Ischemia-Induced Multipotent Stem Cells Isolated from Stroke Patients Exhibit Higher Neurogenic Differentiation Potential than Bone Marrow-Derived Mesenchymal Stem Cells.


Journal

Stem cells and development
ISSN: 1557-8534
Titre abrégé: Stem Cells Dev
Pays: United States
ID NLM: 101197107

Informations de publication

Date de publication:
01 08 2020
Historique:
pubmed: 10 6 2020
medline: 3 9 2021
entrez: 10 6 2020
Statut: ppublish

Résumé

Perivascular areas of the brain harbor multipotent stem cells. We recently demonstrated that after a stroke, brain pericytes exhibit features of multipotent stem cells. Moreover, these ischemia-induced multipotent stem cells (iSCs) are present within ischemic areas of the brain of patients diagnosed with stroke. Although increasing evidence shows that iSCs have traits similar to those of mesenchymal stem cells (MSCs), the phenotypic similarities and differences between iSCs and MSCs remain unclear. In this study, we used iSCs extracted from stroke patients (h-iSCs) and compared their neurogenic potential with that of human MSCs (h-MSCs) in vitro. Microarray analysis, fluorescence-activated cell sorting, immunohistochemistry, and multielectrode array were performed to compare the characteristics of h-iSCs and h-MSCs. Although h-iSCs and h-MSCs had similar gene expression profiles, the percentage expressing the neural stem/progenitor cell marker nestin was significantly higher in h-iSCs than in h-MSCs. Consistent with these findings, h-iSCs, but not h-MSCs, differentiated into electrophysiologically functional neurons. In contrast, although both h-iSCs and h-MSCs were able to differentiate into several mesodermal lineages, including adipocytes, osteocytes, and chondrocytes, the potential of h-iSCs to differentiate into adipocytes and osteocytes was relatively low. These results suggest that compared with h-MSCs, h-iSCs predominantly exhibit neural rather than mesenchymal lineages. In addition, these results indicate that h-iSCs have the potential to repair the injured brain of patients with stroke by directly differentiating into neuronal lineages.

Identifiants

pubmed: 32515302
doi: 10.1089/scd.2020.0031
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

994-1006

Auteurs

Saujanya Rajbhandari (S)

Department of Neurosurgery, Hyogo College of Medicine, Nishinomiya, Japan.

Mikiya Beppu (M)

Department of Neurosurgery, Hyogo College of Medicine, Nishinomiya, Japan.

Toshinori Takagi (T)

Department of Neurosurgery, Hyogo College of Medicine, Nishinomiya, Japan.

Akiko Nakano-Doi (A)

Institute for Advanced Medical Sciences, Departments of Hyogo College of Medicine, Nishinomiya, Japan.
Therapeutic Progress in Brain Diseases and Hyogo College of Medicine, Nishinomiya, Japan.

Nami Nakagomi (N)

Surgical Pathology, Hyogo College of Medicine, Nishinomiya, Japan.

Tomohiro Matsuyama (T)

Therapeutic Progress in Brain Diseases and Hyogo College of Medicine, Nishinomiya, Japan.

Takayuki Nakagomi (T)

Institute for Advanced Medical Sciences, Departments of Hyogo College of Medicine, Nishinomiya, Japan.
Therapeutic Progress in Brain Diseases and Hyogo College of Medicine, Nishinomiya, Japan.

Shinichi Yoshimura (S)

Department of Neurosurgery, Hyogo College of Medicine, Nishinomiya, Japan.
Institute for Advanced Medical Sciences, Departments of Hyogo College of Medicine, Nishinomiya, Japan.

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