Transforming growth factor-β inhibits proliferation and maturation of cultured guinea pig gastric pit cells

被引:29
作者
Rokutan, K
Yamada, M
Torigoe, J
Saito, T
机构
[1] Univ Tokushima, Sch Med, Dept Nutr, Tokushima 7708503, Japan
[2] Tokyo Med Coll, Dept Internal Med 4, Tokyo 1600023, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1998年 / 275卷 / 03期
关键词
serum-free culture; pit cell lineage; proliferation and differentiation; mucin synthesis; intracellular signals;
D O I
10.1152/ajpgi.1998.275.3.G526
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We studied the effects of transforming growth factor-beta 1 (TGF-beta 1) on guinea pig gastric mucous cells, cultured in serum-free conditions. Electron microscopy showed that most cells were pre-pit cells, characterized by the presence of a few secretory granules scattered in the cytoplasm. Epidermal growth factor (EGF) stimulated cell growth, [H-3]glucosamine uptake, and accumulation of mucus granules positive for galactose oxidase-Schiff reaction. This EGF-induced maturation into pit cells was confirmed morphologically by the appearance of uniformly dense ovoid or spherical mucus granules packed in the ectoplasm. Western blotting with an antiphosphotyrosine antibody showed that TGF-beta 1 did not inhibit the EGF-initiated tyrosine phosphorylation of the EGF receptor. Northern blotting with cDNA probes for c-fos and c-myc demonstrated that TGF-beta 1 did not affect the EGF-induced expression of the transcripts. However TGF-pl-treated cells did not replicate and remained in an immature stage, even in the presence of EGF, suggesting a potential role of TGF-beta 1 in the regulation of proliferation and differentiation of a pit cell lineage in vivo.
引用
收藏
页码:G526 / G533
页数:8
相关论文
共 43 条
[1]   THE CELL BIOLOGY OF TRANSFORMING GROWTH-FACTOR-BETA [J].
BARNARD, JA ;
LYONS, RM ;
MOSES, HL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1032 (01) :79-87
[2]  
BASSON MD, 1992, SURGERY, V112, P299
[3]   LOCALIZATION OF TRANSFORMING GROWTH FACTOR-ALPHA AND ITS RECEPTOR IN GASTRIC-MUCOSAL CELLS - IMPLICATIONS FOR A REGULATORY ROLE IN ACID-SECRETION AND MUCOSAL RENEWAL [J].
BEAUCHAMP, RD ;
BARNARD, JA ;
MCCUTCHEN, CM ;
CHERNER, JA ;
COFFEY, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :1017-1023
[4]   GROWTH-FACTORS AND WOUND-HEALING - BIOCHEMICAL-PROPERTIES OF GROWTH-FACTORS AND THEIR RECEPTORS [J].
BENNETT, NT ;
SCHULTZ, GS .
AMERICAN JOURNAL OF SURGERY, 1993, 165 (06) :728-737
[5]  
Boivin GP, 1996, LAB INVEST, V74, P513
[6]   CHARACTERIZATION OF MUCOUS CELL SYNTHETIC FUNCTIONS IN A NEW PRIMARY CANINE GASTRIC MUCOUS CELL-CULTURE SYSTEM [J].
BOLAND, CR ;
KRAUS, ER ;
SCHEIMAN, JM ;
BLACK, C ;
DESHMUKH, GD ;
DOBBINS, WO .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (05) :G774-G787
[7]   MITOGENIC RESPONSE OF CANINE FUNDIC EPITHELIAL-CELLS IN SHORT-TERM CULTURE TO TRANSFORMING GROWTH FACTOR-ALPHA AND INSULIN-LIKE GROWTH FACTOR-I [J].
CHEN, MC ;
LEE, AT ;
SOLL, AH .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (05) :1716-1723
[8]   PARACRINE CONTROL OF GASTRIC EPITHELIAL-CELL GROWTH IN CULTURE BY TRANSFORMING GROWTH FACTOR-ALPHA [J].
CHEN, MC ;
LEE, AT ;
KARNES, WE ;
AVEDIAN, D ;
MARTIN, M ;
SORVILLO, JM ;
SOLL, AH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02) :G390-G396
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]  
Ernst H, 1996, J PHYSIOL PHARMACOL, V47, P443