Osteocalcin of maternal and embryonic origins synergize to establish homeostasis in offspring.
Danilo Correa Pinto JuniorIsabella Canal DelgadoHaiyang YangAlisson ClemenceauAndré CorveloGiuseppe NarzisiRajeeva Lochan MusunuriJulian Meyer BergerLauren E HendricksKazuya TokumuraNa LuoHongchao LiFranck OuryPatricia DucyVijay K YadavXiang LiGerard KarsentyPublished in: EMBO reports (2024)
Many physiological osteocalcin-regulated functions are affected in adult offspring of mothers experiencing unhealthy pregnancy. Furthermore, osteocalcin signaling during gestation influences cognition and adrenal steroidogenesis in adult mice. Together these observations suggest that osteocalcin may broadly function during pregnancy to determine organismal homeostasis in adult mammals. To test this hypothesis, we analyzed in unchallenged wildtype and Osteocalcin-deficient, newborn and adult mice of various genotypes and origin maintained on different genetic backgrounds, the functions of osteocalcin in the pancreas, liver and testes and their molecular underpinnings. This analysis revealed that providing mothers are Osteocalcin-deficient, Osteocalcin haploinsufficiency in embryos hampers insulin secretion, liver gluconeogenesis, glucose homeostasis, testes steroidogenesis in adult offspring; inhibits cell proliferation in developing pancreatic islets and testes; and disrupts distinct programs of gene expression in these organs and in the brain. This study indicates that osteocalcin exerts dominant functions in most organs it influences. Furthermore, through their synergistic regulation of multiple physiological functions, osteocalcin of maternal and embryonic origins contributes to the establishment and maintenance of organismal homeostasis in newborn and adult offspring.
Keyphrases
- gene expression
- cell proliferation
- white matter
- dna methylation
- metabolic syndrome
- multiple sclerosis
- adipose tissue
- blood pressure
- body mass index
- preterm infants
- mild cognitive impairment
- transcription factor
- signaling pathway
- young adults
- insulin resistance
- cell cycle
- pregnant women
- copy number
- high fat diet induced
- cancer therapy
- blood glucose
- weight gain