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本文引用的文献

1
Effects of the EGFR Inhibitor Erlotinib on Magnesium Handling.表皮生长因子受体抑制剂厄洛替尼对镁代谢的影响。
J Am Soc Nephrol. 2010 Aug;21(8):1309-16. doi: 10.1681/ASN.2009111153. Epub 2010 Jul 1.
2
Testosterone increases urinary calcium excretion and inhibits expression of renal calcium transport proteins.睾酮可增加尿钙排泄并抑制肾脏钙转运蛋白的表达。
Kidney Int. 2010 Apr;77(7):601-8. doi: 10.1038/ki.2009.522. Epub 2010 Jan 20.
3
Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.遗传性肾小管转运障碍:对肾脏处理钙和镁的影响。
Clin Sci (Lond). 2009 Sep 28;118(1):1-18. doi: 10.1042/CS20090086.
4
Klotho prevents renal calcium loss.α-klotho蛋白可防止肾脏钙流失。
J Am Soc Nephrol. 2009 Nov;20(11):2371-9. doi: 10.1681/ASN.2008121273. Epub 2009 Aug 27.
5
Parathyroid hormone activates TRPV5 via PKA-dependent phosphorylation.甲状旁腺激素通过依赖蛋白激酶A的磷酸化作用激活瞬时受体电位阳离子通道亚家族V成员5(TRPV5)。
J Am Soc Nephrol. 2009 Aug;20(8):1693-704. doi: 10.1681/ASN.2008080873. Epub 2009 May 7.
6
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.癫痫、共济失调、感音神经性耳聋、肾小管病以及KCNJ10基因突变。
N Engl J Med. 2009 May 7;360(19):1960-70. doi: 10.1056/NEJMoa0810276.
7
HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.肝细胞核因子1β(HNF1B)突变与低镁血症及肾性镁流失相关。
J Am Soc Nephrol. 2009 May;20(5):1123-31. doi: 10.1681/ASN.2008060633. Epub 2009 Apr 23.
8
A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia.电压门控钾通道编码基因KCNA1中的错义突变与人类常染色体显性低镁血症有关。
J Clin Invest. 2009 Apr;119(4):936-42. doi: 10.1172/JCI36948. Epub 2009 Mar 23.
9
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.由KCNJ10基因突变引起的癫痫、感音神经性耳聋、共济失调、智力发育迟缓及电解质失衡(SeSAME综合征)。
Proc Natl Acad Sci U S A. 2009 Apr 7;106(14):5842-7. doi: 10.1073/pnas.0901749106. Epub 2009 Mar 16.
10
Active Ca(2+) reabsorption in the connecting tubule.连接小管中的主动钙(Ca²⁺)重吸收。
Pflugers Arch. 2009 May;458(1):99-109. doi: 10.1007/s00424-008-0602-6. Epub 2008 Nov 7.

上皮细胞 Ca2+和 Mg2+转运的分子基础:TRP 通道家族的研究进展。

Molecular basis of epithelial Ca2+ and Mg2+ transport: insights from the TRP channel family.

机构信息

Department of Physiology, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, the Netherlands.

出版信息

J Physiol. 2011 Apr 1;589(Pt 7):1535-42. doi: 10.1113/jphysiol.2010.199869. Epub 2010 Nov 1.

DOI:10.1113/jphysiol.2010.199869
PMID:21041532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3099013/
Abstract

Maintenance of plasma Ca(2+) and Mg(2+) levels is of vital importance for many physiological functions. This is achieved via a coordinated interplay between the intestine, bone and kidney by amending the rate of absorption, storage and excretion, respectively. Discovery of the transient receptor potential (TRP) family identified several new ion channels acting as gatekeepers of Ca(2+) and Mg(2+) transport in these epithelia, greatly increasing our understanding of the molecular processes that facilitate the movement of these minerals. In the intestine, TRP channels contribute to the saturable active transcellular movement of divalent cations from the lumen into the enterocyte. Furthermore, in bone, TRPV channels play important roles by influencing the osteoclastic resorption process, thereby contributing importantly to overall bone mineral content. The divalent cation-permeable TRPV5 and TRPM6 channels are located in the renal distal convolution, the main site of active transcellular Ca(2+) and Mg(2+) transport. The channels are regulated by a multitude of factors and hormones that contribute importantly to keeping the systemic concentrations of Ca(2+) and Mg(2+) within normal limits. Dysregulation of either channel impacts the renal reabsorptive capacity for these cations. This review summarizes the current knowledge related to TRP channels in epithelial Ca(2+) and Mg(2+) transport.

摘要

维持血浆 Ca(2+) 和 Mg(2+) 水平对于许多生理功能至关重要。这是通过肠道、骨骼和肾脏之间的协调相互作用来实现的,分别通过调整吸收、储存和排泄的速度来实现。瞬时受体电位 (TRP) 家族的发现确定了几个新的离子通道,作为这些上皮细胞中 Ca(2+) 和 Mg(2+) 转运的门控,极大地增加了我们对促进这些矿物质运动的分子过程的理解。在肠道中,TRP 通道有助于从腔内向肠细胞中饱和主动转运二价阳离子。此外,在骨骼中,TRPV 通道通过影响破骨细胞的吸收过程发挥重要作用,从而对整体骨矿物质含量有重要贡献。可渗透二价阳离子的 TRPV5 和 TRPM6 通道位于肾脏远曲小管,是主动跨细胞 Ca(2+) 和 Mg(2+) 转运的主要部位。这些通道受多种因素和激素的调节,对维持 Ca(2+) 和 Mg(2+) 的系统浓度在正常范围内起着重要作用。这些通道的失调会影响肾脏对这些阳离子的重吸收能力。本综述总结了与上皮细胞中 Ca(2+) 和 Mg(2+) 转运相关的 TRP 通道的最新知识。