Department of Molecular Nutrition, CSIR-Central Food Technological Research Institute, Mysore, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Cell Mol Life Sci. 2021 Feb;78(4):1729-1744. doi: 10.1007/s00018-020-03608-6. Epub 2020 Jul 30.
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.
母体营养对于后代骨骼发育和晚年骨质疏松症的发生至关重要。虽然低蛋白饮食已被证明会对骨量产生负面影响,但高蛋白饮食(HP)的影响仍未得到探索。在这里,我们发现 C57BL/6 小鼠的 HP 饮食导致后代在出生时骨骼矿化减少,并且由于成骨细胞成熟度下降,其一生中的骨量减少。小 RNA 测序研究表明,HP 组成骨细胞中 miR-24-1-5p 高度上调。靶标预测和验证研究表明,SMAD-5 是 miR-24-1-5p 的直接靶标。此外,模拟物和抑制剂研究表明 miR-24-1-5p 的表达与成骨细胞功能呈负相关。此外,体外抑制 miR-24-1-5p 可逆转 HP 组成骨细胞中成熟度和 SMAD-5 表达的降低。综上所述,我们表明母体 HP 通过 miR-24-1-5p 降低了后代的骨量。