Hypomorphic ATP11c is a novel regulator of decreased efficacy of transfused red blood cells in humans and mice
Year: 2026
Type: article
Study design: Observational Study
Abstract: Chronic red blood cell (RBC) transfusion sustains patients with diverse hematologic disorders, but repeated transfusion leads to iron overload and alloimmunization. Reducing transfusion burden requires identifying donor units that circulate more effectively after storage, yet determinants of this variability remain incompletely defined. Here, we integrate forward genetics in mice, multi-omics analyses of over 13,000 human donors, and studies of two families with hereditary ATP11c mutations to reveal a central role for this phospholipid flippase in transfusion efficacy. We show that common ATP11C variants, including the missense SNP V972M, and rare familial loss-of-function alleles impair RBC survival by disrupting membrane lipid remodeling and cytoskeletal stability-a mechanism distinct from oxidative damage pathways. Together, these findings establish ATP11c as a novel determinant of transfusion outcomes across species and genetic contexts, and highlight opportunities for donor stratification and improved storage technologies to advance precision transfusion medicine.
Source: HemaSphere
DOI: 10.1002/hem3.70288
Language: English
Subfield: Biochemistry
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,480
Awards: G1071959385, G1491012639, G2113296280, G225837024, G2273349799, G2295196357, The Impact of Oxidative Stress on Erythocyte Biology, G3835517529, G4451713954, G4598208154, G6186859056, G629452866, G6296967160, G6624492967, G689272554, G7732282970, G9000024437, The role of ferroptosis in red cell aging in vivo and in vitro
OpenAlex ID: W7119517846
