You Say You Want a Resolution (of Fibrosis)
Overview
Molecular Biology
Affiliations
In pathological fibrosis, aberrant tissue remodeling with excess extracellular matrix leads to organ dysfunction and eventual morbidity. Diseases of fibrosis create significant global health and economic burdens and are often deadly. Although fibrosis has traditionally been thought of as an irreversible process, a growing body of evidence demonstrates that organ fibrosis can reverse in certain circumstances, especially if an underlying cause of injury can be removed. This body of evidence has uncovered more and more contributors to persistent and nonresolving tissue fibrosis. Here, we review the present knowledge on resolution of organ fibrosis and restoration of near-normal tissue architecture. We emphasize three critical areas of tissue homeostasis that are necessary for fibrosis resolution, namely, the elimination of matrix-producing cells, the clearance of excess matrix, and the regeneration of normal tissue constituents. In so doing, we also highlight how profibrotic pathways interact with one another and where there may be therapeutic opportunities to intervene and remediate pathological persistent fibrosis.
Sacchi M, Tomaselli D, Ruggeri M, Aiello F, Sabella P, Dore S Int J Mol Sci. 2025; 26(5).
PMID: 40076946 PMC: 11900438. DOI: 10.3390/ijms26052327.
Baas J, Varga J, Feghali-Bostwick C, Peters-Golden M, Fortier S bioRxiv. 2025; .
PMID: 40060695 PMC: 11888450. DOI: 10.1101/2025.02.26.640163.
Brizio M, Mancini M, Lora M, Joy S, Zhu S, Brilland B Stem Cell Res Ther. 2024; 15(1):329.
PMID: 39334258 PMC: 11438190. DOI: 10.1186/s13287-024-03916-9.
BCL-2 Modulates IRE1α Activation to Attenuate Endoplasmic Reticulum Stress and Pulmonary Fibrosis.
Jourdan Le Saux C, Ho T, Brumwell A, Kathiriya J, Wei Y, Hughes J Am J Respir Cell Mol Biol. 2023; 70(4):247-258.
PMID: 38117250 PMC: 11478128. DOI: 10.1165/rcmb.2023-0109OC.
Zhang Y, Fu J, Li C, Chang Y, Li X, Cheng H Cell Mol Life Sci. 2023; 80(10):308.
PMID: 37768341 PMC: 11072733. DOI: 10.1007/s00018-023-04961-y.