Wood G W, Gollahon K A, Tilzer S A, Vats T, Morantz R A
J Neuropathol Exp Neurol. 1979 Jul;38(4):369-76. doi: 10.1097/00005072-197907000-00002.
The origin of brain macrophages or "reactive microglia" has been the subject of considerable controversy. The fundamental question is whether or not there is a morphologically and functionally distinct population of cells, called microglia, which are resident in normal brain and differentiate into macrophages in response to inflammatory stimuli. The present study was performed to determine if any cells in the normal brain have the common markers of mononuclear phagocytes; phagocytosis, IgGFc receptors or macrophage specific antigens. In studies of the newborn and the adult murine brain and adult human brain no cells were detected which had any of those markers, although the highly sensitive marker methods were capable of detecting mononuclear phagocytes in all other tissues where they are known to occur. The results suggest that microglia, if they exist as a distinct cell type, are unrelated to mononuclear phagocytes. Furthermore, they suggest, but do not prove, that all inflammatory macrophages are derived from hematogenous precursors.
脑巨噬细胞或“反应性小胶质细胞”的起源一直是相当有争议的话题。根本问题在于,是否存在一种形态和功能上独特的细胞群体,称为小胶质细胞,它们驻留在正常大脑中,并在炎症刺激下分化为巨噬细胞。本研究旨在确定正常大脑中的任何细胞是否具有单核吞噬细胞的共同标志物;吞噬作用、IgG Fc受体或巨噬细胞特异性抗原。在对新生和成年小鼠大脑以及成人大脑的研究中,未检测到具有任何这些标志物的细胞,尽管高度敏感的标志物方法能够在已知存在单核吞噬细胞的所有其他组织中检测到它们。结果表明,小胶质细胞(如果它们作为一种独特的细胞类型存在)与单核吞噬细胞无关。此外,结果表明但未证明所有炎性巨噬细胞均源自血源性前体细胞。