Literature DB >> 18045170

Functional domains of aquaporin-1: keys to physiology, and targets for drug discovery.

Andrea J Yool1.   

Abstract

Aquaporins (AQPs) are expressed in physiologically essential tissues and organs in which edema and fluid imbalances are of major concern. Potential roles in brain water homeostasis and edema, angiogenesis, cell migration, development, neuropathological diseases, and cancer suggest that this family of membrane proteins is an attractive set of novel drug targets. A problem in pursuing therapeutic and basic research strategies for dissecting contributions of AQPs to cell and tissue functions is that little is known regarding the pharmacology of AQP channels; currently defined agents such as tetraethylammonium and phloretin as blockers for aquaporins suffer from a lack of specificity and potency. Subtypes of AQPs modulated by signaling pathways could enable discrete localized control of fluid homeostasis, volume and morphology in cells and intracellular organelles, and might be found to participate in many different aspects of physiology, such as the control of paracellular permeability, process extension, growth, migration, and other responses involving changes in cell shape or surface to volume ratios. Recognizing that AQP1 is a water channel and, under permissive conditions, also a cGMP-gated cation channel, evidence in various tissues for a coupling of the cGMP signaling cascade to a physiological outcome that might involve AQP1 dual ion-and-water channel functions is of interest. Groundbreaking advances in defining aquaporin gating mechanisms suggest conformational changes are important elements in regulation and gating across classes of aquaporins. With a rapidly expanding knowledge of aquaporin structure and functional regulation, new avenues for manipulation of aquaporin channels are likely to be discovered. In parallel, a discovery for novel compounds with specificity and potency for aquaporins is a compelling goal. The need for pharmacological agents to dissect the roles of aquaporins in physiological and pathological processes is a clear call for further research in the field.

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Year:  2007        PMID: 18045170     DOI: 10.2174/138161207782341349

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  22 in total

1.  Ion channels in volume regulation of clonal kidney cells.

Authors:  M B da Silva; V M A Costa; V R A Pereira; G J B de Albertim; E B B de Melo; D P Bezerra; R P da Silva; C G Rodrigues; C M M Carneiro; L N Yuldasheva; O V Krasilnikov
Journal:  Cell Prolif       Date:  2010-12       Impact factor: 6.831

2.  Stimulation of aquaporin-mediated fluid transport by cyclic GMP in human retinal pigment epithelium in vitro.

Authors:  Nicholas W Baetz; W Daniel Stamer; Andrea J Yool
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-04-24       Impact factor: 4.799

3.  The over-expression of aquaporin-1 alters erythroid gene expression in human erythroleukemia K562 cells.

Authors:  Min Wei; Rong Shi; Jun Zeng; Nisha Wang; Jueyu Zhou; Wenli Ma
Journal:  Tumour Biol       Date:  2014-09-25

4.  Aquaporin-1 facilitates angiogenic invasion in the pathological neovasculature that accompanies cirrhosis.

Authors:  Robert C Huebert; Meher M Vasdev; Uday Shergill; Amitava Das; Bing Q Huang; Michael R Charlton; Nicholas F LaRusso; Vijay H Shah
Journal:  Hepatology       Date:  2010-07       Impact factor: 17.425

Review 5.  Structure, function and translational relevance of aquaporin dual water and ion channels.

Authors:  Andrea J Yool; Ewan M Campbell
Journal:  Mol Aspects Med       Date:  2012-02-11

6.  Bumetanide Derivatives AqB007 and AqB011 Selectively Block the Aquaporin-1 Ion Channel Conductance and Slow Cancer Cell Migration.

Authors:  Mohamad Kourghi; Jinxin V Pei; Michael L De Ieso; Gary Flynn; Andrea J Yool
Journal:  Mol Pharmacol       Date:  2015-10-14       Impact factor: 4.436

7.  Aquaporin-1 promotes angiogenesis, fibrosis, and portal hypertension through mechanisms dependent on osmotically sensitive microRNAs.

Authors:  Robert C Huebert; Kumaravelu Jagavelu; Helen I Hendrickson; Meher M Vasdev; Juan P Arab; Patrick L Splinter; Christy E Trussoni; Nicholas F Larusso; Vijay H Shah
Journal:  Am J Pathol       Date:  2011-08-18       Impact factor: 4.307

8.  Role of bone marrow-derived mesenchymal stem cells on the parotid glands of streptozotocin induced diabetes rats.

Authors:  Mona Denewar; Laila E Amin
Journal:  J Oral Biol Craniofac Res       Date:  2020-02-08

9.  Yeast-expressed human membrane protein aquaporin-1 yields excellent resolution of solid-state MAS NMR spectra.

Authors:  Sanaz Emami; Ying Fan; Rachel Munro; Vladimir Ladizhansky; Leonid S Brown
Journal:  J Biomol NMR       Date:  2013-01-24       Impact factor: 2.835

10.  Inhibition of aquaporin-1 and aquaporin-4 water permeability by a derivative of the loop diuretic bumetanide acting at an internal pore-occluding binding site.

Authors:  Elton Migliati; Nathalie Meurice; Pascale DuBois; Jennifer S Fang; Suma Somasekharan; Elizabeth Beckett; Gary Flynn; Andrea J Yool
Journal:  Mol Pharmacol       Date:  2009-04-29       Impact factor: 4.436

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