Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 38
Filter
1.
Int J Mol Sci ; 24(15)2023 Jul 26.
Article in English | MEDLINE | ID: mdl-37569323

ABSTRACT

The early failure of glaucoma surgery is mainly caused by over-fibrosis at the subconjunctival space, causing obliteration of the filtration bleb. Because fibrosis has a suspected basis of genetic predisposition, we have undertaken a prospective study to identify upregulated profibrotic genes in a population of glaucoma patients with signs of conjunctival fibrosis and early postoperative surgical failure. Clinical data of re-operated fibrosis patients, hyperfibrosis patients who re-operated more than once in a short time, and control patients with no fibrosis were recorded and analyzed at each follow-up visit. Conjunctival-Tenon surgical specimens were obtained intraoperatively to evaluate the local expression of a panel of genes potentially associated with fibrosis. In order to correlate gene expression signatures with protein levels, we quantified secreted proteins in primary cultures of fibroblasts from patients. Expression of VEGFA, CXCL8, MYC, and CDKN1A was induced in the conjunctiva of hyperfibrosis patients. VEGFA and IL8 protein levels were also increased in fibroblast supernatants. We propose that an increase in these proteins could be useful in detecting conjunctival fibrosis in glaucoma patients undergoing filtering surgery. Molecular markers could be crucial for early detection of patients at high risk of failure of filtration surgery, leading to more optimal and personalized treatments.

2.
Front Pharmacol ; 12: 773871, 2021.
Article in English | MEDLINE | ID: mdl-34899333

ABSTRACT

Protons reaching the eyeball from exogenous acidic substances or released from damaged cells during inflammation, immune cells, after tissue injury or during chronic ophthalmic conditions, activate or modulate ion channels present in sensory nerve fibers that innervate the ocular anterior surface. Their identification as well as their role during disease is critical for the understanding of sensory ocular pathophysiology. They are likely to mediate some of the discomfort sensations accompanying several ophthalmic formulations and may represent novel targets for the development of new therapeutics for ocular pathologies. Among the ion channels expressed in trigeminal nociceptors innervating the anterior surface of the eye (cornea and conjunctiva) and annex ocular structures (eyelids), members of the TRP and ASIC families play a critical role in ocular acidic pain. Low pH (pH 6) activates TRPV1, a polymodal ion channel also activated by heat, capsaicin and hyperosmolar conditions. ASIC1, ASIC3 and heteromeric ASIC1/ASIC3 channels present in ocular nerve terminals are activated at pH 7.2-6.5, inducing pain by moderate acidifications of the ocular surface. These channels, together with TRPA1, are involved in acute ocular pain, as well as in painful sensations during allergic keratoconjunctivitis or other ophthalmic conditions, as blocking or reducing channel expression ameliorates ocular pain. TRPV1, TRPA1 and other ion channels are also present in corneal and conjunctival cells, promoting inflammation of the ocular surface after injury. In addition to the above-mentioned ion channels, members of the K2P and P2X ion channel families are also expressed in trigeminal neurons, however, their role in ocular pain remains unclear to date. In this report, these and other ion channels and receptors involved in acid sensing during ocular pathologies and pain are reviewed.

3.
Front Physiol ; 12: 691045, 2021.
Article in English | MEDLINE | ID: mdl-34658903

ABSTRACT

Volume-regulated anion channel (VRAC), constituted by leucine-rich repeat-containing 8 (LRRC8) heteromers, is crucial for volume homeostasis in vertebrate cells. This widely expressed channel has been associated with membrane potential modulation, proliferation, migration, apoptosis, and glutamate release. VRAC is activated by cell swelling and by low cytoplasmic ionic strength or intracellular guanosine 5'-O-(3-thiotriphosphate) (GTP-γS) in isotonic conditions. Despite the substantial number of studies that characterized the biophysical properties of VRAC, its mechanism of activation remains a mystery. Different evidence suggests a possible effect of caveolins in modulating VRAC activity: (1) Caveolin 1 (Cav1)-deficient cells display insignificant swelling-induced Cl- currents mediated by VRAC, which can be restored by Cav1 expression; (2) Caveolin 3 (Cav3) knockout mice display reduced VRAC currents; and (3) Interaction between LRRC8A, the essential subunit for VRAC, and Cav3 has been found in transfected human embryonic kidney 293 (HEK 293) cells. In this study, we demonstrate a physical interaction between endogenous LRRC8A and Cav1 proteins, that is enhanced by hypotonic stimulation, suggesting that this will increase the availability of the channel to Cav1. In addition, LRRC8A targets plasma membrane regions outside caveolae of HEK 293 cells where it associates with non-caveolar Cav1. We propose that a rise in cell membrane tension by hypotonicity would flatten caveolae, as described previously, increasing the amount of Cav1 outside of caveolar structures interacting with VRAC. Besides, the expression of Cav1 in HEK Cav1- cells increases VRAC current density without changing the main biophysical properties of the channel. The present study provides further evidence on the relevance of Cav1 on the activation of endothelial VRAC through a functional molecular interaction.

