Intravenous Grafts of Human Amniotic Fluid-Derived Stem Cells Reduce Behavioral Deficits in Experimental Ischemic Stroke.
Tatiana Taís SibovLorena Favaro PavonFrancisco Romero CabralIvone Farias CunhaDaniela Mara de OliveiraJean Gabriel de SouzaLuciana Cavalheiro MartiEdgar Ferreira da CruzJackeline Moraes MalheirosFernando F PaivaAlberto TannúsSérgio Mascarenhas de OliveiraMarcos Devanir Silva da CostaPatrícia A DastoliJardel N MendonçaSilvia Regina Caminada de ToledoSuzana M Fleury MalheirosManoel Antonio de Paiva NetoNelma Bastos Bezerra RegoAntônio Fernandes MoronSérgio CavalheiroPublished in: Cell transplantation (2019)
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.
Keyphrases
- cerebral ischemia
- stem cells
- cell therapy
- subarachnoid hemorrhage
- middle cerebral artery
- induced apoptosis
- brain injury
- endothelial cells
- blood brain barrier
- acute myocardial infarction
- single cell
- traumatic brain injury
- white matter
- atrial fibrillation
- cell cycle arrest
- induced pluripotent stem cells
- emergency department
- resting state
- heart failure
- iron oxide nanoparticles
- high dose
- multiple sclerosis
- cell death
- pluripotent stem cells
- mesenchymal stem cells
- drug induced
- high resolution
- umbilical cord
- oxidative stress
- left ventricular