The secretory immune system of the eye is designed to protect the ocular surface against microbial invasion. This system, by acting primarily through secretory IgA (sIgA) antibodies, prevents bacterial colonization, inhibits viral adhesion, abolishes parasitic infestation and blocks toxin-induced damage in mucosal epithelial cells. Thus, sIgA may play a unique and crucial role in preserving corneal integrity and defending against severe visual impairment and possible blindness. The long-range objective of this grant application is to advance our understanding of how the neural-endocrine system regulates the secretory immune system of the eye. Experimental procedures involve rat and mouse models, cell cultures, flow cytometry, autoradiography, sIgA transport studies, ligand binding determinations, immunoassays, chromatographic techniques, immunofluorescence and electron microscopy, image analysis, immune response studies with defined soluble, particulate and viral antigens, autoimmune disorders and endocrine organ ablation and reconstitution studies.
Specific aims are: (1) To identify the hormonal and neuroendocrine factors that regulate lacrimal gland immunity, structure and function. These studies include (a) determination of the endocrine interactions controlling the expression, secretion and function of secretory component (SC) in lacrimal gland acinar cells in vitro; SC is a critical determinant for surface defense and modulates the transport of IgA antibodies in tears. (b) evaluation of the neural-endocrine interrelationships governing the secretory immune system of the eye in vivo. These latter experiments will also identify the hormonal and neuroendocrine factors regulating lacrimal gland morphology and tear production. (2) To analyze the neural-endocrine impact on the ocular secretory immune response to defined soluble, particulate and viral antigens. (3) To develop an endocrine strategy to ameliorate or prevent specific autoimmune disorders of the lacrimal gland. Results from these studies should clarify the extensive and complex interactions between the neural, endocrine and immune systems in the lacrimal gland. In addition, findings may have health relatedness for the eye, because they (a) explore the neural and endocrine mechanisms regulating the ocular secretory immune response to antigenic challenge; (b) examine a possible hormonal strategy to effectively treat specific autoimmune disorders of the lacrimal gland and (c) evaluate hormonal and neural factors that modulate lacrimal gland structure and tear production.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005612-07
Application #
3260813
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1985-09-30
Project End
1993-09-29
Budget Start
1991-09-30
Budget End
1992-09-29
Support Year
7
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Schepens Eye Research Institute
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02114
Chen, Di; Sahin, Afsun; Kam, Wendy R et al. (2018) Influence of lipopolysaccharide on proinflammatory gene expression in human corneal, conjunctival and meibomian gland epithelial cells. Ocul Surf 16:382-389
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Liu, Yang; Knop, Erich; Knop, Nadja et al. (2016) Growth Hormone Influence on the Morphology and Size of the Mouse Meibomian Gland. J Ophthalmol 2016:5728071
Liu, Yang; Kam, Wendy R; Sullivan, David A (2016) Influence of Omega 3 and 6 Fatty Acids on Human Meibomian Gland Epithelial Cells. Cornea 35:1122-6
Kam, Wendy R; Liu, Yang; Ding, Juan et al. (2016) Do Cyclosporine A, an IL-1 Receptor Antagonist, Uridine Triphosphate, Rebamipide, and/or Bimatoprost Regulate Human Meibomian Gland Epithelial Cells? Invest Ophthalmol Vis Sci 57:4287-94
Ding, Juan; Wirostko, Barbara; Sullivan, David A (2015) Human growth hormone promotes corneal epithelial cell migration in vitro. Cornea 34:686-92
Liu, Yang; Kam, Wendy R; Ding, Juan et al. (2015) Can tetracycline antibiotics duplicate the ability of azithromycin to stimulate human meibomian gland epithelial cell differentiation? Cornea 34:342-6
Wirostko, Barbara; Rafii, MaryJane; Sullivan, David A et al. (2015) Novel Therapy to Treat Corneal Epithelial Defects: A Hypothesis with Growth Hormone. Ocul Surf 13:204-212.e1

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