Similar and differential behaviour between the nectin-afadin-ponsin and cadherin-catenin systems during the formation and disruption of the polarized junctional alignment in epithelial cells

被引:81
作者
Asakura, T
Nakanishi, H
Sakisaka, T
Takahashi, K
Mandai, K
Nishimura, M
Sasaki, T
Takai, Y
机构
[1] Osaka Univ, Grad Sch Med, Fac Med, Dept Biochem & Mol Biol, Suita, Osaka 5650871, Japan
[2] JCR Pharmaceut Co, Japan Sci & Technol Corp, ERATO, Takai Biotimer Project,Nishi Ku, Kobe, Hyogo 6512241, Japan
关键词
D O I
10.1046/j.1365-2443.1999.00283.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: We have recently identified a novel cell-cell adhesion system, named NAP system, which is localized at cadherin-based cell-cell adherens junctions (AJs), The NAP system is composed of at least nectin, afadin and ponsin, Nectin is an immunoglobulin-like cell adhesion molecule. Afadin is an actin filament-binding protein which associates nectin with the actin cytoskeleton, Ponsin is an afadin-binding protein which furthermore binds to vinculin and provides a possible linkage of nectin-afadin to cadherin-catenin through vinculin, We compared here the behaviour of the NAP and cadherin-catenin systems during the formation and disruption of the polarized junctional alignment in epithelial cells. Results: At the early stage of the formation of the polarized junctional alignment in MTD-1A cells, primordial spot-like junctions were formed at the tips of thin cellular protrusions radiating from adjacent cells. Nectin, afadin, ponsin, cadherin and catenin were simultaneously recruited to these junctions. As the cell polarization proceeded, the spot-like junctions were gradually fused to form belt-like AJs where all these proteins were concentrated, The disruption of cell-cell AJs in MDCK cells by culturing at a low Ca2+ concentration caused rapid endocytosis of cadherin, but not that of nectin or afadin, Addition of 12-O-tetradecanoylphorbol-13-acetate to the cells formed a tight junction-like structure where nectin and afadin, but not cadherin, accumulated. Conclusion: These results indicate that the NAP and cadherin-catenin systems show similar and differential behaviour during the formation and disruption of the polarized junctional alignment in epithelial cells.
引用
收藏
页码:573 / 581
页数:9
相关论文
共 41 条
[1]  
Ando-Akatsuka Y, 1999, J CELL PHYSIOL, V179, P115, DOI 10.1002/(SICI)1097-4652(199905)179:2<115::AID-JCP1>3.0.CO
[2]  
2-T
[3]   Interspecies diversity of the occludin sequence: cDNA cloning of human, mouse, dog, and rat-kangaroo homologues [J].
AndoAkatsuka, Y ;
Saitou, M ;
Hirase, T ;
Kishi, M ;
Sakakibara, A ;
Itoh, M ;
Yonemura, S ;
Furuse, M ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1996, 133 (01) :43-47
[4]   Mouse homolog of poliovirus receptor-related gene 2 product, mPRR2, mediates homophilic cell aggregation [J].
Aoki, J ;
Koike, S ;
Asou, H ;
Ise, I ;
Suwa, H ;
Tanaka, T ;
Miyasaka, M ;
Nomoto, A .
EXPERIMENTAL CELL RESEARCH, 1997, 235 (02) :374-384
[5]   ASSEMBLY OF THE TIGHT JUNCTION - THE ROLE OF DIACYLGLYCEROL [J].
BALDA, MS ;
GONZALEZMARISCAL, L ;
MATTER, K ;
CEREIJIDO, M ;
ANDERSON, JM .
JOURNAL OF CELL BIOLOGY, 1993, 123 (02) :293-302
[6]  
CIMINO G, 1991, CANCER RES, V51, P6712
[7]   THE HUMAN PRR2 GENE, RELATED TO THE HUMAN POLIOVIRUS RECEPTOR GENE (PVR), IS THE TRUE HOMOLOG OF THE MURINE MPH GENE [J].
EBERLE, F ;
DUBREUIL, P ;
MATTEI, MG ;
DEVILARD, E ;
LOPEZ, M .
GENE, 1995, 159 (02) :267-272
[8]   OCCLUDIN - A NOVEL INTEGRAL MEMBRANE-PROTEIN LOCALIZING AT TIGHT JUNCTIONS [J].
FURUSE, M ;
HIRASE, T ;
ITOH, M ;
NAGAFUCHI, A ;
YONEMURA, S ;
TSUKITA, S ;
TSUKITA, S .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1777-1788
[9]   Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin [J].
Furuse, M ;
Fujita, K ;
Hiiragi, T ;
Fujimoto, K ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1998, 141 (07) :1539-1550
[10]   THE CYTOPLASMIC DOMAIN OF ADHERENS-TYPE JUNCTIONS [J].
GEIGER, B ;
GINSBERG, D .
CELL MOTILITY AND THE CYTOSKELETON, 1991, 20 (01) :1-6