{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13"],"submitter":["Frangi G"],"pubmed_abstract":["The common cellular origin between bone marrow adipocytes (BMAds) and osteoblasts contributes to the intimate link between bone marrow adipose tissue (BMAT) and skeletal health. An imbalance between the differentiation ability of BMSCs towards one of the two lineages occurs in conditions like aging or osteoporosis, where bone mass is decreased. Recently, we showed that the sodium-phosphate co-transporter PiT2/SLC20A2 is an important determinant for bone mineralization, strength and quality. Since bone mass is reduced in homozygous mutant mice, we investigated in this study whether the BMAT was also affected in <i>PiT2<sup>-/-</sup></i> mice by assessing the effect of the absence of PiT2 on BMAT volume between 3 and 16 weeks, as well as in an ovariectomy-induced bone loss model. Here we sho"],"journal":["Frontiers in endocrinology"],"pagination":["921073"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9708882"],"repository":["biostudies-literature"],"pubmed_title":["PiT2 deficiency prevents increase of bone marrow adipose tissue during skeletal maturation but not in OVX-induced osteoporosis."],"pmcid":["PMC9708882"],"pubmed_authors":["Jacquot F","Guihard P","Prieur X","Guicheteau M","Beck L","Veziers J","Sourice S","Feyeux M","Guicheux J","Pyka G","Halgand B","Beck-Cormier S","Kerckhofs G","Frangi G"],"additional_accession":[]},"is_claimable":false,"name":"PiT2 deficiency prevents increase of bone marrow adipose tissue during skeletal maturation but not in OVX-induced osteoporosis.","description":"The common cellular origin between bone marrow adipocytes (BMAds) and osteoblasts contributes to the intimate link between bone marrow adipose tissue (BMAT) and skeletal health. An imbalance between the differentiation ability of BMSCs towards one of the two lineages occurs in conditions like aging or osteoporosis, where bone mass is decreased. Recently, we showed that the sodium-phosphate co-transporter PiT2/SLC20A2 is an important determinant for bone mineralization, strength and quality. Since bone mass is reduced in homozygous mutant mice, we investigated in this study whether the BMAT was also affected in <i>PiT2<sup>-/-</sup></i> mice by assessing the effect of the absence of PiT2 on BMAT volume between 3 and 16 weeks, as well as in an ovariectomy-induced bone loss model. Here we sho","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-04-22T03:58:54.698Z","creation":"2025-04-05T20:53:42.691Z"},"accession":"S-EPMC9708882","cross_references":{"pubmed":["36465661"],"doi":["10.3389/fendo.2022.921073"]}}