(Taken from the application): In recent years, numerous advances have been made towards understanding the molecular regulation of chondrocyte maturation within the growth plate through the production of growth factors and the regulation of their receptors and receptor-mediated transmembrane signaling processes. The growth/differentiation factors (GDFs) represent a distinct subset of the TGF-beta family which may play a role in regulating endochondral bone growth. Evidence for GDF involvement comes largely from the documented mutation in GDF-5/CDMP-1 in individuals with acromesomelic chondrodysplasia of the Hunter-Thompson and Grebe types, and a reduction in the length of the long bones of GDF-5 deficient brachypodism mice. Given the link between GDF-5/CDMP-1 and chondrodysplasia in humans, it is likely that other chondrodysplastic disorders are linked to mutations in related GDF/CDMP family members. The goal of this research is to examine the effect of GDFs 5, 6, & 7 on endochondral bone growth by studying animals with a deficiency in these signaling peptides. We will examine mice with mutations in the genes which code for GDF 5, 6 or 7. For each gene of interest, three groups of ten healthy male mice will be studied, representing mutant (-/-) and heterozygous (+/-) control littermates at 4 weeks of age. Using classical methods of stereology and chondrocyte kinetics, growth plates from the proximal tibia, proximal humerus, and fourth rib will be carefully examined to test the hypothesis that mice deficient in GDF 5, 6, or 7 will exhibit impaired endochondral bone growth. The proposed detailed analyses of stereologic and chondrocyte kinetic parameters will help to identify precisely which growth plate cell populations are affected by the absence of GDFs 5, 6, & 7. Future studies will extend these investigations to double and triple GDF family member mutations, as well as molecular characterization of other important growth plate signaling molecules in the various single, double, and triple GDF mutations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Small Research Grants (R03)
Project #
7R03AR047097-02
Application #
6492244
Study Section
Special Emphasis Panel (ZAR1-AAA-B (M1))
Program Officer
Sharrock, William J
Project Start
2000-09-01
Project End
2003-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
2
Fiscal Year
2001
Total Cost
$66,860
Indirect Cost
Name
Smith College
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
066989427
City
Northampton
State
MA
Country
United States
Zip Code
01063
Mikic, Borjana; Ferreira, Maria P; Battaglia, Todd C et al. (2008) Accelerated hypertrophic chondrocyte kinetics in GDF-7 deficient murine tibial growth plates. J Orthop Res 26:986-90
Mikic, Borjana (2004) Multiple effects of GDF-5 deficiency on skeletal tissues: implications for therapeutic bioengineering. Ann Biomed Eng 32:466-76
Mikic, B; Clark, R T; Battaglia, T C et al. (2004) Altered hypertrophic chondrocyte kinetics in GDF-5 deficient murine tibial growth plates. J Orthop Res 22:552-6
Mikic, Borjana; Battaglia, T C; Taylor, E A et al. (2002) The effect of growth/differentiation factor-5 deficiency on femoral composition and mechanical behavior in mice. Bone 30:733-7