Therapeutics effect of mesenchymal stromal cells in reactive oxygen species-induced damages

Subodh Kumar1, Ranjan Verma1, Nishant Tyagi1

  • 1Stem Cell & Gene Therapy Research Group, Institute of Nuclear Medicine & Allied Sciences (INMAS), Defence Research and Development Organisation (DRDO), Lucknow Road, Timarpur, Delhi, 110054, India.

Human Cell
|November 20, 2021
PubMed

Insights

Reactive Oxygen Species (ROS) cause cellular damage and disease. Mesenchymal stromal cells (MSCs) show promise as a novel therapy for ROS-induced pathologies due to their unique regenerative and immunomodulatory properties.

Area of Science:

  • Biomedical Science
  • Cell Biology
  • Pathology

Background:

  • Reactive Oxygen Species (ROS) are byproducts of aerobic respiration, crucial in cellular signaling but implicated in oxidative damage, inflammation, and cancer when imbalanced.
  • Oxidative damage driven by ROS can trigger signaling pathways promoting cell proliferation, oncogenesis, and metastasis.
  • Mesenchymal stromal cells (MSCs) are being investigated for therapeutic potential across diverse diseases, including cardiovascular, kidney, and neurodegenerative conditions.

Purpose of the Study:

  • To review the potential of Mesenchymal Stromal Cells (MSCs) in targeted therapy against pathologies induced by Reactive Oxygen Species (ROS).
  • To highlight MSCs' regenerative, immunomodulatory, and migratory capacities for treating ROS-related diseases.
  • To explore MSCs as a novel, side-effect-free therapeutic strategy for ROS-induced conditions.

Main Methods:

  • Literature review focusing on the role of ROS in disease pathogenesis.
  • Analysis of Mesenchymal Stromal Cells' biological properties and therapeutic applications.
  • Synthesis of current research on MSCs for ROS-mediated pathologies and anti-tumor strategies.

Main Results:

  • Imbalanced ROS levels lead to oxidative damage, inflammation, and cancer.
  • MSCs possess regenerative, immunomodulatory, and migratory capabilities beneficial for therapeutic interventions.
  • Current anti-tumor drugs show limitations, creating a need for novel therapeutic approaches.

Conclusions:

  • MSCs offer a promising avenue for targeted therapy against ROS-induced pathologies.
  • The unique properties of MSCs position them as potential next-generation therapeutics with minimal side effects.
  • Further research into MSC-based therapies could revolutionize the treatment of oxidative stress-related diseases.