4.
Int J Mol Sci ; 21(15)2020 Jul 23.
Article in English | MEDLINE | ID: mdl-32717813

ABSTRACT

TRESK belongs to the K2P family of potassium channels, also known as background or leak potassium channels due to their biophysical properties and their role regulating membrane potential of cells. Several studies to date have highlighted the role of TRESK in regulating the excitability of specific subtypes of sensory neurons. These findings suggest TRESK could be involved in pain sensitivity. Here, we review the different evidence available that involves the channel in pain and sensory perception, from studies knocking out the channel or overexpressing it to identified mutations that link the channel to migraine pain. In addition, the therapeutic possibilities are discussed, as targeting the channel seems an interesting therapeutic approach to reduce nociceptor activation and to decrease pain.


Subject(s)
Membrane Potentials/genetics , Mutation , Nociception , Pain Management , Pain , Potassium Channels , Sensory Receptor Cells , Humans , Migraine Disorders/genetics , Migraine Disorders/metabolism , Migraine Disorders/pathology , Migraine Disorders/therapy , Pain/genetics , Pain/metabolism , Pain/pathology , Potassium Channels/genetics , Potassium Channels/metabolism , Sensory Receptor Cells/metabolism , Sensory Receptor Cells/pathology
5.
Sci Rep ; 10(1): 11443, 2020 Jul 07.
Article in English | MEDLINE | ID: mdl-32632252

ABSTRACT

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

6.
Sci Adv ; 6(14): eaay4472, 2020 04.
Article in English | MEDLINE | ID: mdl-32270035

ABSTRACT

The potassium channel Kv7.1 associates with the KCNE1 regulatory subunit to trigger cardiac I Ks currents. Although the Kv7.1/KCNE1 complex has received much attention, the subcellular compartment hosting the assembly is the subject of ongoing debate. Evidence suggests that the complex forms either earlier in the endoplasmic reticulum or directly at the plasma membrane. Kv7.1 and KCNE1 mutations, responsible for long QT syndromes, impair association and traffic, thereby altering I Ks currents. We found that Kv7.1 and KCNE1 do not assemble in the first stages of their biogenesis. Data support an unconventional secretory pathway for Kv7.1-KCNE1 that bypasses Golgi. This route targets channels to endoplasmic reticulum-plasma membrane junctions, where Kv7.1-KCNE1 assemble. This mechanism helps to resolve the ongoing controversy about the subcellular compartment hosting the association. Our results also provide new insights into I Ks channel localization at endoplasmic reticulum-plasma membrane junctions, highlighting an alternative anterograde trafficking mechanism for oligomeric ion channels.


Subject(s)
KCNQ1 Potassium Channel/metabolism , Multiprotein Complexes/metabolism , Potassium Channels, Voltage-Gated/metabolism , Biological Transport , Biomarkers , Fluorescent Antibody Technique , Genes, Reporter , Humans , Ion Channel Gating , Myocytes, Cardiac/metabolism , Protein Binding
7.
J Physiol ; 598(5): 1017-1038, 2020 03.
Article in English | MEDLINE | ID: mdl-31919847

ABSTRACT

KEY POINTS: TRESK background K+ channel is expressed in sensory neurons and acts as a brake to reduce neuronal activation. Deletion of the channel enhances the excitability of nociceptors. Skin nociceptive C-fibres show an enhanced activation by cold and mechanical stimulation in TRESK knockout animals. Channel deletion selectively enhances mechanical and cold sensitivity in mice, without altering sensitivity to heat. These results indicate that the channel regulates the excitability of specific neuronal subpopulations involved in mechanosensitivity and cold-sensing. ABSTRACT: Background potassium-permeable ion channels play a critical role in tuning the excitability of nociceptors, yet the precise role played by different subsets of channels is not fully understood. Decreases in TRESK (TWIK-related spinal cord K+ channel) expression/function enhance excitability of sensory neurons, but its role in somatosensory perception and nociception is poorly understood. Here, we used a TRESK knockout (KO) mouse to address these questions. We show that TRESK regulates the sensitivity of sensory neurons in a modality-specific manner, contributing to mechanical and cold sensitivity but without any effect on heat sensitivity. Nociceptive neurons isolated from TRESK KO mice show a decreased threshold for activation and skin nociceptive C-fibres show an enhanced activation by cold and mechanical stimulation that was also observed in behavioural tests in vivo. TRESK is also involved in osmotic pain and in early phases of formalin-induced inflammatory pain, but not in the development of mechanical and heat hyperalgesia during chronic pain. In contrast, mice lacking TRESK present cold allodynia that is not further enhanced by oxaliplatin. In summary, genetic removal of TRESK uncovers enhanced mechanical and cold sensitivity, indicating that the channel regulates the excitability of specific neuronal subpopulations involved in mechanosensitivity and cold-sensing, acting as a brake to prevent activation by innocuous stimuli.


