| Literature DB >> 32783928 |
Zhen Xu1, Yanxia Rao2, Yubin Huang1, Tian Zhou1, Rui Feng1, Shanshan Xiong1, Ti-Fei Yuan2, Shan Qin3, Yijie Lu3, Xin Zhou4, Xiaoyu Li5, Bo Qin6, Ying Mao4, Bo Peng7.
Abstract
Microglia are important immune cells in the central nervous system (CNS). Dysfunctions of gene-deficient microglia contribute to the development and progression of multiple CNS diseases. Microglia replacement by nonself cells has been proposed to treat microglia-associated disorders. However, some attempts have failed due to low replacement efficiency, such as with the traditional bone marrow transplantation approach. In this study, we develop three efficient strategies for microglia replacement: microglia replacement by bone marrow transplantation (mrBMT), microglia replacement by peripheral blood (mrPB), and microglia replacement by microglia transplantation (mrMT). mrBMT and mrPB allow microglia-like cells to efficiently replace resident microglia in the whole CNS. On the other hand, mrMT achieves microglia replacement in brain regions of interest. In summary, the present study offers effective tactics for microglia replacement with diverse application scenarios, which potentially opens up a window on treating microglia-associated CNS disorders.Entities:
Keywords: CSF1R; allograft; allotransplantation; bone marrow transplantation; fate mapping; microglia; parabiosis; replacement; repopulation; transplantation
Mesh:
Year: 2020 PMID: 32783928 DOI: 10.1016/j.celrep.2020.108041
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423