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Mechanisms of ENaC regulation and clinical implications

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JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
卷 19, 期 10, 页码 1845-1854

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AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2008020225

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资金

  1. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK075048, K08DK071648] Funding Source: NIH RePORTER
  2. NIDDK NIH HHS [R01 DK075048-02, R01 DK075048-01A1, R01 DK075048, K08 DK071648] Funding Source: Medline

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The epithelial Na+ channel (ENaC) transports Na+ across tight epithelia, including the distal nephron. Different paradigms of ENaC regulation include extrinsic and intrinsic factors that affect the expression, single-channel properties, and intracellular trafficking of the channel. In particular, recent discoveries highlight new findings regarding proteolytic processing, ubiquitination, and recycling of the channel. Understanding the regulation of this channel is critical to the understanding of various clinical phenomena, including normal physiology and several diseases of kidney and lung epithelia, such as blood pressure (BP) control, edema, and airway fluid clearance. Significant progress has been achieved in this active field of research. Although ENaC is classically thought to be a mediator of BP and volume status through Na+ reabsorption in the distal nephron, several studies in animal models highlight important roles for ENaC in lung pathophysiology, including in cystic fibrosis. The purpose of this review is to highlight the various modes and mechanisms of ENaC regulation, with a focus on more recent studies and their clinical implications.

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