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现代病理学中酶组织化学的当前概念。

Current concepts of enzyme histochemistry in modern pathology.

作者信息

Meier-Ruge William A, Bruder Elisabeth

机构信息

Institute of Pathology, University Hospital Basel, Basel, Switzerland.

出版信息

Pathobiology. 2008;75(4):233-43. doi: 10.1159/000132384. Epub 2008 Jun 26.

Abstract

Enzyme histochemistry serves as a link between biochemistry and morphology. It is based on metabolization of a substrate provided to a tissue enzyme in its orthotopic localization. Visualization is accomplished with an insoluble dye product. It is a sensitive dynamic technique that mirrors even early metabolic imbalance of a pathological tissue lesion, combined with the advantage of histotopographic enzyme localization. With the advent of immunohistochemistry and DNA-oriented molecular pathology techniques, the potential of enzyme histochemistry currently tends to be underrecognized. This review aims to draw attention to the broad range of applications of this simple, rapid and inexpensive method. Alkaline phosphatase represents tissue barrier functions in brain capillaries, duodenal enterocyte and proximal kidney tubule brush borders. Decrease in enzyme histochemical alkaline phosphatase activity indicates serious functional impairment. Enzyme histochemical increase in lysosomal acid phosphatase activity is an early marker of ischemic tissue lesions. Over the last four decades, acetylcholinesterase enzyme histochemistry has proven to be the gold standard for the diagnosis of Hirschsprung disease and is one of the most commonly applied enzyme histochemical methods today. Chloroacetate esterase and tartrate-resistant phosphatase are both resistant to formalin fixation, EDTA decalcification and paraffin embedding. Early enzyme histochemical insight into development of a pathologic tissue lesion and evaluation of function and vitality of tissue enhance our understanding of the pathophysiology of diseases. In this process, enzyme histochemistry constitutes a valuable complement to conventional histology, immunohistochemistry and molecular pathology for both diagnostic and experimental pathology.

摘要

酶组织化学是生物化学与形态学之间的桥梁。它基于向原位定位的组织酶提供的底物的代谢。通过不溶性染料产物实现可视化。它是一种灵敏的动态技术,即使在病理组织病变的早期代谢失衡时也能反映出来,同时具有组织拓扑酶定位的优势。随着免疫组织化学和以DNA为导向的分子病理学技术的出现,酶组织化学的潜力目前往往未得到充分认识。本综述旨在提请人们注意这种简单、快速且廉价方法的广泛应用。碱性磷酸酶代表脑毛细血管、十二指肠肠上皮细胞和近端肾小管刷状缘的组织屏障功能。酶组织化学碱性磷酸酶活性降低表明严重的功能损害。溶酶体酸性磷酸酶活性的酶组织化学增加是缺血性组织病变的早期标志物。在过去的四十年里,乙酰胆碱酯酶酶组织化学已被证明是诊断先天性巨结肠的金标准,并且是当今最常用的酶组织化学方法之一。氯乙酸酯酶和抗酒石酸磷酸酶都对福尔马林固定、EDTA脱钙和石蜡包埋具有抗性。对病理组织病变发展的早期酶组织化学洞察以及对组织功能和活力的评估增强了我们对疾病病理生理学的理解。在此过程中,酶组织化学构成了对传统组织学、免疫组织化学和分子病理学在诊断和实验病理学方面的宝贵补充。

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