Topical administration of orbital fat-derived stem cells promotes corneal tissue regeneration

Ko Jo Lin, Mei Xue Loi, Gi Shih Lien, Chieh Feng Cheng, Hsiang Yin Pao, Yun Chuang Chang, Andrea Tung Qian Ji, Jennifer Hui Chun Ho

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Introduction. Topical administration of eye drops is the major route for drug delivery to the cornea. Orbital fat-derived stem cells (OFSCs) possess an in vitro corneal epithelial differentiation capacity. Both the safety and immunomodulatory ability of systemic OFSC transplantation were demonstrated in our previous work. In this study, we investigated the safety, therapeutic effect, and mechanism(s) of topical OFSC administration in an extensive alkali-induced corneal wound. Methods. Corneal injury was created by contact of a piece of 0.5 N NaOH-containing filter paper on the corneal surface of a male Balb/c mouse for 30 s. The area of the filter paper covered the central 70% or 100% of the corneal surface. OFSCs (2 × 10§ssup§5§ esup§) in 5 μl phosphate-buffered saline (PBS) were given by topical administration (T) twice a day or by two intralimbal (IL) injections in the right cornea, while 5 μl of PBS in the left cornea served as the control. Results: Topical OFSCs promoted corneal re-epithelialization of both the limbal-sparing and limbal-involved corneal wounds. In the first three days, topical OFSCs significantly reduced alkali-induced corneal edema and stromal infiltration according to a histopathological examination. Immunohistochemistry and immunofluorescence staining revealed that transplanted cells were easily detectable in the corneal epithelium, limbal epithelium and stroma, but only some of transplanted cells at the limbal epithelium had differentiated into cytokeratin 3-expressing cells. OFSCs did not alter neutrophil (Ly6G) levels in the cornea, but significantly reduced macrophage (CD68) infiltration and inducible nitrous oxide synthetase (iNOS) production during acute corneal injury as quantified by a Western blot analysis. Continuous topical administration of OFSCs for seven days improved corneal transparency, and this was accompanied by diffuse stromal engraftment of transplanted cells and differentiation into p63-expressing cells at the limbal area. The therapeutic effect of the topical administration of OFSCs was superior to that of the IL injection. OFSCs from the IL injection clustered in the limbal area and central corneal epithelium, which was associated with a persistent corneal haze. Conclusions: Topical OFSC administration is a simple, non-surgical route for stem cell delivery to promote corneal tissue regeneration through ameliorating acute inflammation and corneal epithelial differentiation. The limbal area serves as a niche for OFSCs differentiating into corneal epithelial cells in the first week, while the stroma is a potential site for anti-inflammation of OFSCs. Inhibition of corneal inflammation is related to corneal transparency.

Original languageEnglish
Article number72
JournalStem Cell Research and Therapy
Volume4
Issue number3
DOIs
Publication statusPublished - 2013

Fingerprint

Topical Administration
Tissue regeneration
Stem cells
Regeneration
Stem Cells
Fats
Cornea
Corneal Epithelium
Alkalies
Therapeutic Uses
Inflammation
Injections
Infiltration
Transparency
Keratin-3
Epithelium
Phosphates
Re-Epithelialization
Corneal Edema
Safety

Keywords

  • Corneal injury
  • Inflammation
  • Mesenchymal stem cells
  • Orbital fat-derived stem cells
  • Topical administration

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology (miscellaneous)
  • Molecular Medicine
  • Cell Biology
  • Medicine (miscellaneous)
  • Medicine(all)

Cite this

Topical administration of orbital fat-derived stem cells promotes corneal tissue regeneration. / Lin, Ko Jo; Loi, Mei Xue; Lien, Gi Shih; Cheng, Chieh Feng; Pao, Hsiang Yin; Chang, Yun Chuang; Ji, Andrea Tung Qian; Ho, Jennifer Hui Chun.

In: Stem Cell Research and Therapy, Vol. 4, No. 3, 72, 2013.

Research output: Contribution to journalArticle

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AU - Lien, Gi Shih

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AU - Chang, Yun Chuang

AU - Ji, Andrea Tung Qian

AU - Ho, Jennifer Hui Chun

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