α-catenin-deficient F9 cells differentiate into signet ring cells

被引:34
作者
Maeno, Y
Moroi, S
Nagashima, H
Noda, T
Shiozaki, H
Monden, M
Tsukita, S
Nagafuchi, A [1 ]
机构
[1] Kyoto Univ, Fac Med, Dept Cell Biol, Sakyo Ku, Kyoto 606, Japan
[2] Osaka Univ, Sch Med, Dept Surg 2, Osaka 553, Japan
[3] Tokyo Womens Med Coll, Heart Inst Japan, Tokyo 162, Japan
[4] Japanese Fdn Canc Res, Inst Canc, Dept Cell Biol, Tokyo 170, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1016/S0002-9440(10)65385-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
It has been demonstrated that alpha-catenin is frequently lost in diffuse type adenocarcinomas. We have isolated alpha-catenin-deficient mouse teratocarcinoma F9 cells by gene targeting. Wild-type F9 cell aggregates cultured in the presence of retinoic acid differentiated into embryoid bodies with an outer layer of epithelial cells. In contrast, cell aggregates of alpha-catenin-deficient cells did not develop outer layers under the same conditions. The outer surface cells of alpha-catenin-deficient cell aggregates, however, differentiated into epithelial cells as determined by their expression of epithelial marker proteins. These differentiated cells scattered from aggregates and showed signet ring cell morphology, which is frequently observed in diffuse type adenocarcinomas. We have provided clear evidence that a single mutation in the alpha-catenin gene may be a direct cause not only of the scattered properties of cells but also of signet ring cell formation in diffuse type adenocarcinoma.
引用
收藏
页码:1323 / 1328
页数:6
相关论文
共 35 条
[1]   Expression of wild-type alpha-catenin protein in cells with a mutant alpha-catenin gene restores both growth regulation and tumor suppressor activities [J].
Bullions, LC ;
Notterman, DA ;
Chung, LS ;
Levine, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (08) :4501-4508
[2]  
DUANE GB, 1985, ACTA CYTOL, V29, P211
[3]   PROMOTER TRAPS IN EMBRYONIC STEM-CELLS - A GENETIC SCREEN TO IDENTIFY AND MUTATE DEVELOPMENTAL GENES IN MICE [J].
FRIEDRICH, G ;
SORIANO, P .
GENES & DEVELOPMENT, 1991, 5 (09) :1513-1523
[4]   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
[5]   THE ENCEPHALOMYOCARDITIS VIRUS INTERNAL RIBOSOME ENTRY SITE ALLOWS EFFICIENT COEXPRESSION OF 2 GENES FROM A RECOMBINANT PROVIRUS IN CULTURED-CELLS AND IN EMBRYOS [J].
GHATTAS, IR ;
SANES, JR ;
MAJORS, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :5848-5859
[6]   AN ADHESION-DEFECTIVE VARIANT OF F9 EMBRYONAL CARCINOMA-CELLS FAILS TO DIFFERENTIATE INTO VISCERAL ENDODERM [J].
GROVER, A ;
ROSENTRAUS, MJ ;
STERMAN, B ;
SNOOK, ME ;
ADAMSON, ED .
DEVELOPMENTAL BIOLOGY, 1987, 120 (01) :1-11
[7]   IDENTIFICATION OF A NEURAL ALPHA-CATENIN AS A KEY REGULATOR OF CADHERIN FUNCTION AND MULTICELLULAR ORGANIZATION [J].
HIRANO, S ;
KIMOTO, N ;
SHIMOYAMA, Y ;
HIROHASHI, S ;
TAKEICHI, M .
CELL, 1992, 70 (02) :293-301
[8]   Inactivation of the E-cadherin-mediated cell adhesion system in human cancers [J].
Hirohashi, S .
AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (02) :333-339
[9]   CELL-INTERACTIONS MODULATE EMBRYONAL CARCINOMA CELL-DIFFERENTIATION INTO PARIETAL OR VISCERAL ENDODERM [J].
HOGAN, BLM ;
TAYLOR, A ;
ADAMSON, E .
NATURE, 1981, 291 (5812) :235-237
[10]  
KADOWAKI T, 1994, CANCER RES, V54, P291