磷酸转运蛋白的调控和磷酸代谢的新调节剂

Megumi Koike, Minori Uga, Yuji Shiozaki, K. Miyamoto, H. Segawa
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引用次数: 0

摘要

磷对所有生物都是必不可少的。它在维持生物功能方面发挥着重要作用,如能量代谢、细胞膜形成和骨矿化。肠道、肾脏和骨骼中的各种因素调节体内无机磷酸盐(Pi)浓度的稳态。X连锁低磷血症(XLH)是遗传性低磷血症性软骨病的最常见形式,其特征是骨基质矿化受损,软骨细胞肥大伴低磷血症,儿童期维生素D抵抗活跃。与X染色体上的内肽酶同源的磷酸调节基因被认为是XLH的责任基因。XLH被归类为成纤维细胞生长因子23(FGF23)相关的低磷血症性软骨病。增强的FGF23通过下调近端小管中的钠依赖性Pi协同转运蛋白NaPi2a和NaPi2c蛋白来刺激肾磷酸盐消耗。近年来,跨膜蛋白(Tmem)174已被鉴定为一种新型的磷酸盐转运蛋白调节因子。这篇综述介绍了Tmem174在体内Pi稳态中的作用。
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Regulation of Phosphate Transporters and Novel Regulator of Phosphate Metabolism
Phosphorus is essential for all living organisms. It plays an important role in maintaining biological functions, such as energy metabolism, cell membrane formation, and bone mineralization. Various factors in the intestine, kidneys, and bones regulate the homeostasis of the inorganic phosphate (Pi) concentration in the body. X-linked hypophosphatemia (XLH), the most common form of hereditary hypophosphatemic rickets, is characterized by an impaired mineralization of the bone matrix, hypertrophic chondrocytes with hypophosphatemia, and active vitamin D resistance in childhood. Phosphate-regulating gene with homologies to endopeptidases on the X chromosome was recognized as the responsible gene for XLH. XLH is classified as fibroblast growth factor 23 (FGF23)-related hypophosphatemic rickets. The enhanced FGF23 stimulates renal phosphate wasting by downregulating sodium-dependent Pi cotransporters, NaPi2a and NaPi2c proteins, in the proximal tubules. Recently, transmembrane protein (Tmem) 174 has been identified as a novel regulator of phosphate transporters. This review introduces the role of Tmem174 in the Pi homeostasis in the body.
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