This is a basic research study to analyze the earliest corneal changes induced by an obesogenic diet. We are attempting to understand the pathogenesis of an important corneal condition before it reaches the far advanced stages of the metabolic syndrome. There is a heightened concern given the epidemic of obesity in children. We will use diet-induced obesity and full thickness corneal epithelial abrasion in C57BL/6J mice for studies in vivo. The pathogenic effect of a diet is not simply determined by the nutritive content or quantity of the food source, but includes the timing of food intake as shown by recent investigations. Our studies will incorporate this expanded understanding of dietary influence to provide a database necessary for specific investigations into mechanisms by which an obesogenic diet compromises corneal function.Our most recent data in vivo reveal that 10 week old mice fed a high fat diet for 5 weeks show systemic inflammation with increased proinflammatory cytokines in blood as well as leukocyte activation and infiltration into adipose tissues. These mice exhibit significant reductions in nerve density in the epithelial branches of the corneal nerves, and when challenged, they exhibit abnormal wound healing after corneal abrasion with reduced regeneration of damaged corneal nerves. This extends our analysis of the inflammatory cascade activated by epithelial injury, defines corneal dysfunctions induced by an obesogenic diet, and seeks to define new targets for potential therapeutic intervention. Our most recent data in vitro reveal expression of receptors on human corneal epithelium for cytokines that in the mouse model promote epithelial healing.
Specific Aim 1. Determine changes in the cornea induced by feeding mice an obesogenic diet, the reversibility of these changes, and the contributions of diet-induced systemic inflammation to these changes. Hypothesis 1: Dysregulated inflammation induced by an obesogenic diet contributes to corneal pathology.
Specific Aim 2. Analyze the cascade of events required for normal corneal wound healing in mice fed an obesogenic diet that induces systemic inflammation, and determine if therapeutic intervention directed at restoring specific aspects of the healing cascade will promote efficient corneal wound healing. In addition, analyze the effects of specific interventions derived from the mouse studies on healing functions of human corneal epithelial cells in vitro. Hypothesis 2: The cascade of events required for normal corneal wound healing is disrupted by diet- induced systemic inflammation, thereby leading to poor corneal wounding healing.

Public Health Relevance

This application will study the importance of inflammation to healing of wounds in the surface of the eye, and analyzes the effects of diet-induced obesity on corneal integrity and wound healing. Of particular interest are the cascades of adhesion molecules, cytokines, chemokines and emigrating cells that are critical for maintenance and restoration of corneal integrity after wounding and from which therapeutic concepts can be derived for treating the corneal dysfunction resulting from diet-induced obesity and the accompanying metabolic syndrome.

National Institute of Health (NIH)
National Eye Institute (NEI)
Research Project (R01)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mckie, George Ann
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Baylor College of Medicine
Schools of Medicine
United States
Zip Code
Rodarte, Elsa M; Ramos, Marco A; Davalos, Alfredo J et al. (2018) Munc13 proteins control regulated exocytosis in mast cells. J Biol Chem 293:345-358
Liu, Jun; Wu, Mingjuan; He, Jingxin et al. (2018) Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution. Am J Pathol 188:2786-2799
Xue, Yunxia; He, Jingxin; Xiao, Chengju et al. (2018) The mouse autonomic nervous system modulates inflammation and epithelial renewal after corneal abrasion through the activation of distinct local macrophages. Mucosal Immunol 11:1496-1511
Zhang, Wanyu; Magadi, Sri; Li, Zhijie et al. (2017) IL-20 promotes epithelial healing of the injured mouse cornea. Exp Eye Res 154:22-29
Dai, Yu-Bing; Miao, Yi-Fei; Wu, Wan-Fu et al. (2016) Ablation of Liver X receptors ? and ? leads to spontaneous peripheral squamous cell lung cancer in mice. Proc Natl Acad Sci U S A 113:7614-9
Lam, Fong W; Phillips, Jenny; Landry, Paul et al. (2015) Platelet recruitment promotes keratocyte repopulation following corneal epithelial abrasion in the mouse. PLoS One 10:e0118950
Knight, John M; Lee, Seung-Hyo; Roberts, Luz et al. (2014) CD11a polymorphisms regulate TH2 cell homing and TH2-related disease. J Allergy Clin Immunol 133:189-97.e1-8
Hanlon, Samuel D; Smith, C Wayne; Sauter, Marika N et al. (2014) Integrin-dependent neutrophil migration in the injured mouse cornea. Exp Eye Res 120:61-70
Gao, Yuan; Li, Zhijie; Hassan, Nida et al. (2013) NK cells are necessary for recovery of corneal CD11c+ dendritic cells after epithelial abrasion injury. J Leukoc Biol 94:343-51
Liu, Qiong; Smith, C Wayne; Zhang, Wanyu et al. (2012) NK cells modulate the inflammatory response to corneal epithelial abrasion and thereby support wound healing. Am J Pathol 181:452-62

Showing the most recent 10 out of 17 publications