Warning: Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Deprecated: str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525

Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
  English Wikipedia
Nephropedia Template TP (
Twit Text
DeepDyve Pubget Overpricing |   
lüll "Phosphatonins" and the regulation of phosphorus homeostasis Berndt TJ; Schiavi S; Kumar RAm J Physiol Renal Physiol 2005[Dec]; 289 (6): F1170-82Phosphate ions are critical for normal bone mineralization, and phosphate plays a vital role in a number of other biological processes such as signal transduction, nucleotide metabolism, and enzyme regulation. The study of rare disorders associated with renal phosphate wasting has resulted in the discovery of a number of proteins [fibroblast growth factor 23 (FGF-23), secreted frizzled related protein 4 (sFRP-4), matrix extracellular phosphoglycoprotein, and FGF 7 (FGF-7)] that decrease renal sodium-dependent phosphate transport in vivo and in vitro. The "phosphatonins," FGF-23 and sFRP-4, also inhibit the synthesis of 1alpha,25-dihydroxyvitamin D, leading to decreased intestinal phosphate absorption and further reduction in phosphate retention by the organism. In this review, we discuss the biological properties of these proteins, alterations in their concentrations in various clinical disorders, and their possible physiological role.|Adult[MESH]|Animals[MESH]|Bone Remodeling/physiology[MESH]|Extracellular Matrix Proteins/physiology[MESH]|Female[MESH]|Fibroblast Growth Factor 7/biosynthesis[MESH]|Fibroblast Growth Factor-23[MESH]|Fibroblast Growth Factors/physiology[MESH]|Glycoproteins/physiology[MESH]|Homeostasis/drug effects/*physiology[MESH]|Humans[MESH]|Hypophosphatemia, Familial/physiopathology[MESH]|Intercellular Signaling Peptides and Proteins/physiology[MESH]|Intestinal Absorption/physiology[MESH]|Kidney Failure, Chronic/physiopathology/therapy[MESH]|Kidney/physiology[MESH]|Male[MESH]|Membrane Proteins/physiology[MESH]|Mice[MESH]|Neoplasms/complications[MESH]|Osteomalacia/etiology/physiopathology[MESH]|Phosphoproteins/physiology[MESH]|Phosphorus/*metabolism[MESH] |