Author:

Keywords:

Biochemistry & Molecular Biology, CARRIER, CELLS, FLUORESCENT-PROBE, GENE, GLYPICAN-1, IDENTIFICATION, Life Sciences & Biomedicine, MUTATIONS, PARKINSONISM, Science & Technology, SPERMINE, THERAPIES, ATP13A3, P-type ATPase, P5B-ATPase, polyamine, polyamine transport system, putrescine, transporter, Adenosine Triphosphatases, Animals, Biological Transport, CHO Cells, Cricetinae, Cricetulus, Enzyme Inhibitors, Membrane Transport Proteins, Mitoguazone, Mutation, Polyamines, Putrescine, Whole Genome Sequencing, ATP13A2, ATPase, endosome, transport, G094219N#54971233, 1S77920N|1S77922N#55122585, 03 Chemical Sciences, 06 Biological Sciences, 11 Medical and Health Sciences, 31 Biological sciences, 32 Biomedical and clinical sciences, 34 Chemical sciences

Abstract:

Polyamines, such as putrescine, spermidine, and spermine, are physiologically important polycations, but the transporters responsible for their uptake in mammalian cells remain poorly characterized. Here, we reveal a new component of the mammalian polyamine transport system using CHO-MG cells, a widely used model to study alternative polyamine uptake routes and characterize polyamine transport inhibitors for therapy. CHO-MG cells present polyamine uptake deficiency and resistance to a toxic polyamine biosynthesis inhibitor methylglyoxal bis-(guanylhydrazone) (MGBG), but the molecular defects responsible for these cellular characteristics remain unknown. By genome sequencing of CHO-MG cells, we identified mutations in an unexplored gene, ATP13A3, and found disturbed mRNA and protein expression. ATP13A3 encodes for an orphan P5B-ATPase (ATP13A3), a P-type transport ATPase that represents a candidate polyamine transporter. Interestingly, ATP13A3 complemented the putrescine transport deficiency and MGBG resistance of CHO-MG cells, whereas its knockdown in WT cells induced a CHO-MG phenotype demonstrated as a decrease in putrescine uptake and MGBG sensitivity. Taken together, our findings identify ATP13A3, which has been previously genetically linked with pulmonary arterial hypertension, as a major component of the mammalian polyamine transport system that confers sensitivity to MGBG.