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American Heart Association

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Final ID: 4137935

Adipogenesis in Bone Marrow Niche under Cardiac Stress Worsens Cardiac Function

Abstract Body (Do not enter title and authors here): Background: We have recently reported that repetitive cardiac decompensation with multimorbidity often experienced by patients with heart failure (HF) is attributed to epigenetic modifications of hematopoietic stem cells (HSCs) in the bone marrow (BM). HF reprogrammed HSCs differentiation and altered tissue macrophage homeostasis. These findings demonstrate that the BM can carry an innate immune memory of cardiac stress that may exacerbate HF and predispose other organs to pathology.
Aims: Because the stemness of HSCs is mainly regulated by mesenchymal stromal cells (MSCs) in the BM niche, we investigated phenotypic alterations of MSCs under cardiac stress.
Methods & Results: Transcriptome analysis of MSCs showed preferential differentiation toward adipocytes in murine pressure overload models. In vitro assays and histological BM sections also support this finding. Furthermore, single-cell RNA sequencing of MSCs demonstrated that the percentage of adipocyte-primed MSCs increased in proportion to the severity of cardiac dysfunction, and also correlated with the frequency of myeloid-lineage progenitor cells. To investigate the influence of adipo-lineage MSCs on HSCs, we conducted BM transplantation supplemented with MSCs from control or HF mice. Recipient mice transplanted with HF-MSCs showed significant increases in myeloid-biased multipotent progenitors in BM and myeloid cells in peripheral blood. Additionally, the number of proinflammatory cardiac macrophages was significantly increased in the HF-MSCs group, promoting cardiac fibrosis and dysfunction.
Conclusions: Our results demonstrated that the BM niche could perceive cardiac stress in the form of adipocytic skewing of MSCs in the setting of HF, which changed the differentiation behavior in HSCs and ultimately led to further deterioration of cardiac function through the impaired differentiation of circulating monocytes into cardiac macrophages. Therefore, suppressing the adipocytic differentiation of MSCs could have a novel therapeutic potential to avoid repeated HF events.
  • Goto, Kohsaku  ( The University of Tokyo , Tokyo , Japan )
  • Nakayama, Yukiteru  ( The University of Tokyo , Tokyo , Japan )
  • Manabe, Ichiro  ( Chiba University , Chiba , Japan )
  • Komuro, Issei  ( The University of Tokyo , Tokyo , Japan )
  • Takeda, Norihiko  ( The University of Tokyo , Tokyo , Japan )
  • Fujiu, Katsuhito  ( The University of Tokyo , Tokyo , Japan )
  • Author Disclosures:
    KOHSAKU GOTO: DO NOT have relevant financial relationships | Yukiteru Nakayama: DO NOT have relevant financial relationships | Ichiro Manabe: DO NOT have relevant financial relationships | Issei Komuro: No Answer | Norihiko Takeda: DO have relevant financial relationships ; Research Funding (PI or named investigator):Astra Zeneka:Past (completed) ; Speaker:Kyowa Kirin:Past (completed) ; Research Funding (PI or named investigator):Bristol Myers Scibb:Past (completed) ; Research Funding (PI or named investigator):Ono Pharameutical:Past (completed) | Katsuhito Fujiu: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Melvin L. Marcus Early Career Investigator Award in Cardiovascular Sciences Competition

Saturday, 11/16/2024 , 03:15PM - 04:30PM

Abstract Oral Session

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