Raghavan Ravi, Kruijff Loes de, Sterrenburg Monique D, Rogers Beverly B, Hladik Christa L, White Charles L
Neuropathology Laboratory, Department of Pathology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9073, USA.
Pediatr Dev Pathol. 2004 Sep-Oct;7(5):506-16. doi: 10.1007/s10024-003-7080-9. Epub 2004 Sep 8.
Alpha (alpha)-synuclein is a presynaptic protein, abnormal expression of which has been associated with neurodegenerative and neoplastic diseases. It is abundant in the developing vertebrate central nervous system (CNS), but less is known about its developmental expression in the human CNS. Immunohistochemical expression of alpha-synuclein was studied in 39 fetal, perinatal, pediatric, and adolescent brains. Perikaryal expression of alpha-synuclein is observed as early as 11-wk gestation in the cortical plate. Several discrete neuronal groups in the hippocampus, basal ganglia, and brain stem express perikaryal alpha-synuclein by 20-wk gestation, persisting through the first few years of life. In the cerebellum, alpha-synuclein is present by 21-wk gestation and persists into adult life as a coarse granular neuropil reaction product in the internal granular layer, and as a diffuse neuropil "blush" in the molecular layer. The germinal matrix, glia, endothelial cells, external granular layer, Pukinje cells, and dentate neurons are consistently negative for alpha-synuclein. We conclude that alpha-synuclein is expressed very early in human gestation, and that its distribution and temporal sequence of expression varies in discrete neuronal groups. Perikaryal alpha-synuclein starts disappearing from the neuronal cytosol in early childhood, and only the neuropil retains immunoreactivity into adulthood. The reappearance of alpha-synuclein in the adult neuronal cytosol in certain disease processes may represent reemergence of cues from an earlier developmental stage as part of a stress response.
α-突触核蛋白是一种突触前蛋白,其异常表达与神经退行性疾病和肿瘤性疾病相关。它在发育中的脊椎动物中枢神经系统(CNS)中含量丰富,但对其在人类中枢神经系统中的发育表达了解较少。对39例胎儿、围产期、儿童和青少年大脑进行了α-突触核蛋白的免疫组织化学表达研究。早在妊娠11周时,在皮质板中就观察到α-突触核蛋白的胞体表达。到妊娠20周时,海马、基底神经节和脑干中的几个离散神经元群表达胞体α-突触核蛋白,并持续到生命的最初几年。在小脑中,α-突触核蛋白在妊娠21周时出现,并在成年期持续存在,在内颗粒层表现为粗大颗粒状神经纤维反应产物,在分子层表现为弥漫性神经纤维“红晕”。生发基质、神经胶质细胞、内皮细胞、外颗粒层、浦肯野细胞和齿状神经元的α-突触核蛋白始终为阴性。我们得出结论,α-突触核蛋白在人类妊娠早期就开始表达,其分布和表达的时间顺序在离散的神经元群中有所不同。胞体α-突触核蛋白在儿童早期开始从神经元胞质中消失,只有神经纤维在成年期仍保持免疫反应性。在某些疾病过程中,α-突触核蛋白在成年神经元胞质中的再次出现可能代表了早期发育阶段线索的重新出现,作为应激反应的一部分。