The focus of the proposed experiments centers on the use of monoclonal antibodies which react with unique carbohydrate moieties and provide a high-resolution analysis system of extracellular matrix moieties in human skin. The central hypothesis is that proteoglycans provide unique water- structuring and visco-elastic properties of the extracellular matrix and that subtle changes in these molecules can have profound effects on the properties of human skin, especially those associated with aging. The availability of unique monoclonal antibodies to specific carbohydrate epitopes on proteoglycans allows the identification of a distinct fingerprint for various layers of skin as a function of human age. Preliminary results establish certain monoclonal antibodies to be unique to specific skin layers and to subtly change as a function of age. We propose to build on these preliminary observations to establish a normative data base for skin samples as a function of age. In addition, by using these monoclonal antibodies, we propose to isolate and characterize the epitope- containing macromolecules from human skin specimens, in this case, proteoglycans. Proteoglycans will be isolated and epitope-reactive molecules will be obtained, and these macromolecules characterized. This project draws together technologies ranging from immunocytochemistry to detailed proteoglycan biochemistry and will provide basic information about changes in skin extracellular matrices as a function of human age.
Specific Aims : 1. Identify monoclonal antibodies which react with carbohydrate moieties, which change in discrete layers of human skin as a function of age (focus on chondroitin and keratan sulfate epitopes). 2. Use these antibodies which are specific to discrete layers of skin to isolate and/or characterize the macromolecules which contain these epitopes. 3. Establish new, innovative techniques to characterize the detailed microchemistry of proteoglycans relevant to skin aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG011331-04
Application #
2052503
Study Section
Biological and Clinical Aging Review Committee (BCA)
Project Start
1992-06-01
Project End
1997-05-31
Budget Start
1995-06-10
Budget End
1996-05-31
Support Year
4
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Carrino, D A; Sorrell, J M; Caplan, A I (2000) Age-related changes in the proteoglycans of human skin. Arch Biochem Biophys 373:91-101
Sorrell, J M; Carrino, D A; Baber, M A et al. (1999) Versican in human fetal skin development. Anat Embryol (Berl) 199:45-56
Fleming Jr, J E; Haynesworth, S E; Cassiede, P et al. (1998) Monoclonal antibody against adult marrow-derived mesenchymal stem cells recognizes developing vasculature in embryonic human skin. Dev Dyn 212:119-32
Bruder, S P; Jaiswal, N; Haynesworth, S E (1997) Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subcultivation and following cryopreservation. J Cell Biochem 64:278-94
Lazarus, H M; Haynesworth, S E; Gerson, S L et al. (1997) Human bone marrow-derived mesenchymal (stromal) progenitor cells (MPCs) cannot be recovered from peripheral blood progenitor cell collections. J Hematother 6:447-55
Lazarus, H M; Haynesworth, S E; Gerson, S L et al. (1995) Ex vivo expansion and subsequent infusion of human bone marrow-derived stromal progenitor cells (mesenchymal progenitor cells): implications for therapeutic use. Bone Marrow Transplant 16:557-64