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Role of the mesenchymal stromal cells in bone marrow failure of Fanconi Anemia patients.

Role of the mesenchymal stromal cells in bone marrow failure of Fanconi Anemia patients.

Authors :
Zubicaray J
Ivanova M
Iriondo J
García Martínez J
Muñoz-Viana R
Abad L
García-García L
González de Pablo J
Gálvez E
Sebastián E
Ramírez M
Madero L
Díaz MÁ
González-Murillo Á
Sevilla J
Source :
Frontiers in cell and developmental biology [Front Cell Dev Biol] 2024 Jul 25; Vol. 12, pp. 1286815. Date of Electronic Publication: 2024 Jul 25 (Print Publication: 2024).
Publication Year :
2024

Abstract

Introduction: Fanconi anemia (FA) is an inherited disorder characterized by bone marrow failure, congenital malformations, and predisposition to malignancies. Alterations in hematopoietic stem cells (HSC) have been reported, but little is known regarding the bone marrow (BM) stroma. Thus, the characterization of Mesenchymal Stromal Cells (MSC) would help to elucidate their involvement in the BM failure.<br />Methods: We characterized MSCs of 28 FA patients (FA-MSC) before and after treatment (hematopoietic stem cell transplantation, HSCT; or gene therapy, GT). Phenotypic and functional properties were analyzed and compared with MSCs expanded from 26 healthy donors (HD-MSCs). FA-MSCs were genetically characterized through, mitomycin C-test and chimerism analysis. Furthermore, RNA-seq profiling was used to identify dysregulated metabolic pathways.<br />Results: Overall, FA-MSC had the same phenotypic and functional characteristics as HD-MSC. Of note, MSC-GT had a lower clonogenic efficiency. These findings were not confirmed in the whole FA patients' cohort. Transcriptomic profiling identified dysregulation in HSC self-maintenance pathways in FA-MSC (HOX), and was confirmed by real-time quantitative polymerase chain reaction (RT-qPCR).<br />Discussion: Our study provides a comprehensive characterization of FA-MSCs, including for the first time MSC-GT and constitutes the largest series published to date. Interestingly, transcript profiling revealed dysregulation of metabolic pathways related to HSC self-maintenance. Taken together, our results or findings provide new insights into the pathophysiology of the disease, although whether these niche defects are involved in the hematopoietic defects seen of FA deserves further investigation.<br />Competing Interests: JS reports financial support outside the submitted work for educational lectures by Novartis, Miltenyi, and Amgen; advisory board member for Rocket Pharma, Novartis, Sobi, Agios, and Amgen. JZ reports financial support outside the submitted work for educational lectures by Novartis. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Zubicaray, Ivanova, Iriondo, García Martínez, Muñoz-Viana, Abad, García-García, González de Pablo, Gálvez, Sebastián, Ramírez, Madero, Díaz, González-Murillo and Sevilla.)

Details

Language :
English
ISSN :
2296-634X
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in cell and developmental biology
Publication Type :
Academic Journal
Accession number :
39119037
Full Text :
https://doi.org/10.3389/fcell.2024.1286815