Vitamin D Receptor Deficiency and Low Vitamin D Diet Stimulate Aortic Calcification and Osteogenic Key Factor Expression in Mice

被引:74
作者
Schmidt, Nadine [1 ]
Brandsch, Corinna [1 ]
Kuehne, Hagen [1 ]
Thiele, Alexandra [1 ]
Hirche, Frank [1 ]
Stangl, Gabriele I. [1 ]
机构
[1] Univ Halle Wittenberg, Inst Agr & Nutr Sci, Halle, Saale, Germany
来源
PLOS ONE | 2012年 / 7卷 / 04期
关键词
SMOOTH-MUSCLE-CELL; VASCULAR CALCIFICATION; CARDIOVASCULAR-DISEASE; RISK; ATHEROSCLEROSIS; 25-HYDROXYVITAMIN-D; ASSOCIATION; PREVALENCE; MECHANISMS; CALCITRIOL;
D O I
10.1371/journal.pone.0035316
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Low levels of 25-hydroxy vitamin D (25(OH)D) are associated with cardiovascular diseases. Herein, we tested the hypothesis that vitamin D deficiency could be a causal factor in atherosclerotic vascular changes and vascular calcification. Aortic root sections of vitamin D receptor knockout (VDR-/-) mice that were stained for vascular calcification and immunostained for osteoblastic differentiation factors showed more calcified areas and a higher expression of the osteogenic key factors Msx2, Bmp2, and Runx2 than the wild-type mice (P<0.01). Data from LDL receptor knockout (LDLR-/-) mice that were fed western diet with either low (50 IU/kg), recommended (1,000 IU/kg), or high (10,000 IU/kg) amounts of vitamin D-3 over 16 weeks revealed increasing plasma concentrations of 25(OH)D (P<0.001) with increasing intake of vitamin D, whereas levels of calcium and phosphorus in plasma and femur were not influenced by the dietary treatment. Mice treated with the low vitamin D diet had more calcified lesions and a higher expression of Msx2, Bmp2, and Runx2 in aortic roots than mice fed recommended or high amounts of vitamin D (P<0.001). Taken together, these findings indicate vitamin D deficiency as a risk factor for aortic valve and aortic vessel calcification and a stimulator of osteogenic key factor expression in these vascular areas.
引用
收藏
页数:8
相关论文
共 34 条
[1]   Vascular calcification - Mechanisms and clinical ramifications [J].
Abedin, M ;
Tintut, Y ;
Demer, LL .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (07) :1161-1170
[2]   QUANTIFICATION OF CORONARY-ARTERY CALCIUM USING ULTRAFAST COMPUTED-TOMOGRAPHY [J].
AGATSTON, AS ;
JANOWITZ, WR ;
HILDNER, FJ ;
ZUSMER, NR ;
VIAMONTE, M ;
DETRANO, R .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 15 (04) :827-832
[3]   Patterns and risk factors for systemic calcified atherosclerosis [J].
Allison, MA ;
Criqui, MH ;
Wright, CM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (02) :331-336
[4]   Vitamin D and the Cardiovascular System [J].
Artaza, Jorge N. ;
Mehrotra, Rajnish ;
Norris, Keith C. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 4 (09) :1515-1522
[5]  
BASSLER R, 1993, CHEM UNTERSUCHUNG FU, V2
[6]  
BRAUNWALD, 1997, J MOD, V337, P1360
[7]   Cardiovascular disease burden increases, NIH funding decreases [J].
Breslow, JL .
NATURE MEDICINE, 1997, 3 (06) :600-601
[8]   Vascular calcifications:: Pathogenesis, management, and impact on clinical outcomes [J].
Cannata-Andia, Jorge B. ;
Rodriguez-Garcia, Minerva ;
Carrillo-Lopez, Natalia ;
Naves-Diaz, Manuel ;
Diaz-Lopez, Bernardino .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 :S267-S273
[9]   Independent association of low serum 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels with all-cause and cardiovascular mortality [J].
Dobnig, Harald ;
Pilz, Stefan ;
Scharnagl, Hubert ;
Renner, Wilfried ;
Seelhorst, Ursula ;
Wellnitz, Britta ;
Kinkeldei, Jurgen ;
Boehm, Bernhard O. ;
Weihrauch, Gisela ;
Maerz, Winfried .
ARCHIVES OF INTERNAL MEDICINE, 2008, 168 (12) :1340-1349
[10]   Serum metabolite profiles and target tissue gene expression define the effect of cholecalciferol intake on calcium metabolism in rats and mice [J].
Fleet, James C. ;
Gliniak, Christy ;
Zhang, Zhentao ;
Xue, Yingben ;
Smith, Kathleen B. ;
McCreedy, Rebecca ;
Adedokun, Sunday A. .
JOURNAL OF NUTRITION, 2008, 138 (06) :1114-1120