CD38 and the mitochondrial calcium uniporter contribute to age-related hematopoietic stem cell dysfunction

Hematopoietic stem cells (HSCs) are the multipotent progenitors of all immune cells. During aging, their regenerative capacity decreases for reasons that are not well understood. Recently, Song et al investigated the roles of two metabolic proteins in age-related HSC dysfunction: CD38 (a membrane-bound NADase) and the mitochondrial calcium uniporter that transports calcium into the mitochondrial matrix. They found that the interplay between these proteins is deranged in aged HSCs, contributing to their diminished renewal capacity. These findings implicate compromised nicotinamide adenine dinucleotide metabolism as underlying HSC dysfunction in aging.

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Publication Details

Journal
Immunometabolism
Published
2024-10-01
DOI
https://doi.org/10.1097/in9.0000000000000048
Citations
1
Primary Topic
Calcium signaling and nucleotide metabolism
Type
article
Field-Weighted Citation Impact
0.40

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article

CD38 and the mitochondrial calcium uniporter contribute to age-related hematopoietic stem cell dysfunction

Connor S.R. Jankowski, Thomas Weichhart
1 citations
Immunometabolism
Calcium signaling and nucleotide metabolism
0.40
article

CD38 and the mitochondrial calcium uniporter contribute to age-related hematopoietic stem cell dysfunction

Connor S.R. Jankowski, Thomas Weichhart
article en
1 citations

Abstract

Hematopoietic stem cells (HSCs) are the multipotent progenitors of all immune cells. During aging, their regenerative capacity decreases for reasons that are not well understood. Recently, Song et al investigated the roles of two metabolic proteins in age-related HSC dysfunction: CD38 (a membrane-bound NADase) and the mitochondrial calcium uniporter that transports calcium into the mitochondrial matrix. They found that the interplay between these proteins is deranged in aged HSCs, contributing to their diminished renewal capacity. These findings implicate compromised nicotinamide adenine dinucleotide metabolism as underlying HSC dysfunction in aging.

ImmunometabolismVol. 6(4)
Medical University of Vienna (AT)
Austrian Science Fund
Openalex Percentile: Top 36%
Calcium signaling and nucleotide metabolism
0.40
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