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组织微阵列分析在骨组织学研究中的应用。

Tissue Microarray Analysis Applied to Bone Diagenesis.

机构信息

Escola Paulista de Medicina-Universidade Federal de São Paulo, Department of Pathology, São Paulo 04023-062, Brazil.

Northumbria University, Faculty of Health and Life Sciences, Newcastle Upon Tyne NE1 8ST, United Kingdom.

出版信息

Sci Rep. 2017 Jan 4;7:39987. doi: 10.1038/srep39987.

Abstract

Taphonomic processes affecting bone post mortem are important in forensic, archaeological and palaeontological investigations. In this study, the application of tissue microarray (TMA) analysis to a sample of femoral bone specimens from 20 exhumed individuals of known period of burial and age at death is described. TMA allows multiplexing of subsamples, permitting standardized comparative analysis of adjacent sections in 3-D and of representative cross-sections of a large number of specimens. Standard hematoxylin and eosin, periodic acid-Schiff and silver methenamine, and picrosirius red staining, and CD31 and CD34 immunohistochemistry were applied to TMA sections. Osteocyte and osteocyte lacuna counts, percent bone matrix loss, and fungal spheroid element counts could be measured and collagen fibre bundles observed in all specimens. Decalcification with 7% nitric acid proceeded more rapidly than with 0.5 M EDTA and may offer better preservation of histological and cellular structure. No endothelial cells could be detected using CD31 and CD34 immunohistochemistry. Correlation between osteocytes per lacuna and age at death may reflect reported age-related responses to microdamage. Methodological limitations and caveats, and results of the TMA analysis of post mortem diagenesis in bone are discussed, and implications for DNA survival and recovery considered.

摘要

影响骨骼死后变化的埋藏学过程在法医、考古和古生物学研究中非常重要。本研究描述了组织微阵列(TMA)分析在 20 例挖掘出土的已知埋葬时间和死亡年龄的股骨骨标本中的应用。TMA 允许对亚样本进行多重分析,从而能够对 3D 中相邻切片进行标准化比较分析,并对大量标本的代表性横切片进行比较分析。对 TMA 切片进行了苏木精和伊红、过碘酸-Schiff 和银甲烯胺、以及苦味酸天狼星红染色,以及 CD31 和 CD34 免疫组织化学染色。可以在所有标本中测量骨陷窝内的骨细胞和骨陷窝数量、骨基质损失百分比和真菌球状体元素计数,并观察胶原纤维束。7%硝酸脱钙比 0.5 M EDTA 进行得更快,并且可能更好地保存组织学和细胞结构。使用 CD31 和 CD34 免疫组织化学染色无法检测到内皮细胞。每个骨陷窝中的骨细胞数与死亡年龄之间的相关性可能反映了与年龄相关的对微损伤的反应。讨论了 TMA 分析在骨骼死后变化中的方法学限制和注意事项,以及对 DNA 存活和回收的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aedb/5209720/3feaa46fadba/srep39987-f1.jpg

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