Frontiers in Cell and Developmental Biology (Feb 2021)

Consistent Long-Term Therapeutic Efficacy of Human Umbilical Cord Matrix-Derived Mesenchymal Stromal Cells After Myocardial Infarction Despite Individual Differences and Transient Engraftment

  • Tiago L. Laundos,
  • Tiago L. Laundos,
  • Tiago L. Laundos,
  • Francisco Vasques-Nóvoa,
  • Francisco Vasques-Nóvoa,
  • Francisco Vasques-Nóvoa,
  • Francisco Vasques-Nóvoa,
  • Rita N. Gomes,
  • Rita N. Gomes,
  • Rita N. Gomes,
  • Vasco Sampaio-Pinto,
  • Vasco Sampaio-Pinto,
  • Vasco Sampaio-Pinto,
  • Pedro Cruz,
  • Hélder Cruz,
  • Jorge M. Santos,
  • Rita N. Barcia,
  • Perpétua Pinto-do-Ó,
  • Perpétua Pinto-do-Ó,
  • Perpétua Pinto-do-Ó,
  • Diana S. Nascimento,
  • Diana S. Nascimento,
  • Diana S. Nascimento

DOI
https://doi.org/10.3389/fcell.2021.624601
Journal volume & issue
Vol. 9

Abstract

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Human mesenchymal stem cells gather special interest as a universal and feasible add-on therapy for myocardial infarction (MI). In particular, human umbilical cord matrix-derived mesenchymal stromal cells (UCM-MSC) are advantageous since can be easily obtained and display high expansion potential. Using isolation protocols compliant with cell therapy, we previously showed UCM-MSC preserved cardiac function and attenuated remodeling 2 weeks after MI. In this study, UCM-MSC from two umbilical cords, UC-A and UC-B, were transplanted in a murine MI model to investigate consistency and durability of the therapeutic benefits. Both cellular products improved cardiac function and limited adverse cardiac remodeling 12 weeks post-ischemic injury, supporting sustained and long-term beneficial therapeutic effect. Donor associated variability was found in the modulation of cardiac remodeling and activation of the Akt-mTOR-GSK3β survival pathway. In vitro, the two cell products displayed similar ability to induce the formation of vessel-like structures and comparable transcriptome in normoxia and hypoxia, apart from UCM-MSCs proliferation and expression differences in a small subset of genes associated with MHC Class I. These findings support that UCM-MSC are strong candidates to assist the treatment of MI whilst calling for the discussion on methodologies to characterize and select best performing UCM-MSC before clinical application.

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