Gastrin stimulates the growth of gastric pit with less-differentiated features

被引:30
作者
Konda, Y
Kamimura, H
Yokota, H
Hayashi, N
Sugano, K
Takeuchi, T
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Dept Mol Med, Maebashi, Gumma 3718512, Japan
[2] Jichi Med Sch, Dept Med, Gastrointestinal Div, Minami Kawachi, Tochigi 3290498, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1999年 / 277卷 / 04期
关键词
gastric mucosa; gastric surface mucous cells; gastrin binding;
D O I
10.1152/ajpgi.1999.277.4.G773
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Gastrin stimulates the growth of gastric mucosa by increasing mostly its glandular region but is not known to induce the growth of a pit region where-its major constituent cells, gastric surface mucous (GSM) cells, turn over rapidly. To investigate the effect of gastrin on GSM cells, we generated hypergastrinemic mice by expressing a human gastrin transgene. We obtained a hypergastrinemic mouse line whose average serum gastrin level is 671 +/- 252 pg/ml (normal level <150 pg/ml). Gastrin-positive cells were found in the fundic mucosa. The gastric mucosa exhibited hypertrophic growth, which was characterized by an elongated pit with an active proliferative zone, but the glandular region containing parietal cells was normal or reduced in size. The GSM cells contained fewer mucous granules than those of control littermates and lost reactivity to the GSM cell-specific cholera toxin P-subunit lectin. GSM cells along the foveolar region and many mucous neck cells became Alcian blue positive, suggesting the appearance of sialomucin in these cells. We suggest that gastrin stimulates the growth of the proliferative zone of gastric glands, which results in the elongation of the pit region whose GSM cells exhibit less-differentiated features.
引用
收藏
页码:G773 / G784
页数:12
相关论文
共 54 条
[11]  
EIPPER BA, 1992, J NATL CANCER I MONO, V13, P163
[12]   HELICOBACTER-PYLORI INFECTION AND ABNORMALITIES OF ACID-SECRETION IN PATIENTS WITH DUODENAL-ULCER DISEASE [J].
ELOMAR, EM ;
PENMAN, ID ;
ARDILL, JES ;
CHITTAJALLU, RS ;
HOWIE, C ;
MCCOLL, KEL .
GASTROENTEROLOGY, 1995, 109 (03) :681-691
[13]   MOLUCCELLA LAEVIS LECTIN, A MARKER FOR CELLULAR-DIFFERENTIATION PROGRAMS IN MOUSE GUT EPITHELIUM [J].
FALK, P ;
LORENZ, RG ;
SHARON, N ;
GORDON, JI .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 268 (04) :G553-G567
[14]  
FALK P, 1994, AM J PHYSIOL, V266, P987
[15]  
FENOGLIOPREISER CM, 1989, GASTROINTESTINAL PAT, P133
[16]   MOLECULAR-CLONING AND SEQUENCING OF A RAT PREPROGASTRIN COMPLEMENTARY DEOXYRIBONUCLEIC-ACID [J].
FULLER, PJ ;
STONE, DL ;
BRAND, SJ .
MOLECULAR ENDOCRINOLOGY, 1987, 1 (04) :306-311
[17]   UNDERSTANDING GASTROINTESTINAL EPITHELIAL-CELL BIOLOGY - LESSONS FROM MICE WITH HELP FROM WORMS AND FLIES [J].
GORDON, JI .
GASTROENTEROLOGY, 1993, 105 (02) :315-324
[18]   PRODUCTION OF BIOACTIVE GASTRIN FROM THE NONENDOCRINE CELL-LINES CHO AND COS-7 [J].
HAYASHI, N ;
KAYO, T ;
SUGANO, K ;
TAKEUCHI, T .
FEBS LETTERS, 1994, 337 (01) :27-32
[19]  
Hogan B., 1994, Manipulating the Mouse Embryo, Section E: Production of Transgenic Mice, P217
[20]   Distinct effects of tetragastrin, histamine, and CCh on rat gastric mucin synthesis and contribution of NO [J].
Ichikawa, T ;
Ishihara, K ;
Kusakabe, T ;
Kurihara, M ;
Kawakami, T ;
Takenaka, T ;
Saigenji, K ;
Hotta, K .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (01) :G138-G146