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Updated: Jun 12, 2026

Generation of Induced Pluripotent Stem Cell-Derived iTenocytes via Combined Scleraxis Overexpression and 2D Uniaxial Tension
Published on: March 1, 2024
Interleukins 4 and 13 modulate gene expression and promote proliferation of primary human tenocytes
Jean-Paul Courneya1, Irina G Luzina, Cynthia B Zeller
1Department of Medicine, University of Maryland School of Medicine and Baltimore VA Medical Center, Baltimore, MD, USA. satamas@umaryland.edu.
Background:
Tendon disorders (tendinopathies) pose serious biomedical and socioeconomic problems. Despite diverse treatment approaches, the best treatment strategy remains unclear. Surgery remains the last resort because of the associated morbidity and inconsistent outcomes. We hypothesized that, similar to fibroblasts in various organs, tendon fibroblasts (tenocytes) might be responsive to stimulation with interleukins (ILs), particularly IL-4 and IL-13. These two cytokines share sequence homology, receptor chains and functional effects, including stimulation of fibrogenesis. It is unknown whether tenocytes are responsive to stimulation with IL-4 or IL-13. If true, local use of these cytokines might be used to facilitate tendon repair in patients with tendinopathies or used for tendon tissue-engineering approaches to facilitate tenocyte growth on scaffolds in culture.
Results:
Tendon tissues that would normally be discarded were obtained during reconstructive surgery procedures performed for clinical indications. Primary tenocytes were derived from Achilles, posterior tibial, flexor digitorum longus and flexor hallucis longus tendon tissue samples. Reverse transcriptase quantitative PCR (RT-qPCR) experiments revealed that mRNAs for the receptor (R) chains IL-4Ralpha, IL-13Ralpha1 and IL-13Ralpha2, but not the common gamma-chain were present in all tested tendon tissues and in cultured tenocytes. Levels of IL-13R chain mRNAs were significantly higher than those of IL-4R mRNA. The cultures responded, in a dose-dependent fashion, to stimulation with recombinant human IL-4 or IL-13, by increasing proliferation rates 1.5 to 2.0-fold. The mRNA levels of 84 genes related to cell cycle regulation were measured by RT-qPCR after 6 h and 24 h of activation. The expression levels of several genes, notably CDK6 and CDKN2B changed more than twofold. In contrast to their effects on proliferation, stimulation with IL-4 or IL-13 had little if any effect on the levels of collagen mRNA or protein in cultured primary tenocytes. The mRNA levels of 84 other genes related to extracellular matrix and cell adhesion were also measured by RT-qPCR; expression of only five genes was consistently changed.
Conclusions:
Stimulation with IL-4 or IL-13 could be used to facilitate tendon repair in vivo or to aid in tendon tissue engineering, through stimulation of tenocyte proliferation.
Insights
Interleukin-4 (IL-4) and Interleukin-13 (IL-13) stimulate tendon fibroblast (tenocyte) proliferation, offering potential for tendon repair and tissue engineering. This research explores their role in enhancing cell growth for therapeutic applications.
Area of Science:
- Biomedical Science
- Cell Biology
- Regenerative Medicine
Background:
- Tendon disorders (tendinopathies) present significant biomedical and socioeconomic challenges.
- Current treatments for tendinopathies lack consistent outcomes, and surgery is a last resort.
- The response of tendon fibroblasts (tenocytes) to interleukins (ILs), specifically IL-4 and IL-13, is unknown.
Purpose of the Study:
- To investigate the responsiveness of tenocytes to IL-4 and IL-13 stimulation.
- To explore the potential of IL-4 and IL-13 in facilitating tendon repair and tissue engineering.
Main Methods:
- Primary tenocytes were isolated from human tendon tissue samples.
- Reverse transcriptase quantitative PCR (RT-qPCR) was used to analyze gene expression for IL-4 and IL-13 receptors.
- Cell proliferation assays were performed after stimulation with recombinant human IL-4 or IL-13.
Main Results:
- Tenocytes express mRNAs for IL-4Ralpha, IL-13Ralpha1, and IL-13Ralpha2 receptors.
- IL-4 and IL-13 stimulation significantly increased tenocyte proliferation in a dose-dependent manner (1.5–2.0-fold).
- IL-4 and IL-13 had minimal impact on collagen mRNA or protein levels, but altered expression of cell cycle-related genes.
Conclusions:
- IL-4 and IL-13 can stimulate tenocyte proliferation.
- These cytokines hold promise for enhancing tendon repair in vivo and aiding tenocyte growth in tendon tissue engineering applications.
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