一套预处理试剂,包括改良配方固定和脱钙,有助于对福尔马林固定石蜡包埋骨髓穿刺活检组织进行免疫组化和 DNA 分析。

IF 2.3 4区 生物学 Q4 CELL BIOLOGY Acta histochemica Pub Date : 2024-09-06 DOI:10.1016/j.acthis.2024.152188
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引用次数: 0

摘要

骨髓活检取决于组织形态、免疫组化染色和分子检测。从临床标本采集到病理报告,骨髓样本都需要进行组织预处理,但在这一过程中,蛋白质和核酸往往会因固定和脱钙溶液中的酸而发生改变。在我们的研究中,我们提出了一种简便有效的预处理方案,并利用组织形态学、IHC 染色和分子病理学分析比较了这种新型预处理方案(Set 2)和现有的传统预处理流程(Set 1)。与第一套方案相比,第二套方案样本中的粒细胞 IHC 标记显示出更密集的染色。第2套方案的DNA产量更高,碎片更少;此外,用第2套方案处理的样本随后还可用于FISH和DNA测序检测。与传统预处理相比,我们优化的新型预处理方案能更好地保护蛋白质和 DNA 分子,同时保持良好的细胞形态。新型预处理试剂可为更多实验室对骨髓活检样本进行预处理和科学研究提供参考。
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A set of pretreatment reagents including improved formula fixation and decalcification facilitating immunohistochemistry and DNA analyses of formalin-fixed paraffin-embedded bone marrow trephine biopsy

Bone marrow biopsy depends on tissue morphology, immunohistochemical staining, and moleculardetection. Tissue pretreatment is required for bone marrow samples, from clinical specimen acquisition to pathological reporting, but during the process, proteins and nucleic acids are often altered because of the acid in fixation and decalcification solutions. In our study, we present an easy and effective pretreatment protocol and compared this novel pretreatment protocol (Set 2) with an existing traditional pretreatment process (Set 1) using tissue morphology, IHC staining, and molecular pathological analyses. Granulocytic IHC markers showed more intensive staining in samples of Set 2 than in those of Set 1. The Set 2 protocol provided a higher DNA yield and less fragmentation; moreover, samples processed with the Set 2 protocol could be subsequently used in FISH and DNA sequencing assays. Our optimized novel pretreatment protocol could better protect proteins and DNA molecules while maintaining good cell morphology compared to traditional pretreatment The novel pretreatment reagents could role as a reference by more laboratories for pretreating bone marrow biopsy samples and scientific research.

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来源期刊
Acta histochemica
Acta histochemica 生物-细胞生物学
CiteScore
4.60
自引率
4.00%
发文量
107
审稿时长
23 days
期刊介绍: Acta histochemica, a journal of structural biochemistry of cells and tissues, publishes original research articles, short communications, reviews, letters to the editor, meeting reports and abstracts of meetings. The aim of the journal is to provide a forum for the cytochemical and histochemical research community in the life sciences, including cell biology, biotechnology, neurobiology, immunobiology, pathology, pharmacology, botany, zoology and environmental and toxicological research. The journal focuses on new developments in cytochemistry and histochemistry and their applications. Manuscripts reporting on studies of living cells and tissues are particularly welcome. Understanding the complexity of cells and tissues, i.e. their biocomplexity and biodiversity, is a major goal of the journal and reports on this topic are especially encouraged. Original research articles, short communications and reviews that report on new developments in cytochemistry and histochemistry are welcomed, especially when molecular biology is combined with the use of advanced microscopical techniques including image analysis and cytometry. Letters to the editor should comment or interpret previously published articles in the journal to trigger scientific discussions. Meeting reports are considered to be very important publications in the journal because they are excellent opportunities to present state-of-the-art overviews of fields in research where the developments are fast and hard to follow. Authors of meeting reports should consult the editors before writing a report. The editorial policy of the editors and the editorial board is rapid publication. Once a manuscript is received by one of the editors, an editorial decision about acceptance, revision or rejection will be taken within a month. It is the aim of the publishers to have a manuscript published within three months after the manuscript has been accepted
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