Article
Electrogenic Kinetics of a Mammalian Intestinal Type IIb Na+/Pi Cotransporter
DOI:http://www.ncbi.nlm.nih.gov/pubmed/17342377
Source: OAI
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Article: Phosphatonins–a new perspective on mineral metabolism
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ABSTRACT: The recent five years were the most prolific in scientific publications related to one of the re-emerging theme of human physiology, namely phosphate homeostasis. Classically, the phosphate absorption and excretion were thought to be mediated only by the parathyroid hormone (PTH)/vitamin D endocrine axis. Presently, apart from this traditional well-known control and feedback-loop, newly uncovered factors intervene, fine tuning the complex physiological process of renal phosphate handling and bone mineralization. The discovery of phosphatonins and Klotho gene provided new insights into the pathogenesis of several hypophosphatemic or hyperphosphatemic diseases, such as tumor induced osteomalacia, X-linked hypophosphatemic rickets, autosomal dominant hypophosphatemic rickets, autosomal recessive hypophosphatemia and tumoral calcinosis. Fibroblast growth factor 23 (FGF-23), secreted frizzled-related protein 4 (sFRP-4), fibroblast growth factor 7 (FGF-7) and matrix extracellular phosphoglycoprotein (MEPE) have been shown to be major phosphaturic factors. Whether and in which manner these hormones participate to the developing of secondary hyperparathyroidism, bone remodeling, and renal fibrogenesis needs to be clarified in the future. We review the current literature describing the role and mode of action of this new hormone class.Maedica A Journal of Clinical Medicine. 01/2008; 3. -
Article: Regulation of phosphate homeostasis by the phosphatonins and other novel mediators.
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ABSTRACT: A variety of factors regulate the efficiency of phosphate absorption in the intestine and phosphate reabsorption in kidney. Apart from the well-known regulators of phosphate homeostasis, namely parathyroid hormone (PTH) and the vitamin D-endocrine system, a number of peptides collectively known as the "phosphatonins" have been recently identified as a result of the study of various diseases associated with hypophosphatemia. These factors, fibroblast growth factor 23 (FGF-23), secreted frizzled-related protein 4 (sFRP-4), fibroblast growth factor 7 (FGF-7) and matrix extracellular phosphoglycoprotein (MEPE), have been shown to play a role in the pathogenesis of various hypophosphatemic and hyperphosphatemic disorders, such as oncogenic osteomalacia, X-linked hypophosphatemic rickets, autosomal dominant hypophosphatemic rickets, autosomal recessive hypophosphatemia and tumoral calcinosis. Whether these factors are true hormones, in the sense that they are regulated by the intake of dietary phosphorus and the needs of the organism for higher or lower amounts of phosphorus, remains to be firmly established in humans. Additionally, new information demonstrates that the intestine "senses" luminal concentrations of phosphate and regulates the excretion of phosphate in the kidney by elaborating novel factors that alter renal phosphate reabsorption.Pediatric Nephrology 09/2008; 23(8):1203-10. · 2.52 Impact Factor
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Keywords
apparent affinity constant
charge distribution midpoint potential
curvilinear steady-state cotransport characteristic
divalent Pi
external Na(+)
flounder NaPi-IIb
immobilized pre-steady-state charge movements
membrane hyperpolarization
mouse NaPi-IIb
mouse small intestine
moveable charge
NaPi-IIb
Pi dose dependence
pre-steady-state charge movement
Pre-steady-state currents
steady state
steady-state Pi-induced current
strong dependence
voltage dependence
zebrafish NaPi-IIb2