Tendon microstructural disruption promotes tendon-derived stem cells to express chondrogenic genes by activating

Chang Liu1,2, Tian-Yu Li1, Yong Chen1

  • 1Shenzhen Key Laboratory of Musculoskeletal Tissue Reconstruction and Function Restoration, Division of Hand and Microvascular Surgery, Department of Orthopedic Surgery, Shenzhen People's Hospital (the First Affiliated Hospital, Southern University of Science and Technology the Second Clinical Medical College, Jinan University), Shenzhen, China.

Insights

Tendon microdamage can trigger endoplasmic reticulum (ER) stress, promoting tendon-derived stem cells (TDSCs) to differentiate into chondrocytes. Inhibiting ER stress reduces this chondrogenic differentiation, revealing a key mechanism in tendinopathy development.

Area of Science:

  • Biomedical Engineering
  • Stem Cell Biology
  • Orthopedics

Background:

  • Tendinopathy involves erroneous differentiation of tendon-derived stem cells (TDSCs).
  • Regulatory mechanisms of TDSC differentiation in tendinopathy are not fully understood.
  • Tendon microstructural disruption is a potential factor influencing TDSC differentiation.

Purpose of the Study:

  • To investigate the role of tendon microstructural disruption in TDSC differentiation.
  • To elucidate the underlying mechanisms, focusing on endoplasmic reticulum (ER) stress.

Main Methods:

  • Bovine Achilles tendon slices were subjected to varying tensile strains.
  • TDSCs were cultured on these altered tendon microstructures.
  • Quantitative RT-PCR, immunostaining, and Western blot analyzed TDSC differentiation and ER stress markers (ATF-4, PERK).
  • ER stress inhibition was used to assess its effect on chondrogenic differentiation.

Main Results:

  • Structural alterations (6.4% strain) promoted TDSC chondrogenic gene expression without affecting viability.
  • ER stress markers ATF-4 and PERK were upregulated following structural alteration.
  • Inhibiting ER stress reduced ATF-4 and SOX9 (chondrogenic gene) expression in TDSCs.

Conclusions:

  • Tendon microdamage induces chondrogenic differentiation of TDSCs.
  • This process is mediated by ER stress activation.
  • ER stress leads to the subsequent activation of ATF-4 and SOX9, contributing to tendinopathy development.