Elucidation of the regulatory steps in corneal collagen fibrillogenesis and matrix assembly will provide the foundation for understanding normal corneal development, growth, maturation and repair. In addition, definition of the regulatory steps is critical for understanding the development and maintenance of transparency, regulation of hydration as well as corneal pathobiologies such as edema, wound healing and some dystrophies. Our overall hypothesis is that corneal matrix assembly is a multi-step process with specific regulatory interactions at each step. This application addresses: (1) fibril nucleation at the keratocyte surface and its regulation by collagen I/V interactions; (2) fibril growth steps and their regulation by small leucine-rich proteoglycans; and (3) matrix integration/organization during development, growth and maturation involving fibril-associated collagens.
The specific aims of this application are to:
(aim 1) determine the role(s) of type V collagen in regulation of fibril nucleation, the specific domains responsible for regulation and the sites of action;
(aim 2) determine the regulatory roles of decorin/biglycan and lumican/keratocan in regulation of fibril growth and packing necessary for corneal transparency;
and (aim 3) determine the role(s) of the fibril-associated collagens, types XII and XIV in mediating the integration/maturation of the developing stroma. The hypotheses to be tested are:
(aim 1) type V collagen is the key regulator involved in the nucleation of corneal fibril assembly;
(aim 2) small leucine-rich proteoglycans regulate fibril growth steps and organization involving a coordinate regulation by 2 separate classes: Class I, decorin and biglycan and class II, lumican and keratocan;
and (aim 3) fibril packing, stromal compaction and integration of the developing matrix are mediated by fibril-associated collagen types XII and XIV through their association with fibrils and ability to interact with other matrix molecules. Mouse models deficient in specific matrix molecules will be utilized and stromal development will be analyzed using biochemical, immunochemical, molecular and ultrastructural approaches. Binding assays and in vitro fibrillogenesis studies will be done in parallel to define specific functional interactions. Definition of the regulatory steps in corneal-specific matrix assembly provides the foundation to further our understanding of corneal repair/regeneration, pathobiologies and the modulation of these processes. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY005129-25
Application #
7145110
Study Section
Special Emphasis Panel (ZRG1-BDCN-H (92))
Program Officer
Shen, Grace L
Project Start
1992-09-01
Project End
2011-06-30
Budget Start
2006-08-01
Budget End
2007-06-30
Support Year
25
Fiscal Year
2006
Total Cost
$491,381
Indirect Cost
Name
Thomas Jefferson University
Department
Pathology
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Chen, Shoujun; Mienaltowski, Michael J; Birk, David E (2015) Regulation of corneal stroma extracellular matrix assembly. Exp Eye Res 133:69-80
Espana, Edgar M; Sun, Mei; Birk, David E (2015) Existence of Corneal Endothelial Slow-Cycling Cells. Invest Ophthalmol Vis Sci 56:3827-37
Basu, Sayan; Hertsenberg, Andrew J; Funderburgh, Martha L et al. (2014) Human limbal biopsy-derived stromal stem cells prevent corneal scarring. Sci Transl Med 6:266ra172
Chen, Shoujun; Young, Marian F; Chakravarti, Shukti et al. (2014) Interclass small leucine-rich repeat proteoglycan interactions regulate collagen fibrillogenesis and corneal stromal assembly. Matrix Biol 35:103-11
Chen, Shoujun; Sun, Mei; Iozzo, Renato V et al. (2013) Intracellularly-retained decorin lacking the C-terminal ear repeat causes ER stress: a cell-based etiological mechanism for congenital stromal corneal dystrophy. Am J Pathol 183:247-56
Chen, Shoujun; Birk, David E (2013) The regulatory roles of small leucine-rich proteoglycans in extracellular matrix assembly. FEBS J 280:2120-37
Hemmavanh, Chinda; Koch, Manuel; Birk, David E et al. (2013) Abnormal corneal endothelial maturation in collagen XII and XIV null mice. Invest Ophthalmol Vis Sci 54:3297-308
Chervoneva, Inna; Zhan, Tingting; Iglewicz, Boris et al. (2012) Two-stage hierarchical modeling for analysis of subpopulations in conditional distributions. J Appl Stat 39:445-460
Smith, Simone M; Birk, David E (2012) Focus on molecules: collagens V and XI. Exp Eye Res 98:105-6
Izu, Yayoi; Sun, Mei; Zwolanek, Daniela et al. (2011) Type XII collagen regulates osteoblast polarity and communication during bone formation. J Cell Biol 193:1115-30

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