pH regulates hematopoietic stem cell potential via polyamines

Author:

Kumar Sachin12ORCID,Vassallo Jeffrey D1ORCID,Nattamai Kalpana J1,Hassan Aishlin1ORCID,Karns Rebekah3,Vollmer Angelika4,Soller Karin4,Sakk Vadim4,Sacma Mehmet4ORCID,Nemkov Travis5,D'Alessandro Angelo5ORCID,Geiger Hartmut46ORCID

Affiliation:

1. Division of Experimental Hematology and Cancer Biology Cincinnati Children's Research Foundation Cincinnati OH USA

2. Pharmacology Division CSIR‐Central Drug Research Institute Lucknow India

3. Division of Gastroenterology, Hepatology and Nutrition Cincinnati Children's Hospital Medical Center and University of Cincinnati Cincinnati OH USA

4. Institute of Molecular Medicine Ulm University Ulm Germany

5. University of Colorado Denver ‐ Anschutz Medical Campus Aurora CO USA

6. Aging Research Center Ulm University Ulm Germany

Abstract

AbstractUpon ex vivo culture, hematopoietic stem cells (HSCs) quickly lose potential and differentiate into progenitors. The identification of culture conditions that maintain the potential of HSCs ex vivo is therefore of high clinical interest. Here, we demonstrate that the potential of murine and human HSCs is maintained when cultivated for 2 days ex vivo at a pH of 6.9, in contrast to cultivation at the commonly used pH of 7.4. When cultivated at a pH of 6.9, HSCs remain smaller, less metabolically active, less proliferative and show enhanced reconstitution ability upon transplantation compared to HSC cultivated at pH 7.4. HSCs kept at pH 6.9 show an attenuated polyamine pathway. Pharmacological inhibition of the polyamine pathway in HSCs cultivated at pH 7.4 with DFMO mimics phenotypes and potential of HSCs cultivated at pH 6.9. Ex vivo exposure to a pH of 6.9 is therefore a positive regulator of HSC function by reducing polyamines. These findings might improve HSC short‐term cultivation protocols for transplantation and gene therapy interventions.

Funder

Deutsche Forschungsgemeinschaft

Science and Engineering Research Board

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

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