Subject(s)
Nociceptors , Potassium Channels , Animals , Hyperalgesia/genetics , Mice , Nociception , Sensory Receptor Cells
8.
Sci Rep ; 9(1): 5392, 2019 04 01.
Article in English | MEDLINE | ID: mdl-30931966

ABSTRACT

Regulation of cellular volume is an essential process to balance volume changes during cell proliferation and migration or when intracellular osmolality increases due to transepithelial transport. We previously characterized the key role of volume-regulated anion channels (VRAC) in the modulation of the volume of trabecular meshwork (TM) cells and, in turn, the aqueous humour (AH) outflow from the eye. The balance between the secretion and the drainage of AH determines the intraocular pressure (IOP) that is the major casual risk factor for glaucoma. Glaucoma is an ocular disease that causes irreversible blindness due to the degeneration of retinal ganglion cells. The recent identification of Leucine-Rich Repeat-Containing 8 (LRRC8A-E) proteins as the molecular components of VRAC opens the field to elucidate their function in the physiology of TM and glaucoma. Human TM cells derived from non-glaucomatous donors and from open-angle glaucoma patients were used to determine the expression and the functional activity of LRRC8-mediated channels. Expression levels of LRRC8A-E subunits were decreased in HTM glaucomatous cells compared to normotensive HTM cells. Consequently, the activity of VRAC currents and volume regulation of TM cells were significantly affected. Impaired cell volume regulation will likely contribute to altered aqueous outflow and intraocular pressure.


Subject(s)
Glaucoma, Open-Angle/genetics , Membrane Proteins/genetics , Trabecular Meshwork/metabolism , Voltage-Dependent Anion Channels/genetics , Aged , Aqueous Humor/cytology , Aqueous Humor/metabolism , Aqueous Humor/physiology , Cell Line , Cell Size , Cells, Cultured , Female , Gene Expression Profiling/methods , Glaucoma, Open-Angle/metabolism , Glaucoma, Open-Angle/physiopathology , Humans , Intraocular Pressure/physiology , Male , Membrane Proteins/metabolism , Middle Aged , Protein Subunits/genetics , Protein Subunits/metabolism , Protein Subunits/physiology , Trabecular Meshwork/cytology , Voltage-Dependent Anion Channels/metabolism , Voltage-Dependent Anion Channels/physiology
9.
Cell Mol Life Sci ; 75(21): 4059-4075, 2018 Nov.
Article in English | MEDLINE | ID: mdl-29947924

ABSTRACT

The voltage-dependent potassium channel Kv1.3 participates in peripheral insulin sensitivity. Genetic ablation of Kv1.3 triggers resistance to diet-induced weight gain, thereby pointing to this protein as a pharmacological target for obesity and associated type II diabetes. However, this role is under intense debate because Kv1.3 expression in adipose tissue raises controversy. We demonstrated that Kv1.3 is expressed in white adipose tissue from humans and rodents. Moreover, other channels, such as Kv1.1, Kv1.2, Kv1.4 and especially Kv1.5, from the same Shaker family are also present. Although elevated insulin levels and adipogenesis remodel the Kv phenotype, which could lead to multiple heteromeric complexes, Kv1.3 markedly participates in the insulin-dependent regulation of glucose uptake in mature adipocytes. Adipocyte differentiation increased the expression of Kv1.3, which is targeted to caveolae by molecular interactions with caveolin 1. Using a caveolin 1-deficient 3T3-L1 adipocyte cell line, we demonstrated that the localization of Kv1.3 in caveolar raft structures is important for proper insulin signaling. Insulin-dependent phosphorylation of the channel occurs at the onset of insulin-mediated signaling. However, when Kv1.3 was spatially outside of these lipid microdomains, impaired phosphorylation was exhibited. Our data shed light on the putative role of Kv1.3 in weight gain and insulin-dependent responses contributing to knowledge about adipocyte physiology.


Subject(s)
Adipocytes/metabolism , Insulin/genetics , Kv1.3 Potassium Channel/genetics , Obesity/genetics , 3T3-L1 Cells , Adipogenesis/genetics , Adipose Tissue/metabolism , Adipose Tissue/pathology , Animals , Caveolae/metabolism , Caveolin 1/genetics , Caveolin 1/metabolism , Diabetes Mellitus, Type 2/genetics , Diabetes Mellitus, Type 2/metabolism , Diabetes Mellitus, Type 2/pathology , Gene Expression Regulation , Glucose/metabolism , Humans , Insulin/metabolism , Insulin Resistance/genetics , Kv1.3 Potassium Channel/metabolism , Mice , Muscle, Skeletal/metabolism , Muscle, Skeletal/pathology , Obesity/metabolism , Obesity/pathology
10.
Pain ; 159(1): 92-105, 2018 01.
Article in English | MEDLINE | ID: mdl-28937579

