Regulation of 25-hydroxyvitamin D3-1α-hydroxylase and production of 1α,25-dihydroxyvitamin D3 by human dendritic cells

被引:184
作者
Fritsche, J [1 ]
Mondal, K [1 ]
Ehrnsperger, A [1 ]
Andreesen, R [1 ]
Kreutz, M [1 ]
机构
[1] Univ Regensburg, Dept Hematol & Oncol, D-93042 Regensburg, Germany
关键词
D O I
10.1182/blood-2002-11-3521
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
25-Hydroxyvitamin D-3-1alpha-hydroxylase (25(OH)D-3-1alpha-hydroxylase), the key enzyme of 1alpha,25-dihydroxyvitamin D-3 (1,25(OH)(2)D-3) production, is expressed in monocyte-derived macrophages (MACs). Here we show for the first time constitutive expression of 25(OH)D-3-1alpha-hydroxylase in monocyte-derived dendritic cells (DCs), which was increased after stimulation with lipopolysaccharide (LPS). Accordingly, DCs showed low constitutive production of 1,25(OH)(2)D-3, but activation by LPS increased 1,25(OH)(2)D-3 synthesis. In addition, 25(OH)D-3-1alpha-hydroxylase expression was found in blood DCs but not in CD34(+)-derived DCs. Next we analyzed the functional consequences of these results. Addition of 1,25(OH)(2)D-3 at concentrations comparable with those produced by DCs inhibited the allostimulatory potential of DCs during the early phase of DC differentiation. However, terminal differentiation decreased the responsiveness of DCs to 1,25(OH)(2)D-3. In conclusion, DCs are able to produce 1,25(OH)(2)D-3 especially following stimulation with LIPS. Terminal maturation renders DCs unresponsive to the effects of 1,25(OH)(2)D-3, but those cells are able to suppress the differentiation of their own precursor cells in a paracrine way through the production of 1,25(OH)(2)D-3. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:3314 / 3316
页数:3
相关论文
共 50 条
[41]   Assessment of total and 'free' circulatory 25-hydroxyvitamin D and 1, 25-dihydroxyvitamin D3 status in men with osteoporosis. [J].
Al-Oanzi, ZH ;
Varanasi, SS ;
Tuck, SP ;
Francis, RM ;
Datta, HK .
JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 :S483-S483
[42]   Assessment of total and 'free' circulatory 25-hydroxyvitamin D and 1, 25-dihydroxyvitamin D3 status in men with osteoporosis. [J].
Al-Oanzi, ZH ;
Varanasi, SS ;
Tuck, SP ;
Francis, RM ;
Datta, HK .
JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 :S483-S483
[43]   Human keratinocyte line HaCaT metabolizes 1α-hydroxyvitamin D3 and vitamin D3 to 1α,25-dihydroxyvitamin D3 (calcitriol) [J].
Lehmann, B ;
Pietzsch, J ;
Kampf, A ;
Meurer, M .
JOURNAL OF DERMATOLOGICAL SCIENCE, 1998, 18 (02) :118-127
[44]   New A-ring analogs of the hormone 1α,25-dihydroxyvitamin D3: (2′-hydroxymethyl)tetrahydrofuro[1,2-a]-25-hydroxyvitamin D3 [J].
Jeon, Heung Bae ;
Posner, Gary H. .
TETRAHEDRON, 2009, 65 (07) :1235-1240
[45]   Expression of vitamin D receptor and 25-hydroxyvitamin D3-1α-hydroxylase in normal and malignant human colon [J].
Matusiak, D ;
Murillo, G ;
Carroll, RE ;
Mehta, RG ;
Benya, RV .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2005, 14 (10) :2370-2376
[46]   Pancreatic cancer cells express 25-hydroxyvitamin D-1α-hydroxylase and their proliferation is inhibited by the prohormone 25-hydroxyvitamin D3 [J].
Schwartz, GG ;
Eads, D ;
Rao, A ;
Cramer, SD ;
Willingham, MC ;
Chen, TC ;
Jamieson, DP ;
Wang, LL ;
Burnstein, KL ;
Holick, MF ;
Koumenis, C .
CARCINOGENESIS, 2004, 25 (06) :1015-1026
[47]   Calcitonin:: A major regulator of the 25-hydroxyvitamin D3-1α-hydroxylase gene. [J].
Zhong, Y. ;
Christakos, S. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 :S120-S120
[48]   The ontogeny of 25-hydroxyvitamin D3 1α-hydroxylase expression and decidua [J].
Zehnder, D ;
Evans, KN ;
Kilby, MD ;
Bulmer, JN ;
Innes, BA ;
Stewart, PM ;
Hewison, M .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (01) :105-114
[49]   Calcitonin, a Regulator of the 25-Hydroxyvitamin D3 1α-Hydroxylase Gene [J].
Zhong, Yan ;
Armbrecht, Harvey J. ;
Christakos, Sylvia .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (17) :11059-11069
[50]   Expression of 25 hydroxyvitamin D3-1α-hydroxylase in human endometrial tissue [J].
Becker, Steffi ;
Cordes, Tim ;
Diesing, Dagmar ;
Diedrich, Klaus ;
Friedrich, Michael .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2007, 103 (3-5) :771-775