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Elucidating the Molecular Signatures Associated with Elevated Bone Formation Rate Public Deposited

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Lowery, Jonathan, Jackson, Krista, and Jestes, Kelli. Elucidating the Molecular Signatures Associated with Elevated Bone Formation Rate. . 1192. https://mushare.marian.edu/concern/generic_works/27ec4f44-b06f-4ec1-a92d-8b8e489f68bb?locale=en

APA citation style

Lowery, Jonathan, Jackson, Krista, & Jestes, Kelli. (1192). Elucidating the Molecular Signatures Associated with Elevated Bone Formation Rate. https://mushare.marian.edu/concern/generic_works/27ec4f44-b06f-4ec1-a92d-8b8e489f68bb?locale=en

Chicago citation style

Lowery, Jonathan, Jackson, Krista, and Jestes, Kelli. Elucidating the Molecular Signatures Associated with Elevated Bone Formation Rate. 1192. https://mushare.marian.edu/concern/generic_works/27ec4f44-b06f-4ec1-a92d-8b8e489f68bb?locale=en

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Osteoporosis is a disease of decreased bone density that occurs when bone resorption exceeds bone formation, thereby placing individuals at greater risk of fracture and disability. We previously reported that deletion of the Bmpr2 gene in embryonic skeletal progenitor cells causes substantially elevated bone density in young adulthood and reduced age-related decline in bone density, likely due to elevated bone formation rate. Thus, these mice may serve as a novel model in which to explore the mechanisms regulating bone formation in the aging skeleton. Here, we performed transcriptome profiling and identified a concise gene signature associated with elevated bone formation rate in Bmpr2 mutant mice, with 120 transcripts up-regulated and 131 transcripts down-regulated. Candidate-driven qRT-PCR provided secondary confirmation of this dataset. Notably, only 8 of these differentially-expressed transcripts have been previously implicated in bone physiology (Pak4, Rpl38, B2m, Fgf1, Nmu, Phospho1, Smpd3 and Inbe), thus representing potentially novel regulators of osteoblast function in the aging skeleton. Additionally, we sought to examine the cell communication events that are associated with elevated bone formation rate. Using protein samples from control and mutant mice, we took advantage of recent advancements in high-throughput phospho-profiling antibody arrays, which allow simultaneous detection of >1,300 targets using very small quantities of protein. These results indicate that the phosphorylation status of at least 86 signaling effectors is differentially regulated in Bmpr2 mutant mice as compared to control littermates, including numerous proteins known to regulate osteoblast differentiation and/or activity. Collectively, our work highlights novel factors associated with elevated bone formation rate and may identify new opportunities for treating low bone density in humans.

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