Scientific Reports (Jul 2017)

Intravenous infusion of human bone marrow mesenchymal stromal cells promotes functional recovery and neuroplasticity after ischemic stroke in mice

  • Eliana Sammali,
  • Claudia Alia,
  • Gloria Vegliante,
  • Valentina Colombo,
  • Nadia Giordano,
  • Francesca Pischiutta,
  • Giorgio B. Boncoraglio,
  • Mario Barilani,
  • Lorenza Lazzari,
  • Matteo Caleo,
  • Maria-Grazia De Simoni,
  • Giuseppe Gaipa,
  • Giuseppe Citerio,
  • Elisa R. Zanier

DOI
https://doi.org/10.1038/s41598-017-07274-w
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 13

Abstract

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Abstract Transplantation of human bone marrow mesenchymal stromal cells (hBM-MSC) promotes functional recovery after stroke in animal models, but the mechanisms underlying these effects remain incompletely understood. We tested the efficacy of Good Manufacturing Practices (GMP) compliant hBM-MSC, injected intravenously 3.5 hours after injury in mice subjected to transient middle cerebral artery occlusion (tMCAo). We addressed whether hBM-MSC are efficacious and if this efficacy is associated with cortical circuit reorganization using neuroanatomical analysis of GABAergic neurons (parvalbumin; PV-positive cells) and perineuronal nets (PNN), a specialized extracellular matrix structure which acts as an inhibitor of neural plasticity. tMCAo mice receiving hBM-MSC, showed early and lasting improvement of sensorimotor and cognitive functions compared to control tMCAo mice. Furthermore, 5 weeks post-tMCAo, hBM-MSC induced a significant rescue of ipsilateral cortical neurons; an increased proportion of PV-positive neurons in the perilesional cortex, suggesting GABAergic interneurons preservation; and a lower percentage of PV-positive cells surrounded by PNN, indicating an enhanced plastic potential of the perilesional cortex. These results show that hBM-MSC improve functional recovery and stimulate neuroprotection after stroke. Moreover, the downregulation of “plasticity brakes” such as PNN suggests that hBM-MSC treatment stimulates plasticity and formation of new connections in the perilesional cortex.