ABSTRACT

Pyrethroid insecticides are widely used for pest control in agriculture or in human public health commonly as a topical treatment for scabies and head lice. Exposure to pyrethroids such as permethrin or tetramethrin (TM) causes sensory alterations such as transient pain, burning, stinging sensations, and paraesthesias. Despite the well-known effects of pyrethroids on sodium channels, actions on other channels that control sensory neuron excitability are less studied. Given the role of 2-pore domain potassium (K2P) channels in modulating sensory neuron excitability and firing, both in physiological and pathological conditions, we examined the effect of pyrethroids on K2P channels mainly expressed in sensory neurons. Through electrophysiological and calcium imaging experiments, we show that a high percentage of TM-responding neurons were nociceptors, which were also activated by TRPA1 and/or TRPV1 agonists. This pyrethroid also activated and enhanced the excitability of peripheral saphenous nerve fibers. Pyrethroids produced a significant inhibition of native TRESK, TRAAK, TREK-1, and TREK-2 currents. Similar effects were found in transfected HEK293 cells. At the behavioral level, intradermal TM injection in the mouse paw produced nocifensive responses and caused mechanical allodynia, demonstrating that the effects seen on nociceptors in culture lead to pain-associated behaviors in vivo. In TRESK knockout mice, pain-associated behaviors elicited by TM were enhanced, providing further evidence for a role of this channel in preventing excessive neuronal activation. Our results indicate that inhibition of K2P channels facilitates sensory neuron activation and increases their excitability. These effects contribute to the generation of paraesthesias and pain after pyrethroid exposure.


Subject(s)
Insecticides/pharmacology , Potassium Channel Blockers/pharmacology , Potassium Channels, Tandem Pore Domain/antagonists & inhibitors , Pyrethrins/pharmacology , Sensory Receptor Cells/drug effects , Animals , Behavior, Animal/drug effects , HEK293 Cells , Humans , Mice , Nociceptors/drug effects
11.
FEM (Ed. impr.) ; 20(2): 75-78, mar.-abr. 2017. tab
Article in Spanish | IBECS | ID: ibc-161676

ABSTRACT

La adquisición de valores y actitudes es un aspecto esencial de los resultados del aprendizaje de los estudiantes de medicina junto con los conocimientos y las habilidades prácticas y forma parte de lo que se conoce como profesionalismo médico. El proceso de aprendizaje de un médico implica no sólo el desarrollo de conocimientos y habilidades, sino también un proceso de transformación del alumno en el transcurso del cual aprende a ser diferente y a ser capaz de integrarse en una comunidad profesional. Por ello, debe considerarse seriamente la formación de nuestros estudiantes en este campo. Esta formación debe ser un proceso continuo y desde los primeros momentos del Grado de Medicina. En el contexto de la reforma de Bolonia, la Facultad de Medicina de la Universitat de Barcelona y otras facultades de medicina españolas han definido sus resultados de aprendizaje. Entre ellos, figura que los estudiantes deben ser capaces de aplicar los valores profesionales de excelencia como altruismo, compromiso, responsabilidad, integridad y honestidad en la práctica médica. Sin embargo, esta temática no está suficientemente representada en las actividades de aprendizaje del plan de estudios. Por ello, hace seis años, decidimos implementar un curso introductorio sobre profesionalismo médico dirigido a estudiantes de primer curso de medicina. En este trabajo describimos nuestra experiencia durante esos años. Los resultados de esta experiencia indican que la introducción del profesionalismo desde momentos iniciales del Grado de Medicina es factible y altamente apreciado por los estudiantes


The acquisition of values and attitudes is an essential aspect of the learning outcomes of medical students together with knowledge and practical skills and they are part of what is known as medical professionalism. The learning process of a physician implies not only the development of knowledge and skills but also a transformational process of the learner, whereby he/she also learns to be different and to be able to join a professional community. Therefore we need to consider seriously the training of our students in this field. This training must be a continuous and on-going process throughout the entire educational continuum, beginning from early moments in medical school. In the context of the Bologna reform the Medical School of the University of Barcelona, and other Spanish medical schools, have defined their learning outcomes. Among them, the students must be able to apply the professional values of excellence, altruism, commitment, responsibility, integrity and honesty in medical practice, but this topic is insufficiently represented in the curriculum learning activities. Consequently six years ago, we decided to implement an introductory course on medical professionalism addressed to first year medical students. We describe our experience during the last six years of the implementation and development of this introductory course. Our results indicate that the introduction of professionalism from the earliest moments of the educative process in medical schools is feasible and is highly appreciated by our students


Subject(s)
Humans , Education, Medical/trends , Teaching/methods , Learning , Professional Competence , Educational Measurement/methods , Patient-Centered Care , Social Responsibility , Morals , Attitude of Health Personnel
12.
Sci Rep ; 7: 42395, 2017 02 10.
Article in English | MEDLINE | ID: mdl-28186199

