Connexins: a connection with the skin

被引:131
作者
Richard, G
机构
[1] Thomas Jefferson Univ, Jefferson Med Coll, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Jefferson Inst Mol Med, Philadelphia, PA 19107 USA
关键词
connexin; gap junctional intercellular communication erythrokeratodermia variabilis; palmoplantar keratoderma; Vohwinkel syndrome; hearing loss; mutation; differentiation;
D O I
10.1034/j.1600-0625.2000.009002077.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The intercellular signaling system mediated by connexin channels is crucial for maintaining tissue homeostasis, growth control, development, and synchronized response of cells to stimuli. This review summarizes the structure, assembly, and properties of the components of the complex and diverse connexin system, and their biological functions in skin. The importance of gap junctional intercellular communication for normal development and differentiation of human epidermis as well as the hearing function of the inner ear is illustrated by the examples of erythrokeratodermia variabilis and palmoplantar keratoderma associated with hearing loss. These autosomal dominant inherited disorders are caused by germline mutations in the connexin genes GJB3 (encoding connexin-31) and GJB2 (encoding connexin-26), respectively. Recent functional studies of individual connexin mutations suggest that they may exert a dominant inhibitory effect on normal connexin channel function and perturb gap junctional intercellular communication, resulting in phenotypic manifestation in patients with these disorders.
引用
收藏
页码:77 / 96
页数:20
相关论文
共 131 条
[1]   Tuberculosis: milking the genome for drug targets and vaccines - Novartis Foundation Symposium: Genetics and Tuberculosis - Cape Town, South Africa, 18-20 November 1997 [J].
Abdulla, S .
MOLECULAR MEDICINE TODAY, 1998, 4 (03) :104-105
[2]   Rapid turnover of connexin43 in the adult rat heart [J].
Beardslee, MA ;
Laing, JG ;
Beyer, EC ;
Saffitz, JE .
CIRCULATION RESEARCH, 1998, 83 (06) :629-635
[3]   CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE [J].
BERGOFFEN, J ;
SCHERER, SS ;
WANG, S ;
SCOTT, MO ;
BONE, LJ ;
PAUL, DL ;
CHEN, K ;
LENSCH, MW ;
CHANCE, PF ;
FISCHBECK, KH .
SCIENCE, 1993, 262 (5142) :2039-2042
[4]   Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin [J].
Berry, V ;
Mackay, D ;
Khaliq, S ;
Francis, PJ ;
Hameed, A ;
Anwar, K ;
Mehdi, SQ ;
Newbold, RJ ;
Ionides, A ;
Shiels, A ;
Moore, T ;
Bhattacharya, SS .
HUMAN GENETICS, 1999, 105 (1-2) :168-170
[5]   Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules [J].
Bevans, CG ;
Kordel, M ;
Rhee, SK ;
Harris, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :2808-2816
[6]   Direct high affinity modulation of connexin channel activity by cyclic nucleotides [J].
Bevans, CG ;
Harris, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3720-3725
[7]   MOLECULAR-CLONING AND EXPRESSION OF RAT CONNEXIN40, A GAP JUNCTION PROTEIN EXPRESSED IN VASCULAR SMOOTH-MUSCLE [J].
BEYER, EC ;
REED, KE ;
WESTPHALE, EM ;
KANTER, HL ;
LARSON, DM .
JOURNAL OF MEMBRANE BIOLOGY, 1992, 127 (01) :69-76
[8]   Extent of intercellular calcium wave propagation is related to gap junction permeability and level of connexin-43 expression in astrocytes in primary cultures from four brain regions [J].
Blomstrand, F ;
Åberg, ND ;
Eriksson, PS ;
Hansson, E ;
Rönnbäck, L .
NEUROSCIENCE, 1999, 92 (01) :255-265
[9]   A genetic polymorphism in connexin 37 as a prognostic marker for atherosclerotic plaque development [J].
Boerma, M ;
Forsberg, L ;
Van Zeijl, L ;
Morgenstern, R ;
De Faire, U ;
Lemne, C ;
Erlinge, D ;
Thulin, T ;
Hong, Y ;
Cotgreave, IA .
JOURNAL OF INTERNAL MEDICINE, 1999, 246 (02) :211-218
[10]  
Brink PR, 1998, ACTA PHYSIOL SCAND, V164, P349