1. CD8 + T Cells Drive Plaque Smooth Muscle Cell Dedifferentiation in Experimental Atherosclerosis.
- Author
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Schäfer S, Gogiraju R, Rösch M, Kerstan Y, Beck L, Garbisch J, Saliba AE, Gisterå A, Hermanns HM, Boon L, Kastenmüller W, Schäfer K, Cochain C, and Zernecke A
- Subjects
- Animals, Mice, Mice, Inbred C57BL, Mice, Knockout, Cells, Cultured, Male, Receptors, LDL genetics, Receptors, LDL deficiency, Phenotype, Core Binding Factor Alpha 2 Subunit genetics, Core Binding Factor Alpha 2 Subunit metabolism, Aorta pathology, Aorta immunology, Aorta metabolism, Coculture Techniques, Aortic Diseases pathology, Aortic Diseases genetics, Aortic Diseases immunology, Aortic Diseases metabolism, CD8-Positive T-Lymphocytes immunology, CD8-Positive T-Lymphocytes metabolism, Myocytes, Smooth Muscle pathology, Myocytes, Smooth Muscle metabolism, Myocytes, Smooth Muscle immunology, Cell Dedifferentiation, Plaque, Atherosclerotic, Disease Models, Animal, Atherosclerosis pathology, Atherosclerosis metabolism, Atherosclerosis genetics, Atherosclerosis immunology, Muscle, Smooth, Vascular pathology, Muscle, Smooth, Vascular metabolism, Muscle, Smooth, Vascular immunology
- Abstract
Background: Atherosclerosis is driven by the infiltration of the arterial intima by diverse immune cells and smooth muscle cells (SMCs). CD8
+ T cells promote lesion growth during atherosclerotic lesion development, but their role in advanced atherosclerosis is less clear. Here, we studied the role of CD8+ T cells and their effects on SMCs in established atherosclerosis., Methods: CD8+ T cells were depleted in (SMC reporter) low-density lipoprotein receptor-deficient ( Ldlr-/- ) mice with established atherosclerotic lesions. Atherosclerotic lesion formation was examined, and single-cell RNA sequencing of aortic SMCs and their progeny was performed. Additionally, coculture experiments with primary aortic SMCs and CD8+ T cells were conducted., Results: Although we could not detect differences in atherosclerotic lesion size, an increased plaque SMC content was noted in mice after CD8+ T-cell depletion. Single-cell RNA sequencing of aortic lineage-traced SMCs revealed contractile SMCs and a modulated SMC cluster, expressing macrophage- and osteoblast-related genes. CD8+ T-cell depletion was associated with an increased contractile but decreased macrophage and osteoblast-like gene signature in this modulated aortic SMC cluster. Conversely, exposure of isolated aortic SMCs to activated CD8+ T cells decreased the expression of genes indicative of a contractile SMC phenotype and induced a macrophage and osteoblast-like cell state. Notably, CD8+ T cells triggered calcium deposits in SMCs under osteogenic conditions. Mechanistically, we identified transcription factors highly expressed in modulated SMCs, including Runx1 , to be induced by CD8+ T cells in cultured SMCs in an IFNγ (interferon-γ)-dependent manner., Conclusions: We here uncovered CD8+ T cells to control the SMC phenotype in atherosclerosis. CD8+ T cells promote SMC dedifferentiation and drive SMCs to adopt features of macrophage-like and osteoblast-like, procalcifying cell phenotypes. Given the critical role of SMCs in atherosclerotic plaque stability, CD8+ T cells could thus be explored as therapeutic target cells during lesion progression., Competing Interests: None.- Published
- 2024
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