Key result
Ischemia triggers brain PDGFRβ(+) pericytes to acquire stemness and differentiate into phagocytic microglia-like cells.
BACKGROUND: Microglia are the resident macrophage population of the central nervous system (CNS) and play essential roles, particularly in inflammation-mediated pathological conditions such as ischemic stroke. Increasing evidence shows that the population of vascular cells located around the blood vessels, rather than circulating cells, harbor stem cells and that these resident vascular stem cells (VSCs) are the likely source of some microglia. However, the precise traits and origins of these cells under pathological CNS conditions remain unclear. METHODS: In this study, we used a mouse model of cerebral infarction to investigate whether reactive pericytes (PCs) acquire microglia-producing VSC activity following ischemia. RESULTS: We demonstrated the localization of ionized calcium-binding adaptor molecule 1 (Iba1)-expressing microglia to perivascular regions within ischemic areas. These cells expressed platelet-derived growth factor receptor-β (PDGFRβ), a hallmark of vascular PCs. PDGFRβ(+) PCs isolated from ischemic, but not non-ischemic, areas expressed stem/undifferentiated cell markers and subsequently differentiated into various cell types, including microglia-like cells with phagocytic capacity. CONCLUSIONS: The study results suggest that vascular PCs acquire multipotent VSC activity under pathological conditions and may thus be a novel source of microglia.
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Sakuma et al. (2016) studied Ischemic stroke / cerebral infarction. Cerebral ischemia (PDGFRβ(+) pericytes from ischemic areas) vs. Non-ischemic areas was evaluated on Acquisition of multipotent vascular stem cell activity and differentiation into microglia-like cells. PDGFRβ(+) pericytes from ischemic brain areas in mice expressed stem cell markers and differentiated into phagocytic microglia-like cells, unlike those from non-ischemic areas.
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