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关于组织的荧光和电子显微镜长期储存:从大鼠肝样品中得到的经验教训。

On the long-term storage of tissue for fluorescence and electron microscopy: lessons learned from rat liver samples.

机构信息

University of Sydney, School of Medical Sciences (Molecular and Cellular Biomedicine), Sydney, Australia.

Australian Centre for Microscopy and Microanalysis, The University of Sydney, Sydney, Camperdown, NSW, 2006, Australia.

出版信息

Histochem Cell Biol. 2024 Nov 27;163(1):12. doi: 10.1007/s00418-024-02334-5.

Abstract

Occasionally, tissue samples cannot be processed completely and are stored under varying conditions for extended periods. This is particularly beneficial in interinstitutional studies where a given research setting may lack the expertise or infrastructure for sample processing, imaging and data analysis. Currently, there is limited literature available on the controlled storage of biological tissues in primary fixatives for fluorescence and electron microscopy. In this contribution, we mimicked various tissue storage scenarios by taking different fixation conditions, storage temperatures and storage durations into account. Rat liver tissue was used for its well-known diversity of cellular ultrastructure and microscopy analysis. Fluorescent labelling of actin, DNA and lipids were employed in conjunction with high-resolution electron microscopy imaging. Herein, we tested three different fixative solutions (1.5% glutaraldehyde, 0.4% glutaraldehyde and 4% formaldehyde and 4% formaldehyde) and stored samples for 1-28 days at room temperature and refrigerator temperature. We found that liver tissue can be stored for up to 2 weeks in a 0.4% glutaraldehyde + 4% formaldehyde fixative solution, while still enabling reliable fluorescent labelling and ultrastructural studies. Ultrastructural integrity was eminent up to 1 month using either glutaraldehyde or formaldehyde fixation protocols. When liver tissue is fixed with a mixture of 0.4% glutaraldehyde and 4% formaldehyde and stored at 4 °C, it retains its capacity for electron microscopy analysis for several years, but loses its capacity for reliable fluorescent labelling studies. In conclusion, we demonstrated that liver tissue can be stored for extended periods enabling profound structure-function analysis across length scales.

摘要

偶尔,组织样本无法完全处理,并在不同条件下储存延长时间。这在机构间研究中特别有益,在给定的研究环境中,可能缺乏样本处理、成像和数据分析的专业知识或基础设施。目前,关于生物组织在荧光和电子显微镜中用初始固定剂进行控制储存的文献有限。在本研究中,我们通过考虑不同的固定条件、储存温度和储存时间来模拟各种组织储存情况。大鼠肝脏组织因其细胞超微结构的多样性和显微镜分析而被选用。我们结合使用了肌动蛋白、DNA 和脂质的荧光标记以及高分辨率电子显微镜成像。在此,我们测试了三种不同的固定液(1.5%戊二醛、0.4%戊二醛和 4%甲醛以及 4%甲醛),并将样本在室温下和冰箱温度下储存 1-28 天。我们发现,肝脏组织可以在 0.4%戊二醛+4%甲醛固定液中储存长达 2 周,同时仍然能够进行可靠的荧光标记和超微结构研究。使用戊二醛或甲醛固定方案,超微结构完整性在 1 个月内仍然显著。当肝脏组织用 0.4%戊二醛和 4%甲醛的混合物固定并储存在 4°C 时,它可以保持多年进行电子显微镜分析的能力,但失去了可靠的荧光标记研究的能力。总之,我们证明了肝脏组织可以储存很长时间,从而能够进行跨尺度的结构-功能分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee1/11602835/7ad84d6c8cb4/418_2024_2334_Fig1_HTML.jpg

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