Maternal high protein-diet programs impairment of offspring's bone mass through miR-24-1-5p mediated targeting of SMAD5 in osteoblasts.
Govindraj EllurShinde Vijay SukhdeoMd Touseef KhanKunal SharanPublished in: Cellular and molecular life sciences : CMLS (2020)
Maternal nutrition is crucial for the offspring's skeleton development and the onset of osteoporosis later in life. While maternal low protein diet has been shown to regulate bone mass negatively, the effect of a high protein diet (HP) remains unexplored. Here, we found that C57BL/6 mice fed with HP delivered offspring with decreased skeletal mineralization at birth and reduced bone mass throughout their life due to a decline in their osteoblast maturation. A small RNA sequencing study revealed that miR-24-1-5p was highly upregulated in HP group osteoblasts. Target prediction and validation studies identified SMAD-5 as a direct target of miR-24-1-5p. Furthermore, mimic and inhibitor studies showed a negative correlation between miR-24-1-5p expression and osteoblast function. Moreover, ex vivo inhibition of miR-24-1-5p reversed the reduced maturation and SMAD-5 expression in the HP group osteoblasts. Together, we show that maternal HP diminishes the bone mass of the offspring through miR-24-1-5p.
Keyphrases
- bone mineral density
- bone regeneration
- high fat diet
- birth weight
- physical activity
- pregnancy outcomes
- binding protein
- epithelial mesenchymal transition
- poor prognosis
- weight loss
- transforming growth factor
- soft tissue
- bone loss
- single cell
- gestational age
- protein protein
- body composition
- amino acid
- pregnant women
- adipose tissue
- skeletal muscle