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Hyperplastic Human Macromass Cartilage for Joint Regeneration

Cartilage damage affects millions of people worldwide. Tissue engineering strategies hold the promise to provide off‐the‐shelf cartilage analogs for tissue transplantation in cartilage repair. However, current strategies hardly generate sufficient grafts, as tissues cannot maintain size growth and c...

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Autores principales: Wen, Ya, Chen, Yishan, Wu, Weiliang, Zhang, Hong, Peng, Zhi, Yao, Xudong, Zhang, Xianzhu, Jiang, Wei, Liao, Youguo, Xie, Yuan, Shen, Xilin, Sun, Heng, Hu, Jiajie, Liu, Hua, Chen, Xiao, Chen, Jiansong, Ouyang, Hongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502860/
https://www.ncbi.nlm.nih.gov/pubmed/37395375
http://dx.doi.org/10.1002/advs.202301833
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author Wen, Ya
Chen, Yishan
Wu, Weiliang
Zhang, Hong
Peng, Zhi
Yao, Xudong
Zhang, Xianzhu
Jiang, Wei
Liao, Youguo
Xie, Yuan
Shen, Xilin
Sun, Heng
Hu, Jiajie
Liu, Hua
Chen, Xiao
Chen, Jiansong
Ouyang, Hongwei
author_facet Wen, Ya
Chen, Yishan
Wu, Weiliang
Zhang, Hong
Peng, Zhi
Yao, Xudong
Zhang, Xianzhu
Jiang, Wei
Liao, Youguo
Xie, Yuan
Shen, Xilin
Sun, Heng
Hu, Jiajie
Liu, Hua
Chen, Xiao
Chen, Jiansong
Ouyang, Hongwei
author_sort Wen, Ya
collection PubMed
description Cartilage damage affects millions of people worldwide. Tissue engineering strategies hold the promise to provide off‐the‐shelf cartilage analogs for tissue transplantation in cartilage repair. However, current strategies hardly generate sufficient grafts, as tissues cannot maintain size growth and cartilaginous phenotypes simultaneously. Herein, a step‐wise strategy is developed for fabricating expandable human macromass cartilage (macro‐cartilage) in a 3D condition by employing human polydactyly chondrocytes and a screen‐defined serum‐free customized culture (CC). CC‐induced chondrocytes demonstrate improved cell plasticity, expressing chondrogenic biomarkers after a 14.59‐times expansion. Crucially, CC‐chondrocytes form large‐size cartilage tissues with average diameters of 3.25 ± 0.05 mm, exhibiting abundant homogenous matrix and intact structure without a necrotic core. Compared with typical culture, the cell yield in CC increases 2.57 times, and the expression of cartilage marker collagen type II increases 4.70 times. Transcriptomics reveal that this step‐wise culture drives a proliferation‐to‐differentiation process through an intermediate plastic stage, and CC‐chondrocytes undergo a chondral lineage‐specific differentiation with an activated metabolism. Animal studies show that CC macro‐cartilage maintains a hyaline‐like cartilage phenotype in vivo and significantly promotes the healing of large cartilage defects. Overall, an efficient expansion of human macro‐cartilage with superior regenerative plasticity is achieved, providing a promising strategy for joint regeneration.
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spelling pubmed-105028602023-09-16 Hyperplastic Human Macromass Cartilage for Joint Regeneration Wen, Ya Chen, Yishan Wu, Weiliang Zhang, Hong Peng, Zhi Yao, Xudong Zhang, Xianzhu Jiang, Wei Liao, Youguo Xie, Yuan Shen, Xilin Sun, Heng Hu, Jiajie Liu, Hua Chen, Xiao Chen, Jiansong Ouyang, Hongwei Adv Sci (Weinh) Research Articles Cartilage damage affects millions of people worldwide. Tissue engineering strategies hold the promise to provide off‐the‐shelf cartilage analogs for tissue transplantation in cartilage repair. However, current strategies hardly generate sufficient grafts, as tissues cannot maintain size growth and cartilaginous phenotypes simultaneously. Herein, a step‐wise strategy is developed for fabricating expandable human macromass cartilage (macro‐cartilage) in a 3D condition by employing human polydactyly chondrocytes and a screen‐defined serum‐free customized culture (CC). CC‐induced chondrocytes demonstrate improved cell plasticity, expressing chondrogenic biomarkers after a 14.59‐times expansion. Crucially, CC‐chondrocytes form large‐size cartilage tissues with average diameters of 3.25 ± 0.05 mm, exhibiting abundant homogenous matrix and intact structure without a necrotic core. Compared with typical culture, the cell yield in CC increases 2.57 times, and the expression of cartilage marker collagen type II increases 4.70 times. Transcriptomics reveal that this step‐wise culture drives a proliferation‐to‐differentiation process through an intermediate plastic stage, and CC‐chondrocytes undergo a chondral lineage‐specific differentiation with an activated metabolism. Animal studies show that CC macro‐cartilage maintains a hyaline‐like cartilage phenotype in vivo and significantly promotes the healing of large cartilage defects. Overall, an efficient expansion of human macro‐cartilage with superior regenerative plasticity is achieved, providing a promising strategy for joint regeneration. John Wiley and Sons Inc. 2023-07-03 /pmc/articles/PMC10502860/ /pubmed/37395375 http://dx.doi.org/10.1002/advs.202301833 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
Wen, Ya
Chen, Yishan
Wu, Weiliang
Zhang, Hong
Peng, Zhi
Yao, Xudong
Zhang, Xianzhu
Jiang, Wei
Liao, Youguo
Xie, Yuan
Shen, Xilin
Sun, Heng
Hu, Jiajie
Liu, Hua
Chen, Xiao
Chen, Jiansong
Ouyang, Hongwei
Hyperplastic Human Macromass Cartilage for Joint Regeneration
title Hyperplastic Human Macromass Cartilage for Joint Regeneration
title_full Hyperplastic Human Macromass Cartilage for Joint Regeneration
title_fullStr Hyperplastic Human Macromass Cartilage for Joint Regeneration
title_full_unstemmed Hyperplastic Human Macromass Cartilage for Joint Regeneration
title_short Hyperplastic Human Macromass Cartilage for Joint Regeneration
title_sort hyperplastic human macromass cartilage for joint regeneration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502860/
https://www.ncbi.nlm.nih.gov/pubmed/37395375
http://dx.doi.org/10.1002/advs.202301833
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