Bone loss with aging results from attenuated and unbalanced bone turnover, and is associated with a decreased number of bone-forming osteoblasts, increased number of bone-resorbing osteoclasts, and increased number of fat cells, adipocytes, in the bone marrow. Osteoblasts and adipocytes originate from marrow-derived mesenchymal stroma/stem cells (MSCs). The milieu of intracellular and extracellular signals controls MSC lineage allocation. Emerging evidence indicates that the adipocyte-specific transcription factor peroxisome proliferator- activated receptor-gamma (PPARg) acts as a positive regulator of marrow adipocyte formation and negative regulator of osteoblast development. In vivo, increased activity of PPARg leads to bone loss, similar to bone loss with aging, whereas its decreased activity results in increased bone mass. The pro-adipocytic and the anti- osteoblastic properties of PPARg are determined by the type of ligand and can be distinguished, suggesting separate mechanisms by which PPARg controls bone mass and fat mass in bone. During aging, the status of MSCs changes with respect to both their intrinsic differentiation potential and production of signaling molecules that contribute to the formation of a specific marrow micro-environment. The expression of PPARg and production of its natural activators (e.g., oxidized fatty acids) increases, suggesting increased activity of this nuclear receptor. Increased activity of PPARg down-regulates the expression and activity of multiple regulatory pathways, including Wnt, TGF-beta, and IGF-1, suggesting the role of this transcription factor in the regulation of the extrinsic signaling milieu. We propose that age-related bone loss results from the increased anti-osteoblastic activity of PPARg, which results in both intrinsic changes in the differentiation of MSCs and a decrease in pro-osteoblastic signaling in the marrow micro-environment. The following Specific Aims will test this hypothesis:
Aim 1 : Determine regulatory mechanisms by which PPARg suppresses osteoblast differentiation during aging.
Aim 2 : Determine the effects of PPAR-g controlled intracellular mechanisms and microenvironmental changes on bone formation with the model of distraction osteogenesis (DO). An understanding of the effects of aging on the interrelationship between MSC differentiation potential and the modulatory effects of the bone marrow environment on this process is the starting point for the development of successful therapies for osteoporosis that will specifically target bone and bone marrow stem cells. Completion of the above aims should enable us to determine the role of PPARg in this process and will allow designing therapeutic interventions that will selectively block PPARg anti-osteoblastic activity. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
1R01AG028935-01
Application #
7152348
Study Section
Special Emphasis Panel (ZAG1-ZIJ-2 (M1))
Program Officer
Williams, John
Project Start
2006-08-15
Project End
2007-06-15
Budget Start
2006-08-15
Budget End
2007-06-15
Support Year
1
Fiscal Year
2006
Total Cost
$297,680
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Other Health Professions
Type
Schools of Medicine
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Stechschulte, Lance A; Lecka-Czernik, Beata (2017) Reciprocal regulation of PPAR? and RUNX2 activities in marrow mesenchymal stem cells: Fine balance between p38 MAPK and Protein Phosphatase 5. Curr Mol Biol Rep 3:107-113
Kolli, Vipula; Stechschulte, Lance A; Dowling, Abigail R et al. (2014) Partial agonist, telmisartan, maintains PPAR? serine 112 phosphorylation, and does not affect osteoblast differentiation and bone mass. PLoS One 9:e96323
Liu, Lichu; Aronson, James; Lecka-Czernik, Beata (2013) Rosiglitazone disrupts endosteal bone formation during distraction osteogenesis by local adipocytic infiltration. Bone 52:247-58
Rahman, Sima; Lu, Yalin; Czernik, Piotr J et al. (2013) Inducible brown adipose tissue, or beige fat, is anabolic for the skeleton. Endocrinology 154:2687-701
Lecka-Czernik, Beata (2013) Safety of Anti-Diabetic Therapies on Bone. Clin Rev Bone Miner Metab 11:49-58
Liu, Lichu; Aronson, James; Huang, Shilong et al. (2012) Rosiglitazone inhibits bone regeneration and causes significant accumulation of fat at sites of new bone formation. Calcif Tissue Int 91:139-48
Krings, A; Rahman, S; Huang, S et al. (2012) Bone marrow fat has brown adipose tissue characteristics, which are attenuated with aging and diabetes. Bone 50:546-52
Rahman, Sima; Czernik, Piotr J; Lu, Yalin et al. (2012) ?-catenin directly sequesters adipocytic and insulin sensitizing activities but not osteoblastic activity of PPAR?2 in marrow mesenchymal stem cells. PLoS One 7:e51746
Lecka-Czernik, Beata (2012) Marrow fat metabolism is linked to the systemic energy metabolism. Bone 50:534-9
Huang, S; Kaw, M; Harris, M T et al. (2010) Decreased osteoclastogenesis and high bone mass in mice with impaired insulin clearance due to liver-specific inactivation to CEACAM1. Bone 46:1138-45

Showing the most recent 10 out of 14 publications