Msx1(+) stem cells recruited by bioactive tissue engineering graft for bone regeneration.
Msx1(+) stem cells recruited by bioactive tissue engineering graft for bone regeneration.
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DOI:
10.1038/s41467-022-32868-y
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发表时间:
2022-09-05
影响因子:
16.6
通讯作者:
Ouyang, Hongwei
中科院分区:
文献类型:
--
作者:
Zhang, Xianzhu;Jiang, Wei;Xie, Chang;Wu, Xinyu;Ren, Qian;Wang, Fei;Shen, Xilin;Hong, Yi;Wu, Hongwei;Liao, Youguo;Zhang, Yi;Liang, Renjie;Sun, Wei;Gu, Yuqing;Zhang, Tao;Chen, Yishan;Wei, Wei;Zhang, Shufang;Zou, Weiguo;Ouyang, Hongwei
Critical-sized bone defects often lead to non-union and full-thickness defects of the calvarium specifically still present reconstructive challenges. In this study, we show that neurotrophic supplements induce robust in vitro expansion of mesenchymal stromal cells, and in situ transplantation of neurotrophic supplements-incorporated 3D-printed hydrogel grafts promote full-thickness regeneration of critical-sized bone defects. Single-cell RNA sequencing analysis reveals that a unique atlas of in situ stem/progenitor cells is generated during the calvarial bone healing in vivo. Notably, we find a local expansion of resident Msx1+ skeletal stem cells after transplantation of the in situ cell culture system. Moreover, the enhanced calvarial bone regeneration is accompanied by an increased endochondral ossification that closely correlates to the Msx1+ skeletal stem cells. Our findings illustrate the time-saving and regenerative efficacy of in situ cell culture systems targeting major cell subpopulations in vivo for rapid bone tissue regeneration. Critical-sized bone defects still present clinical challenges. Here the authors show that transplantation of neurotrophic supplement-incorporated hydrogel grafts promote full-thickness regeneration of the calvarium and perform scRNA-seq to reveal contributing stem/progenitor cells, notably a resident Msx1+ skeletal stem cell population.
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影响因子:
3.1
作者:
Bruderer, M.;Richards, R. G.;Stoddart, M. J.
通讯作者:
Stoddart, M. J.
影响因子:
44.1
作者:
He J;Yan J;Wang J;Zhao L;Xin Q;Zeng Y;Sun Y;Zhang H;Bai Z;Li Z;Ni Y;Gong Y;Li Y;He H;Bian Z;Lan Y;Ma C;Bian L;Zhu H;Liu B;Yue R
通讯作者:
Yue R
影响因子:
14
作者:
Ho-Shui-Ling A;Bolander J;Rustom LE;Johnson AW;Luyten FP;Picart C
通讯作者:
Picart C
影响因子:
64.5
作者:
Baryawno, Ninib;Przybylski, Dariusz;Scadden, David T.
通讯作者:
Scadden, David T.
影响因子:
16.6
作者:
Cui, Zhong-Kai;Kim, Soyon;Lee, Min
通讯作者:
Lee, Min