁遗传模式。一名母亲的所有吞噬细胞都正常产生ROI,提示为常染色体遗传模式。总而言之,所介绍的方法为诊断CGD、确定ROI产生的减少或完全缺乏以及确定疾病的遗传模式提供了一种快速且极其简单的工具。

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