The extracellular matrix of connective tissue consists primarily of collagens, glycoproteins and proteoglycans. The collagenous components provide the tensile strength and a structural framework for the glycoproteins and proteoglycans. The non-collagenous components are often tissue specific and provide the functional properties characteristic of that particular tissue. The corneal stroma contains extracellular matrix components that interact, in an unknown way, to produce the optical transparency unique to this connective tissue. The corneal keratan sulfate proteoglycan is crucial to transparency. It appears during the acquisition of transparency and its loss or alteration produces opacities. We have tentatively identified four stromal glycoproteins and expect them to be likewise involved in matrix transparency. The long-term goals of this project are to define the interaction of the stromal matrix components that produce corneal transparency and to identify the genetic elements that regulate their production.
The first aim i s to use chromatographic procedures to isolate the non-collagenous components of the stromal matrix and then use immunological and biochemical procedures to partially characterize them. These studies will establish the general structure of these components and their tissue distribution, and will provide a means to initiate cDNA cloning studies.
The second aim i s to use recombinant DNA technology to isolate cDNA clones to these matrix components. The amino acid sequence deduced from the clones will determine its definitive structure and establish its relationship to other matrix components.
The third aim i s to use affinity chromatography to identify the interacting matrix components and their structural domains that account for the interaction. This information will define the molecular arrangement of the components within the matrix.
The fourth aim i s to initiate studies using recombinant DNA technology to establish the gene structure of these matrix components and identify the genetic elements that regulate their production. These regulatory elements will play an important role in the process involved in corneal development, wound healing and disease.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY008104-01
Application #
3265259
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1989-04-01
Project End
1994-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Eye and Ear Institute of Pittsburgh
Department
Type
DUNS #
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Hassell, John R; Birk, David E (2010) The molecular basis of corneal transparency. Exp Eye Res 91:326-35
Etheredge, LaTia; Kane, Bradley P; Valkov, Nikola et al. (2010) Enhanced cell accumulation and collagen processing by keratocytes cultured under agarose and in media containing IGF-I, TGF-? or PDGF. Matrix Biol 29:519-24
Kane, Bradley P; Jester, James V; Huang, Jiying et al. (2009) IGF-II and collagen expression by keratocytes during postnatal development. Exp Eye Res 89:218-23
Etheredge, Latia; Kane, Bradley P; Hassell, John R (2009) The effect of growth factor signaling on keratocytes in vitro and its relationship to the phases of stromal wound repair. Invest Ophthalmol Vis Sci 50:3128-36
Musselmann, Kurt; Kane, Bradley P; Alexandrou, Bridgette et al. (2008) IGF-II is present in bovine corneal stroma and activates keratocytes to proliferate in vitro. Exp Eye Res 86:506-11
Hassell, John R; Kane, Bradley P; Etheredge, La Tia et al. (2008) Increased stromal extracellular matrix synthesis and assembly by insulin activated bovine keratocytes cultured under agarose. Exp Eye Res 87:604-11
Musselmann, Kurt; Kane, Bradley; Alexandrou, Bridgette et al. (2006) Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Invest Ophthalmol Vis Sci 47:5260-6
Musselmann, Kurt; Alexandrou, Bridgette; Kane, Bradley et al. (2005) Maintenance of the keratocyte phenotype during cell proliferation stimulated by insulin. J Biol Chem 280:32634-9
Liu, Chia-Yang; Birk, David E; Hassell, John R et al. (2003) Keratocan-deficient mice display alterations in corneal structure. J Biol Chem 278:21672-7
Musselmann, Kurt; Kane, Bradley P; Hassell, John R (2003) Isolation of a putative keratocyte activating factor from the corneal stroma. Exp Eye Res 77:273-9

Showing the most recent 10 out of 31 publications