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Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer
BACKGROUND: Cell-assisted lipotransfer (CAL), a modified adipose-derived stromal/stem cells (ADSCs)-based approach for autologous fat grafting that is an ideal option for soft tissue augmentation, has many shortcomings in terms of retention and adverse effects. The objective of our study was to impr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762074/ https://www.ncbi.nlm.nih.gov/pubmed/36582606 http://dx.doi.org/10.1016/j.reth.2022.11.008 |
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author | Fu, Hongtao Dong, Shanshan Li, Kun |
author_facet | Fu, Hongtao Dong, Shanshan Li, Kun |
author_sort | Fu, Hongtao |
collection | PubMed |
description | BACKGROUND: Cell-assisted lipotransfer (CAL), a modified adipose-derived stromal/stem cells (ADSCs)-based approach for autologous fat grafting that is an ideal option for soft tissue augmentation, has many shortcomings in terms of retention and adverse effects. The objective of our study was to improve the treatment efficacy of CAL by adding fibroblasts. METHODS: ADSCs and fibroblasts were isolated from human adipose and dermal tissues, with fibroblasts identified by immunofluorescence and ADSCs identified by the multilineage differentiation method. We performed cell proliferation, apoptosis, migration, adipogenic, and hemangioendothelial differentiation experiments, qPCR and Western blotting analysis in co-cultures of fibroblasts and ADSCs. Subsequently, we conducted animal experiments with BALB/c nude mice. Masson's staining, immunofluorescence staining and ultrasound were used to analyze the occurrence of adverse reactions of the grafted fat, and CT and three-dimensional reconstruction were used to accurately evaluate the volume of the grafted fat. RESULTS: We found that the co-culture of fibroblasts and ADSCs promoted their mutual proliferation, adipogenic differentiation, hemangioendothelial differentiation and proliferation and migration of HUVECs. Fibroblasts inhibit the apoptosis of ADSCs. Moreover, in animal experiments, the autografted adipose group combined with ADSCs and fibroblasts had the least occurrence of oily cysts, and fat had the best form of survival. CONCLUSIONS: We enhanced adipocyte regeneration and angiogenesis in ADSCs and fibroblast cells after adding fibroblasts to conventional CAL autologous fat grafts. In turn, the volume retention rate of the grafted fat is improved, and the adverse reactions are reduced. |
format | Online Article Text |
id | pubmed-9762074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-97620742022-12-28 Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer Fu, Hongtao Dong, Shanshan Li, Kun Regen Ther Original Article BACKGROUND: Cell-assisted lipotransfer (CAL), a modified adipose-derived stromal/stem cells (ADSCs)-based approach for autologous fat grafting that is an ideal option for soft tissue augmentation, has many shortcomings in terms of retention and adverse effects. The objective of our study was to improve the treatment efficacy of CAL by adding fibroblasts. METHODS: ADSCs and fibroblasts were isolated from human adipose and dermal tissues, with fibroblasts identified by immunofluorescence and ADSCs identified by the multilineage differentiation method. We performed cell proliferation, apoptosis, migration, adipogenic, and hemangioendothelial differentiation experiments, qPCR and Western blotting analysis in co-cultures of fibroblasts and ADSCs. Subsequently, we conducted animal experiments with BALB/c nude mice. Masson's staining, immunofluorescence staining and ultrasound were used to analyze the occurrence of adverse reactions of the grafted fat, and CT and three-dimensional reconstruction were used to accurately evaluate the volume of the grafted fat. RESULTS: We found that the co-culture of fibroblasts and ADSCs promoted their mutual proliferation, adipogenic differentiation, hemangioendothelial differentiation and proliferation and migration of HUVECs. Fibroblasts inhibit the apoptosis of ADSCs. Moreover, in animal experiments, the autografted adipose group combined with ADSCs and fibroblasts had the least occurrence of oily cysts, and fat had the best form of survival. CONCLUSIONS: We enhanced adipocyte regeneration and angiogenesis in ADSCs and fibroblast cells after adding fibroblasts to conventional CAL autologous fat grafts. In turn, the volume retention rate of the grafted fat is improved, and the adverse reactions are reduced. Japanese Society for Regenerative Medicine 2022-12-13 /pmc/articles/PMC9762074/ /pubmed/36582606 http://dx.doi.org/10.1016/j.reth.2022.11.008 Text en © 2022 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Fu, Hongtao Dong, Shanshan Li, Kun Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title | Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title_full | Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title_fullStr | Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title_full_unstemmed | Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title_short | Study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
title_sort | study on promoting the regeneration of grafted fat by cell-assisted lipotransfer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762074/ https://www.ncbi.nlm.nih.gov/pubmed/36582606 http://dx.doi.org/10.1016/j.reth.2022.11.008 |
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