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Maternal Western-style diet remodels the transcriptional landscape of fetal hematopoietic stem and progenitor cells in rhesus macaques

Maternal obesity adversely impacts the in utero metabolic environment, but its effect on fetal hematopoiesis remains incompletely understood. During late development, the fetal bone marrow (FBM) becomes the major site where macrophages and B lymphocytes are produced via differentiation of hematopoie...

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Detalles Bibliográficos
Autores principales: Sureshchandra, Suhas, Chan, Chi N., Robino, Jacob J., Parmelee, Lindsay K., Nash, Michael J., Wesolowski, Stephanie R., Pietras, Eric M., Friedman, Jacob E., Takahashi, Diana, Shen, Weining, Jiang, Xiwen, Hennebold, Jon D., Goldman, Devorah, Packwood, William, Lindner, Jonathan R., Roberts, Charles T., Burwitz, Benjamin J., Messaoudi, Ilhem, Varlamov, Oleg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768582/
https://www.ncbi.nlm.nih.gov/pubmed/36332628
http://dx.doi.org/10.1016/j.stemcr.2022.10.003
Descripción
Sumario:Maternal obesity adversely impacts the in utero metabolic environment, but its effect on fetal hematopoiesis remains incompletely understood. During late development, the fetal bone marrow (FBM) becomes the major site where macrophages and B lymphocytes are produced via differentiation of hematopoietic stem and progenitor cells (HSPCs). Here, we analyzed the transcriptional landscape of FBM HSPCs at single-cell resolution in fetal macaques exposed to a maternal high-fat Western-style diet (WSD) or a low-fat control diet. We demonstrate that maternal WSD induces a proinflammatory response in FBM HSPCs and fetal macrophages. In addition, maternal WSD consumption suppresses the expression of B cell development genes and decreases the frequency of FBM B cells. Finally, maternal WSD leads to poor engraftment of fetal HSPCs in nonlethally irradiated immunodeficient NOD/SCID/IL2rγ(−/−) mice. Collectively, these data demonstrate for the first time that maternal WSD impairs fetal HSPC differentiation and function in a translationally relevant nonhuman primate model.