Connexin 43: a New Therapeutic Target Against Chronic Kidney Disease?

被引:33
作者
Prakoura, Niki [1 ]
Kavvadas, Panagiotis [1 ]
Chadjichristos, Christos E. [1 ,2 ]
机构
[1] Tenon Hosp, Inst Natl Sante & Rech Med, UMRS 1155, 4 Rue Chine, F-75020 Paris, France
[2] Sorbonne Univ, Paris, France
关键词
Chronic kidney disease; Inflammation; Fibrosis; Connexin43; Targets of therapy; TO-CELL COMMUNICATION; GAP-JUNCTIONS; UP-REGULATION; INTERCELLULAR COMMUNICATION; GLOMERULAR PODOCYTES; MESANGIAL CELLS; ATP RELEASE; EXPRESSION; HEMICHANNELS; INJURY;
D O I
10.1159/000493230
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic kidney disease is an incurable to date pathology with a continuously growing incidence that contributes to the increase of the number of deaths worldwide. With currently no efficient prognostic or therapeutic options being available, the only possibility for treatment of end-stage renal disease is renal replacement therapy through dialysis or transplantation. Understanding the molecular mechanisms participating in the progression of renal diseases and uncovering the pathways implicated will permit the identification of novel and more efficient targets of therapy. Connexin43 was recently identified as a novel player in the development of chronic kidney disease. It was found de novo expressed and/or differentially localized in various renal cell populations during progression of renal disease, indicating an abnormal connexin signaling, both in patients and animal models. Subsequent in vivo studies demonstrated that connexin43 is involved in mediating inflammatory and fibrotic processes contributing to renal damage. Genetic, pharmaco-genetic or peptide-based inhibition of connexin43 in animal models and cell culture systems was successful in preventing the progression of the pathology and preserving the cell phenotypes. This review will summarize the recent advances on connexin43 in the field of kidney diseases and discuss the potential of future connexin43-based therapies against chronic kidney disease. (C) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:998 / 1009
页数:12
相关论文
共 85 条
  • [1] Targeting connexin 43 protects against the progression of experimental chronic kidney disease in mice
    Abed, Ahmed
    Toubas, Julie
    Kavvadas, Panagiotis
    Authier, Florence
    Cathelin, Dominique
    Alfieri, Carlo
    Boffa, Jean-Jacques
    Dussaule, Jean-Claude
    Chatziantoniou, Christos
    Chadjichristos, Christos E.
    [J]. KIDNEY INTERNATIONAL, 2014, 86 (04) : 768 - 779
  • [2] An angiotensin II- and NF-κB-dependent mechanism increases connexin 43 in murine arteries targeted by renin-dependent hypertension
    Alonso, Florian
    Krattinger, Nathalie
    Mazzolai, Lucia
    Simon, Alexander
    Waeber, Gerard
    Meda, Paolo
    Haefliger, Jacques-Antoine
    [J]. CARDIOVASCULAR RESEARCH, 2010, 87 (01) : 166 - 176
  • [3] LOCALIZATION OF CONNEXIN43 IN RAT-KIDNEY
    BARAJAS, L
    LIU, L
    TUCKER, M
    [J]. KIDNEY INTERNATIONAL, 1994, 46 (03) : 621 - 626
  • [4] Gap junctions and hemichannels in signal transmission, function and development of bone
    Batra, Nidhi
    Kar, Rekha
    Jiang, Jean X.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2012, 1818 (08): : 1909 - 1918
  • [5] Connexins in wound healing; perspectives in diabetic patients
    Becker, David L.
    Thrasivoulou, Christopher
    Phillips, Anthony R. J.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2012, 1818 (08): : 2068 - 2075
  • [6] ANTISERA DIRECTED AGAINST CONNEXIN-43 PEPTIDES REACT WITH A 43-KD PROTEIN LOCALIZED TO GAP-JUNCTIONS IN MYOCARDIUM AND OTHER TISSUES
    BEYER, EC
    KISTLER, J
    PAUL, DL
    GOODENOUGH, DA
    [J]. JOURNAL OF CELL BIOLOGY, 1989, 108 (02) : 595 - 605
  • [7] CONNEXINS: KEY MEDIATORS OF ENDOCRINE FUNCTION
    Bosco, Domenico
    Haefliger, Jacques-Antoine
    Meda, Paolo
    [J]. PHYSIOLOGICAL REVIEWS, 2011, 91 (04) : 1393 - 1445
  • [8] Intravital imaging of podocyte calcium in glomerular injury and disease
    Burford, James L.
    Villanueva, Kane
    Lam, Lisa
    Riquier-Brison, Anne
    Hackl, Matthias J.
    Pippin, Jeffrey
    Shankland, Stuart J.
    Peti-Peterdi, Janos
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (05) : 2050 - 2058
  • [9] A genetically clamped renin transgene for the induction of hypertension
    Caron, KMI
    James, LR
    Kim, HS
    Morham, SG
    Lopez, MLSS
    Gomez, RA
    Reudelhuber, TL
    Smithies, O
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) : 8248 - 8252
  • [10] Connexin 43 a check-point component of cell proliferation implicated in a wide range of human testis diseases
    Chevallier, Daniel
    Carette, Diane
    Segretain, Dominique
    Gilleron, Jerome
    Pointis, Georges
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2013, 70 (07) : 1207 - 1220