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一种新型固定剂改善了人类存档组织中核酸和蛋白质组分析的机会。

A novel fixative improves opportunities of nucleic acids and proteomic analysis in human archive's tissues.

作者信息

Stanta Giorgio, Mucelli Stefano Pozzi, Petrera Francesca, Bonin Serena, Bussolati Gianni

机构信息

Department of Clinical, Morphological and Technological Sciences, University of Trieste, 34149 Trieste, Italy.

出版信息

Diagn Mol Pathol. 2006 Jun;15(2):115-23. doi: 10.1097/00019606-200606000-00009.

Abstract

All tissues from biopsy or surgery origin are fixed and paraffin embedded as a routine procedure in the hospital departments of pathology. The traditional method of tissue preservation is the fixation in formalin, followed by paraffin embedding. In this way tissue's integrity is ensured also for future analyses, because there is no further chemical degradation of nucleic acids and proteins in tissues embedded in paraffin. After few sections for the histopathological examination the tissues are stored for decades in the hospital archives. Even if formalin fixation compromises the quality and integrity of nucleic acids, it has already been demonstrated that it is possible to recover and analyze DNA and RNA from these archive's tissues, even of autopsy origin. Protein analysis is on the contrary completely blocked, due to the fact that formalin fixation creates covalent links between proteins and the only way to study protein expression is immunohistochemistry. In this study we present our results concerning the use of a new formalin free fixative, the FineFIX. After extraction of nucleic acids, PCR and RT-PCR analyses were performed in DNA and RNA respectively. For DNA analysis it was possible to obtain amplicons of 2400 bps, while in formalin-fixed samples the maximum length achieved was less than 400 bps. RT-PCR analysis show that it was possible to study RNA fragments of 600 bps from FineFIX fixed tissues, against a maximum length of about 150 bps achieved by formalin-fixed tissues. These tissues were analyzed also by Western Blot analysis, showing that the proteins obtained from FineFIX treated samples are amenable and comparable in quality with those obtained from fresh frozen tissues. Protein extracts from FineFix treated tissues were also compared with fresh tissues'ones by two dimensional electrophoresis, demonstrating that the protein pattern were well comparable for number and distribution of the spots.

摘要

来自活检或手术的所有组织在医院病理科都按常规程序进行固定和石蜡包埋。传统的组织保存方法是用福尔马林固定,然后进行石蜡包埋。通过这种方式,即使是用于未来的分析,组织的完整性也能得到保证,因为石蜡包埋的组织中的核酸和蛋白质不会进一步发生化学降解。在进行了几部分组织病理学检查后,这些组织会在医院档案中保存数十年。即使福尔马林固定会损害核酸的质量和完整性,但已经证明,即使是来自尸检的存档组织,也有可能从中提取并分析DNA和RNA。相反,蛋白质分析则完全受阻,因为福尔马林固定会在蛋白质之间形成共价键,而研究蛋白质表达的唯一方法是免疫组织化学。在本研究中,我们展示了使用一种新型无福尔马林固定剂FineFIX的结果。提取核酸后,分别对DNA和RNA进行了PCR和RT-PCR分析。对于DNA分析,能够获得2400个碱基对的扩增子,而在福尔马林固定的样本中,获得的最大长度小于400个碱基对。RT-PCR分析表明,从FineFIX固定的组织中可以研究600个碱基对的RNA片段,而福尔马林固定的组织获得的最大长度约为150个碱基对。这些组织还通过蛋白质印迹分析进行了检测,结果表明从FineFIX处理的样本中获得的蛋白质在质量上与从新鲜冷冻组织中获得的蛋白质相当且易于分析。通过二维电泳还将FineFix处理组织的蛋白质提取物与新鲜组织的提取物进行了比较,结果表明蛋白质斑点的数量和分布具有良好的可比性。

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