Intracellular cytoskeleton and junction proteins of endothelial cells in the porcine iris microvasculature. (November 2015)

• Record Type: Journal Article
• Authors: Yang, Hongfang; Yu, Paula K.; Cringle, Stephen J.; Sun, Xinghuai; Yu, Dao-Yi
• Is Part Of: Experimental eye research. Volume 140(2015:Nov.)
• Page Start: 106
• Page End: 116
• Publication Date: 2015-11
• Subjects: Iris microvasculature -- Endothelium -- Micro-perfusion -- Cytoskeleton -- Junction proteins -- Claudin-5 -- VE-cadherin; Ophthalmology -- Periodicals; Eye -- Periodicals; Œil -- Périodiques; Ophthalmology; Periodicals; Electronic journals; 612.8405
• DOI: 10.1016/j.exer.2015.08.025
• Languages: English
• ISSNs: 0014-4835

Abstract

Abstract: Recently we reported studies of the iris microvasculature and its endothelial cells using intra-luminal micro-perfusion, fixation, and silver staining, suggesting that the iris vascular endothelium may be crucial for maintaining homeostasis in the ocular anterior segment. Here we present information regarding the intracellular structure and cell junctions of the iris endothelium. Thirty-seven porcine eyes were used for this study. The temporal long posterior ciliary artery was cannulated to assess the iris microvascular network and its endothelium using intra-luminal micro-perfusion, fixation, and staining with phalloidin for intracellular cytoskeleton f-actin, and with antibodies against claudin-5 and VE-cadherin for junction proteins. Nuclei were counterstained with Hoechst. The iris was flat-mounted for confocal imaging. The iris microvasculature was studied for its distribution, branch orders and endothelial morphometrics with endothelial cell length measured for each vessel order. Our results showed that morphometrics of the iris microvasculature was comparable with our previous silver staining. Abundant stress fibres and peripheral border staining were seen within the endothelial cells in larger arteries. An obvious decrease in cytoplasmic stress fibres was evident further downstream in the smaller arterioles, and they tended to be absent from capillaries and veins. Endothelial intercellular junctions throughout the iris vasculature were VE-cadherin and claudin-5 immuno-positive, indicating the presence of both adherent junctions and tight junctions between vascular endothelial cells throughout the iris microvasculature. Unevenness of claudin-5 staining was noted along the endothelial cell borders in almost every order of vessels, especially in veins and small arterioles. Our results suggest that significant heterogeneity of intracellular structure and junction proteins is present in different orders of the iris vasculature in addition to vascular diameter and shape of the endothelia. Detailed information of the topography and intracellular structure and junction proteins of the endothelium of the iris microvasculature combined with unique structural features of the iris may help us to further understand the physiological and pathogenic roles of the iris vasculature in relevant ocular diseases. Highlights: The endothelium was assessed using staining for f-actin and junction proteins. Abundant stress fibres and peripheral border staining were seen in larger arteries. Intercellular junctions were VE-cadherin and claudin-5 immunopositive. Heterogeneity of intracellular and junctional proteins was revealed. Iris vascular endothelium may be crucial for homeostasis in the anterior segment.