Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts

AIM: To investigate the toxicity of the E-prostanoid 2 (EP2) receptor agonist, butaprost against human subconjunctival (Tenon’s capsule) fibroblasts, and to determine the underlying mechanism. METHODS: We isolated Tenon’s fibroblasts from the subconjunctival area of healthy subjects and evaluated t...

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Main Authors: Jong Hoon Shin, Je Hyun Seo, Jae Ho Jung, Tae Woo Kim
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2017-07-01
Series:International Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.cn/en_publish/2017/7/20170702.pdf
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author Jong Hoon Shin
Je Hyun Seo
Jae Ho Jung
Tae Woo Kim
author_facet Jong Hoon Shin
Je Hyun Seo
Jae Ho Jung
Tae Woo Kim
author_sort Jong Hoon Shin
collection DOAJ
description AIM: To investigate the toxicity of the E-prostanoid 2 (EP2) receptor agonist, butaprost against human subconjunctival (Tenon’s capsule) fibroblasts, and to determine the underlying mechanism. METHODS: We isolated Tenon’s fibroblasts from the subconjunctival area of healthy subjects and evaluated the types of EP receptors expressed using quantitative real-time reverse transcription polymerase chain reaction (RT-PCR). The toxicity of butaprost against the fibroblasts was evaluated using methyl thiazolyl tetrazolium and lactic dehydrogenase assays. The inhibition of conjunctival fibroblast proliferation by butaprost was assessed by measuring α-actin levels. The underlying mechanism was assessed by measuring intracellular cyclic adenosine monophosphate (cAMP) levels. Intergroup differences were statistically analyzed using an independent t-test. Densitometry of the Western blot bands was performed using the Image J software. RESULTS: Quantitative real-time RT-PCR revealed that the fibroblast EP2 receptor levels were higher than those of the other EP receptors. Butaprost did not show toxicity against Tenon’s tissue, but inhibited conjunctival fibroblast proliferation by reducing collagen synthesis. EP2 receptor activation enhanced the cAMP cascade, which might be an important mechanism underlying this effect. CONCLUSION: Butaprost effectively reduces the subconjunctival scarring response. Given the significance of wound healing modulation in blebs, butaprost’s inhibitory effect on subconjunctival Tenon’s fibroblasts may be beneficial in managing postoperative scarring in glaucoma surgery.
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spelling doaj.art-f522c9ff3eef462e94a2f2c776d2a3752022-12-22T02:13:38ZengPress of International Journal of Ophthalmology (IJO PRESS)International Journal of Ophthalmology2222-39592227-48982017-07-011071028103310.18240/ijo.2017.07.02Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblastsJong Hoon Shin0Je Hyun Seo1Jae Ho Jung2Tae Woo Kim3Department of Ophthalmology, Pusan National University Hospital, Busan 49241, KoreaDepartment of Ophthalmology, Pusan National University Yangsan Hospital, Yangsan 50612, Korea; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, KoreaDepartment of Ophthalmology, Pusan National University Yangsan Hospital, Yangsan 50612, Korea; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, KoreaDepartment of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam 13620, KoreaAIM: To investigate the toxicity of the E-prostanoid 2 (EP2) receptor agonist, butaprost against human subconjunctival (Tenon’s capsule) fibroblasts, and to determine the underlying mechanism. METHODS: We isolated Tenon’s fibroblasts from the subconjunctival area of healthy subjects and evaluated the types of EP receptors expressed using quantitative real-time reverse transcription polymerase chain reaction (RT-PCR). The toxicity of butaprost against the fibroblasts was evaluated using methyl thiazolyl tetrazolium and lactic dehydrogenase assays. The inhibition of conjunctival fibroblast proliferation by butaprost was assessed by measuring α-actin levels. The underlying mechanism was assessed by measuring intracellular cyclic adenosine monophosphate (cAMP) levels. Intergroup differences were statistically analyzed using an independent t-test. Densitometry of the Western blot bands was performed using the Image J software. RESULTS: Quantitative real-time RT-PCR revealed that the fibroblast EP2 receptor levels were higher than those of the other EP receptors. Butaprost did not show toxicity against Tenon’s tissue, but inhibited conjunctival fibroblast proliferation by reducing collagen synthesis. EP2 receptor activation enhanced the cAMP cascade, which might be an important mechanism underlying this effect. CONCLUSION: Butaprost effectively reduces the subconjunctival scarring response. Given the significance of wound healing modulation in blebs, butaprost’s inhibitory effect on subconjunctival Tenon’s fibroblasts may be beneficial in managing postoperative scarring in glaucoma surgery.http://www.ijo.cn/en_publish/2017/7/20170702.pdf1033butaprostTenon’s capsuletrabeculectomyfibroblasts
spellingShingle Jong Hoon Shin
Je Hyun Seo
Jae Ho Jung
Tae Woo Kim
Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
International Journal of Ophthalmology
1033
butaprost
Tenon’s capsule
trabeculectomy
fibroblasts
title Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
title_full Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
title_fullStr Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
title_full_unstemmed Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
title_short Anti-scarring effects of butaprost on human subconjunctival Tenon’s fibroblasts
title_sort anti scarring effects of butaprost on human subconjunctival tenon s fibroblasts
topic 1033
butaprost
Tenon’s capsule
trabeculectomy
fibroblasts
url http://www.ijo.cn/en_publish/2017/7/20170702.pdf
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AT jaehojung antiscarringeffectsofbutaprostonhumansubconjunctivaltenonsfibroblasts
AT taewookim antiscarringeffectsofbutaprostonhumansubconjunctivaltenonsfibroblasts