Intravenous Grafts of Human Amniotic Fluid-Derived Stem Cells Reduce Behavioral Deficits in Experimental Ischemic Stroke

Author:

Sibov Tatiana Taís1,Pavon Lorena Favaro1,Cabral Francisco Romero2,Cunha Ivone Farias2,de Oliveira Daniela Mara3,de Souza Jean Gabriel4,Marti Luciana Cavalheiro2,da Cruz Edgar Ferreira5,Malheiros Jackeline Moraes6,Paiva Fernando F.6,Tannús Alberto6,de Oliveira Sérgio Mascarenhas6,da Costa Marcos Devanir Silva1ORCID,Dastoli Patrícia A.1,Mendonça Jardel N.1,de Toledo Silvia Regina Caminada7,Malheiros Suzana M. Fleury28,de Paiva Neto Manoel Antonio1,Rego Nelma Bastos Bezerra9,Moron Antônio Fernandes9,Cavalheiro Sérgio1

Affiliation:

1. Department of Neurology and Neurosurgery, Escola Paulista de Medicina—Universidade Federal de São Paulo (EPM-UNIFESP), São Paulo, Brazil

2. Hospital Israelita Albert Einstein (HIAE), Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, Brazil

3. Department of Genetics and Morphology, Universidade de Brasilia, São Paulo, Brazil

4. Biochemistry and Biophysics Laboratory, Butantan Institute, São Paulo, Brazil

5. Department of Medicine, Discipline of Nephrology, Escola Paulista de Medicina—Universidade Federal de São Paulo (EPM-UNIFESP), São Paulo, Brazil

6. São Carlos Institute of Physics, São Paulo University, São Paulo, Brazil

7. Pediatrics Oncology Institute, GRAACC (Grupo de Apoio ao Adolescente e a Criança com Câncer), Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil

8. Department of Neuro-Oncology, Escola Paulista de Medicina—Universidade Federal de São Paulo (EPM-UNIFESP), São Paulo, Brazil

9. Department of Obstetrics, Escola Paulista de Medicina—Universidade Federal de São Paulo (EPM-UNIFESP), São Paulo, Brazil

Abstract

Amniotic fluid has been investigated as new cell source for stem cells in the development of future cell-based transplantation. This study reports isolation of viable human amniotic fluid-derived stem cells, labeled with multimodal iron oxide nanoparticles, and its effect on focal cerebral ischemia–reperfusion injury in Wistar rats. Middle cerebral artery occlusion of 60 min followed by reperfusion for 1 h, 6 h, and 24 h was employed in the present study to produce ischemia and reperfusion-induced cerebral injury in rats. Tests were employed to assess the functional outcome of the sensorimotor center activity in the brain, through a set of modified neurological severity scores used to assess motor and exploratory capacity 24 h, 14, and 28 days after receiving cellular therapy via tail vein. In our animal model of stroke, transplanted cells migrated to the ischemic focus, infarct volume decreased, and motor deficits improved. Therefore, we concluded that these cells appear to have beneficial effects on the ischemic brain, possibly based on their ability to enhance endogenous repair mechanisms.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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