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Cited 69 time in webofscience Cited 72 time in scopus
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Corneal Wound Healing Effects of Mesenchymal Stem Cell Secretome Delivered Within a Viscoelastic Gel Carrier

Authors
Fernandes-Cunha, Gabriella MariaNa, Kyung-SunPutra, IlhamLee, Hyun JongHull, SarahCheng, Yu-ChiaBlanco, Ignacio JesusEslani, MediDjalilian, Ali R.Myung, David
Issue Date
May-2019
Publisher
WILEY
Keywords
Cellular proliferation; Chondroitin sulfate; Cornea; Mesenchymal stem cells
Citation
STEM CELLS TRANSLATIONAL MEDICINE, v.8, no.5, pp.478 - 489
Journal Title
STEM CELLS TRANSLATIONAL MEDICINE
Volume
8
Number
5
Start Page
478
End Page
489
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/53886
DOI
10.1002/sctm.18-0178
ISSN
2157-6564
Abstract
Severe corneal injuries often result in permanent vision loss and remain a clinical challenge. Human bone marrow-derived mesenchymal stem cells (MSCs) and their secreted factors (secretome) have been studied for their antiscarring, anti-inflammatory, and antiangiogeneic properties. We aimed to deliver lyophilized MSC secretome (MSC-S) within a viscoelastic gel composed of hyaluronic acid (HA) and chondroitin sulfate (CS) as a way to enhance corneal re-epithelialization and reduce complications after mechanical and chemical injuries of the cornea. We hypothesized that delivering MSC-S within HA/CS would have improved wound healing effects compared the with either MSC-S or HA/CS alone. The results showed that a once-daily application of MSC-S in HA/CS enhances epithelial cell proliferation and wound healing after injury to the cornea. It also reduced scar formation, neovascularization, and hemorrhage after alkaline corneal burns. We found that combining MSC-S and HA/CS increased the expression of CD44 receptors colocalized with HA, suggesting that the observed therapeutic effects between the MSC-S and HA/CS are in part mediated by CD44 receptor upregulation and activation by HA. The results from this study demonstrate a reproducible and efficient approach for delivering the MSC-S to the ocular surface for treatment of severe corneal injuries. Stem Cells Translational Medicine 2019;8:478-489
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