Simple method of thawing cryo-stored samples preserves ultrastructural features in electron microscopy
Autor: | Gottfried Dohr, Nadja Kupper, Dagmar Kolb, Markus Galhuber, Grazyna Kwapiszewska, Andrea Olschewski, Andreas Prokesch, Elisabeth Gschwandtner, Martin Gauster, Dagmar Kratky, Gerd Leitinger, Martina Schweiger, Katharina Jandl |
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Rok vydání: | 2021 |
Předmět: |
Biobanking
0301 basic medicine Histology Short Communication Sample preparation 030209 endocrinology & metabolism White adipose tissue Cryo-storage law.invention Mice 03 medical and health sciences 0302 clinical medicine Fresh Tissue law Lipid droplet Freezing Brown adipose tissue medicine Animals Molecular Biology Fixation (histology) Cryopreservation Chemistry Lipid Droplets Cell Biology Mitochondria Mice Inbred C57BL Microscopy Electron Medical Laboratory Technology 030104 developmental biology medicine.anatomical_structure Liver Freeze substitution Cryoprotectant-free TEM Ultrastructure Ultrastructural features Electron microscope Biomedical engineering |
Zdroj: | Histochemistry and Cell Biology |
ISSN: | 1432-119X 0948-6143 |
DOI: | 10.1007/s00418-020-01952-z |
Popis: | Preservation of ultrastructural features in biological samples for electron microscopy (EM) is a challenging task that is routinely accomplished through chemical fixation or high-pressure freezing coupled to automated freeze substitution (AFS) using specialized devices. However, samples from clinical (e.g. “biobanking” of bulk biopsies) and preclinical (e.g. whole mouse tissues) specimens are often not specifically prepared for ultrastructural analyses but simply immersed in liquid nitrogen before long-term cryo-storage. We demonstrate that ultrastructural features of such samples are insufficiently conserved using AFS and developed a simple, rapid, and effective method for thawing that does not require specific instrumentation. This procedure consists of dry ice-cooled pre-trimming of frozen tissue and aldehyde fixation for 3 h at 37 °C followed by standard embedding steps. Herein investigated tissues comprised human term placentae, clinical lung samples, as well as mouse tissues of different composition (brown adipose tissue, white adipose tissue, cardiac muscle, skeletal muscle, liver). For all these tissues, we compared electron micrographs prepared from cryo-stored material with our method to images derived from directly prepared fresh tissues with standard chemical fixation. Our protocol yielded highly conserved ultrastructural features and tissue-specific details, largely matching the quality of fresh tissue samples. Furthermore, morphometric analysis of lipid droplets and mitochondria in livers of fasted mice demonstrated that statistically valid quantifications can be derived from samples prepared with our method. Overall, we provide a simple and effective protocol for accurate ultrastructural and morphometric analyses of cryo-stored bulk tissue samples. Supplementary Information The online version contains supplementary material available at 10.1007/s00418-020-01952-z. |
Databáze: | OpenAIRE |
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