Phosphate toxicity: new insights into an old problem

被引:191
作者
Razzaque, M. Shawkat [1 ]
机构
[1] Harvard Univ, Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA 02115 USA
关键词
calcium; fibroblast growth factor 23 (FGF23); klotho; parathyroid hormone (PTH); sodium-dependent phosphate transporter; vitamin D; FIBROBLAST-GROWTH-FACTOR; SOFT-TISSUE CALCIFICATION; KLOTHO MUTANT MICE; VITAMIN-D; INORGANIC-PHOSPHATE; SEVERE HYPERPHOSPHATEMIA; BONE MINERALIZATION; TUMORAL CALCINOSIS; MISSENSE MUTATION; GENETIC-EVIDENCE;
D O I
10.1042/CS20100377
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Phosphorus is an essential nutrient required for critical biological reactions that maintain the normal homoeostatic control of the cell. This element is an important component of different cellular structures, including nucleic acids and cell membranes. Adequate phosphorus balance is vital for maintaining basic cellular functions, ranging from energy metabolism to cell signalling. In addition, many intracellular pathways utilize phosphate ions for important cellular reactions; therefore, homoeostatic control of phosphate is one of the most delicate biological regulations. Impaired phosphorus balance can affect the functionality of almost every human system, including musculoskeletal and cardiovascular systems, ultimately leading to an increase in morbidity and mortality of the affected patients. Human and experimental studies have found that delicate balance among circulating factors, like vitamin D, PTH (parathyroid hormone) and FGF23 (fibroblast growth factor 23), are essential for regulation of physiological phosphate balance. Dysregulation of these factors, either alone or in combination, can induce phosphorus imbalance. Recent studies have shown that suppression of the FGF23-klotho system can lead to hyperphosphataennia with extensive tissue damage caused by phosphate toxicity. The cause and consequences of phosphate toxicity will be briefly summarized in the present review.
引用
收藏
页码:91 / 97
页数:7
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