Corneal Wound Healing Effects of Mesenchymal Stem Cell Secretome Delivered Within a Viscoelastic Gel Carrier

被引:87
作者
Fernandes-Cunha, Gabriella Maria [1 ]
Na, Kyung-Sun [1 ,2 ]
Putra, Ilham [3 ]
Lee, Hyun Jong [1 ]
Hull, Sarah [4 ]
Cheng, Yu-Chia [1 ]
Blanco, Ignacio Jesus [1 ]
Eslani, Medi [3 ]
Djalilian, Ali R. [3 ]
Myung, David [1 ,4 ,5 ]
机构
[1] Stanford Univ, Sch Med, Dept Ophthalmol, Byers Eye Inst, Palo Alto, CA 94304 USA
[2] Catholic Univ Korea, Yeouido St Marys Hosp, Coll Med, Dept Ophthalmol & Visual Sci, Seoul, South Korea
[3] Univ Illinois, Dept Ophthalmol & Visual Sci, Chicago, IL USA
[4] Stanford Univ, Dept Chem Engn, Palo Alto, CA 94304 USA
[5] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA
基金
美国国家卫生研究院;
关键词
Cellular proliferation; Chondroitin sulfate; Cornea; Mesenchymal stem cells; ADHESION MOLECULE CD44; HYALURONIC-ACID; OCULAR SURFACE; STROMAL CELLS; CHONDROITIN SULFATE; STEM/STROMAL CELLS; EXPRESSION; TRANSPARENCY; INFLAMMATION; MACROPHAGE;
D O I
10.1002/sctm.18-0178
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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
引用
收藏
页码:478 / 489
页数:12
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