The type 3 inositol 1,4,5-trisphosphate receptor is concentrated at the tight junction level in polarized MDCK cells

被引:32
作者
Colosetti, P
Tunwell, REA
Cruttwell, C
Arsanto, JP
Mauger, JP
Cassio, D
机构
[1] Univ Paris 11, INSERM, U442, F-91405 Orsay, France
[2] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[3] Univ Aix Marseille 2, Fac Sci Luminy, Inst Dev Biol,UMR 6156, NMDA,Lab Neurogenese & Morphogenese Dev & Adulte, F-13288 Marseille, France
关键词
inositol 1,4,5-trisphosphate receptor; tight junction; polarity; calcium; endoplasmic reticulum; InsP(3)R-1-EGFP;
D O I
10.1242/jcs.00482
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The subcellular localization of inositol 1,4,5-trisphosphate (InsP(3))-induced Ca2+ signals is important for the activation of many physiological functions. In epithelial cells the spatial distribution of InsP(3) receptor is restricted to specific areas, but little is known about the relationship between the receptor's distribution and cell polarity. To investigate this relationship, the best known polarized cell model, MDCK, was examined. This cell line is characterized by a strong expression of the type 3 InsP(3) receptor and the subcellular localization of this receptor was followed during cell polarization using immunofluorescence and confocal analysis. In non-polarized cells, including ras transformed f3 MDCK cells, the type 3 InsP(3) receptor was found to colocalize with markers of the endoplasmic reticulum in the cytoplasm. In contrast, in polarized cells, this receptor was mostly distributed at the apex of the lateral plasma membrane with the markers of tight junctions, ZO-1 and occludin. The localization of the type 3 InsP(3) receptor in the vicinity of tight junctions was confirmed by immunogold electron microscopy. The culture of MDCK cells in calcium-deprived medium, led to disruption of cell polarity and receptor redistribution in the cytoplasm. Addition of calcium to these deprived cells induced the restoration of polarity and the relocalization of the receptor to the plasma membrane. MDCK cells were stably transfected with a plasmid coding the full-length mouse type 1 InsP(3) receptor tagged with EGFP at the C-terminus. The EGFP-tagged type 1 receptor and the endogenous type 3 co-localized in the cytoplasm of non-polarized cells and at the tight junction level of polarized cells. Thus, the localization of InsP(3) receptor in MDCK depends on polarity.
引用
收藏
页码:2791 / 2803
页数:13
相关论文
共 54 条
[1]   Functional dissociation of paracellular permeability and transepithelial electrical resistance and disruption of the apical-basolateral intramembrane diffusion barrier by expression of a mutant tight junction membrane protein [J].
Balda, MS ;
Whitney, JA ;
Flores, C ;
Gonzalez, S ;
Cereijido, M ;
Matter, K .
JOURNAL OF CELL BIOLOGY, 1996, 134 (04) :1031-1049
[2]  
Baldini A, 2000, ZEI STUD EU ECON LAW, V2, P19
[3]   The structural and functional polarity of the hepatic human/rat hybrid WIF-B is a stable and dominant trait [J].
Bender, V ;
Bravo, P ;
Decaens, C ;
Cassio, D .
HEPATOLOGY, 1999, 30 (04) :1002-1010
[4]   The versatility and universality of calcium signalling [J].
Berridge, MJ ;
Lipp, P ;
Bootman, MD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) :11-21
[5]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[6]   Elementary and global aspects of calcium signalling [J].
Berridge, MJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 499 (02) :291-306
[7]  
BLONDEL O, 1993, J BIOL CHEM, V268, P11356
[8]  
BUSH KT, 1994, J BIOL CHEM, V269, P23694
[9]   HYBRID CELL-LINES CONSTITUTE A POTENTIAL RESERVOIR OF POLARIZED CELLS - ISOLATION AND STUDY OF HIGHLY DIFFERENTIATED HEPATOMA-DERIVED HYBRID-CELLS ABLE TO FORM FUNCTIONAL BILE CANALICULI INVITRO [J].
CASSIO, D ;
HAMONBENAIS, C ;
GUERIN, M ;
LECOQ, O .
JOURNAL OF CELL BIOLOGY, 1991, 115 (05) :1397-1408
[10]   Restoration of tight junction structure and barrier function by down-regulation of the mitogen-activated protein kinase pathway in Ras-transformed Madin-Darby canine kidney cells [J].
Chen, YH ;
Lu, Q ;
Schneeberger, EE ;
Goodenough, DA .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :849-862