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Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material
Interest in cell-penetrating peptides (CPPs) as delivery agents has fuelled a large number of studies conducted on cultured cells and in mice. However, only a few studies have been devoted to the behaviour of CPPs in human tissues. Therefore, we performed ex vivo tissue-dipping experiments where we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033972/ https://www.ncbi.nlm.nih.gov/pubmed/27713271 http://dx.doi.org/10.3390/ph3030621 |
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author | Saar, Külliki Saar, Helgi Hansen, Mats Langel, Ülo Pooga, Margus |
author_facet | Saar, Külliki Saar, Helgi Hansen, Mats Langel, Ülo Pooga, Margus |
author_sort | Saar, Külliki |
collection | PubMed |
description | Interest in cell-penetrating peptides (CPPs) as delivery agents has fuelled a large number of studies conducted on cultured cells and in mice. However, only a few studies have been devoted to the behaviour of CPPs in human tissues. Therefore, we performed ex vivo tissue-dipping experiments where we studied the distribution of CPP-protein complexes in samples of freshly harvested human tissue material. We used the carcinoma or hyperplasia-containing specimens of the uterus and the cervix, obtained as surgical waste from nine hysterectomies. Our aim was to evaluate the tissue of preference (epithelial versus muscular/connective tissue, carcinoma versus adjacent histologically normal tissue) for two well-studied CPPs, the transportan and the TAT-peptide. We complexed biotinylated CPPs with avidin-β-galactosidase (ABG), which enabled us to apply whole-mount X-gal staining as a robust detection method. Our results demonstrate that both peptides enhanced the tissue distribution of ABG. The enhancing effect of the tested CPPs was more obvious in the normal tissue and in some specimens we detected a striking selectivity of CPP-ABG complexes for the normal tissue. This unexpected finding encourages the evaluation of CPPs as local delivery agents in non-malignant situations, for example in the intrauterine gene therapy of benign gynaecological diseases. |
format | Online Article Text |
id | pubmed-4033972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-40339722014-05-27 Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material Saar, Külliki Saar, Helgi Hansen, Mats Langel, Ülo Pooga, Margus Pharmaceuticals (Basel) Article Interest in cell-penetrating peptides (CPPs) as delivery agents has fuelled a large number of studies conducted on cultured cells and in mice. However, only a few studies have been devoted to the behaviour of CPPs in human tissues. Therefore, we performed ex vivo tissue-dipping experiments where we studied the distribution of CPP-protein complexes in samples of freshly harvested human tissue material. We used the carcinoma or hyperplasia-containing specimens of the uterus and the cervix, obtained as surgical waste from nine hysterectomies. Our aim was to evaluate the tissue of preference (epithelial versus muscular/connective tissue, carcinoma versus adjacent histologically normal tissue) for two well-studied CPPs, the transportan and the TAT-peptide. We complexed biotinylated CPPs with avidin-β-galactosidase (ABG), which enabled us to apply whole-mount X-gal staining as a robust detection method. Our results demonstrate that both peptides enhanced the tissue distribution of ABG. The enhancing effect of the tested CPPs was more obvious in the normal tissue and in some specimens we detected a striking selectivity of CPP-ABG complexes for the normal tissue. This unexpected finding encourages the evaluation of CPPs as local delivery agents in non-malignant situations, for example in the intrauterine gene therapy of benign gynaecological diseases. Molecular Diversity Preservation International 2010-03-12 /pmc/articles/PMC4033972/ /pubmed/27713271 http://dx.doi.org/10.3390/ph3030621 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Saar, Külliki Saar, Helgi Hansen, Mats Langel, Ülo Pooga, Margus Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title | Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title_full | Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title_fullStr | Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title_full_unstemmed | Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title_short | Distribution of CPP-Protein Complexes in Freshly Resected Human Tissue Material |
title_sort | distribution of cpp-protein complexes in freshly resected human tissue material |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033972/ https://www.ncbi.nlm.nih.gov/pubmed/27713271 http://dx.doi.org/10.3390/ph3030621 |
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