Meng S Z, Arai Y, Deguchi K, Takashima S
Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry.
Brain Dev. 1997 Nov;19(7):480-4. doi: 10.1016/s0387-7604(97)00068-5.
The expression of beta-amyloid precursor protein (beta-APP) immunoreactivity was investigated in 16 cases of prenatal-onset periventricular leukomalacia (PVL). beta-APP positive axons were found in the early stage of prenatal PVL, which included coagulation necrosis, microglial activation, axonal swelling or astrogliosis, but were not detectable in the late stage of prenatal PVL. Furthermore, beta-APP immunoreactive neurons were also observed in the fifth layer of pyramidal neurons of the cerebral cortex, corresponding to the beta-APP positive axons in PVL. Thus, beta-APP is detected as an early sign of axonal and neuronal lesions in prenatal-onset PVL, and neuronal beta-APP in the cerebral cortex may function to repair cell damage. In addition, prenatal PVL occurred at various stages before birth.
对16例产前脑室周围白质软化症(PVL)患者的β-淀粉样前体蛋白(β-APP)免疫反应性表达进行了研究。在产前PVL的早期发现了β-APP阳性轴突,早期表现为凝固性坏死、小胶质细胞活化、轴突肿胀或星形胶质细胞增生,但在产前PVL的晚期未检测到。此外,在大脑皮质锥体细胞的第五层也观察到β-APP免疫反应性神经元,这与PVL中β-APP阳性轴突相对应。因此,β-APP被检测为产前PVL中轴突和神经元损伤的早期迹象,大脑皮质中的神经元β-APP可能具有修复细胞损伤的功能。此外,产前PVL发生在出生前的不同阶段。