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瞬时受体电位香草酸亚型6和7通道、镁转运与血管生物学:对高血压的影响

Transient receptor potential melastatin 6 and 7 channels, magnesium transport, and vascular biology: implications in hypertension.

作者信息

Touyz Rhian M

机构信息

Kidney Research Center, Ottawa Heallth Research Institute, University of Ottawa, Ottawa, Ontario, Canada K1H 8M5.

出版信息

Am J Physiol Heart Circ Physiol. 2008 Mar;294(3):H1103-18. doi: 10.1152/ajpheart.00903.2007. Epub 2008 Jan 11.

Abstract

Magnesium, an essential intracellular cation, is critically involved in many biochemical reactions involved in the regulation of vascular tone and integrity. Decreased magnesium concentration has been implicated in altered vascular reactivity, endothelial dysfunction, vascular inflammation, and structural remodeling, processes important in vascular changes and target organ damage associated with hypertension. Until recently, very little was known about mechanisms regulating cellular magnesium homeostasis, and processes controlling transmembrane magnesium transport had been demonstrated only at the functional level. Two cation channels of the transient receptor potential melastatin (TRPM) cation channel family have now been identified as magnesium transporters, TRPM6 and TRPM7. These unique proteins, termed chanzymes because they possess a channel and a kinase domain, are differentially expressed, with TRPM6 being found primarily in epithelial cells and TRPM7 occurring ubiquitously. Vascular TRPM7 is modulated by vasoactive agents, pressure, stretch, and osmotic changes and may be a novel mechanotransducer. In addition to its magnesium transporter function, TRPM7 has been implicated as a signaling kinase involved in vascular smooth muscle cell growth, apoptosis, adhesion, contraction, cytoskeletal organization, and migration, important processes involved in vascular remodeling associated with hypertension and other vascular diseases. Emerging evidence suggests that vascular TRPM7 function may be altered in hypertension. This review discusses the importance of magnesium in vascular biology and implications in hypertension and highlights the transport systems, particularly TRPM6 and TRPM7, which may play a role in the control of vascular magnesium homeostasis. Since the recent identification and characterization of Mg2+-selective transporters, there has been enormous interest in the field. However, there is still a paucity of information, and much research is needed to clarify the exact mechanisms of magnesium regulation in the cardiovascular system and the implications of aberrant transmembrane magnesium transport in the pathogenesis of hypertension and other vascular diseases.

摘要

镁是一种必需的细胞内阳离子,在许多参与血管张力和完整性调节的生化反应中起着关键作用。镁浓度降低与血管反应性改变、内皮功能障碍、血管炎症和结构重塑有关,这些过程在与高血压相关的血管变化和靶器官损伤中很重要。直到最近,人们对调节细胞镁稳态的机制知之甚少,控制跨膜镁转运的过程仅在功能水平上得到证实。瞬时受体电位褪黑素(TRPM)阳离子通道家族的两个阳离子通道现已被确定为镁转运体,即TRPM6和TRPM7。这些独特的蛋白质被称为通道酶,因为它们具有一个通道和一个激酶结构域,它们的表达存在差异,TRPM6主要在上皮细胞中发现,而TRPM7普遍存在。血管TRPM7受血管活性物质、压力、牵张和渗透压变化的调节,可能是一种新型的机械转导器。除了其镁转运功能外,TRPM7还被认为是一种信号激酶,参与血管平滑肌细胞的生长、凋亡、粘附、收缩、细胞骨架组织和迁移,这些都是与高血压和其他血管疾病相关的血管重塑中的重要过程。新出现的证据表明,高血压患者血管TRPM7的功能可能会发生改变。本综述讨论了镁在血管生物学中的重要性及其在高血压中的意义,并强调了可能在控制血管镁稳态中起作用的转运系统,特别是TRPM6和TRPM7。自从最近对Mg2+选择性转运体进行鉴定和表征以来,该领域引起了极大的兴趣。然而,仍然缺乏信息,需要进行大量研究来阐明心血管系统中镁调节的确切机制以及异常跨膜镁转运在高血压和其他血管疾病发病机制中的意义。

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