Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSPSILVA, Rafael Andre daRODA, Vinicius Moraes de PaivaMATSUDA, MoniqueSIQUEIRA, Paula VelosoLUSTOZA-COSTA, Gabriela JesusWU, Davi ChenHAMASSAKI, Dania Emi2022-06-202022-06-202022GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, v.260, n.5, p.1435-1444, 20220721-832Xhttps://observatorio.fm.usp.br/handle/OPI/47473Idiopathic epiretinal membrane (iERM) is a fibrocellular proliferation on the inner surface of the retina, which leads to decreased visual acuity and even central visual loss. As iERM is associated to advanced age and posterior vitreous detachment, a higher prevalence is expected with increasing life expectancy and aging of the global population. Although various cell types of retinal and extra-retinal origin have been described in iERMs (Muller glial cells, astrocytes, hyalocytes, retinal pigment epithelium cells, myofibroblasts, and fibroblasts), myofibroblasts have a central role in collagen production and contractile activity. Thus, myofibroblast differentiation is considered a key event for the iERM formation and progression, and fibroblasts, Muller glial cells, hyalocytes, and retinal pigment epithelium have been identified as myofibroblast precursors. On the other side, the different cell types synthesize growth factors, cytokines, and extracellular matrix, which have a crucial role in ERM pathogenesis. In the present review, the major cellular components and their functions are summarized, and their possible roles in the iERM formation are discussed. By exploring in detail the cellular and molecular aspects of iERM, we seek to contribute for better understanding of this fibrotic disease and the origin of myofibroblasts, which may eventually drive to more targeted therapeutic approaches.engrestrictedAccessEpiretinal membraneHyalocyteMuller cellMyofibroblastRetinal pigment epithelium cellTransdifferentiationproliferative vitreoretinal diseasesgrowth-factormuller cellstgf-betahyalocytestissueoverexpressiondetachmentcollagensgliaarticleCopyright SPRINGER10.1007/s00417-021-05492-7Clinical Neurology1435-702X