Cardiac matrix-bound Nanovesicles provide insight into mechanisms of clinical heart disease progression to failure

Remodeling of the extracellular matrix (ECM) is critical for effective wound healing and maintaining organ homeostasis. The ECM of soft tissues, including cardiac, contains embedded nanovesicles; or matrix-bound nanovesicles (MBV). The luminal cargo of MBV consists of lipids, microRNAs (miRNAs), and...

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Veröffentlicht in:International journal of cardiology 2024-12, Vol.421, p.132892, Article 132892
Hauptverfasser: Cramer, Madeline, Borrelli, Matt, Mathews, Lisa, Dewey, Marley, Schwarzmann, William, Soman, Vishal, Sembrat, John, Rojas, Mauricio, McTiernan, Charlie, Chandran, Uma, Hussey, George S., Badylak, Stephen F., Turnquist, Heth R.
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container_title International journal of cardiology
container_volume 421
creator Cramer, Madeline
Borrelli, Matt
Mathews, Lisa
Dewey, Marley
Schwarzmann, William
Soman, Vishal
Sembrat, John
Rojas, Mauricio
McTiernan, Charlie
Chandran, Uma
Hussey, George S.
Badylak, Stephen F.
Turnquist, Heth R.
description Remodeling of the extracellular matrix (ECM) is critical for effective wound healing and maintaining organ homeostasis. The ECM of soft tissues, including cardiac, contains embedded nanovesicles; or matrix-bound nanovesicles (MBV). The luminal cargo of MBV consists of lipids, microRNAs (miRNAs), and proteins that influence the function of immune and stromal cells. ECM remodeling is extensive during heart disease, yet it is unknown if MBV are altered during the development of heart disease. We conducted the present study to answer this question. MBV were isolated from de-identified human left ventricle (LV) tissue samples from: 1) non-ischemic, failing hearts (failing) and 2) non-failing, non-ischemic hearts (control). MBV morphology was analyzed and the protein and miRNA cargo were quantified. Immunomodulatory capacity of MBV was assessed on macrophages. Failing and control heart tissue had similar concentrations of MBV, however, their size and cargo differed. MBV from failing tissue had increased levels of Apolipoprotein A-1 and decreased levels of C-Reactive Protein. Over 600 unique miRNA were detected. Of these, 5 % showed significantly different levels, with most being downregulated in MBV from failing heart tissue. Ex vivo stimulation of human macrophages with MBV isolated from control ventricular tissue, but not failing ventricles, induced gene expression suggesting increased reparative functions. These data reveal that MBV are present within the human heart and suggests that disease progression alters MBV cargo (lipids, microRNAs, and proteins). Furthermore, it is suggested that alterations in local MBV cargo may perpetuate pathology when their capacity to modulate reparative immune cells is diminished. [Display omitted] •This is an early investigation into disease state changes in human cardiac extracellular matrix-bound vesicles (MBV).•Cardiac MBV display significant changes to their protein and RNA cargo.•MBV from diseased hearts contain several markers of heart disease.•This work suggests altered MBV cargo have a functional effect on macrophages.
doi_str_mv 10.1016/j.ijcard.2024.132892
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subjects Extracellular matrix
Extracellular vesicles
Heart failure
Immunomodulation
Macrophages
title Cardiac matrix-bound Nanovesicles provide insight into mechanisms of clinical heart disease progression to failure
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