Ginhoux Florent, Prinz Marco
Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Singapore 138648.
Institute of Neuropathology, University of Freiburg, 79106 Freiburg, Germany BIOSS Centre for Biological Signalling Studies, University of Freiburg, 79106 Freiburg, Germany.
Cold Spring Harb Perspect Biol. 2015 Jul 1;7(8):a020537. doi: 10.1101/cshperspect.a020537.
Microglia are the resident macrophages of the central nervous system (CNS), which sit in close proximity to neural structures and are intimately involved in brain homeostasis. The microglial population also plays fundamental roles during neuronal expansion and differentiation, as well as in the perinatal establishment of synaptic circuits. Any change in the normal brain environment results in microglial activation, which can be detrimental if not appropriately regulated. Aberrant microglial function has been linked to the development of several neurological and psychiatric diseases. However, microglia also possess potent immunoregulatory and regenerative capacities, making them attractive targets for therapeutic manipulation. Such rationale manipulations will, however, require in-depth knowledge of their origins and the molecular mechanisms underlying their homeostasis. Here, we discuss the latest advances in our understanding of the origin, differentiation, and homeostasis of microglial cells and their myelomonocytic relatives in the CNS.
小胶质细胞是中枢神经系统(CNS)中的常驻巨噬细胞,它们紧邻神经结构,密切参与脑内稳态。小胶质细胞群体在神经元增殖和分化过程中以及在围产期突触回路的建立中也发挥着重要作用。正常脑环境中的任何变化都会导致小胶质细胞激活,如果调节不当,可能会产生有害影响。异常的小胶质细胞功能与多种神经和精神疾病的发生有关。然而,小胶质细胞也具有强大的免疫调节和再生能力,使其成为治疗干预的有吸引力的靶点。然而,这种合理的干预将需要深入了解它们的起源以及其稳态背后的分子机制。在这里,我们讨论了我们对中枢神经系统中小胶质细胞及其骨髓单核细胞亲属的起源、分化和稳态的最新认识进展。