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首页> 外文期刊>Journal of Alzheimer's disease: JAD >Localization of active forms of C-jun kinase (JNK) and p38 kinase in Alzheimer's disease brains at different stages of neurofibrillary degeneration.
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Localization of active forms of C-jun kinase (JNK) and p38 kinase in Alzheimer's disease brains at different stages of neurofibrillary degeneration.

机译:C-jun激酶(JNK)和p38激酶的活性形式在神经原纤维变性不同阶段在阿尔茨海默氏病脑中的定位。

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The principal protein component of paired helical filaments (PHFs) in Alzheimer disease is abnormally hyperphosphorylated tau (PHF-tau). The stress activated protein kinases JNK and p38 have been shown to phosphorylate tau at some sites only seen in PHF-tau. If JNK and p38 are involved in the abnormal hyperphosphorylation of tau, they should be activated in neurons undergoing neurofibrillary degeneration. In the present study, we determined the intracellular and regional distribution of the active forms of JNK and p38 kinase in entorhinal, hippocampal, and temporal cortices of brains staged for neurofibrillary changes according to Braak and Braak. Neurons with tangle-like inclusions positive for active forms of JNK and p38 kinase were found to appear first in the Pre-alpha layer of the entorhinal cortex, and then extend into other brain regions co-incident with the progressive sequence of neurofibrillary changes. The intraneuronal accumulation of active forms of JNK and p38 kinase apeared to precede the deposition of amyloid in the extracellular space. These data indicate that increased activation of the stress related kinases JNK and p38 occurs very early in the disease and might be involved in the intraneuronal protein phosphorylation/dephosphorylation imbalance that leads to neurofibrillary degeneration in Alzheimer disease.
机译:阿尔茨海默病中成对的螺旋细丝(PHF)的主要蛋白质成分是异常的过度磷酸化tau(PHF-tau)。应力激活的蛋白激酶JNK和p38已显示在仅在PHF-tau中可见的某些位点使tau磷酸化。如果JNK和p38参与了tau的异常过度磷酸化,则应在经历神经原纤维变性的神经元中激活它们。在本研究中,我们确定了根据Braak和Braak进行神经原纤维改变的脑的内嗅,海马和颞皮质的JNK和p38激酶活性形式的细胞内和区域分布。发现具有对JNK和p38激酶活性形式呈阳性的缠结状内含物的神经元首先出现在内嗅皮层的Pre-alpha层中,然后扩展到与神经原纤维变化进行性顺序一致的其他大脑区域。 JNK和p38激酶的活性形式在神经元内积累在淀粉样蛋白沉积到细胞外空间之前开始。这些数据表明,与疾病相关的应激相关激酶JNK和p38的活化增强在疾病中很早就发生,并且可能与神经元内蛋白磷酸化/去磷酸化失衡有关,从而导致阿尔茨海默病的神经原纤维变性。

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