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Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review

Acellular adipose matrix (AAM) has received increasing attention for soft tissue reconstruction, due to its abundant source, high long-term retention rate and in vivo adipogenic induction ability. However, the current decellularization methods inevitably affect native extracellular matrix (ECM) prop...

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Detalles Bibliográficos
Autores principales: Liu, Kaiyang, He, Yunfan, Lu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207478/
https://www.ncbi.nlm.nih.gov/pubmed/35733521
http://dx.doi.org/10.3389/fbioe.2022.881523
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author Liu, Kaiyang
He, Yunfan
Lu, Feng
author_facet Liu, Kaiyang
He, Yunfan
Lu, Feng
author_sort Liu, Kaiyang
collection PubMed
description Acellular adipose matrix (AAM) has received increasing attention for soft tissue reconstruction, due to its abundant source, high long-term retention rate and in vivo adipogenic induction ability. However, the current decellularization methods inevitably affect native extracellular matrix (ECM) properties, and the residual antigens can trigger adverse immune reactions after transplantation. The behavior of host inflammatory cells mainly decides the regeneration of AAM after transplantation. In this review, recent knowledge of inflammatory cells for acellular matrix regeneration will be discussed. These advancements will inform further development of AAM products with better properties.
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spelling pubmed-92074782022-06-21 Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review Liu, Kaiyang He, Yunfan Lu, Feng Front Bioeng Biotechnol Bioengineering and Biotechnology Acellular adipose matrix (AAM) has received increasing attention for soft tissue reconstruction, due to its abundant source, high long-term retention rate and in vivo adipogenic induction ability. However, the current decellularization methods inevitably affect native extracellular matrix (ECM) properties, and the residual antigens can trigger adverse immune reactions after transplantation. The behavior of host inflammatory cells mainly decides the regeneration of AAM after transplantation. In this review, recent knowledge of inflammatory cells for acellular matrix regeneration will be discussed. These advancements will inform further development of AAM products with better properties. Frontiers Media S.A. 2022-06-06 /pmc/articles/PMC9207478/ /pubmed/35733521 http://dx.doi.org/10.3389/fbioe.2022.881523 Text en Copyright © 2022 Liu, He and Lu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Liu, Kaiyang
He, Yunfan
Lu, Feng
Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title_full Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title_fullStr Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title_full_unstemmed Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title_short Research Progress on the Immunogenicity and Regeneration of Acellular Adipose Matrix: A Mini Review
title_sort research progress on the immunogenicity and regeneration of acellular adipose matrix: a mini review
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207478/
https://www.ncbi.nlm.nih.gov/pubmed/35733521
http://dx.doi.org/10.3389/fbioe.2022.881523
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