Multiple strategies, one mission: mesenchymal stromal cell-based mechanisms of action in osteoarthritis

Maid Junuzović1, Antonia Troillet2, Janina Burk1

  • 1Physiology and Pathophysiology, Department of Biological Sciences and Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.

Insights

Mesenchymal stromal cells (MSCs) show therapeutic potential for osteoarthritis (OA) by modulating immune responses and promoting tissue repair. Mitochondrial transfer is an emerging mechanism for MSCs to restore joint homeostasis in OA.

Area of Science:

  • Orthopedics
  • Immunology
  • Regenerative Medicine

Background:

  • Osteoarthritis (OA) is a degenerative joint disease involving cartilage breakdown, bone remodeling, and inflammation.
  • Chronic inflammation and cellular imbalance drive OA progression, affecting all joint tissues.
  • Mesenchymal stromal cells (MSCs) are investigated for OA due to their immune-modulating and regenerative properties.

Purpose of the Study:

  • To review the mechanisms by which MSCs exert therapeutic effects in OA.
  • To explore MSCs' indirect therapeutic actions, including paracrine signaling and mitochondrial transfer.
  • To highlight the role of MSCs in restoring joint homeostasis and attenuating OA pathology.

Main Methods:

  • Literature review of current research on MSCs in OA.
  • Analysis of MSC-mediated immunomodulation and regenerative capacities.
  • Focus on indirect therapeutic mechanisms within the articular microenvironment.

Main Results:

  • MSCs primarily act indirectly via paracrine factors, extracellular vesicles, and mitochondrial transfer.
  • MSC-derived mitochondria can be transferred to damaged joint cells, promoting repair.
  • These mechanisms modulate immune responses and support tissue regeneration in OA.

Conclusions:

  • MSCs offer a promising therapeutic strategy for OA through multifaceted indirect mechanisms.
  • Mitochondrial transfer represents a key, emerging pathway for MSCs to rescue joint homeostasis.
  • Further research into MSC mechanisms can optimize OA treatment strategies.