Core2 O-glycan structure is essential for the cell surface expression of sucrase isomaltase and dipeptidyl peptidase-IV during intestinal cell differentiation

Journal of Biological Chemistry

Volumn 285, Issue 48, 2010, Pages 37683-37692

  Lee, Seung Ho ^a,f   Yu, Shin Yi ^b   Nakayama, Jun ^c   Khoo, Kai Hooi ^b   Stone, Erica L ^d   Fukuda, Michiko N ^a   Marth, Jamey D ^e   Fukuda, Minoru ^a  

^a BURNHAM INSTITUTE   (United States)

^b INSTITUTE OF BIOLOGICAL CHEMISTRY   (Taiwan)

^c SHINSHU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^d UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f Scripps Korea Antibody Institute   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CACO-2 CELLS; CELL SURFACE EXPRESSION; DIFFERENTIAL EXPRESSIONS; DIFFERENTIATION MARKERS; DIPEPTIDYL PEPTIDASE; GLYCAN STRUCTURES; GLYCOSYLATED; IN-VIVO; INTESTINAL CELLS; KNOCK OUTS; OVER-EXPRESSION; SYNTHASES;

CELL MEMBRANES; MASS SPECTROMETRY; SURFACE STRUCTURE;

CYTOLOGY;

CORE2 BETA1,6 N ACETYLGLUCOSAMINYLTRANSFERASE 1 3; CORE2 BETA1,6 N ACETYLGLUCOSAMINYLTRANSFERASE 2; DIPEPTIDYL PEPTIDASE IV; N ACETYLGLUCOSAMINYLTRANSFERASE; RNA; SUCRASE ISOMALTASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CARBOHYDRATE ANALYSIS; CELL DIFFERENTIATION; CELL MATURATION; CELL PROLIFERATION; CELL STRAIN CACO 2; CELL SURFACE; CONTROLLED STUDY; ENZYME ACTIVITY; GENE SILENCING; GLYCOSYLATION; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; INTESTINE CELL; MASS SPECTROMETRY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ANALYSIS; RNA INTERFERENCE; STRUCTURE ANALYSIS; WILD ANIMAL;

ANIMALS; CACO-2 CELLS; CELL DIFFERENTIATION; DIPEPTIDYL PEPTIDASE 4; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GLYCOSYLATION; HT29 CELLS; HUMANS; INTESTINES; MICE; MICE, KNOCKOUT; N-ACETYLGLUCOSAMINYLTRANSFERASES; SUCRASE-ISOMALTASE COMPLEX;

MUS;

EID: 78549246798     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.162735     Document Type: Article

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