Origin and differentiation of microglia

被引:608
作者
Ginhoux, Florent [1 ]
Lim, Shawn [2 ]
Hoeffel, Guillaume [1 ]
Low, Donovan [1 ]
Huber, Tara [2 ,3 ]
机构
[1] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore, Singapore
[2] Agcy Sci Technol & Res, Genome Inst Singapore, Singapore, Singapore
[3] Natl Univ Singapore, Dept Biol Sci, Singapore 117548, Singapore
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2013年 / 7卷
关键词
microglia; macrophage; central nervous system; origin; yolk sac; CENTRAL-NERVOUS-SYSTEM; PLURIPOTENT STEM-CELLS; BLOOD-BRAIN-BARRIER; SPLEEN MACROPHAGES DIFFERENTIATE; IN-VITRO DIFFERENTIATION; YOLK-SAC HEMATOPOIESIS; RESIDENT MICROGLIA; CORPUS-CALLOSUM; IMMUNOHISTOCHEMICAL LOCALIZATION; EMBRYONIC-DEVELOPMENT;
D O I
10.3389/fncel.2013.00045
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglia are the resident macrophage population of the central nervous system (CNS). Adequate microglial function is crucial for a healthy CNS. Microglia are not only the first immune sentinels of infection, contributing to both innate and adaptive immune responses locally, but are also involved in the maintenance of brain homeostasis. Emerging data are showing new and fundamental roles for microglia in the control of neuronal proliferation and differentiation, as well as in the formation of synaptic connections. While microglia have been studied for decades, a long history of experimental misinterpretation meant that their true origins remained debated. However, recent studies on microglial origin indicate that these cells in fact arise early during development from progenitors in the embryonic yolk sac (YS) that seed the brain rudiment and, remarkably, appear to persist there into adulthood. Here, we review the history of microglial cells and discuss the latest advances in our understanding of their origin, differentiation, and homeostasis, which provides new insights into their roles in health and disease.
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页数:14
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共 152 条
  • [1] Local self-renewal can sustain CNS microglia maintenance and function throughout adult life
    Ajami, Bahareh
    Bennett, Jami L.
    Krieger, Charles
    Tetzlaff, Wolfram
    Rossi, Fabio M. V.
    [J]. NATURE NEUROSCIENCE, 2007, 10 (12) : 1538 - 1543
  • [2] Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool
    Ajami, Bahareh
    Bennett, Jami L.
    Krieger, Charles
    McNagny, Kelly M.
    Rossi, Fabio M. V.
    [J]. NATURE NEUROSCIENCE, 2011, 14 (09) : 1142 - U263
  • [3] BRAIN MICROGLIA CONSTITUTIVELY EXPRESS BETA-2 INTEGRINS
    AKIYAMA, H
    MCGEER, PL
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1990, 30 (01) : 81 - 93
  • [4] MICROGLIAL PROGENITORS WITH A HIGH PROLIFERATIVE POTENTIAL IN THE EMBRYONIC AND ADULT-MOUSE BRAIN
    ALLIOT, F
    LECAIN, E
    GRIMA, B
    PESSAC, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) : 1541 - 1545
  • [5] Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain
    Alliot, F
    Godin, I
    Pessac, B
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02): : 145 - 152
  • [6] Myeloid development is selectively disrupted in PU.1 null mice
    Anderson, KL
    Smith, KA
    Conners, K
    McKercher, SR
    Maki, RA
    Torbett, BE
    [J]. BLOOD, 1998, 91 (10) : 3702 - 3710
  • [7] Temporospatial relationships between macroglia and microglia during in vitro differentiation of murine stem cells
    Angelov, DN
    Arnhold, S
    Andressen, C
    Grabsch, H
    Puschmann, M
    Hescheler, J
    Addicks, K
    [J]. DEVELOPMENTAL NEUROSCIENCE, 1998, 20 (01) : 42 - 51
  • [8] [Anonymous], 1932, CYTOLOGY CELLULAR PA
  • [9] MICROGLIA AND CELL-DEATH IN THE DEVELOPING MOUSE CEREBELLUM
    ASHWELL, K
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1990, 55 (02): : 219 - 230
  • [10] CELL-DEATH IN THE DEVELOPING TRIGEMINAL NUCLEAR-COMPLEX OF THE RAT
    ASHWELL, KWS
    WAITE, PME
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1991, 63 (1-2): : 291 - 295