Eltrombopag increases the hematopoietic supporting ability of mesenchymal stem/stromal cells

Author:

Muntión Sandra123ORCID,Preciado Silvia423,Sánchez-Luis Elena5,Corchete Luis6,Díez-Campelo María278,Osugui Lika43,Martí-Chillón Gerardo-Javier43,Vidriales María-Belén7,Navarro-Bailón Almudena423,De Las Rivas Javier5,Sánchez-Guijo Fermín42378ORCID

Affiliation:

1. Cell Therapy Area, Department of Hematology, Institute of Biomedical Research of Salamanca-Hospital Universitario de Salamanca (IBSAL-HUS), Paseo de San Vicente 58-182, 37007 Salamanca, Spain

2. RICORS TERAV, ISCIII, Madrid, Spain

3. Centro en Red de Medicina Regenerativa y Terapia Celular de Castilla y León, Valladolid, Spain

4. Cell Therapy Area, Department of Hematology, Institute of Biomedical Research of Salamanca-Hospital Universitario de Salamanca (IBSAL-HUS), Salamanca, Spain

5. Bioinformatics and Functional Genomics Group, Cancer Research Center (CiC-IBMCC), Consejo Superior de Investigaciones Científicas (CSIC) and University of Salamanca (USAL), Salamanca, Spain

6. Institute of Biomedical Research of Salamanca (IBSAL), Cancer Research Center (CiC-IBMCC, CSIC/USAL), Center for Biomedical Research in Network of Cancer (CIBERONC), Hematology Department, University Hospital of Salamanca, Salamanca, Spain

7. Center for Biomedical Research in Network of Cancer (CIBERONC), Department of Hematology, University Hospital of Salamanca (IBSAL-HUS), Salamanca, Spain

8. Department of Medicine, University of Salamanca (USAL), Salamanca, Spain

Abstract

Background: Eltrombopag (EP) is a small molecule that acts directly on hematopoietic stem cells (HSCs) and megakaryocytes to stimulate the hematopoietic process. Mesenchymal stem/stromal cells (MSCs) are key hematopoietic niche regulators. Objectives: We aimed to determine whether EP has any effect on MSC function and properties (especially on their hematopoietic-supporting ability) and if so, what changes (e.g. genome-wide transcriptomic alterations) are induced in MSC after EP treatment. Design/Methods: MSCs were isolated from 12 healthy donors and treated with 15 µM and 50 µM of EP for 24 h. The toxicity of the drug on MSCs and their differentiation ability were analyzed, as well as the transcriptomic profile, reactive oxygen species (ROS) and DNA damage and the changes induced in the clonogenic capacity of HSCs. Results: The results show that EP also modifies MSC functions, decreasing their adipogenic differentiation, increasing the expression of genes involved in hypoxia and other pathways related to oxygen homeostasis, and enhancing their ability to support hematopoiesis in vitro. Conclusion: Our findings support the use of EP in cases where hematopoiesis is defective, despite its well-known direct effects on hematopoietic cells. Our findings suggest that further studies on the effects of EP on MSCs from patients with aplastic anemia are warranted.

Funder

Ministerio de Ciencia e Innovación

european regional development fund

Fundación Española de Hematología y Hemoterapia

Novartis Pharmaceuticals Corporation

Publisher

SAGE Publications

Subject

Hematology

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