Vitamin D treatment of senescence accelerated mice (SAM-P/6) induces several regulators of stromal cell plasticity

被引:31
作者
Duque, G
Macoritto, M
Kremer, R
机构
[1] McGill Univ, Div Geriatr Med, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Jewish Gen Hosp, Bloomfield Ctr Studies Aging, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Ctr Bone & Periodontal Res, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
adipogenesis; microarrays; osteoblastogenesis; SAM-P/6; senile osteoporosis; vitamin D;
D O I
10.1007/s10522-004-3192-5
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
In an attempt to understand the regulation of bone marrow multipotential cells plasticity in vivo, we treated 4-month-old SAM-P/6 mice with a constant infusion of either 18 pmol/24 h of 1,25(OH)(2)D-3 or vehicle alone for 6 weeks. In vehicle treated animals 78% +/- 4 adipose volume vs. total volume was stained positive with oil red O as compared to only 32 +/- 3% in 1,25(OH)(2)D(3)treated animals (P < 0.001). Furthermore, we aimed to identify the changes in gene expression induced by 1,25(OH)(2)D-3 in bone marrow cells by analyzing a set of 5440 genes in the NIA 15K Mouse cDNA microarray. Overall, a coordinated regulation of genes which both stimulate osteoblastogenesis and inhibit adipogenesis was observed in 1,25(OH)(2)D-3-treated mice when compared to vehicle treated mice. In summary, this study illustrates the anti-adipogenic effect of 1,25(OH)(2)D-3 in bone cells and identifies some of the possible key signals involved in bone cell plasticity.
引用
收藏
页码:421 / 429
页数:9
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