Vitamin D and the vitamin D receptor in liver pathophysiology

被引:65
作者
Zunigaa, Silvia [1 ,2 ,3 ]
Firrincieli, Delphine [1 ,2 ]
Housset, Chantal [1 ,2 ,4 ]
Chignard, Nicolas [1 ,2 ]
机构
[1] Univ Paris 06, UMR S 938, CdR St Antoine, F-75005 Paris, France
[2] INSERM, UMR S 938, CdR St Antoine, F-75012 Paris, France
[3] Pontificia Univ Catolica Chile, Santiago, Chile
[4] Hop St Antoine, Serv Hepatol, AP HP, F-75020 Paris, France
关键词
PRIMARY BILIARY-CIRRHOSIS; D-BINDING PROTEIN; ISOLATED EPITHELIAL-CELLS; FARNESOID-X-RECEPTOR; CHRONIC HEPATITIS-C; BILE-ACID SYNTHESIS; D NUCLEAR RECEPTOR; GENE POLYMORPHISMS; IN-VITRO; 1,25-DIHYDROXYVITAMIN D-3;
D O I
10.1016/j.clinre.2011.02.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Vitamin D through the vitamin D nuclear receptor (VDR) plays a key role in mineral ion homeostasis. The liver is central in vitamin D synthesis, however the direct involvement of the vitamin D-VDR axis on the liver remains to be evaluated. In this review, we will describe vitamin D metabolism and the mechanisms of homeostatic control. We will also address the associations between the vitamin D-VDR axis and pathological liver entities, such as non-alcoholic fatty liver disease, autoimmune liver disease, viral hepatitis and liver cancer. The link between liver diseases and the vitamin D-VDR axis will be discussed in light of evidences arising from in vitro and in vivo studies. Finally, we will consider the therapeutic potential of the vitamin D-VDR axis in liver diseases. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 91 条
  • [51] Vitamin effects on the immune system: vitamins A and D take centre stage
    Mora, J. Rodrigo
    Iwata, Makoto
    von Andrian, Ulrich H.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2008, 8 (09) : 685 - 698
  • [52] The promoter of the human 25-hydroxyvitamin D3 1α-hydroxylase gene confers positive and negative responsiveness to PTH, calcitonin, and 1α,25(OH)2D3
    Murayama, A
    Takeyama, K
    Kitanaka, S
    Kodera, Y
    Hosoya, T
    Kato, S
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 249 (01) : 11 - 16
  • [53] NAKANO T, 2010, J HEPATOL, DOI DOI 10.1016/J.JHEP.201011.028
  • [54] EARLY ACTIONS OF PARATHYROID-HORMONE AND 1,25-DIHYDROXYCHOLECALCIFEROL ON ISOLATED EPITHELIAL-CELLS FROM RAT INTESTINE .2. ANALYSES OF ADDITIVITY, CONTRIBUTION OF CALCIUM, AND MODULATORY INFLUENCE OF INDOMETHACIN
    NEMERE, I
    SZEGO, CM
    [J]. ENDOCRINOLOGY, 1981, 109 (06) : 2180 - 2187
  • [55] EARLY ACTIONS OF PARATHYROID-HORMONE AND 1,25-DIHYDROXYCHOLECALCIFEROL ON ISOLATED EPITHELIAL-CELLS FROM RAT INTESTINE .1. LIMITED LYSOSOMAL ENZYME-RELEASE AND CALCIUM-UPTAKE
    NEMERE, I
    SZEGO, CM
    [J]. ENDOCRINOLOGY, 1981, 108 (04) : 1450 - 1462
  • [56] NEMERE I, 1994, J BIOL CHEM, V269, P23750
  • [57] Ribozyme knockdown functionally links a 1,25(OH)2D3 membrane binding protein (1,25D3-MARRS) and phosphate uptake in intestinal cells
    Nemere, I
    Farach-Carson, MC
    Rohe, B
    Sterling, TM
    Norman, AW
    Boyan, BD
    Safford, SE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) : 7392 - 7397
  • [58] Identification and characterization of 1,25D3-membrane-associated rapid response, steroid (1,25D3-MARRS) binding protein
    Nemere, K
    Safford, SE
    Rohe, B
    DeSouza, MM
    Farach-Carson, MC
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 89-90 (1-5) : 281 - 285
  • [59] Modulation of Bile Acid Metabolism by 1α-Hydroxyvitamin D3 Administration in Mice
    Nishida, Shigeru
    Ozeki, Jun
    Makishima, Makoto
    [J]. DRUG METABOLISM AND DISPOSITION, 2009, 37 (10) : 2037 - 2044
  • [60] Vitamin D3 Modulates the Expression of Bile Acid Regulatory Genes and Represses Inflammation in Bile Duct-Ligated Mice
    Ogura, Michitaka
    Nishida, Shigeru
    Ishizawa, Michiyasu
    Sakurai, Kenichi
    Shimizu, Makoto
    Matsuo, Sadanori
    Amano, Sadao
    Uno, Shigeyuki
    Makishima, Makoto
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2009, 328 (02) : 564 - 570