<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(7)</volume><submitter>Moor MB</submitter><funding>Swiss National Science Foundation</funding><funding>Novartis Foundation</funding><pubmed_abstract>Mediator of cell motility 1 (MEMO1) is a ubiquitously expressed modulator of cellular responses to growth factors including FGF23 signaling, and Memo1-deficient mice share some phenotypic traits with Fgf23- or Klotho-deficient mouse models. Here, we tested whether Memo1 gene expression is regulated by calciotropic hormones or by changing the dietary mineral load. MLO-Y4 osteocyte-like cells were cultured and treated with 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/sub> . Wild-type C57BL/6N mice underwent treatments with 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/sub> , parathyroid hormone, 17β-estradiol or vehicle. Other cohorts of C57BL/6N mice were fed diets varying in calcium or phosphate content. Expression of Memo1 and control genes was assessed by qPCR. 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/</pubmed_abstract><journal>Physiological reports</journal><pagination>e14410</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7156332</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Memo1 gene expression in kidney and bone is unaffected by dietary mineral load and calciotropic hormones.</pubmed_title><pmcid>PMC7156332</pmcid><pubmed_authors>Moor MB</pubmed_authors><pubmed_authors>Bonny O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Memo1 gene expression in kidney and bone is unaffected by dietary mineral load and calciotropic hormones.</name><description>Mediator of cell motility 1 (MEMO1) is a ubiquitously expressed modulator of cellular responses to growth factors including FGF23 signaling, and Memo1-deficient mice share some phenotypic traits with Fgf23- or Klotho-deficient mouse models. Here, we tested whether Memo1 gene expression is regulated by calciotropic hormones or by changing the dietary mineral load. MLO-Y4 osteocyte-like cells were cultured and treated with 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/sub> . Wild-type C57BL/6N mice underwent treatments with 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/sub> , parathyroid hormone, 17β-estradiol or vehicle. Other cohorts of C57BL/6N mice were fed diets varying in calcium or phosphate content. Expression of Memo1 and control genes was assessed by qPCR. 1,25(OH)&lt;sub>2&lt;/sub> -vitamin D&lt;sub>3&lt;/</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2025-04-04T22:34:27.087Z</modification><creation>2020-05-22T17:34:40Z</creation></dates><accession>S-EPMC7156332</accession><cross_references><pubmed>32291966</pubmed><doi>10.14814/phy2.14410</doi></cross_references></HashMap>