4.5 Article

Transforming growth factor beta-3 localization in the corneal response to epithelial-stromal injury and effects on corneal fibroblast transition to myofibroblasts

Journal

EXPERIMENTAL EYE RESEARCH
Volume 235, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exer.2023.109631

Keywords

Corneal scarring fibrosis; TGF beta-3; Basement membrane regeneration; Histopathology; Wound healing; Corneal fibrosis; Myofibroblasts; Corneal fibroblasts; Keratocytes; Alpha-smooth muscle actin; Collagen type IV; Jess automated western blotting

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The localization of TGF beta-3 in unwounded and injured rabbit corneas was evaluated, as well as its effects on corneal fibroblasts in vitro. TGF beta-3 was found to have a different distribution pattern compared to TGF beta-1 and TGF beta-2, but had similar effects to TGF beta-1 on corneal fibroblast development.
The purpose of this study was to evaluate the localization of TGF beta-3 in situ in unwounded rabbit corneas and corneas that had epithelial-stromal injuries produced by photorefractive keratectomy (PRK) in rabbits and to evaluate the in vitro effects of TGF beta-3 compared to TGF beta-1 on alpha-smooth muscle actin (alpha-SMA) protein expression and myofibroblast development in corneal fibroblasts. Forty-eight New Zealand white rabbits underwent either -3 diopter (D) or -9D PRK and were studied from one to eight weeks (four corneas in each group at each time point) after surgery with immunohistochemistry for TGF beta-3, laminin alpha-5, and alpha-smooth muscle actin (alpha-SMA). Rabbit corneal fibroblasts were treated with activated TGF beta-1 and/or TGF beta-3 at different concentrations and duration of exposure and studied with immunocytochemistry for myofibroblast development and the expression of alpha-SMA using Jess automated Western blotting. TGF beta-3 was detected at high levels in the stroma of unwounded corneas and corneas at one to eight weeks after -3D or -9D PRK, as well as in the epithelium and epithelial basement membrane (EBM). No difference was noted between corneas that healed with and without myofibroblast-mediated fibrosis, although TGF beta-3 was commonly associated with myofibroblasts. TGF beta-3 effects on corneal fibroblasts in vitro were similar to TGF beta-1 in stimulating transition to alpha-SMA-positive myofibroblasts and promoting alpha-SMA protein expression. The corneal stromal localization pattern of TGF beta-3 protein in unwounded corneas and corneas after epithelial-stromal injury was found to be higher and different from TGF beta-1 and TGF beta-2 reported in previous studies. TGF beta-3 had similar effects to TGF beta-1 in driving myofibroblast development and alpha-SMA expression in corneal fibroblasts cultured in medium with 1% fetal bovine serum.

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