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Immunohistochemical expression of Fibrillin-1 in idiopathic epiretinal membranes.

Authors :
Tien, Luu Viet
Yamamoto, Manabu
Tagami, Mizuki
Misawa, Norihiko
Honda, Shigeru
Source :
Graefe's Archive of Clinical & Experimental Ophthalmology. Feb2025, Vol. 263 Issue 2, p415-424. 10p.
Publication Year :
2025

Abstract

Purpose: To investigate the expression patterns of Fibrillin-1 in idiopathic epiretinal membranes (iERM) and identify Fibrillin-1-secreting cells. Methods: iERM samples were collected via standard 27-gauge vitrectomy and subsequently subjected to flat-mount immunohistochemistry with double staining for the following markers: Fibrillin-1, glial acidic fibrillary protein (GFAP), cellular retinaldehyde-binding protein (CRALBP), retinoid isomerohydrolase RPE65 (RPE65), and α-smooth muscle actin (α-SMA). Results: Fibrillin-1 was detected throughout the iERM. The colocalization of Fibrillin-1 with α-SMA, CRALBP, and RPE65 suggested that myofibroblasts and retinal pigment epithelial (RPE) cells secreted Fibrillin-1. The lack of colocalization between GFAP and Fibrillin-1 indicated that GFAP-positive glial cells did not secrete Fibrillin-1. The colocalization of CRALBP and RPE65 with α-SMA indicated the transformation of RPE cells into myofibroblasts. This suggested that RPE cells transformed into myofibroblasts and secreted Fibrillin-1. The lack of colocalization between GFAP and α-SMA implied that GFAP-positive glial cells did not express α-SMA. Conclusions: Fibrillin-1 is widely distributed in iERMs, and myofibroblasts were the primary sources of Fibrillin-1 secretion. Additionally, during their transformation into myofibroblasts, RPE cells secreted Fibrillin-1. GFAP-positive glial cells did not express α-SMA nor secrete Fibrillin-1. Key messages: What is known Idiopathic epiretinal membranes are a common cause of visual acuity and quality impairment. The protein and cell components of idiopathic epiretinal membrane exhibit diversity. What is new Fibrillin-1 is present throughout the idiopathic epiretinal membrane. Myofibroblasts are the most important source of Fibrillin-1 secretion. Retinal pigment epithelial cells also secrete Fibrillin-1 when transforming into myofibroblast. Glial cells do not transform to myofibroblast and do not secrete Fibrillin-1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0721832X
Volume :
263
Issue :
2
Database :
Academic Search Index
Journal :
Graefe's Archive of Clinical & Experimental Ophthalmology
Publication Type :
Academic Journal
Accession number :
183353566
Full Text :
https://doi.org/10.1007/s00417-024-06667-8