Graeber M B, Streit W J, Kiefer R, Schoen S W, Kreutzberg G W
Department of Neuromorphology, Max-Planck-Institute for Psychiatry, Martinsried, F.R.G.
J Neuroimmunol. 1990 May;27(2-3):121-32. doi: 10.1016/0165-5728(90)90061-q.
The results of the present study demonstrate that following lethal motor neuron injury microglia and perivascular cells, as well as brain macrophages derived from the latter two cell types, newly express antigens of the myelomonocytic lineage as recognized by the monoclonal antibodies ED1 and ED3. It is suggested that differences in the immunophenotype of resident brain macrophage precursor cells, i.e. microglia and perivascular cells, and macrophages occurring outside the central nervous system (CNS) may be explained by differences in local macrophage antigen expression rather than by a different embryological lineage. The new appearance of antigens common to peripheral macrophages on neural phagocytes in CNS lesions may therefore not necessarily imply that most or all of these cells are of recent blood origin.
本研究结果表明,在运动神经元发生致命性损伤后,小胶质细胞和血管周围细胞,以及源自后两种细胞类型的脑巨噬细胞,会新表达髓单核细胞系抗原,这些抗原可被单克隆抗体ED1和ED3识别。有人提出,脑内常驻巨噬细胞前体细胞(即小胶质细胞和血管周围细胞)与中枢神经系统(CNS)外出现的巨噬细胞在免疫表型上的差异,可能是由局部巨噬细胞抗原表达的差异而非不同的胚胎谱系所解释。因此,中枢神经系统病变中神经吞噬细胞上出现外周巨噬细胞共有的抗原,不一定意味着这些细胞中的大多数或全部都来自近期血液。