The long term objective of this project is to improve cemented arthroplasty longevity by avoiding or delaying the occurrence of aseptic loosening which would: 1) broaden the indications for cemented arthroplasty to younger individuals, 2) avoid or delay the need for revision surgery in all patients, 3) improve results in those patients who have poor bone quality or quantity. To obtain this objective, the specific goal of this project is to improve our understanding of the mechanism of aseptic loosening. This will be an in - vitro study involving two groups of experiments over a five year period. In the first group, we will determine the role for each cell type present at the bone-cement interface (i.e. osteoblast, osteoclast, macrophage) in the bone resorption that leads to aseptic loosening by coculturing macrophages exposed to PMMA particles with: 1. rat calvaria and measuring 45 Ca release, 2. osteoclasts cultured on dentin strips and measuring numbers of excavations in bone via scanning E.M., 3. first with osteoblasts and then adding the new secondarily conditioned media to: a. rat calvaria and measuring 45 Ca release, and to; b. osteoclasts cultured on dentin strips and measuring numbers of excavations in bone via scanning E.M. In the second groups of studies, we will determine the relative role of each of the three major bone resorbing mediators in bone resorption at the interface by repeating the experiments in group 1 and attempting to block 45 Ca release or osteoclast excavations with; 1. indomethacin (block prostaglandin E2 synthesis), 2. antibodies to tumor necrosis factor and 3. antibodies to interleukin 1.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29AR041164-02
Application #
2080525
Study Section
Orthopedics and Musculoskeletal Study Section (ORTH)
Project Start
1994-01-01
Project End
1995-08-31
Budget Start
1995-01-01
Budget End
1995-08-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Orthopedics
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Horowitz, S M; Luchetti, W T; Gonzales, J B et al. (1998) The effects of cobalt chromium upon macrophages. J Biomed Mater Res 41:468-73
Horowitz, S M; Gonzales, J B (1997) Effects of polyethylene on macrophages. J Orthop Res 15:50-6
Horowitz, S M; Algan, S A; Purdon, M A (1996) Pharmacologic inhibition of particulate-induced bone resorption. J Biomed Mater Res 31:91-6
Algan, S M; Purdon, M; Horowitz, S M (1996) Role of tumor necrosis factor alpha in particulate-induced bone resorption. J Orthop Res 14:30-5
Gonzales, J B; Purdon, M A; Horowitz, S M (1996) In vitro studies on the role of titanium in aseptic loosening. Clin Orthop Relat Res :244-50
Horowitz, S M; Gonzales, J B (1996) Inflammatory response to implant particulates in a macrophage/osteoblast coculture model. Calcif Tissue Int 59:392-6
Horowitz, S M; Purdon, M A (1995) Mediator interactions in macrophage/particulate bone resorption. J Biomed Mater Res 29:477-84
Horowitz, S M; Purdon, M A (1995) Mechanisms of cellular recruitment in aseptic loosening of prosthetic joint implants. Calcif Tissue Int 57:301-5