| Literature DB >> 29802840 |
Hiroshi Nagahama1, Masahito Nakazaki1, Masanori Sasaki2, Yuko Kataoka-Sasaki1, Takahiro Namioka1, Ai Namioka1, Shinichi Oka1, Rie Onodera1, Junpei Suzuki1, Yuichi Sasaki1, Jeffery D Kocsis3, Osamu Honmou4.
Abstract
Systemic administration of mesenchymal stem cells (MSCs) following cerebral infarction exerts functional improvements. Previous research has suggested potential therapeutic mechanisms that promote neuroprotection and synaptogenesis. These include secretion of neurotrophic factors, remodeling of neural circuits, restoration of the blood brain barrier, reduction of inflammatory infiltration and demyelination, and elevation of trophic factors. In addition to these mechanisms, we hypothesized that restored interhemispheric bilateral motor cortex connectivity might be an additional mechanism of functional recovery. In the present study, we have shown, with both MRI diffusion tensor imaging (DTI) and neuroanatomical tracing techniques using an adeno-associated virus (AAV) expressing GFP, that there was anatomical restoration of cortical interhemispheric connections through the corpus callosum after intravenous infusion of MSCs in a rat middle cerebral artery occlusion (MCAO) stroke model. Moreover, the degree of connectivity was greater in the MSC-treated group than in the vehicle-infused group. In accordance, both the thickness of corpus callosum and synaptic puncta in the contralateral (non-infarcted) motor cortex connected to the corpus callosum were greater in the MSC-treated group than in the vehicle group. Together, these results suggest that distinct preservation of interhemispheric cortical connections through corpus callosum was promoted by intravenous infusion of MSCs. This anatomical preservation of the motor cortex in the contralateral hemisphere may contribute to functional improvements following MSC therapy for cerebral stroke.Entities:
Keywords: Mesenchymal stem cell; Stroke; Transplantation
Mesh:
Year: 2018 PMID: 29802840 DOI: 10.1016/j.brainres.2018.05.033
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252