ABSTRACT

The voltage-dependent potassium channel Kv1.3 plays essential physiological functions in the immune system. Kv1.3, regulating the membrane potential, facilitates downstream Ca2+ -dependent pathways and becomes concentrated in specific membrane microdomains that serve as signaling platforms. Increased and/or delocalized expression of the channel is observed at the onset of several autoimmune diseases. In this work, we show that adenosine (ADO), which is a potent endogenous modulator, stimulates PKC, thereby causing immunosuppression. PKC activation triggers down-regulation of Kv1.3 by inducing a clathrin-mediated endocytic event that targets the channel to lysosomal-degradative compartments. Therefore, the abundance of Kv1.3 at the cell surface decreases, which is clearly compatible with an effective anti-inflammatory response. This mechanism requires ubiquitination of Kv1.3, catalyzed by the E3 ubiquitin-ligase Nedd4-2. Postsynaptic density protein 95 (PSD-95), a member of the MAGUK family, recruits Kv1.3 into lipid-raft microdomains and protects the channel against ubiquitination and endocytosis. Therefore, the Kv1.3/PSD-95 association fine-tunes the anti-inflammatory response in leukocytes. Because Kv1.3 is a promising multi-therapeutic target against human pathologies, our results have physiological relevance. In addition, this work elucidates the ADO-dependent PKC-mediated molecular mechanism that triggers immunomodulation by targeting Kv1.3 in leukocytes.


Subject(s)
Endocytosis , Kv1.3 Potassium Channel/metabolism , Protein Kinase C/metabolism , Ubiquitination , Adenosine/pharmacology , Animals , Clathrin/metabolism , Dendritic Cells/drug effects , Dendritic Cells/metabolism , Disks Large Homolog 4 Protein/metabolism , Down-Regulation/drug effects , Endocytosis/drug effects , HEK293 Cells , Humans , Lipopolysaccharides/pharmacology , Lysosomes/drug effects , Lysosomes/metabolism , Macrophage Activation/drug effects , Membrane Microdomains/drug effects , Membrane Microdomains/metabolism , Mice , Nedd4 Ubiquitin Protein Ligases/metabolism , Protein Stability/drug effects , Rats , Tetradecanoylphorbol Acetate/pharmacology , Ubiquitination/drug effects
13.
Adv Protein Chem Struct Biol ; 104: 157-231, 2016.
Article in English | MEDLINE | ID: mdl-27038375

ABSTRACT

The eye is the sensory organ of vision. There, the retina transforms photons into electrical signals that are sent to higher brain areas to produce visual sensations. In the light path to the retina, different types of cells and tissues are involved in maintaining the transparency of avascular structures like the cornea or lens, while others, like the retinal pigment epithelium, have a critical role in the maintenance of photoreceptor function by regenerating the visual pigment. Here, we have reviewed the roles of different ion channels expressed in ocular tissues (cornea, conjunctiva and neurons innervating the ocular surface, lens, retina, retinal pigment epithelium, and the inflow and outflow systems of the aqueous humor) that are involved in ocular disease pathophysiologies and those whose deletion or pharmacological modulation leads to specific diseases of the eye. These include pathologies such as retinitis pigmentosa, macular degeneration, achromatopsia, glaucoma, cataracts, dry eye, or keratoconjunctivitis among others. Several disease-associated ion channels are potential targets for pharmacological intervention or other therapeutic approaches, thus highlighting the importance of these channels in ocular physiology and pathophysiology.


Subject(s)
Cyclic Nucleotide-Gated Cation Channels/genetics , Eye Diseases/genetics , Eye/metabolism , Retina/metabolism , Aqueous Humor/metabolism , Cornea/metabolism , Cornea/pathology , Cyclic Nucleotide-Gated Cation Channels/metabolism , Eye/innervation , Eye/pathology , Eye Diseases/metabolism , Eye Diseases/pathology , Humans , Lens, Crystalline/innervation , Lens, Crystalline/metabolism , Lens, Crystalline/pathology , Mutation , Retina/pathology , Retinal Pigment Epithelium/metabolism , Retinal Pigment Epithelium/pathology
14.
Sci Rep ; 6: 22453, 2016 Mar 02.
Article in English | MEDLINE | ID: mdl-26931497

ABSTRACT

The spatial localization of ion channels at the cell surface is crucial for their functional role. Many channels localize in lipid raft microdomains, which are enriched in cholesterol and sphingolipids. Caveolae, specific lipid rafts which concentrate caveolins, harbor signaling molecules and their targets becoming signaling platforms crucial in cell physiology. However, the molecular mechanisms involved in such spatial localization are under debate. Kv1.3 localizes in lipid rafts and participates in the immunological response. We sought to elucidate the mechanisms of Kv1.3 surface targeting, which govern leukocyte physiology. Kv1 channels share a putative caveolin-binding domain located at the intracellular N-terminal of the channel. This motif, lying close to the S1 transmembrane segment, is situated near the T1 tetramerization domain and the determinants involved in the Kvß subunit association. The highly hydrophobic domain (FQRQVWLLF) interacts with caveolin 1 targeting Kv1.3 to caveolar rafts. However, subtle variations of this cluster, putative ancillary associations and different structural conformations can impair the caveolin recognition, thereby altering channel's spatial localization. Our results identify a caveolin-binding domain in Kv1 channels and highlight the mechanisms that govern the regulation of channel surface localization during cellular processes.


