Brain Vascular Pericytes Following Ischemia Have Multipotential Stem Cell Activity to Differentiate Into Neural and Vascular Lineage Cells

Author:

Nakagomi Takayuki1,Kubo Shuji2,Nakano-Doi Akiko1,Sakuma Rika1,Lu Shan13,Narita Aya1,Kawahara Maiko14,Taguchi Akihiko5,Matsuyama Tomohiro1

Affiliation:

1. Institute for Advanced Medical Sciences, Nishinomiya, Hyogo, Japan

2. Department of Genetics Hyogo College of Medicine, Nishinomiya, Hyogo, Japan

3. Department of Neurology of Hangzhou First People's Hospital, Hangzhou, People's Republic of China

4. Graduate School of Science and Technology Kwansei Gakuin University, Sanda, Hyogo, Japan

5. Department of Regenerative Medicine Research Institute of Biomedical Research and Innovation, Kobe, Hyogo, Japan

Abstract

Abstract Brain vascular pericytes (PCs) are a key component of the blood-brain barrier (BBB)/neurovascular unit, along with neural and endothelial cells. Besides their crucial role in maintaining the BBB, increasing evidence shows that PCs have multipotential stem cell activity. However, their multipotency has not been considered in the pathological brain, such as after an ischemic stroke. Here, we examined whether brain vascular PCs following ischemia (iPCs) have multipotential stem cell activity and differentiate into neural and vascular lineage cells to reconstruct the BBB/neurovascular unit. Using PCs extracted from ischemic regions (iPCs) from mouse brains and human brain PCs cultured under oxygen/glucose deprivation, we show that PCs developed stemness presumably through reprogramming. The iPCs revealed a complex phenotype of angioblasts, in addition to their original mesenchymal properties, and multidifferentiated into cells from both a neural and vascular lineage. These data indicate that under ischemic/hypoxic conditions, PCs can acquire multipotential stem cell activity and can differentiate into major components of the BBB/neurovascular unit. Thus, these findings support the novel concept that iPCs can contribute to both neurogenesis and vasculogenesis at the site of brain injuries. Stem Cells  2015;33:1962–1974

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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