Abstract

Tissues and organs in vivo are under a hypoxic condition; that is, the oxygen tension is typically much lower than in ambient air. However, the effects of such a hypoxic condition on tendon stem cells, a recently identified tendon cell, remain incompletely defined. In cell culture experiments, we subjected human tendon stem cells (hTSCs) to a hypoxic condition with 5% O2, while subjecting control cells to a normaxic condition with 20% O2. We found that hTSCs at 5% O2 had significantly greater cell proliferation than those at 20% O2. Moreover, the expression of two stem cell marker genes, Nanog and Oct-4, was upregulated in the cells cultured in 5% O2. Finally, in cultures under 5% O2, more hTSCs expressed the stem cell markers nucleostemin, Oct-4, Nanog and SSEA-4. In an in vivo experiment, we found that when both cell groups were implanted with tendon-derived matrix, more tendon-like structures formed in the 5% O2 treated hTSCs than in 20% O2 treated hTSCs. Additionally, when both cell groups were implanted with Matrigel, the 5% O2 treated hTSCs showed more extensive formation of fatty, cartilage-like and bone-like tissues than the 20% O2 treated cells. Together, the findings of this study show that oxygen tension is a niche factor that regulates the stemness of hTSCs, and that less oxygen is better for maintaining hTSCs in culture and expanding them for cell therapy of tendon injuries.

Highlights

  • Tendons connect muscles to bones to enable joint movement

  • Expression of stem cell markers NS, octamer-binding transcription factor 4 (Oct-4), Nanog and stage-specific embryonic antigen-4 (SSEA-4) determined by immunocytochemistry was higher in colonies cultured in 5% O2 compared to human tendon stem cells (hTSCs) grown in 20% O2 (Figure 3A)

  • Semi-quantification of the immuno-stained cells further showed that more than 90% of hTSCs cultured in 5% O2 were NS positive compared to 66% in hTSCs cultured in 20% O2

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Summary

Introduction

Tendons connect muscles to bones to enable joint movement As a result, they are subjected to large mechanical loads and are frequently injured. Healed tendons consist of scar tissue that has lower mechanical strength than normal tendon tissue. This mechanical weakness impairs normal tendon function and joint kinematics, and predisposes patients to further tendon injury [1]. ESCs implantation could result in teratoma formation, which occurs due to difficulty in controlling ESCs differentiation in vivo when compared to adult stem cells such as BMSCs. ESCs implantation could result in teratoma formation, which occurs due to difficulty in controlling ESCs differentiation in vivo when compared to adult stem cells such as BMSCs These and other studies clearly indicate that stem cells from non-tendinous tissues may not be optimal to restore the normal structure and function of injured tendons using cell therapy

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