Subject(s)
Caveolins/metabolism , Kv1.3 Potassium Channel/metabolism , Membrane Microdomains/metabolism , Amino Acid Sequence , Biopolymers/chemistry , Biopolymers/metabolism , HEK293 Cells , Humans , Hydrophobic and Hydrophilic Interactions , Kv1.3 Potassium Channel/chemistry , Membrane Microdomains/chemistry , Protein Binding
15.
Cell Mol Life Sci ; 73(7): 1515-28, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26542799

ABSTRACT

The potassium channel Kv1.3 plays roles in immunity, neuronal development and sensory discrimination. Regulation of Kv1.3 by kinase signaling has been studied. In this context, EGF binds to specific receptors (EGFR) and triggers tyrosine kinase-dependent signaling, which down-regulates Kv1.3 currents. We show that Kv1.3 undergoes EGF-dependent endocytosis. This EGF-mediated mechanism is relevant because is involved in adult neural stem cell fate determination. We demonstrated that changes in Kv1.3 subcellular distribution upon EGFR activation were due to Kv1.3 clathrin-dependent endocytosis, which targets the Kv1.3 channels to the lysosomal degradative pathway. Interestingly, our results further revealed that relevant tyrosines and other interacting motifs, such as PDZ and SH3 domains, were not involved in the EGF-dependent Kv1.3 internalization. However, a new, and yet undescribed mechanism, of ERK1/2-mediated threonine phosphorylation is crucial for the EGF-mediated Kv1.3 endocytosis. Our results demonstrate that EGF triggers the down-regulation of Kv1.3 activity and its expression at the cell surface, which is important for the development and migration of adult neural progenitors.


Subject(s)
Endocytosis/drug effects , Epidermal Growth Factor/pharmacology , Kv1.3 Potassium Channel/metabolism , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3/metabolism , Animals , Butadienes/pharmacology , Cells, Cultured , Clathrin/antagonists & inhibitors , Clathrin/genetics , Clathrin/metabolism , Down-Regulation/drug effects , Dynamin II/antagonists & inhibitors , Dynamin II/genetics , Dynamin II/metabolism , ErbB Receptors/genetics , ErbB Receptors/metabolism , HEK293 Cells , HeLa Cells , Humans , Kv1.3 Potassium Channel/genetics , Lateral Ventricles/cytology , Lateral Ventricles/metabolism , Mice , Mitogen-Activated Protein Kinase 1/antagonists & inhibitors , Mitogen-Activated Protein Kinase 3/antagonists & inhibitors , Neural Stem Cells/cytology , Neural Stem Cells/metabolism , Nitriles/pharmacology , Phosphorylation/drug effects , RNA Interference , Signal Transduction/drug effects
16.
Cardiovasc Res ; 107(4): 613-23, 2015 Sep 01.
Article in English | MEDLINE | ID: mdl-26168993

ABSTRACT

AIMS: KCNQ1 and KCNE1 encode Kv7.1 and KCNE1, respectively, the pore-forming and the accessory subunits of the slow delayed rectifier potassium current, IKs. KCNQ1 mutations are associated with long and short QT syndrome. The aim of this study was to characterize the biophysical and cellular phenotype of a KCNQ1 missense mutation, F279I, found in a 23-year-old man with a corrected QT interval (QTc) of 356 ms and a family history of sudden cardiac death. METHODS AND RESULTS: Experiments were performed using perforated patch-clamp, western blot, co-immunoprecipitation, biotinylation, and immunocytochemistry techniques in HEK293, COS7 cells and in cardiomyocytes transfected with WT Kv7.1/KCNE1 or F279I Kv7.1/KCNE1 channels. In the absence of KCNE1, F279I Kv7.1 current exhibited a lesser degree of inactivation than WT Kv7.1. Also, functional analysis of F279I Kv7.1 in the presence of KCNE1 revealed a negative shift in the activation curve and an acceleration of the activation kinetics leading to a gain of function in IKs. The co-assembly between F279I Kv7.1 channels and KCNE1 was markedly decreased compared with WT Kv7.1 channels, as revealed by co-immunoprecipitation and Föster Resonance Energy Transfer experiments. All these effects contribute to the increase of IKs when channels incorporate F279I Kv7.1 subunits, as shown by a computer model simulation of these data that predicts a shortening of the action potential (AP) consistent with the patient phenotype. CONCLUSION: The F279I mutation induces a gain of function of IKs due to an impaired gating modulation of Kv7.1 induced by KCNE1, leading to a shortening of the cardiac AP.


