The Indian hedgehog-parathyroid hormone-related protein (Ihh/PTHrP) axis regulates the growth chondrocyte differentiation program (round ? flat ? prehypertrophic ? hypertrophic) that drives endochondral bone development. We have found that the Ihh-PTHrP axis is operative also in embryonic and in established articular cartilage. In the embryo, the Ihh-PTHrP axis prevents mineralization of the nascent joint. In established articular cartilage the axis is regulated by mechanical loading, with PTHrP lying upstream of Ihh in the signaling sequence. Our working hypothesis is that PTHrP and Ihh are involved in regulating the maintenance of established articular cartilage, and we propose to test this hypothesis by conditional deletion of PTHrP, Ihh signaling, or both in mice.
In Specific Aim 1, we will test the hypothesis that PTHrP regulates the differentiation of articular chondrocytes and in so doing is a player in articular cartilage maintenance. We will test this idea via two sub-aims: 1) by conditionally deleting PTHrP in mid-zone articular chondrocytes via the Gdf5 promoter and b) by challenging these mice with a protocol(s) designed to highlight dysregulation of maintenance, if present.
In Specific Aim 2, we propose to test the putative role of Ihh in articular cartilage maintenance by conditionally deleting Smoothened (Smo) in mid-zone articular chondrocytes via GDF5-Cre targeting. We further propose to study the combinatorial effects of the axis in articular chondrocytes by conditionally deleting PTHrP and Smo together.

Public Health Relevance

The chondrocytes that make up articular cartilage must remain in their native, undifferentiated state in order for this cartilage to carry out its normal functions, which include lubricating the joints and cushioning load in weight-bearing joints. When chondrocytes differentiate, they begin to mineralize and degenerate, and these are hallmarks of osteoarthritis, the most common form of arthritis, and a leading cause of disability worldwide. We describe here two regulatory molecules that together seem to regulate articular chondrocyte differentiation and describe models that may provide insight into the cause of osteoarthritis at a cellular and molecular level.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AR057243-01A1
Application #
7788286
Study Section
Skeletal Biology Structure and Regeneration Study Section (SBSR)
Program Officer
Tyree, Bernadette
Project Start
2010-01-15
Project End
2011-12-31
Budget Start
2010-01-15
Budget End
2010-12-31
Support Year
1
Fiscal Year
2010
Total Cost
$223,425
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Wang, Meina; VanHouten, Joshua N; Nasiri, Ali R et al. (2013) PTHrP regulates the modeling of cortical bone surfaces at fibrous insertion sites during growth. J Bone Miner Res 28:598-607
Macica, Carolyn; Liang, Guoying; Nasiri, Ali et al. (2011) Genetic evidence of the regulatory role of parathyroid hormone-related protein in articular chondrocyte maintenance in an experimental mouse model. Arthritis Rheum 63:3333-43