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维生素 D 缺乏下调 Notch 通路导致老年 Wistar 大鼠骨骼肌萎缩。

Vitamin D deficiency down-regulates Notch pathway contributing to skeletal muscle atrophy in old wistar rats.

机构信息

Université d'Auvergne, Unité de Nutrition Humaine, Equipe ECREIN, CLARA, CRNH Auvergne; INRA, UMR 1019, UNH, CRNH Auvergne, Clermont Université, 63000 Clermont-Ferrand, France ; Université d'Auvergne, Unité de Nutrition Humaine, Equipe NuTriM, CRNH Auvergne; INRA, UMR 1019, UNH, CRNH Auvergne, Clermont Université, 63000 Clermont-Ferrand, France ; INRA, UMR1019, UNH, CRNH Auvergne, 63000 Clermont-Ferrand, France.

Université d'Auvergne, Unité de Nutrition Humaine, Equipe NuTriM, CRNH Auvergne; INRA, UMR 1019, UNH, CRNH Auvergne, Clermont Université, 63000 Clermont-Ferrand, France ; INRA, UMR1019, UNH, CRNH Auvergne, 63000 Clermont-Ferrand, France.

出版信息

Nutr Metab (Lond). 2014 Sep 30;11(1):47. doi: 10.1186/1743-7075-11-47. eCollection 2014.

Abstract

BACKGROUND

The diminished ability of aged muscle to self-repair is a factor behind sarcopenia and contributes to muscle atrophy. Muscle repair depends on satellite cells whose pool size is diminished with aging. A reduction in Notch pathway activity may explain the age-related decrease in satellite cell proliferation, as this pathway has been implicated in satellite cell self-renewal. Skeletal muscle is a target of vitamin D which modulates muscle cell proliferation and differentiation in vitro and stimulates muscle regeneration in vivo. Vitamin D status is positively correlated to muscle strength/function, and elderly populations develop a vitamin D deficiency. The aim of this study was to evaluate how vitamin D deficiency induces skeletal muscle atrophy in old rats through a reduction in Notch pathway activity and proliferation potential in muscle.

METHODS

15-month-old male rats were vitamin D-depleted or not (control) for 9 months (n = 10 per group). Rats were 24-month-old at the end of the experiment. Gene and/or protein expression of markers of proliferation, or modulating proliferation, and of Notch signalling pathway were studied in the tibialis anterior muscle by qPCR and western blot. An unpaired student's t-test was performed to test the effect of the experimental conditions.

RESULTS

Vitamin D depletion led to a drop in concentrations of plasma 25-hydroxyvitamin D in depleted rats compared to controls (-74%, p < 0.01). Tibialis anterior weight was decreased in D-depleted rats (-25%, p < 0.05). The D-depleted group showed -39%, -31% drops in expression of two markers known to modulate proliferation (Bmp4, Fgf-2 mRNA levels) and -56% drop in one marker of cell proliferation (PCNA protein expression) compared to controls (p < 0.05). Notch pathway activity was blunted in tibialis anterior of D-depleted rats compared to controls, seen as a down-regulation of cleaved Notch (-53%, p < 0.05) and its target Hes1 (-35%, p < 0.05).

CONCLUSIONS

A 9-month vitamin D depletion induced vitamin D deficiency in old rats. Vitamin D depletion induces skeletal muscle atrophy in old rats through a reduction in Notch pathway activity and proliferation potential. Vitamin D deficiency could aggravate the age-related decrease in muscle regeneration capacity.

摘要

背景

衰老肌肉自我修复能力的下降是导致肌肉减少症和肌肉萎缩的一个因素。肌肉修复依赖于卫星细胞,其数量随年龄的增长而减少。Notch 通路活性的降低可能解释了与年龄相关的卫星细胞增殖减少,因为该通路与卫星细胞自我更新有关。骨骼肌是维生素 D 的靶标,维生素 D 可调节体外肌细胞增殖和分化,并刺激体内肌肉再生。维生素 D 状态与肌肉力量/功能呈正相关,老年人群会出现维生素 D 缺乏。本研究旨在评估维生素 D 缺乏如何通过降低 Notch 通路活性和肌肉增殖潜力导致老年大鼠的骨骼肌萎缩。

方法

15 月龄雄性大鼠接受维生素 D 耗竭或不耗竭(对照)处理 9 个月(每组 10 只)。实验结束时,大鼠为 24 月龄。通过 qPCR 和 Western blot 研究前胫骨肌中增殖标志物或调节增殖的标志物以及 Notch 信号通路的基因和/或蛋白表达。使用未配对的学生 t 检验测试实验条件的影响。

结果

维生素 D 耗竭导致耗竭组大鼠血浆 25-羟维生素 D 浓度下降(与对照组相比,-74%,p<0.01)。D 耗竭组大鼠前胫骨重量下降(-25%,p<0.05)。与对照组相比,D 耗竭组两种已知调节增殖的标志物(Bmp4、Fgf-2 mRNA 水平)的表达下降了-39%和-31%,一种细胞增殖标志物(PCNA 蛋白表达)下降了-56%(p<0.05)。与对照组相比,D 耗竭大鼠前胫骨中的 Notch 通路活性减弱,表现为 Notch 裂解减少(-53%,p<0.05)和其靶基因 Hes1 减少(-35%,p<0.05)。

结论

9 个月的维生素 D 耗竭导致老年大鼠发生维生素 D 缺乏。维生素 D 缺乏通过降低 Notch 通路活性和增殖潜力导致老年大鼠的骨骼肌萎缩。维生素 D 缺乏可能会加重与年龄相关的肌肉再生能力下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba69/4195890/3ffe93b73993/12986_2014_619_Fig1_HTML.jpg

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