Changes in peripheral HCN2 channels during persistent inflammation.

Abstract:

:Nociceptor sensitization following nerve injury or inflammation leads to chronic pain. An increase in the nociceptor hyperpolarization-activated current, Ih, is observed in many models of pathological pain. Pharmacological blockade of Ih prevents the mechanical and thermal hypersensitivity that occurs during pathological pain. Alterations in the Hyperpolarization-activated Cyclic Nucleotide-gated ion channel 2 (HCN2) mediate Ih-dependent thermal and mechanical hyperalgesia. Limited knowledge exists regarding the nature of these changes during chronic inflammatory pain. Modifications in HCN2 expression and post-translational SUMOylation have been observed in the Complete Freund's Adjuvant (CFA) model of chronic inflammatory pain. Intra-plantar injection of CFA into the rat hindpaw induces unilateral hyperalgesia that is sustained for up to 14 days following injection. The hindpaw is innervated by primary afferents in lumbar DRG, L4-6. Adjustments in HCN2 expression and SUMOylation have been well-documented for L5 DRG during the first 7 days of CFA-induced inflammation. Here, we examine bilateral L4 and L6 DRG at day 1 and day 3 post-CFA. Using L4 and L6 DRG cryosections, HCN2 expression and SUMOylation were measured with immunohistochemistry and proximity ligation assays, respectively. Our findings indicate that intra-plantar injection of CFA elicited a bilateral increase in HCN2 expression in L4 and L6 DRG at day 1, but not day 3, and enhanced HCN2 SUMOylation in ipsilateral L6 DRG at day 1 and day 3. Changes in HCN2 expression and SUMOylation were transient over this time course. Our study suggests that HCN2 is regulated by multiple mechanisms during CFA-induced inflammation.

journal_name

Channels (Austin)

journal_title

Channels (Austin, Tex.)

authors

Jansen LR,Forster LA,Smith XL,Rubaharan M,Murphy AZ,Baro DJ

doi

10.1080/19336950.2020.1870086

keywords:

["CFA","DRG","HCN2","SUMO","inflammation"]

subject

Has Abstract

pub_date

2021-12-01 00:00:00

pages

165-179

issue

1

eissn

1933-6950

issn

1933-6969

journal_volume

15

pub_type

杂志文章

相关文献

文献大全
  • Potassium channel gating in the absence of the highly conserved glycine of the inner transmembrane helix.

    abstract::Potassium channel activation regulates cellular excitability, such as in neuronal and cardiac cells. Regulation of ion channel activity relies on a switching mechanism between two major conformations, the open and closed states, known as gating. It has been suggested that potassium channels are generally gated via a p...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.4475

    authors: Rosenhouse-Dantsker A,Logothetis DE

    更新日期:2007-05-01 00:00:00

  • Control of pH and PIP2 gating in heteromeric Kir4.1/Kir5.1 channels by H-Bonding at the helix-bundle crossing.

    abstract::Inhibition by intracellular H(+) (pH gating) and activation by phosphoinositides such as PIP(2) (PIP(2)-gating) are key regulatory mechanisms in the physiology of inwardly-rectifying potassium (Kir) channels. Our recent findings suggest that PIP(2) gating and pH gating are controlled by an intra-subunit H-bond at the ...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.5176

    authors: Rapedius M,Paynter JJ,Fowler PW,Shang L,Sansom MS,Tucker SJ,Baukrowitz T

    更新日期:2007-09-01 00:00:00

  • Differences between ion binding to eag and HERG voltage sensors contribute to differential regulation of activation and deactivation gating.

    abstract::HERG (KCNH2) and ether-à-go-go (eag) (KCNH1) are members of the same subfamily of voltage-gated K+ channels. In eag, voltage-dependent activation is significantly slowed by extracellular divalent cations. To exert this effect, ions bind to a site located between transmembrane segments S2 and S3 in the voltage sensor d...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.1.6.5760

    authors: Lin MC,Papazian DM

    更新日期:2007-11-01 00:00:00

  • Random assembly of SUR subunits in K(ATP) channel complexes.

