Regulation of C-terminal and intact FGF-23 by dietary phosphate in men and women

被引:358
作者
Burnett, Sherri-Ann M.
Gunawardene, Samantha C.
Bringhurst, F. Richard
Juppner, Harald
Lee, Hang
Finkelstein, Joel S.
机构
[1] Massachusetts Gen Hosp, Endocrine Unit, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Biostat, Boston, MA 02114 USA
关键词
fibroblast growth factor 23; phosphate; homeostasis; nutrition;
D O I
10.1359/JBMR.060507
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
FGF-23 is a novel regulator of phosphate metabolism. We studied the regulation of FGF-23 by dietary phosphate in 66 men and women using two assays. Dietary phosphate restriction decreased FGF-23 and loading increased FGF-23 significantly. An assay that measured intact FGF-23 showed the effects of dietary phosphate much more clearly than an assay that also measures presumed biologically inactive fragments. Dietary phosphate is a key regulator of circulating FGF-23; choice of assay is critical when studying FGF-23 physiology.
引用
收藏
页码:1187 / 1196
页数:10
相关论文
共 52 条
[31]   MEPE has the properties of an osteoblastic phosphatonin and minhibin [J].
Rowe, PSN ;
Kumagai, Y ;
Gutierrez, G ;
Garrett, IR ;
Blacher, R ;
Rosen, D ;
Cundy, J ;
Navvab, S ;
Chen, D ;
Drezner, MK ;
Quarles, LD ;
Mundy, GR .
BONE, 2004, 34 (02) :303-319
[32]   MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia [J].
Rowe, PSN ;
de Zoysa, PA ;
Dong, R ;
Wang, HR ;
White, KE ;
Econs, MJ ;
Oudet, CL .
GENOMICS, 2000, 67 (01) :54-68
[33]   Human fibroblast growth factor-23 mutants suppress Na+ -dependent phosphate co-transport activity and 1α,25-dihydroxyvitamin D3 production [J].
Saito, H ;
Kusano, K ;
Kinosaki, M ;
Ito, H ;
Hirata, M ;
Segawa, H ;
Miyamoto, K ;
Fukushima, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (04) :2206-2211
[34]   Circulating FGF-23 is regulated by 1α,25-dihydroxyvitamin D3 and phosphorus in vivo [J].
Saito, H ;
Maeda, A ;
Ohtomo, S ;
Hirata, M ;
Kusano, K ;
Kato, S ;
Ogata, E ;
Segawa, H ;
Miyamoto, K ;
Fukushima, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (04) :2543-2549
[35]   Effect of hydrolysis-resistant FGF23-R179Q on dietary phosphate regulation of the renal type-II Na/Pi transporter [J].
Segawa, H ;
Kawakami, E ;
Kaneko, I ;
Kuwahata, M ;
Ito, M ;
Kusano, K ;
Saito, H ;
Fukushima, N ;
Miyamoto, K .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2003, 446 (05) :585-592
[36]   Tumor-induced osteomalacia: Clinical and basic studies [J].
Shane, E ;
Parisien, M ;
Henderson, JE ;
Dempster, DW ;
Feldman, F ;
Hardy, MA ;
Tohme, JF ;
Karaplis, AC ;
Clemens, TL .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (09) :1502-1511
[37]   Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism [J].
Shimada, T ;
Kakitani, M ;
Yamazaki, Y ;
Hasegawa, H ;
Takeuchi, Y ;
Fujita, T ;
Fukumoto, S ;
Tomizuka, K ;
Yamashita, T .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (04) :561-568
[38]   FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa [J].
Shimada, T ;
Urakawa, I ;
Yamazaki, Y ;
Hasegawa, H ;
Hino, R ;
Yoneya, T ;
Takeuchi, Y ;
Fujita, T ;
Fukumoto, S ;
Yamashita, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 314 (02) :409-414
[39]   Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia [J].
Shimada, T ;
Mizutani, S ;
Muto, T ;
Yoneya, T ;
Hino, R ;
Takeda, S ;
Takeuchi, Y ;
Fujita, T ;
Fukumoto, S ;
Yamashita, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (11) :6500-6505
[40]   Mutant FGF-23 responsible for autosomal dominant hypophosphatemic, rickets is resistant to proteolytic cleavage and causes hypophosphatemia in vivo [J].
Shimada, T ;
Muto, T ;
Urakawa, I ;
Yoneya, T ;
Yamazaki, Y ;
Okawa, K ;
Takeuchi, Y ;
Fujita, T ;
Fukumoto, S ;
Yamashita, T .
ENDOCRINOLOGY, 2002, 143 (08) :3179-3182