Stromal Tissue Rigidity Promotes Mesenchymal Stem Cell-Mediated Corneal Wound Healing Through the Transforming Growth Factor β Signaling Pathway

Yun Hsiang Yang, Ting Lieh Hsieh, Andrea Tung Qian Ji, Wei Tse Hsu, Chia Yu Liu, Oscar Kuang Sheng Lee, Jennifer Hui Chun Ho

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

The healing of a corneal epithelial defect is essential for preventing infectious corneal ulcers and subsequent blindness. We previously demonstrated that mesenchymal stem cells (MSCs) in the corneal stroma, through a paracrine mechanism, yield a more favorable therapeutic benefit for corneal wound re-epithelialization than do MSCs in the corneal epithelium. In this study, MSCs were grown on a matrix with the rigidity of the physiological human vitreous (1 kPa), corneal epithelium (8 kPa), or corneal stroma (25 kPa) for investigating the role of corneal tissue rigidity in MSC functions regarding re-epithelialization promotion. MSC growth on a 25-kPa dish significantly promoted the wound healing of human corneal epithelial (HCE-T) cells. Among growth factors contributing to corneal epithelial wound healing, corneal stromal rigidity selectively enhanced transforming growth factor-beta (TGF-β) secretion from MSCs. Inhibitors of TGF-β pan receptor, TGF-β receptor 1, and Smad2 dose dependently abrogated MSC-mediated HCE-T wound healing. Furthermore, MSCs growth on a matrix with corneal stromal rigidity enhanced the ability of themselves to promote corneal re-epithelialization by activating matrix metalloproteinase (MMP) expression and integrin β1 production in HCE-T cells through TGF-β signaling pathway activation. Smad2 activation resulted in the upregulation of MMP-2 and −13 expression in HCE-T cells, whereas integrin β1 production favored a Smad2-independent TGF-β pathway. Altogether, we conclude that corneal stromal rigidity is a critical factor for MSC-induced promotion of corneal re-epithelialization. The activation of the TGF-β signaling pathway, which maintains the balance between integrin and MMP expression, in HCE-T cells is the major pathway responsible for MSC-mediated wound healing. Stem Cells 2016;34:2525–2535.

Original languageEnglish
Pages (from-to)2525-2535
Number of pages11
JournalStem Cells
Volume34
Issue number10
DOIs
Publication statusPublished - Oct 1 2016

Fingerprint

Transforming Growth Factors
Mesenchymal Stromal Cells
Wound Healing
Re-Epithelialization
Transforming Growth Factor beta
Epithelial Cells
Integrins
Corneal Stroma
Corneal Epithelium
Matrix Metalloproteinases
Matrix Metalloproteinase 13
Corneal Ulcer
Transforming Growth Factor beta Receptors
Matrix Metalloproteinase 2
Blindness
Growth
Intercellular Signaling Peptides and Proteins
Up-Regulation
Stem Cells

Keywords

  • Corneal stroma
  • Matrix rigidity
  • Mesenchymal stem cells
  • Transforming growth factor-β
  • Wound healing

ASJC Scopus subject areas

  • Molecular Medicine
  • Developmental Biology
  • Cell Biology

Cite this

Stromal Tissue Rigidity Promotes Mesenchymal Stem Cell-Mediated Corneal Wound Healing Through the Transforming Growth Factor β Signaling Pathway. / Yang, Yun Hsiang; Hsieh, Ting Lieh; Ji, Andrea Tung Qian; Hsu, Wei Tse; Liu, Chia Yu; Lee, Oscar Kuang Sheng; Ho, Jennifer Hui Chun.

In: Stem Cells, Vol. 34, No. 10, 01.10.2016, p. 2525-2535.

Research output: Contribution to journalArticle

Yang, Yun Hsiang ; Hsieh, Ting Lieh ; Ji, Andrea Tung Qian ; Hsu, Wei Tse ; Liu, Chia Yu ; Lee, Oscar Kuang Sheng ; Ho, Jennifer Hui Chun. / Stromal Tissue Rigidity Promotes Mesenchymal Stem Cell-Mediated Corneal Wound Healing Through the Transforming Growth Factor β Signaling Pathway. In: Stem Cells. 2016 ; Vol. 34, No. 10. pp. 2525-2535.
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