Whole transcriptome analysis on blue light-induced eye damage.

AIM: To analyze abnormal gene expressions of mice eyes exposed to blue light using RNA-seq and analyze the related signaling pathways. METHODS: Kunming mice were divided into an experimental group that was exposed to blue light and a control group that was exposed to natural light. After 14d, the mice were euthanized and their eyeballs were collected. Whole transcriptome analysis was attempted to analyze the gene expression of the eyeballs using RNA-seq to reconstruct genetic networks. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were used to reveal the related signaling pathways. RESULTS: The 737 differentially expressed genes were identified, including 430 up and 307 down regulated genes, by calculating the gene FPKM in each sample and conducting differential gene analysis. GO and KEGG pathway enrichment analysis showed that blue light damage may associated with the visual perception, sensory perception of light stimulus, phototransduction, and JAK-STAT signaling pathways. Differential lncRNA, circRNA and miRNA analysis showed that blue light exposure affected pathways for retinal cone cell development and phototransduction, among others. CONCLUSION: Exposure to blue light can cause a certain degree of abnormal gene expression and modulate signaling pathways in the eye.

Mechanisms of blue light-induced eye hazard and protective measures: a review.

The risk of blue light exposure to human health has attracted increased research attention. Blue light, with relatively high energy, can cause irreversible photochemical damage to eye tissue. Excessive exposure of the eye to blue light tends to cause a series of alterations, such as oxidative stress, mitochondrial apoptosis, inflammatory apoptosis, mitochondrial apoptosis and DNA damage, resulting in the development of dry eye disease, glaucoma, and keratitis. Accordingly, physical protection, chemical and pharmaceutical protective measures, gene therapy, and other methods are widely used in the clinical treatment of blue light hazard. We reviewed the studies on possible blue light-induced signaling pathways and mechanisms in the eye and summarized the therapeutic approaches to addressing blue light hazard.

Co-culture and Mechanical Stimulation on Mesenchymal Stem Cells and Chondrocytes for Cartilage Tissue Engineering.

Defects in articular cartilage injury and chronic osteoarthritis are very widespread and common, and the ability of injured cartilage to repair itself is limited. Stem cell-based cartilage tissue engineering provides a promising therapeutic option for articular cartilage damage. However, the application of the technique is limited by the number, source, proliferation, and differentiation of stem cells. The co-culture of mesenchymal stem cells and chondrocytes is available for cartilage tissue engineering, and mechanical stimulation is an important factor that should not be ignored. A combination of these two approaches, i.e., co-culture of mesenchymal stem cells and chondrocytes under mechanical stimulation, can provide sufficient quantity and quality of cells for cartilage tissue engineering, and when combined with scaffold materials and cytokines, this approach ultimately achieves the purpose of cartilage repair and reconstruction. In this review, we focus on the effects of co-culture and mechanical stimulation on mesenchymal stem cells and chondrocytes for articular cartilage tissue engineering. An in-depth understanding of the impact of co-culture and mechanical stimulation of mesenchymal stem cells and chondrocytes can facilitate the development of additional strategies for articular cartilage tissue engineering.

The collagen metabolism affects the scleral mechanical properties in the different processes of scleral remodeling.

PURPOSE: To increase the understanding of collagen metabolism as related to scleral remodeling in the process of emmetropization and myopization. METHODS: An eyelid suture that lasted 60 days was performed on one-month-old rabbits to establish an experimental monocular visual deprivation myopia model and the axial length was recorded. HE staining and transmission electron microscope were used to observe the scleral structure. The Instron 5544 was used to measure scleral elastic modulus after measuring the scleral thickness. The content of scleral tissue collagen was determined by detecting the hydroxyproline quantity and the collagen I α1, MMP-2, and TIMP-2 mRNA expression were detected by RT-PCR Kit. RESULTS: During regular emmetropization, the scleral collagen synthesis was higher than decomposition and the diameter of collagen fibrils increased, and then the sclera thickened and mechanical properties improved. During myopization, the scleral collagen decomposition was higher than synthesis and the diameter of collagen fibrils was smaller, and then the sclera thinner and mechanical properties lower, which resulted in a difference in scleral tissue strain. CONCLUSION: The results suggested that there were different scleral remodeling process between the emmetropization and myopization, and the collagen metabolism affected the scleral mechanical properties and scleral remodeling and then affected the scleral growth, axial elongation, and even myopization.