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2
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本文引用的文献

1
Control of metabolic homeostasis by stress signaling is mediated by the lipocalin NLaz.应激信号对代谢稳态的调控由脂质运载蛋白NLaz介导。
PLoS Genet. 2009 Apr;5(4):e1000460. doi: 10.1371/journal.pgen.1000460. Epub 2009 Apr 24.
2
Meta-analysis of age-related gene expression profiles identifies common signatures of aging.与年龄相关基因表达谱的荟萃分析确定了衰老的共同特征。
Bioinformatics. 2009 Apr 1;25(7):875-81. doi: 10.1093/bioinformatics/btp073. Epub 2009 Feb 2.
3
Human apolipoprotein D overexpression in transgenic mice induces insulin resistance and alters lipid metabolism.转基因小鼠中人类载脂蛋白D的过表达会诱导胰岛素抵抗并改变脂质代谢。
Am J Physiol Endocrinol Metab. 2009 Apr;296(4):E802-11. doi: 10.1152/ajpendo.90725.2008. Epub 2009 Jan 27.
4
p53 family members regulate the expression of the apolipoprotein D gene.p53家族成员调控载脂蛋白D基因的表达。
J Biol Chem. 2009 Jan 9;284(2):872-83. doi: 10.1074/jbc.M807185200. Epub 2008 Nov 11.
5
Neuroprotective effect of apolipoprotein D against human coronavirus OC43-induced encephalitis in mice.载脂蛋白D对小鼠人冠状病毒OC43诱导的脑炎的神经保护作用。
J Neurosci. 2008 Oct 8;28(41):10330-8. doi: 10.1523/JNEUROSCI.2644-08.2008.
6
Evolution of the aging brain transcriptome and synaptic regulation.衰老大脑转录组的演变与突触调节。
PLoS One. 2008 Oct 2;3(10):e3329. doi: 10.1371/journal.pone.0003329.
7
The plant Apolipoprotein D ortholog protects Arabidopsis against oxidative stress.植物载脂蛋白D直系同源物保护拟南芥免受氧化应激。
BMC Plant Biol. 2008 Jul 31;8:86. doi: 10.1186/1471-2229-8-86.
8
Human ApoD, an apolipoprotein up-regulated in neurodegenerative diseases, extends lifespan and increases stress resistance in Drosophila.人类载脂蛋白D(ApoD)是一种在神经退行性疾病中上调的载脂蛋白,可延长果蝇的寿命并增强其抗应激能力。
Proc Natl Acad Sci U S A. 2008 May 13;105(19):7088-93. doi: 10.1073/pnas.0800896105. Epub 2008 May 5.
9
Apolipoprotein D is involved in the mechanisms regulating protection from oxidative stress.载脂蛋白D参与调节抗氧化应激保护的机制。
Aging Cell. 2008 Aug;7(4):506-15. doi: 10.1111/j.1474-9726.2008.00395.x. Epub 2008 Apr 14.
10
Seymour Benzer (1921-2007).
Curr Biol. 2008 Feb 12;18(3):R106-10. doi: 10.1016/j.cub.2007.12.039.

载脂蛋白 D:在衰老和与年龄相关疾病中的作用概述。

Apolipoprotein D: an overview of its role in aging and age-related diseases.

机构信息

Division of Biology, California Institute of Technology, Pasadena, CA, USA.

出版信息

Cell Cycle. 2010 Jan 15;9(2):269-73. doi: 10.4161/cc.9.2.10433. Epub 2010 Jan 26.

DOI:10.4161/cc.9.2.10433
PMID:20023409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3691099/
Abstract

“” —Seymour Benzer, reflecting on the observation that ApoD mRNA levels increase 500-fold following neuronal crush injury. Seymour Benzer’s curiosity was legendary and seemingly limitless. Towards the end of his life, one of the (many) questions that kept him awake at night concerned the emerging role of Apolipoprotein D (ApoD) in aging and neurological disease. In this perspective, we will discuss the clinical and biochemical data on ApoD, and the input from the recent genetic studies in model systems, including those from the Benzer lab.

摘要

——西摩·本泽尔(Seymour Benzer),在观察到神经元挤压损伤后 ApoD mRNA 水平增加 500 倍时的感想。西摩·本泽尔(Seymour Benzer)的好奇心是出了名的,而且似乎是无穷无尽的。在他生命的最后阶段,困扰他夜不能寐的(众多)问题之一是载脂蛋白 D(ApoD)在衰老和神经疾病中的新作用。在这篇观点文章中,我们将讨论 ApoD 的临床和生化数据,以及最近来自模型系统的遗传研究的结果,包括本泽尔实验室的研究。