Investigations from our laboratory have revealed that Notch1 plays a critical role in osteoblastic cell differentiation and function, and its expression n immature osteoblasts causes osteopenia secondary to an inhibitory effect on osteoblastogenesis. Although Notch2 appears to have an important and distinct function from Notch1, most of the work conducted in skeletal cells has examined the effects of Notch1, and there is limited information on the function of Notch2 in the skeleton. Hajdu-Cheney Syndrome (HCS), a devastating disease characterized by acro-osteolysis, osteoporosis and fractures, was recently attributed to gain-of-function mutations of NOTCH2 leading to NOTCH2 protein stabilization.
The aim of the proposed research is to create and study mouse models of HCS, to understand the skeletal disease and mechanisms involved in HCS. As a consequence, the function of Notch2 in the skeleton will be defined.
Our specific aims are: (1) To characterize the HCS and determine the function of Notch2 by studying global and conditional mouse models of Notch2HCS mutant activation in skeletal cells. The skeletal phenotype of global and cell lineage-specific Notch2HCS conditional by inversion (COIN) mutants will be compared to that of wild type mice and determined by contact radiography, densitometry, micro CT scanning and histomorphometry. The biomechanical properties of the skeleton from HCS mutant mice will be analyzed;(2) To determine the mechanism responsible for HCS in the skeleton. To this end, mechanisms responsible for the skeletal phenotype will be established, and we will determine whether the Notch canonical signaling pathway is responsible for the HCS phenotype. In addition, we will explore interactions with Wnt signaling, and determine whether Notch2 mRNA and protein are stabilized in cells from Notch2HCS mutants and explain the phenotype observed. Levels of transcriptional and post-transcriptional regulation of genes modified by Notch2HCS mutants will be examined in vitro;and (3) To determine the role of Notch target gene(s) in the skeleton and in the HCS. To this end, we will determine whether the Notch2HCS mutant phenotype is secondary to the activation of Hairy-Enhancer of Split (Hes) 1. Notch2HCS mutants will be studied in the context (or not) of the conditional Hes1 inactivation for changes in their skeletal phenotype determined by micro CT scanning and histomorphometry and for changes in osteoblastic gene expression.
|Zanotti, Stefano; Canalis, Ernesto (2017) Parathyroid hormone inhibits Notch signaling in osteoblasts and osteocytes. Bone 103:159-167|
|Canalis, Ernesto; Zanotti, Stefano (2017) Hairy and Enhancer of Split-Related With YRPW Motif-Like (HeyL) Is Dispensable for Bone Remodeling in Mice. J Cell Biochem 118:1819-1826|
|Zanotti, Stefano; Yu, Jungeun; Sanjay, Archana et al. (2017) Sustained Notch2 signaling in osteoblasts, but not in osteoclasts, is linked to osteopenia in a mouse model of Hajdu-Cheney syndrome. J Biol Chem 292:12232-12244|
|Canalis, Ernesto (2017) Clinical and experimental aspects of notch receptor signaling: Hajdu-Cheney syndrome and related disorders. Metabolism :|
|Canalis, Ernesto; Sanjay, Archana; Yu, Jungeun et al. (2017) An Antibody to Notch2 Reverses the Osteopenic Phenotype of Hajdu-Cheney Mutant Male Mice. Endocrinology 158:730-742|
|Zanotti, Stefano; Canalis, Ernesto (2016) Notch Signaling and the Skeleton. Endocr Rev 37:223-53|
|Adami, Giovanni; Rossini, Maurizio; Gatti, Davide et al. (2016) Hajdu Cheney Syndrome; report of a novel NOTCH2 mutation and treatment with denosumab. Bone 92:150-156|
|Canalis, Ernesto; Schilling, Lauren; Yee, Siu-Pok et al. (2016) Hajdu Cheney Mouse Mutants Exhibit Osteopenia, Increased Osteoclastogenesis, and Bone Resorption. J Biol Chem 291:1538-51|
|Canalis, Ernesto; Zanotti, Stefano (2016) Hajdu-Cheney Syndrome, a Disease Associated with NOTCH2 Mutations. Curr Osteoporos Rep 14:126-31|
|Mirza, Faryal; Canalis, Ernesto (2015) Management of endocrine disease: Secondary osteoporosis: pathophysiology and management. Eur J Endocrinol 173:R131-51|
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