Adult cartilage is known to have little ability for repair, due primarily to a lack of active chondrogenic progenitor cells. As a result, there are limited alternatives for the treatment of osteoarthritis, most of which are targeted at the symptoms of the disease and not at a cure. Mesenchymal stem cells and cultured pre-chondrocytes isolated from a patient have the potential to be applied to the repair of cartilage if they can be delivered to the sites where needed. It is hypothesized that pre-chondrogenic cells coated with antibodies specific for cartilage matrix could be used as a method to regenerate or repair damaged cartilage. The focus of this proposal is to develop a targeting strategy for pre-chondrocytes so that these cells can be used to repair an articular cartilage defect in vivo. To achieve this goal, MSCs and pre-chondrocytes will be coated with palmitated protein G (or A [PPG/A]) and then incubated with antibodies to type II collagen or to epitopes on aggrecan molecules. These antibodies will bind to the PPNG and their antigen binding sites will be oriented outward. These cells coated with different antibodies, alone or in combination, will be tested for their ability to bind cartilage matrix on frozen sections and on explants of rabbit articular cartilage. Pre-chondrocytes will be stained with a vital fluorescent dye, coated with targeting antibodies, added to sections or explants, washed and then observed for the presence of fluorescent cells. In vitro studies will be carried out on coated cells to confirm that the coating procedure does not significantly impede the cells ability to proliferate or to differentiate into chondrocytes. Once targeting and synthesis of cartilage matrix have been demonstrated, these targeted pre-chondrocytes will be tested for their ability to repair a standard articular cartilage defect in rabbits, in vivo. The degree of repair will be assessed by histologic examination and morphometric examination of the articular cartilage defects. Experimental groups to be tested are: (1) control untreated defects, (2) targeted cell-injected, (3) PPA/g coated, and (4) untreated cell-injected. These experiments will determine if this novel cell targeting methodology effectively directs pre-chondrocytes to cartilage matrix and whether these targeted cells can contribute to the repair of damaged cartilage. The long-term goal of these studies is to develop a treatment for osteoarthritis. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR049785-02
Application #
6879161
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Program Officer
Tyree, Bernadette
Project Start
2004-06-01
Project End
2009-05-31
Budget Start
2005-06-01
Budget End
2006-05-31
Support Year
2
Fiscal Year
2005
Total Cost
$302,940
Indirect Cost
Name
Case Western Reserve University
Department
Orthopedics
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Lin, Paul; Correa, Diego; Kean, Thomas J et al. (2014) Serial transplantation and long-term engraftment of intra-arterially delivered clonally derived mesenchymal stem cells to injured bone marrow. Mol Ther 22:160-8
Kean, Thomas J; Duesler, Lori; Young, Randell G et al. (2012) Development of a peptide-targeted, myocardial ischemia-homing, mesenchymal stem cell. J Drug Target 20:23-32
Maeda, Toru; Sakabe, Tomoya; Sunaga, Ataru et al. (2011) Conversion of mechanical force into TGF-?-mediated biochemical signals. Curr Biol 21:933-41
Sarkar, Saheli; Bustard, Bethany L; Welter, Jean F et al. (2011) Combined experimental and mathematical approach for development of microfabrication-based cancer migration assay. Ann Biomed Eng 39:2346-59
Diekman, Brian O; Rowland, Christopher R; Lennon, Donald P et al. (2010) Chondrogenesis of adult stem cells from adipose tissue and bone marrow: induction by growth factors and cartilage-derived matrix. Tissue Eng Part A 16:523-33
Ko, In Kap; Kim, Byung-Gyu; Awadallah, Amad et al. (2010) Targeting improves MSC treatment of inflammatory bowel disease. Mol Ther 18:1365-72
Song, In-Hwan; Dennis, James E (2010) A novel method for large-scale immuno-SEM using protein G coupled polystyrene beads. J Electron Microsc (Tokyo) 59:527-30
Wang, Fangjing; Dennis, James E; Awadallah, Amad et al. (2009) Transcriptional profiling of human mesenchymal stem cells transduced with reporter genes for imaging. Physiol Genomics 37:23-34
Ko, In Kap; Kean, Thomas J; Dennis, James E (2009) Targeting mesenchymal stem cells to activated endothelial cells. Biomaterials 30:3702-10
Lee, Zhenghong; Dennis, James E; Gerson, Stanton L (2008) Imaging stem cell implant for cellular-based therapies. Exp Biol Med (Maywood) 233:930-40

Showing the most recent 10 out of 11 publications