    abstract::Sulfonylurea receptors (SURs) associate with Kir6.x subunits to form tetradimeric K(ATP) channel complexes. SUR1 and SUR2 confer differential channel sensitivities to nucleotides and pharmacological agents, and are expressed in specific, but overlapping, tissues. This raises the question of whether these different SUR...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.2.1.6046

    authors: Cheng WW,Tong A,Flagg TP,Nichols CG

    更新日期:2008-01-01 00:00:00

  • Modulation of neuronal voltage-activated calcium and sodium channels by polyamines and pH.

    abstract::The endogenous polyamines spermine, spermidine and putrescine are present at high concentrations inside neurons and can be released into the extracellular space where they have been shown to modulate ion channels. Here, we have examined polyamine modulation of voltage-activated Ca(2+) channels (VACCs) and voltage-acti...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.4988

    authors: Chen W,Harnett MT,Smith SM

    更新日期:2007-07-01 00:00:00

  • Molecular determinants of sensitivity and conductivity of human TRPM7 to Mg2+ and Ca2+.

    abstract::It is known that extracellular Mg(2+) and Ca(2+) can permeate TRPM7 and at the same time block the permeation by monovalent cations. In the present study, we examined the molecular basis for the conductivity and sensitivity of human TRPM7 to these divalent cations. Extracellular acidification to pH 4.0 markedly reduce...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.2.4.6695

    authors: Numata T,Okada Y

    更新日期:2008-07-01 00:00:00

  • TRPC3/6/7: Topical aspects of biophysics and pathophysiology.

    abstract::Nonselective and lipid-regulated cation channels formed by TRPC3, TRPC6 and TRPC7 have recently obtained attention in view their potential pathophysiological impact. It appears as a particular challenge to understand the molecular basis of TRPC3/6/7-related diseases in order to further delineate their value as therape...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章,评审

    doi:10.4161/chan.2.2.6015

    authors: Eder P,Groschner K

    更新日期:2008-03-01 00:00:00

  • Connexin and pannexin hemichannels of neurons and astrocytes.

    abstract::Hemichannels are large pore ion channels that in the traditional view are formed when half a gap connexin junction opens to the extracellular space. It is now evident that other ion channel families, including the newly discovered pannexin family can form channels with all the nascent properties of hemichannels. This ...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章,评审

    doi:10.4161/chan.2.2.6003

    authors: Thompson RJ,Macvicar BA

    更新日期:2008-03-01 00:00:00

  • The role of 14-3-3 dimerization in its modulation of the CaV2.2 channel.

    abstract::Voltage-dependent inactivation is an important property of voltage-gated calcium channels. Recently, we have reported that 14-3-3 proteins profoundly reduce inactivation of the Ca(V)2.2 channel at both open- and closed-states. Using a combination of molecular, biochemical and electrophysiological approaches, we have s...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章,评审

    doi:

    authors: Li Y,Wu Y,Li R,Zhou Y

    更新日期:2007-01-01 00:00:00

  • Distribution of the AQP4 water channel in normal human tissues: protein and tissue microarrays reveal expression in several new anatomical locations, including the prostate gland and seminal vesicles.

    abstract::Aquaporins facilitate osmotically driven water movement across cell membranes. Aquaporin 4 (AQP4) is a major water channel in the central nervous system where it participates in cerebral water balance. AQP4 is also present in basolateral membranes of lower respiratory tract airway and renal collecting duct epithelial ...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:

    authors: Mobasheri A,Marples D,Young IS,Floyd RV,Moskaluk CA,Frigeri A

    更新日期:2007-01-01 00:00:00

  • Mitsugumin 53-mediated maintenance of K+ currents in cardiac myocytes.

