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In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration
Current clinical treatments on lymphedema provide promising results, but also result in donor site morbidities. The establishment of a microenvironment optimized for lymphangiogenesis can be an alternative way to enhance lymphatic tissue formation. Hemodynamic flow stimuli have been confirmed to hav...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472829/ https://www.ncbi.nlm.nih.gov/pubmed/37661967 http://dx.doi.org/10.1177/20417314231196212 |
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author | Hsiao, Hui-Yi Mackert, Gina Alicia Chang, Yung-Chun Liu, Jia-Wei Chang, Frank Chun-Shin Huang, Jung-Ju |
author_facet | Hsiao, Hui-Yi Mackert, Gina Alicia Chang, Yung-Chun Liu, Jia-Wei Chang, Frank Chun-Shin Huang, Jung-Ju |
author_sort | Hsiao, Hui-Yi |
collection | PubMed |
description | Current clinical treatments on lymphedema provide promising results, but also result in donor site morbidities. The establishment of a microenvironment optimized for lymphangiogenesis can be an alternative way to enhance lymphatic tissue formation. Hemodynamic flow stimuli have been confirmed to have an influential effect on angiogenesis in tissue engineering, but not on lymphatic vessel formation. Here, the three in vivo scaffolds generated from different blood stimuli in the subcutaneous layer, in the flow through pedicle, and in an arterio-venous (AV) loop model, were created to investigate potential of lymphangiogenesis of scaffolds containing lymphatic endothelial cells (LECs). Our results indicated that AV loop model displayed better lymphangiogenesis in comparison to the other two models with slower flow or no stimuli. Other than hemodynamic force, the supplement of LECs is required for lymphatic vessel regeneration. The in vivo scaffold generated from AV loop model provides an effective approach for engineering lymphatic tissue in the clinical treatment of lymphedema. |
format | Online Article Text |
id | pubmed-10472829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-104728292023-09-02 In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration Hsiao, Hui-Yi Mackert, Gina Alicia Chang, Yung-Chun Liu, Jia-Wei Chang, Frank Chun-Shin Huang, Jung-Ju J Tissue Eng Original Article Current clinical treatments on lymphedema provide promising results, but also result in donor site morbidities. The establishment of a microenvironment optimized for lymphangiogenesis can be an alternative way to enhance lymphatic tissue formation. Hemodynamic flow stimuli have been confirmed to have an influential effect on angiogenesis in tissue engineering, but not on lymphatic vessel formation. Here, the three in vivo scaffolds generated from different blood stimuli in the subcutaneous layer, in the flow through pedicle, and in an arterio-venous (AV) loop model, were created to investigate potential of lymphangiogenesis of scaffolds containing lymphatic endothelial cells (LECs). Our results indicated that AV loop model displayed better lymphangiogenesis in comparison to the other two models with slower flow or no stimuli. Other than hemodynamic force, the supplement of LECs is required for lymphatic vessel regeneration. The in vivo scaffold generated from AV loop model provides an effective approach for engineering lymphatic tissue in the clinical treatment of lymphedema. SAGE Publications 2023-08-31 /pmc/articles/PMC10472829/ /pubmed/37661967 http://dx.doi.org/10.1177/20417314231196212 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Hsiao, Hui-Yi Mackert, Gina Alicia Chang, Yung-Chun Liu, Jia-Wei Chang, Frank Chun-Shin Huang, Jung-Ju In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title | In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title_full | In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title_fullStr | In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title_full_unstemmed | In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title_short | In vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
title_sort | in vivo vascularized scaffold with different shear-exposed models for lymphatic tissue regeneration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472829/ https://www.ncbi.nlm.nih.gov/pubmed/37661967 http://dx.doi.org/10.1177/20417314231196212 |
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