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The distinct metabolic profile of hematopoietic stem cells reflects their location in a hypoxic niche.


ABSTRACT: Bone marrow transplantation is the primary therapy for numerous hematopoietic disorders. The efficiency of bone marrow transplantation depends on the function of long-term hematopoietic stem cells (LT-HSCs), which is markedly influenced by their hypoxic niche. Survival in this low-oxygen microenvironment requires significant metabolic adaptation. Here, we show that LT-HSCs utilize glycolysis instead of mitochondrial oxidative phosphorylation to meet their energy demands. We used flow cytometry to identify a unique low mitochondrial activity/glycolysis-dependent subpopulation that houses the majority of hematopoietic progenitors and LT-HSCs. Finally, we demonstrate that Meis1 and Hif-1alpha are markedly enriched in LT-HSCs and that Meis1 regulates HSC metabolism through transcriptional activation of Hif-1alpha. These findings reveal an important transcriptional network that regulates HSC metabolism.

SUBMITTER: Simsek T 

PROVIDER: S-EPMC4159713 | biostudies-literature | 2010 Sep

REPOSITORIES: biostudies-literature

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The distinct metabolic profile of hematopoietic stem cells reflects their location in a hypoxic niche.

Simsek Tugba T   Kocabas Fatih F   Kocabas Fatih F   Zheng Junke J   Deberardinis Ralph J RJ   Mahmoud Ahmed I AI   Olson Eric N EN   Schneider Jay W JW   Zhang Cheng Cheng CC   Sadek Hesham A HA  

Cell stem cell 20100901 3


Bone marrow transplantation is the primary therapy for numerous hematopoietic disorders. The efficiency of bone marrow transplantation depends on the function of long-term hematopoietic stem cells (LT-HSCs), which is markedly influenced by their hypoxic niche. Survival in this low-oxygen microenvironment requires significant metabolic adaptation. Here, we show that LT-HSCs utilize glycolysis instead of mitochondrial oxidative phosphorylation to meet their energy demands. We used flow cytometry t  ...[more]

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