Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis

Authors

Haarin Chun, University of Maryland
Tracy Catterson, University of Maryland
Heejeong Kim, University of Nebraska-LincolnFollow
Jaekwon Lee, University of Nebraska-LincolnFollow
Byung-Eun Kim, University of Maryland & University of Nebraska- LincolnFollow

Date of this Version

9-20-2017

Citation

Scientific Reports | 7: 12001 | DOI:10.1038/s41598-017-11961-z Pages 1-13

Comments

Creative Commons Attribution 4.0 International License,

Abstract

Copper (Cu) is an essential cofactor for various enzymatic activities including mitochondrial electron transport, iron mobilization, and peptide hormone maturation. Consequently, Cu dysregulation is associated with fatal neonatal disease, liver and cardiac dysfunction, and anemia. While the Cu transporter ATP7A plays a major role in both intestinal Cu mobilization to the periphery and prevention of Cu over-accumulation, it is unclear how regulation of ATP7A contributes to Cu homeostasis in response to systemic Cu fluctuation. Here we show, using Cu-deficient mouse models, that steadystate levels of ATP7A are lower in peripheral tissues (including the heart, spleen, and liver) under Cu deficiency and that subcutaneous administration of Cu to these animals restore normal ATP7A levels in these tissues. Strikingly, ATP7A in the intestine is regulated in the opposite manner - low systemic Cu increases ATP7A while subcutaneous Cu administration decreases ATP7A suggesting that intestinespecific non-autonomous regulation of ATP7A abundance may serve as a key homeostatic control for Cu export into the circulation. Our results support a systemic model for how a single transporter can be inversely regulated in a tissue-specific manner to maintain organismal Cu homeostasis.