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Enhanced tenogenic differentiation and tendon-like tissue formation by Scleraxis overexpression in human amniotic mesenchymal stem cells

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Abstract

Tendon and ligament injuries are not uncommon in clinics and have poor self-healing capacity due to their bloodless and slow-proliferative nature. Promoting the repair or reconstruction of an injured structure is an urgent problem. While Scleraxis (Scx) is a highly specific tendon cell marker, its function has not been explored to a large extent. Hence, Recombinant adenovirus was used to study the influence of Scx overexpression on directional differentiation of human amniotic mesenchymal stem cells (hMSCAs). hAMSCs modified with Scx could dramatically enhance the gene expression of tendon-related molecules, containing Scx, collagens I and III, Tenascin-C, fibronectin, matrix metalloproteinase-2 (MMP-2), lysyl oxidase-1 (LOX-1) and Tenomodulin at all-time points (P < 0.05), and the secretion of collagen I and III, fibronectin and Tenascin-C over time (P < 0.05) but did not impact the cell proliferation capacity (P > 0.05). Immunofluorescence staining showed the cobweb-like fusion of collagen I and fibronectin in the AdScx group on day 7, with higher average fluorescence intensity than the control (P < 0.05). After mixing with Matrigel, transplants were subcutaneously implanted in nude mice, obvious inflammation and rejection of immune response were not observed and HE staining showed a histological feature of swirl of fibers is closely linked in parallel in hAMSCs modified with Scx. On the contrary, in the control group, an unorganized connective structure with cell distributed randomly was spotted. The results of promoted directional differentiation of stem cells and the spatial structure of the normal tendon tissue in three-dimensional space manifested that Scx can be used as a specific marker for tendon cells, and as a positive regulator for directional differentiation of hAMSCs, which is possible to be applied to novel therapeutics for clinical tendon and ligament injury by hAMSCs modified with Scx.

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Data availability

We declared that materials described in the manuscript, including all relevant raw data, will be freely available to any scientist wishing to use them for non-commercial purposes, without breaching participant confidentiality.

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All data, models, and code generated or used during the study appear in the submitted article.

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Acknowledgements

The authors sincerely thank Prof. Xiaolin Tu from Chongqing Medical University for technical and experimental support and Dr. Chenghao Zhang from the Mayo Clinic, University of Rochester, for manuscript editing and submission consultation. This work was supported by grants awarded to Shuhong Wu from the Science & Technology Program of Guizhou Province (No. SY [2012]172; No. SY [2017]2882); Huazhang Xiong from the Science & Technology Program of Guizhou Province (No. LH [2016]7477) and Qian Wei Ji Ban Han No. 2017-24.

Funding

This work was supported by grants awarded to Shuhong Wu from the Science & Technology Program of Guizhou Province (No. SY [2012]172; No. SY [2017]2882) and Huazhang Xiong from the Science & Technology Program of Guizhou Province (No. LH [2016]7477); and Qian Wei Ji Ban Han No. 2017-24.

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SW and YL conceived and designed the study. XZ, JY, YJ, JZ and YL performed the experiments. ZL provided the mutants. XZ and HX wrote the paper. GZ, XT and CZ reviewed and edited the manuscript. All authors read and approved the manuscript.

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Correspondence to Yi Liu.

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The authors declare that they have no conflict of interest.

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This study has been approved by the Research Ethics Committee of the Affiliated Hospital of Zunyi Medical College.

Research involving human participants and/or animals

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. All procedures performed in studies involving animals were in accordance with the ethical standards of the Zunyi Medical University.

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Informed consent was obtained from all individual participants included in the study.

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Zhu, X., Liu, Z., Wu, S. et al. Enhanced tenogenic differentiation and tendon-like tissue formation by Scleraxis overexpression in human amniotic mesenchymal stem cells. J Mol Hist 51, 209–220 (2020). https://doi.org/10.1007/s10735-020-09873-w

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  • DOI: https://doi.org/10.1007/s10735-020-09873-w

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