Cx36 preferentially connects β-cells within pancreatic islets

被引:133
作者
Serre-Beinier, V
Le Gurun, S
Belluardo, N
Trovato-Salinaro, A
Charollais, A
Haefliger, JA
Condorelli, DF
Meda, P
机构
[1] Univ Geneva, Sch Med, Dept Morphol, CH-1211 Geneva, Switzerland
[2] Univ Lausanne Hosp, Dept Internal Med B, Lausanne, Switzerland
[3] Univ Palermo, Inst Human Physiol, Palermo, Italy
[4] Univ Catania, Sch Med, Dept Chem Sci, Catania, Italy
关键词
D O I
10.2337/diabetes.49.5.727
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies have provided evidence for the transcripts of Cx43 and Cx45 within pancreatic islets. As of yet, however, it has proven difficult to unambiguously demonstrate the expression of these proteins by islet cells. me have investigated whether Cx36, a new connexin species recently identified in mammalian brain and retina, may also be expressed in pancreatic islets. Using probes that permitted the original identification of Cx36 in the central nervous system, we show that a transcript for Cx36 is clearly detectable in rat pancreatic islets. Using novel and affinity-purified polyclonal antibodies, we have found that Cx36 is actually expressed in pancreatic islets. Both in situ hybridization and immunolabeling indicated that this connexin is abundant in the centrally located insulin-producing beta-cells and is expressed much less, if at all, by the other endocrine cell types. This differential expression was further confirmed on fluorescence-activated cell sorter-purified preparations enriched in either beta- or non-beta-cells. The finding of a differential distribution of Cx36 within distinct regions of pancreatic islets creates the possibility that this connexin may provide the establishment of selective pathways of communication between the different types of endocrine cells comprising the pancreatic islet.
引用
收藏
页码:727 / 734
页数:8
相关论文
共 53 条
[1]   HYBRID INSULIN GENES REVEAL A DEVELOPMENTAL LINEAGE FOR PANCREATIC ENDOCRINE-CELLS AND IMPLY A RELATIONSHIP WITH NEURONS [J].
ALPERT, S ;
HANAHAN, D ;
TEITELMAN, G .
CELL, 1988, 53 (02) :295-308
[2]   ESTABLISHMENT OF 2-MERCAPTOETHANOL-DEPENDENT DIFFERENTIATED INSULIN-SECRETING CELL-LINES [J].
ASFARI, M ;
JANJIC, D ;
MEDA, P ;
LI, GD ;
HALBAN, PA ;
WOLLHEIM, CB .
ENDOCRINOLOGY, 1992, 130 (01) :167-178
[3]   IDENTIFICATION OF THE 64K AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES AS THE GABA-SYNTHESIZING ENZYME GLUTAMIC-ACID DECARBOXYLASE [J].
BAEKKESKOV, S ;
AANSTOOT, HJ ;
CHRISTGAU, S ;
REETZ, A ;
SOLIMENA, M ;
CASCALHO, M ;
FOLLI, F ;
RICHTEROLESEN, H ;
CAMILLI, PD .
NATURE, 1990, 347 (6289) :151-156
[4]  
BENNETT MVL, 1991, NEURON, V6, P305, DOI 10.1016/0896-6273(91)90241-Q
[5]   CONNEXIN FAMILY OF GAP JUNCTION PROTEINS [J].
BEYER, EC ;
PAUL, DL ;
GOODENOUGH, DA .
JOURNAL OF MEMBRANE BIOLOGY, 1990, 116 (03) :187-194
[6]   IB1, a JIP-1-related nuclear protein present in insulin-secreting cells [J].
Bonny, C ;
Nicod, P ;
Waeber, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :1843-1846
[7]  
BRUZZONE R, 1994, J CELL SCI, V107, P955
[8]  
Charollais A, 1999, DEV GENET, V24, P13, DOI 10.1002/(SICI)1520-6408(1999)24:1/2<13::AID-DVG3>3.0.CO
[9]  
2-N
[10]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159