Parathyroid hormone (PTH) dramatically increases bone formation but also increases bone resorption and causes hypercalcemia. PTH's anabolic actions may make this hormone an attractive part of strategies designed to restore the lost bone of osteoporotics. Incomplete understanding of the mechanisms of PTH action limit its effective use however. This SCOR proposes to define better the actions of parathyroid hormone (PTH) in humans and to use genetically manipulated animals to learn how PTH functions in living bone, in order to exploit fully the therapeutic potential of PTH. Project I: Bone formation-resorption coupling and osteoporosis (Robert Neer, PI) will address the relationship between PTH's anabolic and catabolic actions in osteoporotic women to explore basic mechanisms and to improve current therapies. Project II: Anabolic actions of PTH in early post-menopausal women (Joel Finkelstein, PI will define the actions of PTH on the normal bone of women who have recently become estrogen deficient. This work will provide insight into PTH action and how age and bone loss affect the response to PTH. Project Ill PTH action and skeletal collagen degradation (Stephen Krane, PI) will use mice resistant to collagenase to define the role of matrix resorption in the anabolic actions of PTH and of interstitial collagenase in normal bone physiology. Project IV: Osteoblast-specific ablation of the PTH/PTHrP receptor (Henry Kronenberg, PI) will use the cre-lox system to ablate the PTH/PTHrP receptor gene from populations of cells in the osteoblast lineage in living mice to define the cell-cell cooperation needed for responses to PTH and PTHrP. Project V: Constitutively active PTH/PTHrP receptors in osteoblasts (Ernestina Schipani, PI) will use transgenic animals expressing a constitutively active PTH/PTHrP receptor in different populations of cells of the osteoblast lineage to define how activation of this receptor in osteoblasts leads to anabolic and catabolic actions of PTH. A Bone Analysis Core Facility (Beate Lanske, PI) will provide expert and efficient histologic analysis of bone and performance of serological tests. These projects and associated cores should lead to more effective use of anabolic agents in the treatment of osteoporosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Specialized Center (P50)
Project #
1P50AR044855-01
Application #
2450024
Study Section
Special Emphasis Panel (ZAR1-TLB-B (O1))
Project Start
1997-09-22
Project End
2001-08-31
Budget Start
1997-09-22
Budget End
1998-08-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Yu, Elaine W; Neer, Robert M; Lee, Hang et al. (2011) Time-dependent changes in skeletal response to teriparatide: escalating vs. constant dose teriparatide (PTH 1-34) in osteoporotic women. Bone 48:713-9
Finkelstein, Joel S; Wyland, Jason J; Lee, Hang et al. (2010) Effects of teriparatide, alendronate, or both in women with postmenopausal osteoporosis. J Clin Endocrinol Metab 95:1838-45
Finkelstein, Joel S; Wyland, Jason J; Leder, Benjamin Z et al. (2009) Effects of teriparatide retreatment in osteoporotic men and women. J Clin Endocrinol Metab 94:2495-501
Leder, Benjamin Z; Neer, Robert M; Wyland, Jason J et al. (2009) Effects of teriparatide treatment and discontinuation in postmenopausal women and eugonadal men with osteoporosis. J Clin Endocrinol Metab 94:2915-21
Finkelstein, Joel S; Leder, Benjamin Z; Burnett, Sherri-Ann M et al. (2006) Effects of teriparatide, alendronate, or both on bone turnover in osteoporotic men. J Clin Endocrinol Metab 91:2882-7
Kobayashi, Tatsuya; Kronenberg, Henry M; Foley, John (2005) Reduced expression of the PTH/PTHrP receptor during development of the mammary gland influences the function of the nipple during lactation. Dev Dyn 233:794-803
Miao, Dengshun; He, Bin; Jiang, Yebin et al. (2005) Osteoblast-derived PTHrP is a potent endogenous bone anabolic agent that modifies the therapeutic efficacy of administered PTH 1-34. J Clin Invest 115:2402-11
Inada, Masaki; Wang, Yingmin; Byrne, Michael H et al. (2004) Critical roles for collagenase-3 (Mmp13) in development of growth plate cartilage and in endochondral ossification. Proc Natl Acad Sci U S A 101:17192-7
Kuznetsov, Sergei A; Riminucci, Mara; Ziran, Navid et al. (2004) The interplay of osteogenesis and hematopoiesis: expression of a constitutively active PTH/PTHrP receptor in osteogenic cells perturbs the establishment of hematopoiesis in bone and of skeletal stem cells in the bone marrow. J Cell Biol 167:1113-22
Chiusaroli, R; Maier, A; Knight, M C et al. (2003) Collagenase cleavage of type I collagen is essential for both basal and parathyroid hormone (PTH)/PTH-related peptide receptor-induced osteoclast activation and has differential effects on discrete bone compartments. Endocrinology 144:4106-16

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