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Cortical bone stem cells modify cardiac inflammation after myocardial infarction by inducing a novel macrophage phenotype.
- Source :
-
American journal of physiology. Heart and circulatory physiology [Am J Physiol Heart Circ Physiol] 2021 Oct 01; Vol. 321 (4), pp. H684-H701. Date of Electronic Publication: 2021 Aug 20. - Publication Year :
- 2021
-
Abstract
- Acute damage to the heart, as in the case of myocardial infarction (MI), triggers a robust inflammatory response to the sterile injury that is part of a complex and highly organized wound-healing process. Cortical bone stem cell (CBSC) therapy after MI has been shown to reduce adverse structural and functional remodeling of the heart after MI in both mouse and swine models. The basis for these CBSC treatment effects on wound healing are unknown. The present experiments show that CBSCs secrete paracrine factors known to have immunomodulatory properties, most notably macrophage colony-stimulating factor (M-CSF) and transforming growth factor-β, but not IL-4. CBSC therapy increased the number of galectin-3 <superscript>+</superscript> macrophages, CD4 <superscript>+</superscript> T cells, and fibroblasts in the heart while decreasing apoptosis in an in vivo swine model of MI. Macrophages treated with CBSC medium in vitro polarized to a proreparative phenotype are characterized by increased CD206 expression, increased efferocytic ability, increased IL-10, TGF-β, and IL-1RA secretion, and increased mitochondrial respiration. Next generation sequencing revealed a transcriptome significantly different from M2a or M2c macrophage phenotypes. Paracrine factors from CBSC-treated macrophages increased proliferation, decreased α-smooth muscle actin expression, and decreased contraction by fibroblasts in vitro. These data support the idea that CBSCs are modulating the immune response to MI to favor cardiac repair through a unique macrophage polarization that ultimately reduces cell death and alters fibroblast populations that may result in smaller scar size and preserved cardiac geometry and function. NEW & NOTEWORTHY Cortical bone stem cell (CBSC) therapy after myocardial infarction alters the inflammatory response to cardiac injury. We found that cortical bone stem cell therapy induces a unique macrophage phenotype in vitro and can modulate macrophage/fibroblast cross talk.
- Subjects :
- Animals
Apoptosis
Cells, Cultured
Cortical Bone cytology
Disease Models, Animal
Female
Fibroblasts immunology
Fibroblasts metabolism
Fibrosis
Humans
Macrophages immunology
Mice, Inbred C57BL
Myocardial Infarction genetics
Myocardial Infarction immunology
Myocardial Infarction metabolism
Myocardium immunology
Phenotype
Signal Transduction
Swine
Swine, Miniature
T-Lymphocytes immunology
T-Lymphocytes metabolism
Transcriptome
Mice
Inflammation Mediators metabolism
Macrophage Activation
Macrophages metabolism
Myocardial Infarction surgery
Myocardium metabolism
Paracrine Communication
Stem Cell Transplantation
Stem Cells metabolism
Wound Healing
Subjects
Details
- Language :
- English
- ISSN :
- 1522-1539
- Volume :
- 321
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- American journal of physiology. Heart and circulatory physiology
- Publication Type :
- Academic Journal
- Accession number :
- 34415185
- Full Text :
- https://doi.org/10.1152/ajpheart.00304.2021