    abstract::Mitsugumin 53 (MG53) is a muscle-specific RBCC/TRIM family member predominantly localized on small vesicles underneath the plasma membrane. Upon cell-surface lesion MG53 recruits the vesicles to the repair site in an oxidation-dependent manner and MG53-knockout mice develop progressive myopathy associated with defecti...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.3.1.7571

    authors: Masumiya H,Asaumi Y,Nishi M,Minamisawa S,Adachi-Akahane S,Yoshida M,Kangawa K,Ito K,Kagaya Y,Yanagisawa T,Yamazaki T,Ma J,Takeshima H

    更新日期:2009-01-01 00:00:00

  • Phasic and tonic modes of depolarization-exocytosis coupling in beta-cells of porcine islets of Langerhans.

    abstract::In response to depolarizations that open voltage dependent Ca2+ channels single porcine beta-cells display heterogeneous time courses of exocytosis. Some cells display phasic exocytosis that is triggered by individual or short burst of action potentials typically characteristic of glucose-induced electrical activity o...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.3.2.7866

    authors: Misler S,Silva AM,Barnett D,Dickey AS

    更新日期:2009-03-01 00:00:00

  • Activation gating kinetics of GIRK channels are mediated by cytoplasmic residues adjacent to transmembrane domains.

    abstract::G-protein-coupled inwardly rectifying potassium channels (GIRK/Kir3.x) are involved in neurotransmission-mediated reduction of excitability. The gating mechanism following G protein activation of these channels likely proceeds from movement of inner transmembrane helices to allow K(+) ions movement through the pore of...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.3.3.9136

    authors: Sadja R,Reuveny E

    更新日期:2009-05-01 00:00:00

  • Extracellular potassium dependency of block of HERG by quinidine and cisapride is primarily determined by the permeant ion and not by inactivation.

    abstract::Drug induced Long QT syndrome results primarily from block of the cardiac potassium channel HERG (human-ether-a-go-go related gene). In some cases prolongation of the QT interval can result in the lethal arrhythmia torsade de pointes, an arrhythmia characterized by a rapid heart rate and severely compromised cardiac o...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:

    authors: Barrows B,Cheung K,Bialobrzeski T,Foster J,Schulze J,Miller A

    更新日期:2009-07-01 00:00:00

  • Synaptic NMDAR activity suppresses FOXO1 expression via a cis-acting FOXO binding site: FOXO1 is a FOXO target gene.

    abstract::Activation of gene expression by FOXO transcription factors can promote neuronal death in response to loss of trophic support, or oxidative stress. The predominant neuronal FOXOs, FOXO1 and FOXO3, promote the expression of pro-death genes, such as Fas Ligand, Bim and Txnip. Neuroprotective signals initiated by neurotr...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.3.4.9381

    authors: Al-Mubarak B,Soriano FX,Hardingham GE

    更新日期:2009-07-01 00:00:00

  • Elevated InsP3R expression underlies enhanced calcium fluxes and spontaneous extra-systolic calcium release events in hypertrophic cardiac myocytes.

    abstract::Cardiac hypertrophy is associated with profound remodeling of Ca(2+) signaling pathways. During the early, compensated stages of hypertrophy, Ca(2+) fluxes may be enhanced to facilitate greater contraction, whereas as the hypertrophic heart decompensates, Ca(2+) homeostatic mechanisms are dysregulated leading to decre...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.4.1.10531

    authors: Harzheim D,Talasila A,Movassagh M,Foo RS,Figg N,Bootman MD,Roderick HL

    更新日期:2010-01-01 00:00:00

  • Fast, repetitive light-activation of CaV3.2 using channelrhodopsin 2.

    abstract::Channelrhodopsin-2 (ChR2) is a light-gated ion channel that is successfully used in neurosciences to depolarize cells with blue light. In this regard control of membrane voltage with light opens new perspectives for the characterization of ion channels and the search for inhibitors or modulators. Here, we report a con...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.4.3.11888

    authors: Prigge M,Rösler A,Hegemann P

    更新日期:2010-05-01 00:00:00

  • Unified modeling of the mammalian and fish proton-dependent oligopeptide transporter PepT1.

