Zhang Z, Chopp M, Powers C
Department of Neurology, Henry Ford Health Science Center, Detroit, MI 48202, USA.
Brain Res. 1997 Jan 9;744(2):189-98. doi: 10.1016/S0006-8993(96)01085-2.
We measured the time-dependent morphological changes of microglial cells reacting to ischemic cell damage after transient (2 h) middle cerebral artery occlusion in the rat by means of lectin histochemistry with the B4-isolectin from Griffonia simplicifolia as well as immunohistochemistry with monoclonal antibodies directed against monocyte/microphage (ED1) and major histocompatibility complex (MHC) class II (OX-6) antigens. As early as 1 h after onset of reperfusion, microglia were absent in the severely neuronal damaged preoptic area. However, ameboid-like microglia were evident in an adjacent area containing scattered shrunken neurons. Rod, round and ameboid-like microglia were present in the ischemic lesion between 2 to 10 h of reperfusion. Round and ameboid cells became predominant in the ischemic core lesion and were mingled with highly ramified microglia to the boundary at 22 h of reperfusion. Highly ramified microglia were found in an adjacent area containing morphologically intact neurons. Round and ameboid cells were localized to the inner boundary of the ischemic lesion surrounding the infarct zone at 46 of reperfusion. Round and ameboid cells were present throughout the entire ischemic lesion in the infarct zone from 70-166 h of reperfusion. A marked increase in number and in intensity of highly ramified microglial cells were present in the outer boundary of the lesion during this period. In addition, a significant increase in both ED1- and OX-6-immunoreactive cells in the ischemic region was detected after 10 h of reperfusion and persisted up to 166 h of reperfusion. These data demonstrate that microglia exhibit a time dependent change in morphology after reperfusion and that the severity of injury may be reflected in the state of microglial activation.
我们通过用来自西非豆科植物的B4异凝集素进行凝集素组织化学以及用针对单核细胞/巨噬细胞(ED1)和主要组织相容性复合体(MHC)II类(OX-6)抗原的单克隆抗体进行免疫组织化学,来测量大鼠大脑中动脉短暂闭塞(2小时)后小胶质细胞对缺血性细胞损伤反应的时间依赖性形态变化。早在再灌注开始后1小时,严重神经元损伤的视前区就没有小胶质细胞了。然而,在含有散在萎缩神经元的相邻区域,类阿米巴样小胶质细胞很明显。在再灌注2至10小时之间,缺血性病变中存在杆状、圆形和类阿米巴样小胶质细胞。圆形和类阿米巴样细胞在缺血核心病变中占主导地位,并在再灌注22小时时与高度分支的小胶质细胞混合至边界处。在含有形态完整神经元的相邻区域发现了高度分支的小胶质细胞。在再灌注46小时时,圆形和类阿米巴样细胞位于梗死灶周围缺血性病变的内边界处。在再灌注70至166小时期间,梗死灶内整个缺血性病变中都存在圆形和类阿米巴样细胞。在此期间,病变外边界处高度分支的小胶质细胞数量和强度显著增加。此外,再灌注10小时后,缺血区域中ED1和OX-6免疫反应性细胞均显著增加,并持续至再灌注166小时。这些数据表明,再灌注后小胶质细胞形态呈现时间依赖性变化,损伤的严重程度可能反映在小胶质细胞的激活状态中。