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Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique
In vivo cryotechnique (IVCT), which immediately cryofixes target organs in situ, was used to clarify the morphological features of beating heart tissue of living mice. IVCT was performed for diastolic heart tissue under the condition of monitoring with electrocardiogram (ECG). Other mouse hearts wer...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Japan Society of Histochemistry and Cytochemistry
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096083/ https://www.ncbi.nlm.nih.gov/pubmed/21614167 http://dx.doi.org/10.1267/ahc.11007 |
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author | Shi, Liye Terada, Nobuo Saitoh, Yurika Saitoh, Sei Ohno, Shinichi |
author_facet | Shi, Liye Terada, Nobuo Saitoh, Yurika Saitoh, Sei Ohno, Shinichi |
author_sort | Shi, Liye |
collection | PubMed |
description | In vivo cryotechnique (IVCT), which immediately cryofixes target organs in situ, was used to clarify the morphological features of beating heart tissue of living mice. IVCT was performed for diastolic heart tissue under the condition of monitoring with electrocardiogram (ECG). Other mouse hearts were prepared with conventional perfusion-fixation (PF-DH) or immersion-fixation followed by dehydration (IM-DH), and quick-freezing of resected heart tissues (FQF). Immunolocalizations of albumin, immunoglobulin G1 (IgG1), intravenously injected bovine serum albumin (BSA), and connexin 43 were examined after different intervals of BSA injection. In the case of IVCT, the exact stop time of beating mouse hearts was recorded by ECG, and open blood vessels with flowing erythrocytes were observed with less artificial tissue shrinkage than with conventional preparation methods. Both albumin and BSA were well preserved in intercalated discs and t-tubules of cardiomyocytes in addition to blood vessels and interstitial matrices. IgG1 was immunolocalized in interstitial matrices of heart tissues in addition to their blood vessels. At 4 hr after BSA injection, it was immunolocalized in the intercalated discs of cardiomyocytes and lost later at 8 hr. IVCT should prove to be more useful for the morphofunctional examination of dynamically changing heart tissue than conventional preparation methods. |
format | Text |
id | pubmed-3096083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Japan Society of Histochemistry and Cytochemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-30960832011-05-25 Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique Shi, Liye Terada, Nobuo Saitoh, Yurika Saitoh, Sei Ohno, Shinichi Acta Histochem Cytochem Regular Article In vivo cryotechnique (IVCT), which immediately cryofixes target organs in situ, was used to clarify the morphological features of beating heart tissue of living mice. IVCT was performed for diastolic heart tissue under the condition of monitoring with electrocardiogram (ECG). Other mouse hearts were prepared with conventional perfusion-fixation (PF-DH) or immersion-fixation followed by dehydration (IM-DH), and quick-freezing of resected heart tissues (FQF). Immunolocalizations of albumin, immunoglobulin G1 (IgG1), intravenously injected bovine serum albumin (BSA), and connexin 43 were examined after different intervals of BSA injection. In the case of IVCT, the exact stop time of beating mouse hearts was recorded by ECG, and open blood vessels with flowing erythrocytes were observed with less artificial tissue shrinkage than with conventional preparation methods. Both albumin and BSA were well preserved in intercalated discs and t-tubules of cardiomyocytes in addition to blood vessels and interstitial matrices. IgG1 was immunolocalized in interstitial matrices of heart tissues in addition to their blood vessels. At 4 hr after BSA injection, it was immunolocalized in the intercalated discs of cardiomyocytes and lost later at 8 hr. IVCT should prove to be more useful for the morphofunctional examination of dynamically changing heart tissue than conventional preparation methods. Japan Society of Histochemistry and Cytochemistry 2011-04-28 2011-03-29 /pmc/articles/PMC3096083/ /pubmed/21614167 http://dx.doi.org/10.1267/ahc.11007 Text en © 2011 The Japan Society of Histochemistry and Cytochemistry This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Article Shi, Liye Terada, Nobuo Saitoh, Yurika Saitoh, Sei Ohno, Shinichi Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title | Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title_full | Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title_fullStr | Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title_full_unstemmed | Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title_short | Immunohistochemical Distribution of Serum Proteins in Living Mouse Heart with In Vivo Cryotechnique |
title_sort | immunohistochemical distribution of serum proteins in living mouse heart with in vivo cryotechnique |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096083/ https://www.ncbi.nlm.nih.gov/pubmed/21614167 http://dx.doi.org/10.1267/ahc.11007 |
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