Brierley J B, Brown A W
J Comp Neurol. 1982 Nov 10;211(4):397-406. doi: 10.1002/cne.902110406.
The potential for the transformation of the normal microglial cell to a lipid phagocyte was studied by light and electron microscopy in the brains of rodents and by light microscopy only in primates. All were subjected to some form of hypoxia-ischemia and the microglial response was examined in regions of selective neuronal destruction (SND) so that infarction was deliberately excluded. In vivo perfusion-fixation was employed in all animals and light microscopic examination was carried out on paraffin- and sometimes celloidin-embedded material. Semithin plastic sections from several regions of the rodent brains were used for light microscopy but ultrastructural studies were confined to the hippocampus. In all animals the microglia were activated and transformed into rod cells exhibiting phagocytic properties but only a minority gave rise to lipid phagocytes. Blood vessels were normal in all animals and no hematogenous elements were identifed in the the parenchyma. As neuronal ghosts could be identified for up to 3 weeks it was concluded that the capacity of the microglia for phagocytic activity was limited.
通过光学显微镜和电子显微镜在啮齿动物脑内研究了正常小胶质细胞转变为脂质吞噬细胞的可能性,而在灵长类动物中仅通过光学显微镜进行研究。所有动物均经历了某种形式的缺氧缺血,并在选择性神经元破坏(SND)区域检查小胶质细胞反应,从而刻意排除梗死情况。所有动物均采用体内灌注固定法,并对石蜡包埋以及有时火棉胶包埋的材料进行光学显微镜检查。来自啮齿动物脑多个区域的半薄塑料切片用于光学显微镜检查,但超微结构研究仅限于海马体。在所有动物中,小胶质细胞均被激活并转变为具有吞噬特性的杆状细胞,但只有少数会产生脂质吞噬细胞。所有动物的血管均正常,实质内未发现血源性成分。由于在长达3周的时间内都能识别出神经元残影,因此得出结论,小胶质细胞的吞噬活性能力有限。