Bockman D E, Sharp R, Merlino G
Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta.
Gastroenterology. 1995 Feb;108(2):447-54. doi: 10.1016/0016-5085(95)90073-x.
BACKGROUND/AIMS: Transforming growth factor (TGF) alpha affects the growth of gastric mucosa. Its overexpression alters the mucosa. The aim of this study was to test the possibility that it regulates differentiation of gland cells.
Transgenic mice that overexpress TGF-alpha were used to detect its effect on zymogenic (chief) cells in the stomach. To test for a general regulatory role of TGF-alpha in differentiation of zymogen-producing cells, salivary glands from transgenic mice were studied.
In these mice, messenger RNA for pepsinogen C is present in the stomach at normal levels during the neonatal period and then decreases markedly. Zymogenic cells are present in the stomach during the neonatal period but are missing in transgenic adults. The bases of gastric glands, normally rich in zymogenic cells, are occupied by undifferentiated cells and mucous neck cells, the precursors of zymogenic cells. Zymogen granules in submandibular glands of transgenic female mice are reduced in number. Zymogen granule-containing cells in the parotid gland undergo redifferentiation to form tubular complexes, collections of ductularlike structures like those formed in the transgenic pancreas.
TGF-alpha is a major participant in the regulation of terminal differentiation of zymogenic cells in the stomach and salivary glands.
背景/目的:转化生长因子(TGF)α影响胃黏膜的生长。其过表达会改变黏膜。本研究的目的是测试其调节腺细胞分化的可能性。
使用过表达TGF-α的转基因小鼠来检测其对胃中胃酶原(主)细胞的影响。为了测试TGF-α在胃酶原产生细胞分化中的一般调节作用,研究了转基因小鼠的唾液腺。
在这些小鼠中,胃蛋白酶原C的信使核糖核酸在新生儿期胃中以正常水平存在,然后显著减少。胃酶原细胞在新生儿期存在于胃中,但在转基因成年小鼠中缺失。通常富含胃酶原细胞的胃腺底部被未分化细胞和黏液颈细胞占据,黏液颈细胞是胃酶原细胞的前体。转基因雌性小鼠下颌下腺中的胃酶原颗粒数量减少。腮腺中含胃酶原颗粒的细胞发生再分化,形成管状复合体,这是一种类似于转基因胰腺中形成的导管样结构的集合。
TGF-α是胃和唾液腺中胃酶原细胞终末分化调节的主要参与者。