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A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair
Stem cells play critical roles in cell therapies and tissue engineering for nerve repair. However, achieving effective delivery of high cell density remains a challenge. Here, a novel cell delivery platform termed the hyper expansion scaffold (HES) is developed to enable high cell loading. HES facil...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667844/ https://www.ncbi.nlm.nih.gov/pubmed/37870182 http://dx.doi.org/10.1002/advs.202301639 |
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author | Qiu, Chen Sun, Yuan Li, Jinying Zhou, Jiayi Xu, Yuchen Qiu, Cong Yu, Kang Liu, Jia Jiang, Yuanqing Cui, Wenyu Wang, Guanghao Liu, He Yuan, Weixin Jiang, Tuoying Kou, Yaohui Ge, Zhen He, Zhiying Zhang, Shaomin He, Yong Yu, Luyang |
author_facet | Qiu, Chen Sun, Yuan Li, Jinying Zhou, Jiayi Xu, Yuchen Qiu, Cong Yu, Kang Liu, Jia Jiang, Yuanqing Cui, Wenyu Wang, Guanghao Liu, He Yuan, Weixin Jiang, Tuoying Kou, Yaohui Ge, Zhen He, Zhiying Zhang, Shaomin He, Yong Yu, Luyang |
author_sort | Qiu, Chen |
collection | PubMed |
description | Stem cells play critical roles in cell therapies and tissue engineering for nerve repair. However, achieving effective delivery of high cell density remains a challenge. Here, a novel cell delivery platform termed the hyper expansion scaffold (HES) is developed to enable high cell loading. HES facilitated self‐promoted and efficient cell absorption via a dual driving force model. In vitro tests revealed that the HES rapidly expanded 80‐fold in size upon absorbing 2.6 million human amniotic epithelial stem cells (hAESCs) within 2 min, representing over a 400% increase in loading capacity versus controls. This enhanced uptake benefited from macroscopic swelling forces as well as microscale capillary action. In spinal cord injury (SCI) rats, HES–hAESCs promoted functional recovery and axonal projection by reducing neuroinflammation and improving the neurotrophic microenvironment surrounding the lesions. In summary, the dual driving forces model provides a new rationale for engineering hydrogel scaffolds to facilitate self‐promoted cell absorption. The HES platform demonstrates great potential as a powerful and efficient vehicle for delivering high densities of hAESCs to promote clinical treatment and repair of SCI. |
format | Online Article Text |
id | pubmed-10667844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106678442023-10-23 A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair Qiu, Chen Sun, Yuan Li, Jinying Zhou, Jiayi Xu, Yuchen Qiu, Cong Yu, Kang Liu, Jia Jiang, Yuanqing Cui, Wenyu Wang, Guanghao Liu, He Yuan, Weixin Jiang, Tuoying Kou, Yaohui Ge, Zhen He, Zhiying Zhang, Shaomin He, Yong Yu, Luyang Adv Sci (Weinh) Research Articles Stem cells play critical roles in cell therapies and tissue engineering for nerve repair. However, achieving effective delivery of high cell density remains a challenge. Here, a novel cell delivery platform termed the hyper expansion scaffold (HES) is developed to enable high cell loading. HES facilitated self‐promoted and efficient cell absorption via a dual driving force model. In vitro tests revealed that the HES rapidly expanded 80‐fold in size upon absorbing 2.6 million human amniotic epithelial stem cells (hAESCs) within 2 min, representing over a 400% increase in loading capacity versus controls. This enhanced uptake benefited from macroscopic swelling forces as well as microscale capillary action. In spinal cord injury (SCI) rats, HES–hAESCs promoted functional recovery and axonal projection by reducing neuroinflammation and improving the neurotrophic microenvironment surrounding the lesions. In summary, the dual driving forces model provides a new rationale for engineering hydrogel scaffolds to facilitate self‐promoted cell absorption. The HES platform demonstrates great potential as a powerful and efficient vehicle for delivering high densities of hAESCs to promote clinical treatment and repair of SCI. John Wiley and Sons Inc. 2023-10-23 /pmc/articles/PMC10667844/ /pubmed/37870182 http://dx.doi.org/10.1002/advs.202301639 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Qiu, Chen Sun, Yuan Li, Jinying Zhou, Jiayi Xu, Yuchen Qiu, Cong Yu, Kang Liu, Jia Jiang, Yuanqing Cui, Wenyu Wang, Guanghao Liu, He Yuan, Weixin Jiang, Tuoying Kou, Yaohui Ge, Zhen He, Zhiying Zhang, Shaomin He, Yong Yu, Luyang A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title | A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title_full | A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title_fullStr | A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title_full_unstemmed | A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title_short | A 3D‐Printed Dual Driving Forces Scaffold with Self‐Promoted Cell Absorption for Spinal Cord Injury Repair |
title_sort | 3d‐printed dual driving forces scaffold with self‐promoted cell absorption for spinal cord injury repair |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667844/ https://www.ncbi.nlm.nih.gov/pubmed/37870182 http://dx.doi.org/10.1002/advs.202301639 |
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