    abstract::Electrophysiological and biophysical analyses were used to compare the partial and complete transport cycles of the intestinal oligopeptide transporter PepT1 among three species (seabass, zebrafish and rabbit). On the whole, the presteady-state currents of the fish transporters were similar to each other. Rabbit PepT1...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.5.1.13505

    authors: Renna MD,Sangaletti R,Bossi E,Cherubino F,Kottra G,Peres A

    更新日期:2011-01-01 00:00:00

  • Regulation of voltage-gated ion channels in excitable cells by the ubiquitin ligases Nedd4 and Nedd4-2.

    abstract::The electrical excitability of neurons is mediated primarily by voltage-gated ion channels, particularly voltage-gated Na(+) (Na(v)), K(+) (K(v)) and Cl(-) (ClC) channels. Cells regulate their electrical excitability by controlling not only the activity, but also the number of individual ion channels in the plasma mem...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章,评审

    doi:10.4161/chan.5.1.13967

    authors: Bongiorno D,Schuetz F,Poronnik P,Adams DJ

    更新日期:2011-01-01 00:00:00

  • Induction of a fast inactivation gating on delayed rectifier Shab K(+) channels by the anti-inflammatory drug celecoxib.

    abstract::Celecoxib is a drug designed to selectively inhibit COX-2, an inflammation-inducible cyclooxygenase isoform, over the constitutively expressed COX-1 isoform. In addition to this selective inhibition it is now known that celecoxib exerts a variety of effects on several types of ion channels, thus producing secondary ph...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.5.1.13972

    authors: Arias-Olguin II,Carrillo E,Meza-Torres B,Barriga-Montoya C,Balleza D,Gomez-Lagunas F

    更新日期:2011-01-01 00:00:00

  • Common allosteric mechanisms between ryanodine and inositol-1,4,5-trisphosphate receptors.

    abstract::Ryanodine receptors (RyRs) are calcium release channels found in the membrane of the endoplasmic reticulum (ER). We recently described the crystal structure of the RyR1 N-terminal disease hot spot. It is built up by three domains that show clear structural homology with the inositol-1,4,5-triphosphate (IP3) binding co...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.5.2.14313

    authors: Yuchi Z,Van Petegem F

    更新日期:2011-03-01 00:00:00

  • Acute modulation of calcium currents and synaptic transmission by gabapentinoids.

    abstract::Gabapentin and pregabalin are anticonvulsant drugs that are extensively used for the treatment of several neurological and psychiatric disorders. Gabapentinoids (GBPs) are known to have a high affinity binding to α2δ-1 and α2δ-2 auxiliary subunit of specific voltage-gated calcium channels. Despite the confusing effect...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章,评审

    doi:10.4161/chan.4.6.12864

    authors: Uchitel OD,Di Guilmi MN,Urbano FJ,Gonzalez-Inchauspe C

    更新日期:2010-11-01 00:00:00

  • Motoneuron subtypes show specificity in glycine receptor channel abnormalities in a transgenic mouse model of amyotrophic lateral sclerosis.

    abstract::Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease characterized by selective loss of motoneurons. Recently we studied glycine receptors (GlyRs) in motoneurons in an ALS mouse model expressing a mutant form of human superoxide dismutase-1 with a Gly93→Ala substitution (G93A-SOD1). Living mo...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.5.4.16206

    authors: Chang Q,Martin LJ

    更新日期:2011-07-01 00:00:00

  • Structural remodeling of the N-terminus tunes TRPA1 channel activation and regulates behavioral responses in Drosophila.

