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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Phosphatidylinositol 3-kinase: increased activity and protein level in amyotrophic lateral sclerosis.
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Phosphatidylinositol 3-kinase: increased activity and protein level in amyotrophic lateral sclerosis.

机译:磷脂酰肌醇3-激酶:肌萎缩性侧索硬化症的活动和蛋白质水平增加。

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Enzyme activities and protein levels of several protein and lipid kinases were measured in postmortem tissue from patients who died with amyotrophic lateral sclerosis (ALS) as well as from control subjects. Patients who died with ALS had increased activities and protein levels of phosphatidylinositol 3-kinase (PI 3-K) in particulate fractions of spinal cord tissue compared with control subjects. The PI 3-K activity increased with PI 3-K protein level, indicating no change in specific PI 3-K activity in ALS. No differences in PI 3-K activities were found in cytosolic fractions of spinal cord, or in motor and visual cortices, from ALS patients compared with those from controls. PI 3-K activities and protein levels were unchanged in brain tissue from patients who died with Alzheimer's disease compared with those from controls. PI 3-K is a lipid kinase that is important for cell survival and is activated in response to many growth factors. Increased PI 3-K activities in particulate fractions of spinal cord from ALS patients may be related to the increase of PI 3-K protein levels found in this tissue. The protein kinases Erk2, protein kinase B (PKB), and p70 ribosomal S6 kinase (S6K) showed no differences in activities in spinal cord tissue between ALS patients and controls. However, the amounts of PKB and S6K protein were significantly higher in ALS patients, whereas Erk2 protein amount was unchanged compared with controls. Protein kinase C activity was increased in spinal cord tissue from ALS patients, which is consistent with our previous report. The increased activity of PI 3-K in spinal cord tissue from patients with ALS implicates the involvement or activation of PI 3-K in ALS, as either a cause or a consequence of the neuron loss. The lack of up-regulation in the activities of PKB and S6K in ALS tissue supports an impairment in signal transduction cascades mediated by PI 3-K in this neurodegenerative disease.
机译:在死于肌萎缩性侧索硬化症(ALS)的患者以及对照组的死后组织中,测量了几种蛋白质和脂质激酶的酶活性和蛋白质水平。与对照组相比,死于ALS的患者的脊髓组织颗粒级分中磷脂酰肌醇3-激酶(PI 3-K)的活性和蛋白质水平增加。 PI 3-K活性随PI 3-K蛋白水平的升高而增加,表明ALS中特定PI 3-K活性没有变化。与对照组相比,ALS患者的脊髓,运动皮质和视觉皮质的PI 3-K活性均未发现差异。与对照组相比,死于阿尔茨海默氏病的患者脑组织中的PI 3-K活性和蛋白质水平没有变化。 PI 3-K是一种脂质激酶,对细胞存活很重要,并响应许多生长因子而被激活。 ALS患者脊髓颗粒中PI 3-K活性的增加可能与该组织中PI 3-K蛋白水平的提高有关。蛋白激酶Erk2,蛋白激酶B(PKB)和p70核糖体S6激酶(S6K)在ALS患者和对照组之间的脊髓组织活动无差异。但是,ALS患者中PKB和S6K蛋白的含量明显高于对照组,而Erk2蛋白的含量与对照组相比没有变化。 ALS患者脊髓组织中的蛋白激酶C活性增加,这与我们先前的报道一致。患有ALS的患者脊髓组织中PI 3-K活性的增加暗示ALS 3-PI的参与或激活是神经元丢失的原因或结果。 ALS组织中PKB和S6K活性缺乏上调支持了这种神经退行性疾病中PI 3-K介导的信号转导级联的损伤。

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