A Comparative Study of Three Different Types of Stem Cells for Treatment of Rat Spinal Cord Injury

Author:

Ruzicka Jiri1,Machova-Urdzikova Lucia1,Gillick John2,Amemori Takashi1,Romanyuk Nataliya1,Karova Kristyna13,Zaviskova Kristyna13,Dubisova Jana13,Kubinova Sarka1,Murali Raj2,Sykova Eva13,Jhanwar-Uniyal Meena2,Jendelova Pavla13

Affiliation:

1. Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic

2. New York Medical College, Valhalla, NY, USA

3. Department of Neuroscience, Charles University, Second Faculty of Medicine, Prague, Czech Republic

Abstract

Three different sources of human stem cells—bone marrow-derived mesenchymal stem cells (BM-MSCs), neural progenitors (NPs) derived from immortalized spinal fetal cell line (SPC-01), and induced pluripotent stem cells (iPSCs)—were compared in the treatment of a balloon-induced spinal cord compression lesion in rats. One week after lesioning, the rats received either BM-MSCs (intrathecally) or NPs (SPC-01 cells or iPSC-NPs, both intraspinally), or saline. The rats were assessed for their locomotor skills (BBB, flat beam test, and rotarod). Morphometric analyses of spared white and gray matter, axonal sprouting, and glial scar formation, as well as qPCR and Luminex assay, were conducted to detect endogenous gene expression, while inflammatory cytokine levels were performed to evaluate the host tissue response to stem cell therapy. The highest locomotor recovery was observed in iPSC-NP-grafted animals, which also displayed the highest amount of preserved white and gray matter. Grafted iPSC-NPs and SPC-01 cells significantly increased the number of growth-associated protein 43 (GAP43+) axons, reduced astrogliosis, downregulated Casp3 expression, and increased IL-6 and IL-12 levels. hMSCs transiently decreased levels of inflammatory IL-2 and TNF-α. These findings correlate with the short survival of hMSCs, while NPs survived for 2 months and matured slowly into glia- and tissue-specific neuronal precursors. SPC-01 cells differentiated more in astroglial phenotypes with a dense structure of the implant, whereas iPSC-NPs displayed a more neuronal phenotype with a loose structure of the graft. We concluded that the BBB scores of iPSC-NP- and hMSC-injected rats were superior to the SPC-01-treated group. The iPSC-NP treatment of spinal cord injury (SCI) provided the highest recovery of locomotor function due to robust graft survival and its effect on tissue sparing, reduction of glial scarring, and increased axonal sprouting.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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