New tools for studying microglia in the mouse and human CNS

被引:1389
作者
Bennett, Mariko L. [1 ]
Bennett, F. Chris [1 ,2 ]
Liddelow, Shane A. [1 ,3 ]
Ajami, Bahareh [4 ]
Zamanian, Jennifer L. [1 ]
Fernhoff, Nathaniel B. [5 ,6 ,7 ,8 ]
Mulinyawe, Sara B. [1 ]
Bohlen, Christopher J. [1 ]
Adil, Aykezar [1 ]
Tucker, Andrew [1 ]
Weissman, Irving L. [5 ,6 ,7 ,8 ]
Chang, Edward F. [9 ]
Li, Gordon [10 ]
Grant, Gerald A. [10 ]
Gephart, Melanie G. Hayden [10 ]
Barres, Ben A. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurobiol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[3] Univ Melbourne, Dept Pharmacol & Therapeut, Melbourne, Vic 3010, Australia
[4] Stanford Univ, Dept Neurol, Sch Med, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Ludwig Ctr Canc Stem Cell Res & Med, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Stanford Canc Inst, Stanford, CA 94305 USA
[8] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[9] Univ Calif San Francisco, San Francisco Epilepsy Ctr, San Francisco, CA 94143 USA
[10] Stanford Univ, Sch Med, Dept Neurosurg, Stanford, CA 94305 USA
基金
英国医学研究理事会; 加拿大健康研究院; 美国国家卫生研究院;
关键词
microglia; glia; developmental neuroscience; RNAseq; macrophage; PERIPHERAL-NERVE INJURY; GENE-EXPRESSION; BRAIN-INJURY; CELLS; MACROPHAGES; RECEPTOR; REVEALS; PROGENITORS; ACTIVATION; MONOCYTES;
D O I
10.1073/pnas.1525528113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The specific function of microglia, the tissue resident macrophages of the brain and spinal cord, has been difficult to ascertain because of a lack of tools to distinguish microglia from other immune cells, thereby limiting specific immunostaining, purification, and manipulation. Because of their unique developmental origins and predicted functions, the distinction of microglia from other myeloid cells is critically important for understanding brain development and disease; better tools would greatly facilitate studies of microglia function in the developing, adult, and injured CNS. Here, we identify transmembrane protein 119 (Tmem119), a cell-surface protein of unknown function, as a highly expressed microglia-specific marker in both mouse and human. We developed monoclonal antibodies to its intracellular and extracellular domains that enable the immunostaining of microglia in histological sections in healthy and diseased brains, as well as isolation of pure nonactivated microglia by FACS. Using our antibodies, we provide, to our knowledge, the first RNAseq profiles of highly pure mouse microglia during development and after an immune challenge. We used these to demonstrate that mouse microglia mature by the second postnatal week and to predict novel microglial functions. Together, we anticipate these resources will be valuable for the future study and understanding of microglia in health and disease.
引用
收藏
页码:E1738 / E1746
页数:9
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