Mesenchymal stem cells overexpressing Ihh promote bone repair

Shasha Zou, Tingting Chen, Yanan Wang, Ruhui Tian, Lingling Zhang, Pingping Song, Shi Yang, Yong Zhu, Xizhi Guo, Yiran Huang, Zheng Li, Lixin Kan, Hongliang Hu

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


BACKGROUND: Indian hedgehog (Ihh) signaling pathway is known to play key roles in various aspects of normal endochondral bone development. This study tested the potential roles of high Ihh signaling in the context of injury-induced bone regeneration.

METHODS: A rabbit tibia defect model was established to test the effects of the implant of Ihh/mesenchymal stem cells (MSCs)/scaffold complex. Computed tomography (CT), gross observation, and standard histological and immunohistological techniques were used to evaluate the effectiveness of the treatment. In vitro studies with MSCs and C3H10T1/2 cells were also employed to further understand the cellular and molecular mechanisms.

RESULTS: We found that the implanted Ihh/MSCs/scaffold complex promoted bone repair. Consistently, in vitro study found that Ihh induced the upregulation of chondrocytic, osteogenic, and vascular cell markers, both in C3H10T1/2 cells and MSCs.

CONCLUSIONS: Our study has demonstrated that high Ihh signaling in a complex with MSCs enhanced bone regeneration effectively in a clinically relevant acute injury model. Even though the exact underlying mechanisms are still far from clear, our primary data suggested that enhanced chondrogenesis, osteogenesis, and angiogenesis of MSCs at least partially contribute to the process. This study not only has implications for basic research of MSCs and Ihh signaling pathway but also points to the possibility of direct application of this specific paradigm to clinical bone repair.

Original languageEnglish (US)
Pages (from-to)102
Number of pages1
JournalJournal of Orthopaedic Surgery and Research
StatePublished - Oct 28 2014
Externally publishedYes

Bibliographical note

Funding Information:
We thank Dr. Suli Cheng for the technical advice on retrovirus production. The work was supported by the National Natural Science Foundation of China (grant number 30973069, 30672146) and the Foundation of Pujiang (grant number 08PJ14100).


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