    abstract::Our bodies are constantly bombarded by a diversity of environmental stimuli, such as touch, taste, sound, smell, light, etc. To detect and process this broad array of signals, nature has evolved a variety of cellular sensory mechanisms and pathways that interface with the environment and transmit neural signals back t...

    journal_title:Channels (Austin, Tex.)

    pub_type: 评论,杂志文章

    doi:10.4161/chan.19351

    authors: Braun AP

    更新日期:2012-01-01 00:00:00

  • Tryptophan scanning mutagenesis reveals distortions in the helical structure of the δM4 transmembrane domain of the Torpedo californica nicotinic acetylcholine receptor.

    abstract::The lipid-protein interface is an important domain of the nicotinic acetylcholine receptor (nAChR) that has recently garnered increased relevance. Several studies have made significant advances toward determining the structure and dynamics of the lipid-exposed domains of the nAChR. However, there is still a need to ga...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.19540

    authors: Caballero-Rivera D,Cruz-Nieves OA,Oyola-Cintrón J,Torres-Nunez DA,Otero-Cruz JD,Lasalde-Dominicci JA

    更新日期:2012-03-01 00:00:00

  • Two-pore domain potassium channels: variation on a structural theme.

    abstract::The ability of cells to reliably fire action potentials is critically dependent upon the maintenance of a hyperpolarized resting potential, which allows voltage-gated Na(+) and Ca(2+) channels to recover from inactivation and open in response to a subsequent stimulus. Hodgkin and Huxley first recognized the functional...

    journal_title:Channels (Austin, Tex.)

    pub_type: 评论,杂志文章

    doi:10.4161/chan.20973

    authors: Braun AP

    更新日期:2012-05-01 00:00:00

  • Structural determinants of CaV1.3 L-type calcium channel gating.

    abstract::A C-terminal modulatory domain (CTM) tightly regulates the biophysical properties of Ca(v)1.3 L-type Ca(2+) channels, in particular the voltage dependence of activation (V(0.5)) and Ca(2+) dependent inactivation (CDI). A functional CTM is present in the long C-terminus of human and mouse Ca(v)1.3 (Ca(v)1.3(L)), but no...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.21002

    authors: Lieb A,Scharinger A,Sartori S,Sinnegger-Brauns MJ,Striessnig J

    更新日期:2012-05-01 00:00:00

  • The dynamics of protein-protein interactions between domains of MscL at the cytoplasmic-lipid interface.

    abstract::The bacterial mechanosensitive channel of large conductance, MscL, is one of the best characterized mechanosensitive channels serving as a paradigm for how proteins can sense and transduce mechanical forces. The physiological role of MscL is that of an emergency release valve that opens a large pore upon a sudden drop...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.20756

    authors: Iscla I,Wray R,Blount P

    更新日期:2012-07-01 00:00:00

  • Molecular and functional determinants of local anesthetic inhibition of NaChBac.

    abstract::In our recent publication, we describe the local anesthetic (LA) inhibition of the prokaryotic voltage gated sodium channel NaChBac. Despite the numerous functional and putative structural differences with the mammalian sodium channels, the data show that LA compounds effectively and reversibly inhibit NaChBac channel...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.21807

    authors: Lee S,Goodchild SJ,Ahern CA

    更新日期:2012-09-01 00:00:00

  • Nitric oxide-induced calcium release: activation of type 1 ryanodine receptor by endogenous nitric oxide.

    abstract::Ryanodine receptors (RyRs), located in the sarcoplasmic/endoplasmic reticulum (SR/ER) membrane, are required for intracellular Ca2+ release that is involved in a wide range of cellular functions. In addition to Ca2+-induced Ca2+ release in cardiac cells and voltage-induced Ca2+ release in skeletal muscle cells, we rec...

    journal_title:Channels (Austin, Tex.)

    pub_type: 杂志文章

    doi:10.4161/chan.22555

    authors: Kakizawa S,Yamazawa T,Iino M

    更新日期:2013-01-01 00:00:00