Bugando Medical Centre, Department of Molecular Histopathology, Catholic University Health Allied Sciences, P.O. Box 1464 Mwanza, Tanzania.
Department of Pathology, Catholic University of Leuven, B-3000 Leuven, Belgium.
Int J Mol Sci. 2021 Mar 12;22(6):2899. doi: 10.3390/ijms22062899.
The revolutionary evolution in science and technology over the last few decades has made it possible to face more adequately three main challenges of modern medicine: changes in old diseases, the appearance of new diseases, and diseases that are unknown (mostly genetic), despite research efforts. In this paper we review the road travelled by pathologists in search of a method based upon the use of routine instruments and techniques which once were available for research only. The application to tissue studies of techniques from immunology, molecular biology, and genetics has allowed dynamic interpretations of biological phenomena with special regard to gene regulation and expression. That implies stepwise investigations, including light microscopy, immunohistochemistry, in situ hybridization, electron microscopy, molecular histopathology, protein crystallography, and gene sequencing, in order to progress from suggestive features detectable in routinely stained preparations to more characteristic, specific, and finally, pathognomonic features. Hematoxylin and Eosin (H&E)-stained preparations and appropriate immunohistochemical stains have enabled the recognition of phenotypic changes which may reflect genotypic alterations. That has been the case with hepatocytic inclusions detected in H&E-stained preparations, which appeared to correspond to secretory proteins that, due to genetic mutations, were retained within the rough endoplasmic reticulum (RER) and were deficient in plasma. The identification of this phenomenon affecting the molecules alpha-1-antitrypsin and fibrinogen has led to the discovery of a new field of cell organelle pathology, endoplasmic reticulum storage disease(s) (ERSD). Over fifty years, pathologists have wandered through a dark forest of complicated molecules with strange conformations, and by detailed observations in simple histopathological sections, accompanied by a growing background of molecular techniques and revelations, have been able to recognize and identify arrays of grotesque polypeptide arrangements.
在过去几十年中,科学技术的革命性发展使得我们能够更好地应对现代医学的三大主要挑战:旧疾病的变化、新疾病的出现以及尽管进行了研究但仍未知的疾病(主要是遗传疾病)。在本文中,我们回顾了病理学家在寻找一种基于常规仪器和技术的方法方面所走过的道路,这些技术以前仅可用于研究。将免疫学、分子生物学和遗传学技术应用于组织研究,使得可以对基因调控和表达等生物现象进行动态解释。这意味着需要进行逐步的研究,包括光镜、免疫组织化学、原位杂交、电子显微镜、分子组织病理学、蛋白质晶体学和基因测序,以便从常规染色标本中可检测到的提示性特征发展为更具特征性、特异性,最终为特征性的特征。苏木精和伊红(H&E)染色标本和适当的免疫组织化学染色使得能够识别可能反映基因型改变的表型变化。在 H&E 染色标本中检测到的肝细胞包涵体就是这种情况,这些包涵体似乎对应于分泌蛋白,由于基因突变,这些蛋白被保留在内质网(RER)中并缺乏血浆。鉴定出这种影响分子α-1-抗胰蛋白酶和纤维蛋白原的现象,导致了细胞细胞器病理学的一个新领域的发现,即内质网贮积病(ERSD)。在过去的五十年中,病理学家在一个充满复杂分子和奇异构象的黑暗森林中徘徊,通过对简单组织病理学切片的详细观察,结合不断发展的分子技术和启示,能够识别和鉴定一系列奇异的多肽排列。