Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Mesenchymal stem cell treatment in corneal nerve damage-an animal model
Author Affiliations & Notes
  • Chia-Ying Tsai
    Ophthalmology, Fu Jen Catholic University Hospital, New Taipei City, Taiwan
    Medicine, Fu Jen Catholic University, Taipei, Taiwan
  • Shan-Chi Yang
    Ophthalmology, National Taiwan University Hospital, Taipei, Taiwan
  • Wei-Li Chen
    Ophthalmology, National Taiwan University Hospital, Taipei, Taiwan
  • Footnotes
    Commercial Relationships   Chia-Ying Tsai None; Shan-Chi Yang None; Wei-Li Chen None
  • Footnotes
    Support  PL-2021080XX
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 4496. doi:
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    • Get Citation

      Chia-Ying Tsai, Shan-Chi Yang, Wei-Li Chen; Mesenchymal stem cell treatment in corneal nerve damage-an animal model. Invest. Ophthalmol. Vis. Sci. 2024;65(7):4496.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To investigate the neural regeneration potential of adipocyte-derived mesenchymal stem cells (AD-MSCs) in a rabbit corneal nerve damage model.

Methods : The characteristics of the AD-MSCs were verified by MSC marker expression through immunocytochemical analysis (ICC) and flow cytometry. The chondrogenic and neurogenic differentiation procedures were used to confirm the multipotency of the AD-MSCs. Intrastromal corneal injection of AD-MSCs was performed after corneal epithelial debridement in the rabbit corneal nerve damage model. The location of the injected MSCs was verified by in vivo confocal microscopy and H & E staining. The process of corneal epithelial wound healing was detected by fluorescein staining. The corneal nerve regeneration was evaluated by in vivo confocal microscope (IVCM) and immunohistochemistry staining (IHC) in the treated region.

Results : The AD-MSCs showed expression of MSC markers (α-SMA+, vimentin+, CD44+, and CD11b-) in ICC and flow cytometry analysis. The multipotency of AD-MSCs was confirmed by chondrocytes and neural stem cells differentiation. The injected AD-MSCs were detectable on post-injection day 1 in the central cornea through in vivo confocal images and the H & E staining analysis. Corneal nerve regeneration in the AD-MSCs treated group was observed on day 14 while on day 21 in the control group through IVCM analysis.(Fig.1) The results of IHC (SMI-312, βIII-tubulin) confirmed the regenerated corneal nerve at the subbasal cornea and epithelium. (Fig.2)

Conclusions : Our results showed AD-MSCs injection benefits corneal nerve regeneration in the rabbit corneal nerve damage model and could be a potential treatment for ocular surface diseases related to corneal nerve injury.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Confocal microscope images of the epithelium, basal epithelium and stroma of mesenchymal stem cells and control groups at Day 7,14,21, and 28 after single intrastromal injection of mesenchymal stem cells or PBS on Day 0 at central cornea. The nerve budding (white arrow) firstly appeared on D14 in the MSC group, and on D21 in the control group.

Confocal microscope images of the epithelium, basal epithelium and stroma of mesenchymal stem cells and control groups at Day 7,14,21, and 28 after single intrastromal injection of mesenchymal stem cells or PBS on Day 0 at central cornea. The nerve budding (white arrow) firstly appeared on D14 in the MSC group, and on D21 in the control group.

 

Immunofluorescence analysis of MSC treated cornea after intrastromal injection. Staining of neurofilament (SMI312, red) and (βIII-tubulin, green), showed regenerated nerves (arrows) on Day28 in MSC treatment and control group.

Immunofluorescence analysis of MSC treated cornea after intrastromal injection. Staining of neurofilament (SMI312, red) and (βIII-tubulin, green), showed regenerated nerves (arrows) on Day28 in MSC treatment and control group.

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