Subject(s)
KCNQ1 Potassium Channel/genetics , Mutation , Myocytes, Cardiac/metabolism , Potassium Channels, Voltage-Gated/genetics , Action Potentials , HEK293 Cells , Heart Diseases/genetics , Humans , Immunoprecipitation/methods , Mutation/genetics
17.
Cardiovasc Res ; 105(2): 223-32, 2015 Feb 01.
Article in English | MEDLINE | ID: mdl-25497550

ABSTRACT

AIMS: Polyunsaturated fatty n-3 acids (PUFAs) have been reported to exhibit antiarrhythmic properties. However, the mechanisms of action remain unclear. We studied the electrophysiological effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on IKs, and on the expression and location of Kv7.1 and KCNE1. METHODS AND RESULTS: Experiments were performed using patch-clamp, western blot, and sucrose gradient techniques in COS7 cells transfected with Kv7.1/KCNE1 channels. Acute perfusion with both PUFAs increased Kv7.1/KCNE1 current, this effect being greater for DHA than for EPA. Similar results were found in guinea pig cardiomyocytes. Acute perfusion of either PUFA slowed the activation kinetics and EPA shifted the activation curve to the left. Conversely, chronic EPA did not modify Kv7.1/KCNE1 current magnitude and shifted the activation curve to the right. Chronic PUFAs decreased the expression of Kv7.1, but not of KCNE1, and induced spatial redistribution of Kv7.1 over the cell membrane. Cholesterol depletion with methyl-ß-cyclodextrin increased Kv7.1/KCNE1 current magnitude. Under these conditions, acute EPA produced similar effects than those induced in non-cholesterol-depleted cells. A ventricular action potential computational model suggested antiarrhythmic efficacy of acute PUFA application under IKr block. CONCLUSIONS: We provide evidence that acute application of PUFAs increases Kv7.1/KCNE1 through a probably direct effect, and shows antiarrhythmic efficacy under IKr block. Conversely, chronic EPA application modifies the channel activity through a change in the Kv7.1/KCNE1 voltage-dependence, correlated with a redistribution of Kv7.1 over the cell membrane. This loss of function may be pro-arrhythmic. This shed light on the controversial effects of PUFAs regarding arrhythmias.


Subject(s)
Eicosapentaenoic Acid/pharmacology , Fatty Acids, Unsaturated/metabolism , Ion Channel Gating , Membrane Microdomains/metabolism , Potassium Channels, Voltage-Gated/metabolism , Action Potentials/drug effects , Animals , Anti-Arrhythmia Agents/pharmacology , COS Cells , Chlorocebus aethiops , Docosahexaenoic Acids/pharmacology , Humans , Ion Channel Gating/drug effects , Myocytes, Cardiac/drug effects , Myocytes, Cardiac/metabolism
18.
Biochim Biophys Acta ; 1848(10 Pt B): 2477-92, 2015 Oct.
Article in English | MEDLINE | ID: mdl-25517985

ABSTRACT

Potassium channels are a diverse group of pore-forming transmembrane proteins that selectively facilitate potassium flow through an electrochemical gradient. They participate in the control of the membrane potential and cell excitability in addition to different cell functions such as cell volume regulation, proliferation, cell migration, angiogenesis as well as apoptosis. Because these physiological processes are essential for the correct cell function, K+ channels have been associated with a growing number of diseases including cancer. In fact, different K+ channel families such as the voltage-gated K+ channels, the ether à-go-go K+ channels, the two pore domain K+ channels and the Ca2+-activated K+ channels have been associated to tumor biology. Potassium channels have a role in neoplastic cell-cycle progression and their expression has been found abnormal in many types of tumors and cancer cells. In addition, the expression and activity of specific K+ channels have shown a significant correlation with the tumor malignancy grade. The aim of this overview is to summarize published data on K+ channels that exhibit oncogenic properties and have been linked to a more malignant cancer phenotype. This article is part of a Special Issue entitled: Membrane channels and transporters in cancers.


