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引用次数: 104
摘要
人体的血管系统被认为是为了向细胞提供氧气和营养物质而发展起来的,而不是简单的扩散。因此,生长中的中枢神经系统(CNS)的相对缺氧是为其服务的复杂血管床进入和细化的主要驱动力。然而,即使在中枢神经系统血管系统建立之前,中枢神经系统特异性巨噬细胞(小胶质细胞)就已经迁移到大脑中。最近对小鼠的研究表明,小胶质细胞在发育过程中形成中枢神经系统血管,并在病理损伤过程中重塑这些血管的基本重要性。在这篇综述中,我们讨论了中枢神经系统小胶质细胞的起源和它们在大脑中的定位基于小鼠获得的数据。然后我们回顾了支持这些小胶质细胞在发育性血管生成中的功能作用的证据。尽管中枢神经系统缺血等病理过程可能会破坏小胶质细胞/巨噬细胞的发育功能,并对脑新生血管生成产生重大影响,但我们将这一主题留给了最近的其他综述(Nat Rev Immunol 9:259- 270,2009和Trends Mol Med 17:743-752, 2011)。
The importance of microglia in the development of the vasculature in the central nervous system.
The body's vascular system is thought to have developed in order to supply oxygen and nutrients to cells beyond the reach of simple diffusion. Hence, relative hypoxia in the growing central nervous system (CNS) is a major driving force for the ingression and refinement of the complex vascular bed that serves it. However, even before the establishment of this CNS vascular system, CNS-specific macrophages (microglia) migrate into the brain. Recent studies in mice point to the fundamental importance of microglia in shaping CNS vasculature during development, and re-shaping these vessels during pathological insults. In this review, we discuss the origin of CNS microglia and their localization within the brain based on data obtained in mice. We then review evidence supporting a functional role of these microglia in developmental angiogenesis. Although pathologic processes such as CNS ischemia may subvert the developmental functions of microglia/macrophages with significant effects on brain neo-angiogenesis, we have left this topic to other recent reviews (Nat Rev Immunol 9:259-270, 2009 and Trends Mol Med 17:743-752, 2011).