The hallmark of amyloid diseases is deposition of misfolded proteins as amyloid fibrils in the interstitium of target organs. Amyloid deposits surround cells, distorting the micro and macro-architecture of the extracellular space and profoundly changing the physical and molecular properties of this compartment. In the heart, extracellular matrix (ECM) remodeling has a profound impact on the mechanical properties of this target organ and on the physiology and metabolism of resident cells. This review critically summarizes the available knowledge on ECM alterations in cardiac amyloidosis, with the goal of providing an overview on how biochemical, biophysical and anatomical modifications are interrelated, and how ECM remodeling participates in the pathophysiology of this unique type of cardiopathy.

Role of extracellular space and matrix remodeling in cardiac amyloidosis

Lavatelli, Francesca;Marchese, Loredana;Mangione, Palma Patrizia;Raimondi, Sara;Canetti, Diana;Verona, Guglielmo;Arbustini, Eloisa;Obici, Laura;Bellotti, Vittorio;Giorgetti, Sofia
2025-01-01

Abstract

The hallmark of amyloid diseases is deposition of misfolded proteins as amyloid fibrils in the interstitium of target organs. Amyloid deposits surround cells, distorting the micro and macro-architecture of the extracellular space and profoundly changing the physical and molecular properties of this compartment. In the heart, extracellular matrix (ECM) remodeling has a profound impact on the mechanical properties of this target organ and on the physiology and metabolism of resident cells. This review critically summarizes the available knowledge on ECM alterations in cardiac amyloidosis, with the goal of providing an overview on how biochemical, biophysical and anatomical modifications are interrelated, and how ECM remodeling participates in the pathophysiology of this unique type of cardiopathy.
2025
Inglese
140
100
112
13
Aging; Amyloid fibrils; Amyloidosis; Cardiomyopathy; ECM remodeling; Molecular imaging; Protein misfolding
https://www.sciencedirect.com/science/article/pii/S0945053X25000630?via=ihub
12
info:eu-repo/semantics/article
262
Lavatelli, Francesca; Marchese, Loredana; Mangione, Palma Patrizia; Raimondi, Sara; Canetti, Diana; Verona, Guglielmo; Venneri, Lucia; Arbustini, Eloi...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1547275
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