Analysis of Mouse Growth Plate Development
Overview
Affiliations
To investigate skeletal development, pathophysiological mechanisms of cartilage and bone disease, and eventually assess innovative treatments, the mouse is a very important resource. During embryonic development, mesenchymal condensations are formed, and cells within these mesenchymal condensations either directly differentiate into osteoblasts and give origin to intramembranous bone, or differentiate into chondrocytes and form a cartilaginous anlage. The cartilaginous anlage or fetal growth plate is then replaced with bone. This process is also called endochondral bone development, and it is responsible for the generation of most of our skeleton. Here we discuss in detail the most common in vivo and in vitro techniques our laboratory is currently using for the analysis of the mouse fetal growth plate during development.
Osteoblastic erythropoietin is not required for bone mass accrual.
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PMID: 38764792 PMC: 11102573. DOI: 10.1093/jbmrpl/ziae052.
The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice.
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PMID: 37330524 PMC: 10276814. DOI: 10.1038/s41467-023-39392-7.
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PMID: 34502142 PMC: 8431545. DOI: 10.3390/ijms22179239.
ERα Signaling in GHRH/Kiss1 Dual-Phenotype Neurons Plays Sex-Specific Roles in Growth and Puberty.
Garcia-Galiano D, Cara A, Tata Z, Allen S, Myers Jr M, Schipani E J Neurosci. 2020; 40(49):9455-9466.
PMID: 33158965 PMC: 7724138. DOI: 10.1523/JNEUROSCI.2069-20.2020.
genes maintain critical roles in the adult skeleton.
Song J, Pineault K, Dones J, Raines R, Wellik D Proc Natl Acad Sci U S A. 2020; 117(13):7296-7304.
PMID: 32170021 PMC: 7132104. DOI: 10.1073/pnas.1920860117.