AI Article Synopsis

  • Mesenchymal stem cells (MSCs) show potential for treating chronic degenerative diseases due to their ability to regenerate tissues, differentiate into other cell types, and secrete factors that aid in healing and immune response.
  • Despite their promise, MSC research faces challenges, especially related to their low survival and migration rates when infused into the body, which raises questions about their effectiveness as a therapy.
  • Recent studies suggest that MSCs can migrate to injured organs, such as the heart and lymph nodes, even though they weren't detectable at the end of the investigation, indicating that their beneficial effects might stem from the secretion of exosomes rather than their physical presence.

Article Abstract

Mesenchymal stem cells (MSC) are promising candidates to combat the growing rates of chronic degenerative diseases. These cells provide regeneration and/or differentiation into other cell types, and secrete various trophic factors that participate in migration, proliferation, and immunomodulation. However, the novelty of MSC research has noticeably declined as common barriers and unresolved challenges prevent further progress. A common issue is the low survivability and migration of systemically infused MSC towards targeted regions. Nevertheless, successful clinical treatment of various chronic diseases suggests that the MSCs may have an alternative mechanism. Recent advancements have shown labelling and imaging techniques to be a reliable source of data. These data not only illustrate the biodistribution but can be referenced to either support and/or improve the specificities of the cellular therapy construct. In this review, we compile recent studies between 2017 and 2021 to determine the homing and migration of MSCs by specific and peripherally-targeted organs. We also compare the different cell-tracking assays with the safety and efficacy of their therapeutic construct. We found that the common route of MSCs occurred in the lungs, liver, kidney and spleen. Furthermore, MSCs were also able to home and migrate towards targeted or injured organs such as the heart and lymph nodes. Although the MSCs were not detectable by the end of the study, the tested animals had significantly improved in terms of the disease symptoms and their related comorbidities. Thus, we hypothesize that the secretion of exosomes had contributed to this phenomenon.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091132PMC

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