Subject(s)
Gene Expression Regulation, Neoplastic , Neoplasms/metabolism , Potassium Channels, Calcium-Activated/metabolism , Potassium Channels, Tandem Pore Domain/metabolism , Potassium Channels, Voltage-Gated/metabolism , Potassium/metabolism , Apoptosis/drug effects , Cell Movement/drug effects , Cell Proliferation/drug effects , Cell Size/drug effects , Disease Progression , Humans , Membrane Potentials/drug effects , Neoplasms/blood supply , Neoplasms/drug therapy , Neoplasms/pathology , Neovascularization, Pathologic/prevention & control , Phenotype , Potassium Channel Blockers/therapeutic use , Potassium Channels, Calcium-Activated/antagonists & inhibitors , Potassium Channels, Calcium-Activated/genetics , Potassium Channels, Tandem Pore Domain/antagonists & inhibitors , Potassium Channels, Tandem Pore Domain/genetics , Potassium Channels, Voltage-Gated/antagonists & inhibitors , Potassium Channels, Voltage-Gated/genetics
19.
Arterioscler Thromb Vasc Biol ; 34(7): 1522-30, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24855057

ABSTRACT

OBJECTIVE: Voltage-dependent K(+) (Kv) channels from the Kv7 family are expressed in blood vessels and contribute to cardiovascular physiology. Although Kv7 channel blockers trigger muscle contractions, Kv7 activators act as vasorelaxants. Kv7.1 and Kv7.5 are expressed in many vessels. Kv7.1 is under intense investigation because Kv7.1 blockers fail to modulate smooth muscle reactivity. In this study, we analyzed whether Kv7.1 and Kv7.5 may form functional heterotetrameric channels increasing the channel diversity in vascular smooth muscles. APPROACH AND RESULTS: Kv7.1 and Kv7.5 currents elicited in arterial myocytes, oocyte, and mammalian expression systems suggest the formation of heterotetrameric complexes. Kv7.1/Kv7.5 heteromers, exhibiting different pharmacological characteristics, participate in the arterial tone. Kv7.1/Kv7.5 associations were confirmed by coimmunoprecipitation, fluorescence resonance energy transfer, and fluorescence recovery after photobleaching experiments. Kv7.1/Kv7.5 heterotetramers were highly retained at the endoplasmic reticulum. Studies in HEK-293 cells, heart, brain, and smooth and skeletal muscles demonstrated that the predominant presence of Kv7.5 stimulates release of Kv7.1/Kv7.5 oligomers out of lipid raft microdomains. Electrophysiological studies supported that KCNE1 and KCNE3 regulatory subunits further increased the channel diversity. Finally, the analysis of rat isolated myocytes and human blood vessels demonstrated that Kv7.1 and Kv7.5 exhibited a differential expression, which may lead to channel diversity. CONCLUSIONS: Kv7.1 and Kv7.5 form heterotetrameric channels increasing the diversity of structures which fine-tune blood vessel reactivity. Because the lipid raft localization of ion channels is crucial for cardiovascular physiology, Kv7.1/Kv7.5 heteromers provide efficient spatial and temporal regulation of smooth muscle function. Our results shed light on the debate about the contribution of Kv7 channels to vasoconstriction and hypertension.


Subject(s)
KCNQ Potassium Channels/metabolism , KCNQ1 Potassium Channel/metabolism , Muscle, Smooth, Vascular/metabolism , Myocytes, Smooth Muscle/metabolism , Potassium/metabolism , Animals , COS Cells , Chlorocebus aethiops , HEK293 Cells , Humans , KCNQ Potassium Channels/chemistry , KCNQ Potassium Channels/drug effects , KCNQ Potassium Channels/genetics , KCNQ1 Potassium Channel/chemistry , KCNQ1 Potassium Channel/drug effects , KCNQ1 Potassium Channel/genetics , Membrane Microdomains/metabolism , Membrane Potentials , Muscle, Smooth, Vascular/drug effects , Myocytes, Cardiac/metabolism , Myocytes, Smooth Muscle/drug effects , Protein Structure, Quaternary , Rats , Transfection , Xenopus
20.
Front Physiol ; 4: 283, 2013 Oct 10.
Article in English | MEDLINE | ID: mdl-24133455

ABSTRACT

Voltage-dependent K(+) channels (Kv) are involved in a number of physiological processes, including immunomodulation, cell volume regulation, apoptosis as well as differentiation. Some Kv channels participate in the proliferation and migration of normal and tumor cells, contributing to metastasis. Altered expression of Kv1.3 and Kv1.5 channels has been found in several types of tumors and cancer cells. In general, while the expression of Kv1.3 apparently exhibits no clear pattern, Kv1.5 is induced in many of the analyzed metastatic tissues. Interestingly, evidence indicates that Kv1.5 channel shows inversed correlation with malignancy in some gliomas and non-Hodgkin's lymphomas. However, Kv1.3 and Kv1.5 are similarly remodeled in some cancers. For instance, expression of Kv1.3 and Kv1.5 correlates with a certain grade of tumorigenicity in muscle sarcomas. Differential remodeling of Kv1.3 and Kv1.5 expression in human cancers may indicate their role in tumor growth and their importance as potential tumor markers. However, despite of this increasing body of information, which considers Kv1.3 and Kv1.5 as emerging tumoral markers, further research must be performed to reach any conclusion. In this review, we summarize what it has been lately documented about Kv1.3 and Kv1.5 channels in human cancer.

SELECTION OF CITATIONS
SEARCH DETAIL
...