Connexins and Pannexins in Bone and Skeletal Muscle

被引:36
作者
Plotkin, Lilian I. [1 ,2 ,3 ]
Davis, Hannah M. [1 ]
Cisterna, Bruno A. [4 ]
Saez, Juan C. [4 ,5 ]
机构
[1] Indiana Univ, Sch Med, Dept Anat & Cell Biol, 635 Barnhill Dr,MS5045, Indianapolis, IN 46202 USA
[2] Richard L Roudebush Vet Adm Med Ctr, Indianapolis, IN 46222 USA
[3] Indiana Ctr Musculoskeletal Hlth, Indianapolis, IN 46202 USA
[4] Pontificia Univ Catolica Chile, Dept Fisiol, Av Alameda 340, Santiago, Chile
[5] Ctr Interdisciplinario Neurociencias Valparaiso, Valparaiso, Chile
来源
CURRENT OSTEOPOROSIS REPORTS | 2017年 / 15卷 / 04期
基金
美国国家卫生研究院;
关键词
Gap junctions; Hemichannels; Connexon; Inflammation; DENTO-DIGITAL DYSPLASIA; GJA1 MISSENSE MUTATION; NEONATAL MICE LACKING; DEFICIENT MDX MICE; OCULODENTODIGITAL DYSPLASIA; GAP-JUNCTIONS; OSTEOBLASTIC CELLS; INTERCELLULAR COMMUNICATION; MEMBRANE-PERMEABILITY; MUSCULAR-DYSTROPHY;
D O I
10.1007/s11914-017-0374-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review To discuss current knowledge on the role of connexins and pannexins in the musculoskeletal system. Recent findings Connexins and pannexins are crucial for the development and maintenance of both bone and skeletal muscle. In bone, the presence of connexin and more recently of pannexin channels in osteoblasts, osteoclasts, and osteocytes has been described and shown to be essential for normal skeletal development and bone adaptation. In skeletal muscles, connexins and pannexins play important roles during development and regeneration through coordinated regulation of metabolic functions via cell-to-cell communication. Further, under pathological conditions, altered expression of these proteins can promote muscle atrophy and degeneration by stimulating inflammasome activity. Summary In this review, we highlight the important roles of connexins and pannexins in the development, maintenance, and regeneration of musculoskeletal tissues, with emphasis on the mechanisms by which these molecules mediate chemical (e.g., ATP and prostaglandin E2) and physical (e.g., mechanical stimulation) stimuli that target the musculoskeletal system and their involvement in the pathophysiological changes in both genetic and acquired diseases.
引用
收藏
页码:326 / 334
页数:9
相关论文
共 106 条
  • [81] Regulation of pannexin and connexin channels and their functional role in skeletal muscles
    Saez, Juan C.
    Cisterna, Bruno A.
    Vargas, Anibal
    Cardozo, Christopher P.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2015, 72 (15) : 2929 - 2935
  • [82] Connexin hemichannel composition determines the FGF-1-induced membrane permeability and free [Ca2+]i responses
    Schalper, Kurt A.
    Palacios-Prado, Nicolas
    Retamal, Mauricio A.
    Shoji, Kenji F.
    Martinez, Agustin D.
    Saez, Juan C.
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (08) : 3501 - 3513
  • [83] Connexin 43 hemichannels mediate the Ca2+ influx induced by extracellular alkalinization
    Schalper, Kurt A.
    Sanchez, Helmuth A.
    Lee, Sung C.
    Altenberg, Guillermo A.
    Nathanson, Michael H.
    Saez, Juan C.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 299 (06): : C1504 - C1515
  • [84] A Germline Variant in the PANX1 Gene Has Reduced Channel Function and Is Associated with Multisystem Dysfunction
    Shao, Qing
    Lindstrom, Kristin
    Shi, Ruoyang
    Kelly, John
    Schroeder, Audrey
    Juusola, Jane
    Levine, Kara L.
    Esseltine, Jessica L.
    Penuela, Silvia
    Jackson, Michael F.
    Laird, Dale W.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (24) : 12432 - 12443
  • [85] Deletion of Connexin43 in Osteoblasts/Osteocytes Leads to Impaired Muscle Formation in Mice
    Shen, Hua
    Grimston, Susan
    Civitelli, Roberto
    Thomopoulos, Stavros
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2015, 30 (04) : 596 - 605
  • [86] Pannexin channels are not gap junction hemichannels
    Sosinsky, Gina E.
    Boassa, Daniela
    Dermietzel, Rolf
    Duffy, Heather S.
    Laird, Dale W.
    MacVicar, Brian A.
    Naus, Christian C.
    Penuela, Silvia
    Scemes, Eliana
    Spray, David C.
    Thompson, Roger J.
    Zhao, Hong-Bo
    Dahl, Gerhard
    [J]. CHANNELS, 2011, 5 (03) : 193 - 197
  • [87] Helper (CD4+) and cytotoxic (CD8+)T cells promote the pathology of dystrophin-deficient muscle
    Spencer, MJ
    Montecino-Rodriguez, E
    Dorshkind, K
    Tidball, JG
    [J]. CLINICAL IMMUNOLOGY, 2001, 98 (02) : 235 - 243
  • [88] Connexins in the skeleton
    Stains, Joseph P.
    Civitelli, Roberto
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2016, 50 : 31 - 39
  • [89] Gap junctions in skeletal development and function
    Stains, JP
    Civitelli, R
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2005, 1719 (1-2): : 69 - 81
  • [90] Characterization of hTERT-immortalized osteoblast cell lines generated from wild-type and connexin43-null mouse calvaria
    Thi, Mia M.
    Urban-Maldonado, Marcia
    Spray, David C.
    Suadicani, Sylvia O.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 299 (05): : C994 - C1006