Kyrkanides S, Olschowka J A, Williams J P, Hansen J T, O'Banion M K
Department of Neurobiology and Anatomy, School of Medicine and Dentistry, University of Rochester, NY 14642, USA.
J Neuroimmunol. 1999 Mar 1;95(1-2):95-106. doi: 10.1016/s0165-5728(98)00270-7.
Radiation injury to the central nervous system (CNS) results in glial activation accompanied by expression of pro-inflammatory cytokines and adhesion molecules. In this study we demonstrate intercellular adhesion molecule-1 (ICAM-1) induction in the irradiated mouse brain at the mRNA and protein levels. Immunocytochemical analysis revealed that ICAM-1 protein was primarily expressed in endothelial cells and microglia. In vitro, ionizing radiation significantly induces TNF alpha, IL-1beta and ICAM-1 mRNA in primary microglia cultures. Interestingly, although ionizing radiation activated primary astrocyte cultures, it did not induce ICAM-1 expression. However, exposure of astrocytes to conditioned medium collected from irradiated microglia resulted in ICAM-1 induction, which was abrogated when the conditioned medium was pre-incubated with neutralizing antibodies raised against murine TNF alpha and IL-1beta. These results indicate that pro-inflammatory cytokines may be necessary for ICAM-1 expression in astrocytes in CNS radiation injury.
中枢神经系统(CNS)的辐射损伤会导致胶质细胞活化,并伴有促炎细胞因子和黏附分子的表达。在本研究中,我们证明了在受辐照的小鼠脑中,细胞间黏附分子-1(ICAM-1)在mRNA和蛋白质水平上均有诱导表达。免疫细胞化学分析显示,ICAM-1蛋白主要在内皮细胞和小胶质细胞中表达。在体外,电离辐射可显著诱导原代小胶质细胞培养物中肿瘤坏死因子α(TNFα)、白细胞介素-1β(IL-1β)和ICAM-1 mRNA的表达。有趣的是,虽然电离辐射激活了原代星形胶质细胞培养物,但并未诱导ICAM-1表达。然而,将星形胶质细胞暴露于从辐照后的小胶质细胞收集的条件培养基中会导致ICAM-1诱导表达,当该条件培养基与针对小鼠TNFα和IL-1β的中和抗体预孵育时,这种诱导作用被消除。这些结果表明,促炎细胞因子可能是中枢神经系统辐射损伤中星形胶质细胞ICAM-1表达所必需的。