| Literature DB >> 31018125 |
Thành Chung Đặng1, Yoko Ishii2, Van De Nguyen3, Seiji Yamamoto4, Takeru Hamashima5, Noriko Okuno5, Quang Linh Nguyen5, Yang Sang5, Noriaki Ohkawa6, Yoshito Saitoh6, Mohammad Shehata6, Nobuyuki Takakura7, Toshihiko Fujimori8, Kaoru Inokuchi6, Hisashi Mori9, Johanna Andrae10, Christer Betsholtz11, Masakiyo Sasahara12.
Abstract
Oligodendrocyte progenitor cells (OPCs) are widely distributed cells of ramified morphology in adult brain that express PDGFRα and NG2. They retain mitotic activities in adulthood and contribute to oligodendrogenesis and myelin turnover; however, the regulatory mechanisms of their cell dynamics in adult brain largely remain unknown. Here, we found that global Pdgfra inactivation in adult mice rapidly led to elimination of OPCs due to synchronous maturation toward oligodendrocytes. Surprisingly, OPC densities were robustly reconstituted by the active expansion of Nestin+ immature cells activated in meninges and brain parenchyma, as well as a few OPCs that escaped from Pdgfra inactivation. The multipotent immature cells were induced in the meninges of Pdgfra-inactivated mice, but not of control mice. Our findings revealed powerful homeostatic control of adult OPCs, engaging dual cellular sources of adult OPC formation. These properties of the adult oligodendrocyte lineage and the alternative OPC source may be exploited in regenerative medicine.Entities:
Keywords: PDGFRα; adult brain; differentiation; mesenchymal cell; oligodendrocyte progenitor cell; pericyte; regeneration
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Year: 2019 PMID: 31018125 DOI: 10.1016/j.celrep.2019.03.084
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423