Effects of 1,25-Vitamin D3 and 24,25-Vitamin D3 on Corneal Nerve Regeneration in Diabetic Mice.
Xiaowen LuZhong ChenJerry LuMitchell A WatskyPublished in: Biomolecules (2023)
Corneal nerve homeostasis is essential for the functional integrity of the ocular surface. Vitamin D deficiency (VDD) and vitamin D receptor knockout (VDR KO) have been found to reduce corneal nerve density in diabetic mice. This is the first study to comprehensively examine the influence of vitamin D on nerve regeneration following corneal epithelial injury in diabetic mice. Corneal nerve regeneration was significantly retarded by diabetes, VDR KO, and VDD, and it was accelerated following topical 1,25 Vit D and 24,25 Vit D administration. Furthermore, topical 1,25 Vit D and 24,25 Vit D increased nerve growth factor, glial cell line-derived neurotropic factor, and neurotropin-3 protein expression, and it increased secretion of GDNF protein from human corneal epithelial cells. CD45+ cells and macrophage numbers were significantly decreased, and vitamin D increased CD45+ cell and macrophage recruitment in these wounded diabetic mouse corneas. The accelerated nerve regeneration observed in these corneas following topical 1,25 Vit D and 24,25 Vit D administration may be related to the vitamin D-stimulated expression, secretion of neurotrophic factors, and recruitment of immune cells.
Keyphrases
- wound healing
- peripheral nerve
- stem cells
- growth factor
- optical coherence tomography
- type diabetes
- adipose tissue
- cardiovascular disease
- induced apoptosis
- single cell
- poor prognosis
- spinal cord
- cell death
- binding protein
- small molecule
- skeletal muscle
- metabolic syndrome
- oxidative stress
- mesenchymal stem cells
- cell cycle arrest
- bone marrow
- weight loss
- induced pluripotent stem cells