Arai T, Uéda K, Ikeda K, Akiyama H, Haga C, Kondo H, Kuroki N, Niizato K, Iritani S, Tsuchiya K
Department of Neuropathology, Institute of Psychiatry, Tokyo, Japan.
Neurosci Lett. 1999 Jan 8;259(2):83-6. doi: 10.1016/s0304-3940(98)00890-8.
Argyrophilic glial inclusions occur in the midbrain of patients with Parkinson's disease (PD) and diffuse Lewy body disease (DLBD). These inclusions are immunohistochemically positive for NACP/alpha-synuclein but negative for tau protein. The results of the present study suggest that a primary degenerative process involves NACP/alpha-synuclein in PD and DLBD and that the process takes place not only in neurons but also in glial cells. Argyrophilic cytoplasmic inclusions, both glial and neuronal, in a variety of degenerative diseases may be grouped into two major categories; one related to aggregates of abnormally phosphorylated tau protein and the other to unusual accumulations of NACP/alpha-synuclein.
嗜银性胶质包涵体出现在帕金森病(PD)和弥漫性路易体病(DLBD)患者的中脑中。这些包涵体免疫组化检测NACP/α-突触核蛋白呈阳性,但tau蛋白呈阴性。本研究结果表明,原发性变性过程涉及PD和DLBD中的NACP/α-突触核蛋白,且该过程不仅发生在神经元中,也发生在胶质细胞中。在各种退行性疾病中,嗜银性细胞质包涵体,包括胶质和神经元的,可分为两大类;一类与异常磷酸化tau蛋白的聚集体有关,另一类与NACP/α-突触核蛋白的异常积聚有关。