Zhu X, Rottkamp C A, Hartzler A, Sun Z, Takeda A, Boux H, Shimohama S, Perry G, Smith M A
Institute of Pathology, Case Western Reserve University, Cleveland, Ohio 44106, USA.
J Neurochem. 2001 Oct;79(2):311-8. doi: 10.1046/j.1471-4159.2001.00597.x.
Mitogen-activated protein kinase (MAPK) p38 has been implicated in the pathogenesis of Alzheimer's disease, but the upstream cascade leading to p38 activation has not been elucidated in the disease. In the present study, we focused on mitogen-activated protein kinase kinase 6 (MKK6), one of the upstream activators of p38 MAPK. We found that MKK6 was not only increased but also specifically associated with granular structures in the susceptible neurons in the hippocampus and cortex of Alzheimer's disease patients, but was only weakly diffuse in the cytoplasm in neurons in control cases. Immunoblot analysis demonstrated a significant increase of MKK6 level in Alzheimer's disease compared with age-matched controls. In this regard, in hippocampal and cortical regions of individuals with Alzheimer's disease, the activated phospho-MKK6 was localized exclusively in association with pathological alterations including neurofibrillary tangles, senile plaques, neuropil threads and granular structures, overlapping with activated p38 MAPK suggesting both a functional and mechanic link. By immunoblot analysis, phospho-MKK6 is also significantly increased in AD compared with control cases. Together, these findings lend further credence to the notion that the p38 MAPK pathway is dysregulated in Alzheimer's disease and also indicates an active role for this pathway in disease pathogenesis.
丝裂原活化蛋白激酶(MAPK)p38与阿尔茨海默病的发病机制有关,但该疾病中导致p38激活的上游级联反应尚未阐明。在本研究中,我们聚焦于丝裂原活化蛋白激酶激酶6(MKK6),它是p38 MAPK的上游激活剂之一。我们发现,MKK6不仅在阿尔茨海默病患者海马体和皮质的易感神经元中增加,而且与颗粒结构特异性相关,而在对照病例的神经元中,它仅在细胞质中呈弱弥漫性分布。免疫印迹分析表明,与年龄匹配的对照组相比,阿尔茨海默病患者中MKK6水平显著升高。在这方面,在阿尔茨海默病患者的海马体和皮质区域,活化的磷酸化MKK6仅与包括神经原纤维缠结、老年斑、神经毡丝和颗粒结构在内的病理改变相关,与活化的p38 MAPK重叠,提示存在功能和机械联系。通过免疫印迹分析,与对照病例相比,阿尔茨海默病患者中磷酸化MKK6也显著增加。总之,这些发现进一步支持了p38 MAPK通路在阿尔茨海默病中失调的观点,也表明该通路在疾病发病机制中起积极作用。