Isolation, culture, and characterisation of human macular inner choroidal microvascular endothelial cells. Issue 10 (16th September 2005)

• Record Type: Journal Article
• Authors: Browning, A C; Gray, T; Amoaku, W M
• Is Part Of: British journal of ophthalmology. Volume 89:Issue 10(2005)
• Page Start: 1343
• Page End: 1347
• Publication Date: 2005-09-16
• Subjects: α-SMA, α smooth muscle actin -- ARMD, age related macular degeneration -- EGM, endothelial growth medium -- FITC, fluorescein isothiocyanate -- ICECs, inner choroidal endothelial cells -- MEM, minimum essential medium -- PBS, phosphate buffered saline -- RPE, retinal pigment epithelium -- TEM, transmission electron microscopy -- VEGF, vascular endothelial growth factor; choroid -- endothelial cells -- macula; Ophthalmology -- Periodicals; 617.7
• DOI: 10.1136/bjo.2004.063602
• Languages: English
• ISSNs: 0007-1161

Abstract

Abstract : Aim: To develop a method for the reliable isolation of adult human macular inner choroidal endothelial cells (ICECs) and to subsequently characterise them for their expression of a range of endothelial cell associated surface markers. Method: Human ICECs were isolated after manual dissection of maculas from fresh human posterior segments. Following enzyme digestion to form a single cell suspension, the ICECs were isolated using anti-CD31 coated Dynabeads. The isolated cells were grown in culture and examined for typical endothelial cell morphology, surface expression of vWf, CD 31, CD 105, VEGF receptors 1 and 2, and expression of E-selectin after stimulation with TNF-α. The cells were also examined for their ability to form fenestrations and capillary-like tubes in Matrigel. Results: The method enabled the rapid isolation of viable cells that demonstrated typical endothelial cobblestone morphology in culture. The cells stained positive for CD31, vWf, CD105, VEGF receptors 1 and 2, and E-selectin (after stimulation with TNF-α). The cells stained negative for α smooth muscle actin and fibroblast surface protein. The cells also developed fenestrations when cultured on fibronectin coated plates and formed capillary-like tubes structures when cultured on Matrigel. Conclusions: This technique isolates cells from the human macular inner choroid that display features consistent with vascular endothelial cells. These cells could subsequently be used to further the understanding of the pathophysiological mechanisms of diseases of the inner choroid, such as choroidal neovascularisation.