LOCALIZATION OF MUCIN (MUC2 AND MUC3) MESSENGER-RNA AND PEPTIDE EXPRESSION IN HUMAN NORMAL INTESTINE AND COLON-CANCER

被引:260
作者
CHANG, SK
DOHRMAN, AF
BASBAUM, CB
HO, SB
TSUDA, T
TORIBARA, NW
GUM, JR
KIM, YS
机构
[1] VET AFFAIRS MED CTR,GASTROINTESTINAL RES LAB 151M2,SAN FRANCISCO,CA 94121
[2] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,DEPT MED,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,DEPT PATHOL,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,DEPT ANAT,SAN FRANCISCO,CA 94143
[5] UNIV MINNESOTA,DEPT MED,MINNEAPOLIS,MN 55455
[6] VET AFFAIRS MED CTR,MINNEAPOLIS,MN
关键词
D O I
10.1016/0016-5085(94)90057-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Several studies have reported Northern blot data showing that mucin is expressed in a tissue-specific manner. To determine whether expression is limited to specific cell types within these tissues requires histological analysis. Methods: Both immunocytochemistry and in situ hybridization were used to identify cell types expressing the MUC2 and MUC3 mucins in the human small intestine, colon, and colon carcinoma. Results: In the normal small intestine and colon, an antibody recognizing the MUC2 apomucin stained goblet cells. In contrast, an antibody recognizing the MUC3 apomucin stained both goblet and absorptive cells. Consistent with this, in situ hybridization showed MUC2 messenger RNA (mRNA) only in goblet cells and MUC3 mRNA in both goblet and absorptive cells. In several samples of moderately well-differentiated colon cancer, MUC2 and MUC3 showed distinct patterns of expression, but the expression level of each was reduced compared with levels in normal tissue; there was considerable tumor-to-tumor and cell-to-cell variability using both mucin antibodies and complementary DNA probes. Conclusions: Individual mucin genes have distinct patterns of expression within mucin-producing tissues, suggesting that the various mucin gene products play distinct functional roles. © 1994.
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页码:28 / 36
页数:9
相关论文
共 29 条
[1]  
Angerer L.M., 1992, IN SITU HYBRIDIZATIO, P15
[2]  
Basbaum C, 1989, LUNG CELL BIOL, P37
[3]  
BOBEK LA, 1993, J BIOL CHEM, V268, P20563
[4]   ALTERATIONS IN HUMAN COLONIC MUCIN OCCURRING WITH CELLULAR-DIFFERENTIATION AND MALIGNANT TRANSFORMATION [J].
BOLAND, CR ;
MONTGOMERY, CK ;
KIM, YS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :2051-2055
[5]   DEGLYCOSYLATION OF MUCIN FROM LS174T COLON CANCER-CELLS BY HYDROGEN-FLUORIDE TREATMENT [J].
BYRD, JC ;
LAMPORT, DTA ;
SIDDIQUI, B ;
KUAN, SF ;
ERICKSON, R ;
ITZKOWITZ, SH ;
KIM, YS .
BIOCHEMICAL JOURNAL, 1989, 261 (02) :617-625
[6]  
CHANTLER E, 1982, MUCUS HLTH DISEASE, V2, P251
[7]   REGIONAL LOCALIZATION OF THE INTESTINAL MUCIN GENE MUC3 TO CHROMOSOME 7Q22 [J].
FOX, MF ;
LAHBIB, F ;
PRATT, W ;
ATTWOOD, J ;
GUM, J ;
KIM, Y ;
SWALLOW, DM .
ANNALS OF HUMAN GENETICS, 1992, 56 :281-287
[8]  
GENDLER SJ, 1990, J BIOL CHEM, V265, P15286
[9]   THE CORE POLYPEPTIDE OF CYSTIC-FIBROSIS TRACHEAL MUCIN CONTAINS A TANDEM REPEAT STRUCTURE - EVIDENCE FOR A COMMON MUCIN IN AIRWAY AND GASTROINTESTINAL TISSUE [J].
GERARD, C ;
EDDY, RL ;
SHOWS, TB .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (06) :1921-1927
[10]   ASSIGNMENT OF THE POLYMORPHIC INTESTINAL MUCIN GENE (MUC2) TO CHROMOSOME-11P15 [J].
GRIFFITHS, B ;
MATTHEWS, DJ ;
WEST, L ;
ATTWOOD, J ;
POVEY, S ;
SWALLOW, DM ;
GUM, JR ;
KIM, YS .
ANNALS OF HUMAN GENETICS, 1990, 54 :277-285