Dariush Fahimi H
Division of Medical Cell Biology, Department of Anatomy and Cell Biology, University of Heidelberg, Im Neuenheimer Feld 307, 69120 Heidelberg, Germany.
Histochem Cell Biol. 2009 Apr;131(4):437-40. doi: 10.1007/s00418-009-0562-8. Epub 2009 Feb 14.
The historical circumstances that led to the discovery of the 3,3'-diamino-benzidine (DAB) method for staining of peroxisomes 40 years ago are reviewed. In the course of studies on the uptake and absorption of horse radish peroxidase in mammalian liver, in sections incubated for detection of peroxidase activity in DAB, it was noted that peroxisomes also stained positively for peroxidase activity. Subsequently, it was revealed that the peroxidatic activity of catalase, which is abundantly present in peroxisomes, is responsible for that staining. This notion was confirmed in quantitative biochemical studies with crystalline beef liver catalase and in tracer studies using catalase as an ultrastructural tracer. The application of the DAB method led to the discovery of peroxisomes as a ubiquitous eukaryotic cell organelle, attracting great interest in their investigation in biomedical research.
回顾了40年前导致发现用于过氧化物酶体染色的3,3'-二氨基联苯胺(DAB)方法的历史背景。在对哺乳动物肝脏中辣根过氧化物酶的摄取和吸收进行研究的过程中,在为检测DAB中的过氧化物酶活性而孵育的切片中,注意到过氧化物酶体对过氧化物酶活性也呈阳性染色。随后发现,过氧化物酶体中大量存在的过氧化氢酶的过氧化物酶活性是导致这种染色的原因。这一观点在使用结晶牛肝过氧化氢酶的定量生化研究以及使用过氧化氢酶作为超微结构示踪剂的示踪研究中得到了证实。DAB方法的应用导致了过氧化物酶体作为一种普遍存在的真核细胞器的发现,引起了生物医学研究中对其研究的极大兴趣。