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Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber
Background: Breast reconstruction with fat grafting has an unstable retention rate due to insufficient revascularization. Tissue Engineering Chamber (TEC) model can promote tissue regeneration in the chamber by introducing ligated vessels around the tissue. We introduced ligated vessels with free fa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153550/ https://www.ncbi.nlm.nih.gov/pubmed/32125221 http://dx.doi.org/10.1080/21623945.2020.1735025 |
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author | Lei, Chen Cai, Beichen Chen, Xiaobin Huang, Zhiyong Wang, Biao |
author_facet | Lei, Chen Cai, Beichen Chen, Xiaobin Huang, Zhiyong Wang, Biao |
author_sort | Lei, Chen |
collection | PubMed |
description | Background: Breast reconstruction with fat grafting has an unstable retention rate due to insufficient revascularization. Tissue Engineering Chamber (TEC) model can promote tissue regeneration in the chamber by introducing ligated vessels around the tissue. We introduced ligated vessels with free fat graft to investigate the retention rate and revascularization of grafted fat that in TEC model. Methods: SD rats (n=24) was divided into 3 groups randomly. Group A: Standard TEC model was constructed; Group B: the epigastric vessel bundles were dissected from the fat flap and ligated, fat flap was cut into granules and planted into the chamber; Group C: Free fat was planted in the chamber. At week 6, samples in the chamber were harvested. Results: Significant volume increase was observed in group A and B, while the volume decreased in group C (P<0.05). Regeneration morphology could be found according to the histological observation in A and B. Micro CT results showed the ligated vessels into grafted fat sprouting robustly, coordinated with volume changes. Conclusion: Fat grafts in TEC model could not only survive but also regenerate. The combination of fat graft and TEC could fabricate a vascularized fat flap, which was a promising method in breast reconstruction. Abbreviations: VOI: Volumes of Interest; TEC: Tissue Engineering Chamber; CAL: Cell Assisted Lipotransfer. |
format | Online Article Text |
id | pubmed-7153550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-71535502020-04-16 Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber Lei, Chen Cai, Beichen Chen, Xiaobin Huang, Zhiyong Wang, Biao Adipocyte Research Article Background: Breast reconstruction with fat grafting has an unstable retention rate due to insufficient revascularization. Tissue Engineering Chamber (TEC) model can promote tissue regeneration in the chamber by introducing ligated vessels around the tissue. We introduced ligated vessels with free fat graft to investigate the retention rate and revascularization of grafted fat that in TEC model. Methods: SD rats (n=24) was divided into 3 groups randomly. Group A: Standard TEC model was constructed; Group B: the epigastric vessel bundles were dissected from the fat flap and ligated, fat flap was cut into granules and planted into the chamber; Group C: Free fat was planted in the chamber. At week 6, samples in the chamber were harvested. Results: Significant volume increase was observed in group A and B, while the volume decreased in group C (P<0.05). Regeneration morphology could be found according to the histological observation in A and B. Micro CT results showed the ligated vessels into grafted fat sprouting robustly, coordinated with volume changes. Conclusion: Fat grafts in TEC model could not only survive but also regenerate. The combination of fat graft and TEC could fabricate a vascularized fat flap, which was a promising method in breast reconstruction. Abbreviations: VOI: Volumes of Interest; TEC: Tissue Engineering Chamber; CAL: Cell Assisted Lipotransfer. Taylor & Francis 2020-03-03 /pmc/articles/PMC7153550/ /pubmed/32125221 http://dx.doi.org/10.1080/21623945.2020.1735025 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lei, Chen Cai, Beichen Chen, Xiaobin Huang, Zhiyong Wang, Biao Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title | Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title_full | Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title_fullStr | Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title_full_unstemmed | Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title_short | Introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
title_sort | introduction of ligated vessels promote the retention and regeneration of free fat: constructing a fat flap in tissue engineering chamber |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153550/ https://www.ncbi.nlm.nih.gov/pubmed/32125221 http://dx.doi.org/10.1080/21623945.2020.1735025 |
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