Suppr超能文献

心脏铜缺乏会激活一个与铜摄取和储存器官进行通讯的系统性信号机制。

Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs.

机构信息

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Cell Metab. 2010 May 5;11(5):353-63. doi: 10.1016/j.cmet.2010.04.003.

Abstract

Copper (Cu) is an essential cofactor for a variety of metabolic functions, and the regulation of systemic Cu metabolism is critical to human health. Dietary Cu is absorbed through the intestine, stored in the liver, and mobilized into the circulation; however, systemic Cu homeostasis is poorly understood. We generated mice with a cardiac-specific knockout of the Ctr1 Cu transporter (Ctr1(hrt/hrt)), resulting in cardiac Cu deficiency and severe cardiomyopathy. Unexpectedly, Ctr1(hrt/hrt) mice exhibited increased serum Cu levels and a concomitant decrease in hepatic Cu stores. Expression of the ATP7A Cu exporter, thought to function predominantly in intestinal Cu acquisition, was strongly increased in liver and intestine of Ctr1(hrt/hrt) mice. These studies identify ATP7A as a candidate for hepatic Cu mobilization in response to peripheral tissue demand, and illuminate a systemic regulation in which the Cu status of the heart is signaled to organs that take up and store Cu.

摘要

铜(Cu)是多种代谢功能的必需辅助因子,而全身铜代谢的调节对人类健康至关重要。膳食中的铜通过肠道吸收,储存在肝脏中,并动员到循环中;然而,全身铜的动态平衡仍知之甚少。我们生成了心脏特异性敲除 Ctr1 铜转运蛋白(Ctr1(hrt/hrt))的小鼠,导致心脏铜缺乏和严重的心肌病。出乎意料的是,Ctr1(hrt/hrt) 小鼠表现出血清铜水平升高,而肝铜储存量相应降低。被认为主要在肠道铜摄取中起作用的 ATP7A 铜外排泵的表达在 Ctr1(hrt/hrt) 小鼠的肝脏和肠道中强烈增加。这些研究确定 ATP7A 是响应外周组织需求进行肝铜动员的候选蛋白,并阐明了一种系统调节机制,其中心脏的铜状态向摄取和储存铜的器官发出信号。

相似文献

2
How copper traverses cellular membranes through the mammalian copper transporter 1, Ctr1.
Ann N Y Acad Sci. 2014 May;1314:32-41. doi: 10.1111/nyas.12371. Epub 2014 Feb 20.
3
Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis.
Sci Rep. 2017 Sep 20;7(1):12001. doi: 10.1038/s41598-017-11961-z.
4
Involvement of CTR1 and ATP7A in lead (Pb)-induced copper (Cu) accumulation in choroidal epithelial cells.
Toxicol Lett. 2014 Feb 10;225(1):110-8. doi: 10.1016/j.toxlet.2013.11.034. Epub 2013 Dec 6.
5
Intestinal regulation of copper homeostasis: a developmental perspective.
Am J Clin Nutr. 2008 Sep;88(3):846S-50S. doi: 10.1093/ajcn/88.3.846S.
6
ATP7A transgenic and nontransgenic mice are resistant to high copper exposure.
J Nutr. 2008 Apr;138(4):693-7. doi: 10.1093/jn/138.4.693.
7
Functional and molecular responses of suckling rat pups and human intestinal Caco-2 cells to copper treatment.
J Nutr Biochem. 2004 Mar;15(3):155-62. doi: 10.1016/j.jnutbio.2003.10.008.
9
Advances in the understanding of mammalian copper transporters.
Adv Nutr. 2011 Mar;2(2):129-37. doi: 10.3945/an.110.000273. Epub 2011 Mar 10.

引用本文的文献

1
Signal Transduction Strategies for DNAzyme-Based Sensing and Imaging of Metal Ions in Cells and .
Chem Biomed Imaging. 2025 Mar 20;3(8):473-498. doi: 10.1021/cbmi.4c00090. eCollection 2025 Aug 25.
2
Copper metabolism in hepatocellular carcinoma: from molecular mechanisms to therapeutic opportunities.
Front Mol Biosci. 2025 May 13;12:1578693. doi: 10.3389/fmolb.2025.1578693. eCollection 2025.
3
Identification of Cuproptosis-Related Genes and Their Potential Role in COPD Pathogenesis: A Bioinformatics Analysis.
Int J Chron Obstruct Pulmon Dis. 2025 Apr 15;20:1083-1096. doi: 10.2147/COPD.S497473. eCollection 2025.
4
The role of metal ion metabolism in the pathogenesis of diabetes and associated complications.
Front Endocrinol (Lausanne). 2025 Apr 3;16:1541809. doi: 10.3389/fendo.2025.1541809. eCollection 2025.
5
Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegeneration.
Mol Biol Cell. 2025 Mar 1;36(3):ar33. doi: 10.1091/mbc.E24-11-0512. Epub 2025 Jan 29.
7
Adaptive protein synthesis in genetic models of copper deficiency and childhood neurodegeneration.
bioRxiv. 2024 Nov 18:2024.09.09.612106. doi: 10.1101/2024.09.09.612106.
8
Mammalian copper homeostasis: physiological roles and molecular mechanisms.
Physiol Rev. 2025 Jan 1;105(1):441-491. doi: 10.1152/physrev.00011.2024. Epub 2024 Aug 22.
9
Cuproptosis and Cu: a new paradigm in cellular death and their role in non-cancerous diseases.
Apoptosis. 2024 Oct;29(9-10):1330-1360. doi: 10.1007/s10495-024-01993-y. Epub 2024 Jul 16.

本文引用的文献

1
Human copper transporter Ctr1 is functional in Drosophila, revealing a high degree of conservation between mammals and insects.
J Biol Inorg Chem. 2010 Jan;15(1):107-13. doi: 10.1007/s00775-009-0599-0. Epub 2009 Oct 25.
2
A role for the ATP7A copper-transporting ATPase in macrophage bactericidal activity.
J Biol Chem. 2009 Dec 4;284(49):33949-56. doi: 10.1074/jbc.M109.070201. Epub 2009 Oct 5.
4
Role of Menkes ATPase in angiotensin II-induced hypertension: a key modulator for extracellular superoxide dismutase function.
Hypertension. 2008 Nov;52(5):945-51. doi: 10.1161/HYPERTENSIONAHA.108.116467. Epub 2008 Sep 2.
5
Fine tuning of hepcidin expression by positive and negative regulators.
Cell Metab. 2008 Jul;8(1):1-3. doi: 10.1016/j.cmet.2008.06.009.
6
Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balance.
Arch Biochem Biophys. 2008 Aug 1;476(1):22-32. doi: 10.1016/j.abb.2008.05.005. Epub 2008 May 21.
7
Mechanisms for copper acquisition, distribution and regulation.
Nat Chem Biol. 2008 Mar;4(3):176-85. doi: 10.1038/nchembio.72.
8
ATP7B expression in human breast epithelial cells is mediated by lactational hormones.
J Histochem Cytochem. 2008 Apr;56(4):389-99. doi: 10.1369/jhc.7A7300.2008. Epub 2008 Jan 7.
9
Copper deficient rats and mice both develop anemia but only rats have lower plasma and brain iron levels.
Comp Biochem Physiol C Toxicol Pharmacol. 2008 Apr;147(3):316-23. doi: 10.1016/j.cbpc.2007.11.008. Epub 2007 Dec 4.
10
Copper-transporting ATPases ATP7A and ATP7B: cousins, not twins.
J Bioenerg Biomembr. 2007 Dec;39(5-6):403-7. doi: 10.1007/s10863-007-9101-2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验