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寿命延长因子α-klotho可增强认知能力。

Life extension factor klotho enhances cognition.

作者信息

Dubal Dena B, Yokoyama Jennifer S, Zhu Lei, Broestl Lauren, Worden Kurtresha, Wang Dan, Sturm Virginia E, Kim Daniel, Klein Eric, Yu Gui-Qiu, Ho Kaitlyn, Eilertson Kirsten E, Yu Lei, Kuro-o Makoto, De Jager Philip L, Coppola Giovanni, Small Gary W, Bennett David A, Kramer Joel H, Abraham Carmela R, Miller Bruce L, Mucke Lennart

机构信息

Gladstone Institute of Neurological Disease, San Francisco, CA 94158, USA; Department of Neurology, University of California, San Francisco, San Francisco, CA 94158, USA.

Department of Neurology, University of California, San Francisco, San Francisco, CA 94158, USA.

出版信息

Cell Rep. 2014 May 22;7(4):1065-76. doi: 10.1016/j.celrep.2014.03.076. Epub 2014 May 10.

Abstract

Aging is the primary risk factor for cognitive decline, an emerging health threat to aging societies worldwide. Whether anti-aging factors such as klotho can counteract cognitive decline is unknown. We show that a lifespan-extending variant of the human KLOTHO gene, KL-VS, is associated with enhanced cognition in heterozygous carriers. Because this allele increased klotho levels in serum, we analyzed transgenic mice with systemic overexpression of klotho. They performed better than controls in multiple tests of learning and memory. Elevating klotho in mice also enhanced long-term potentiation, a form of synaptic plasticity, and enriched synaptic GluN2B, an N-methyl-D-aspartate receptor (NMDAR) subunit with key functions in learning and memory. Blockade of GluN2B abolished klotho-mediated effects. Surprisingly, klotho effects were evident also in young mice and did not correlate with age in humans, suggesting independence from the aging process. Augmenting klotho or its effects may enhance cognition and counteract cognitive deficits at different life stages.

摘要

衰老 是认知能力下降的主要风险因素,这对全球老龄化社会来说是一种新出现的健康威胁。诸如α-klotho等抗衰老因素是否能抵消认知能力下降尚不清楚。我们发现,人类KLOTHO基因的一个延长寿命的变体KL-VS与杂合携带者的认知增强有关。由于该等位基因增加了血清中的α-klotho水平,我们分析了全身性过表达α-klotho的转基因小鼠。它们在多项学习和记忆测试中的表现优于对照组。提高小鼠体内的α-klotho水平还增强了长时程增强效应(一种突触可塑性形式),并增加了突触中的GluN2B(一种在学习和记忆中具有关键功能的N-甲基-D-天冬氨酸受体(NMDAR)亚基)。阻断GluN2B可消除α-klotho介导的效应。令人惊讶的是,α-klotho的作用在年轻小鼠中也很明显,并且与人类的年龄无关,这表明其作用独立于衰老过程。增强α-klotho或其作用可能会在不同生命阶段增强认知能力并抵消认知缺陷。

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