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Tendon stem/progenitor cells regulate inflammation in tendon healing via JNK and STAT3 signaling
Solaiman Tarafder1, Esther Chen1, Yena Jun1
1Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
Abstract:
Tendon stem/progenitor cells (TSCs) have been found in different anatomic locations and showed a promising regenerative potential. We identified a role of TSCs in the regulation of inflammation during healing of acute tendon injuries. Delivery of connective tissue growth factor (CTGF) into full-transected rat patellar tendons significantly increased the number of CD146+ TSCs, leading to enhanced healing. In parallel, CTGF delivery significantly reduced the number of iNOS+ M1 macrophages and increased the expression of anti-inflammatory IL-10 at 2 d after surgery, with over 85% CD146+ TSCs expressing IL-10. By 1 wk, the elevated IL-10 expression remained, and IL-6 expression was significantly attenuated in CTGF-delivered tendon healing. Matrix metalloproteinase (MMP)-3 expression in CTGF-delivered tendon was organized along with the reorienting collagen fibers by 1 wk after surgery, in comparison with the control group showing the abundant MMP-3 expression localized at healing junction. Tissue inhibitor of metalloprotease (TIMP)-3 was expressed in CD146+ TSCs at 1 wk with CTGF, in contrast to control with no TIMP-3 expression. In vitro, IL-10 expression was detected only when tendon cells were stimulated with IL-1β, and CTGF and significantly higher in CD146+ TSCs than CD146- tendon cells. Similarly, TIMP-3 expression was detected only when treated with CTGF or CTGF and IL-1β that is significantly higher in CD146+ TSCs compared to CD146- tendon cells. Signaling study with specific inhibitors and Western blot analysis demonstrated that CTGF-induced expression of IL-10 and TIMP-3 in CD146+ TSCs are regulated by JNK/signal transducer and activator of transcription 3 signaling. Taken together, these findings suggest anti-inflammatory roles of CTGF-stimulated TSCs that are likely associated with improved tendon healing.-Tarafder, S., Chen, E., Jun, Y., Kao, K., Sim, K. H., Back, J., Lee, F. Y., Lee, C. H. Tendon stem/progenitor cells regulate inflammation in tendon healing via JNK and STAT3 signaling.
Insights
Connective tissue growth factor (CTGF) enhances tendon healing by boosting tendon stem/progenitor cells (TSCs). These CTGF-stimulated TSCs reduce inflammation and promote tissue repair through JNK/STAT3 signaling pathways.
Area of Science:
- Regenerative Medicine
- Cell Biology
- Biochemistry
Background:
- Tendon stem/progenitor cells (TSCs) exhibit regenerative potential and are found in various anatomical locations.
- TSCs play a role in regulating inflammation during the healing process of acute tendon injuries.
Purpose of the Study:
- To investigate the role of TSCs in tendon healing and inflammation.
- To determine the effect of connective tissue growth factor (CTGF) on TSCs and their contribution to tendon repair.
Main Methods:
- Delivery of CTGF into transected rat patellar tendons.
- Analysis of cell populations (CD146+ TSCs, iNOS+ M1 macrophages) and gene/protein expression (IL-10, IL-6, MMP-3, TIMP-3).
- In vitro studies using tendon cells stimulated with IL-1β and CTGF, followed by signaling pathway analysis (JNK/STAT3).
Main Results:
- CTGF delivery increased CD146+ TSCs, enhanced healing, reduced M1 macrophages, and increased anti-inflammatory IL-10 expression.
- CTGF promoted organized collagen fiber alignment and TIMP-3 expression in TSCs.
- In vitro, CTGF and IL-1β significantly upregulated IL-10 and TIMP-3 in CD146+ TSCs via JNK/STAT3 signaling.
Conclusions:
- CTGF-stimulated TSCs possess anti-inflammatory properties crucial for tendon healing.
- The JNK/STAT3 signaling pathway mediates the CTGF-induced expression of IL-10 and TIMP-3 in TSCs.
- These findings highlight TSCs as key regulators of inflammation in tendon repair, offering potential therapeutic targets.
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