Grant Abstract: Molecular Mechanisms of Active Copper Transport

Grant Number: 2R01DK071865-14A1
PI Name: Lutensko
Project Title: Molecular Mechanisms of Active Copper Transport

Abstract: Copper (Cu) is essential for the growth, development, and normal function of human organisms. The defects in Cu homeostasis are associated with a broad spectrum of pathologies including Menkes disease, Wilson disease, MEDNIK syndrome, and others. So far, the studies of human Cu homeostasis have focused primarily on the function and regulation of Cu transporters and small Cu carriers. With this program of study, we will begin to learn how mammalian Cu transporters and their regulators work together to modulate the nutrient transport in intestine. The small intestine is responsible for the absorption of all essential nutrients. We discovered that the availability of Cu in enterocytes strongly influenced the abundance of chylomicrons, the primary carriers of dietary fat. We have also identified the fat-responsive protein ANKRD9 as a regulator of Cu transport and hypothesize that ANKRD9 is a molecular integrator of the pathways involved in the intestinal fat and Cu transport. The proposed program of studies will test the central hypothesis that the Cu homeostasis and lipid (fat) metabolism in enterocytes are functionally linked and co-regulated. Studies under Specific Aim 1 will characterize the mechanism of ATP7B regulation and investigate how the intestinal Cu storage compartments are formed. Specific Aim 2 will determine how Cu and dietary fat affect each other transport in enterocytes and elucidate the mechanism behind the Cu-dependent formation of chylomicrons. Specific Aim 3 will characterize the function of ANKRD9 in the small intestine and its role in coupling copper and fat metabolism. The studies will open a new chapter in understanding of intestinal Cu physiology, contribute to better understanding of human disorders associated with Cu misbalance and, ultimately, help to design better treatments for these disorders.

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