Hypoxic metabolism in human hematopoietic stem cells

Fatih Kocabas, Li Xie, Jingjing Xie, Zhuo Yu, Ralph J. DeBerardinis, Wataru Kimura, SuWannee W. Thet, Ahmed F. Elshamy, Hesham Abouellail, Shalini Muralidhar, Xiaoye Liu, Chiqi Chen, Hesham A. Sadek, Cheng Cheng Zhang, Junke Zheng

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Adult hematopoietic stem cells (HSCs) are maintained in a microenvironment, known as niche in the endosteal regions of the bone marrow. This stem cell niche with low oxygen tension requires HSCs to adopt a unique metabolic profile. We have recently demonstrated that mouse long-term hematopoietic stem cells (LT-HSCs) utilize glycolysis instead of mitochondrial oxidative phosphorylation as their main energy source. However, the metabolic phenotype of human hematopoietic progenitor and stem cells (HPSCs) remains unknown. Results: We show that HPSCs have a similar metabolic phenotype, as shown by high rates of glycolysis, and low rates of oxygen consumption. Fractionation of human mobilized peripheral blood cells based on their metabolic footprint shows that cells with a low mitochondrial potential are highly enriched for HPSCs. Remarkably, low MP cells had much better repopulation ability as compared to high MP cells. Moreover, similar to their murine counterparts, we show that Hif-1aα is upregulated in human HPSCs, where it is transcriptionally regulated by Meis1. Finally, we show that Meis1 and its cofactors Pbx1 and HoxA9 play an important role in transcriptional activation of Hif-1aα in a cooperative manner. Conclusions: These findings highlight the unique metabolic properties of human HPSCs and the transcriptional network that regulates their metabolic phenotype.

Original languageEnglish (US)
Article number39
JournalCell and Bioscience
Volume5
Issue number1
DOIs
StatePublished - Jul 17 2015

Fingerprint

Hematopoietic Stem Cells
Stem cells
Metabolism
Glycolysis
Oxygen
Phenotype
Fractionation
Stem Cell Niche
Adult Stem Cells
Bone
Metabolome
Blood
Gene Regulatory Networks
Oxidative Phosphorylation
Chemical activation
Cells
Oxygen Consumption
Transcriptional Activation
Blood Cells
Bone Marrow

Keywords

  • HPSCs
  • Human hematopoietic progenitor and stem cells
  • Hypoxia
  • Hypoxic regulation of metabolism
  • Metabolism
  • Stem cells

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Kocabas, F., Xie, L., Xie, J., Yu, Z., DeBerardinis, R. J., Kimura, W., ... Zheng, J. (2015). Hypoxic metabolism in human hematopoietic stem cells. Cell and Bioscience, 5(1), [39]. https://doi.org/10.1186/s13578-015-0020-3

Hypoxic metabolism in human hematopoietic stem cells. / Kocabas, Fatih; Xie, Li; Xie, Jingjing; Yu, Zhuo; DeBerardinis, Ralph J.; Kimura, Wataru; Thet, SuWannee W.; Elshamy, Ahmed F.; Abouellail, Hesham; Muralidhar, Shalini; Liu, Xiaoye; Chen, Chiqi; Sadek, Hesham A.; Zhang, Cheng Cheng; Zheng, Junke.

In: Cell and Bioscience, Vol. 5, No. 1, 39, 17.07.2015.

Research output: Contribution to journalArticle

Kocabas, F, Xie, L, Xie, J, Yu, Z, DeBerardinis, RJ, Kimura, W, Thet, SW, Elshamy, AF, Abouellail, H, Muralidhar, S, Liu, X, Chen, C, Sadek, HA, Zhang, CC & Zheng, J 2015, 'Hypoxic metabolism in human hematopoietic stem cells', Cell and Bioscience, vol. 5, no. 1, 39. https://doi.org/10.1186/s13578-015-0020-3
Kocabas, Fatih ; Xie, Li ; Xie, Jingjing ; Yu, Zhuo ; DeBerardinis, Ralph J. ; Kimura, Wataru ; Thet, SuWannee W. ; Elshamy, Ahmed F. ; Abouellail, Hesham ; Muralidhar, Shalini ; Liu, Xiaoye ; Chen, Chiqi ; Sadek, Hesham A. ; Zhang, Cheng Cheng ; Zheng, Junke. / Hypoxic metabolism in human hematopoietic stem cells. In: Cell and Bioscience. 2015 ; Vol. 5, No. 1.
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AU - Kimura, Wataru

AU - Thet, SuWannee W.

AU - Elshamy, Ahmed F.

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AU - Muralidhar, Shalini

AU - Liu, Xiaoye

AU - Chen, Chiqi

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