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Ontogenic expression of TGFβ 1, 2, and 3 and its receptors in the rat gastric mucosa
Author(s) -
de Andrade Sá Eunice Ribeiro,
Jordão Luciana Renata,
Takahashi Cassia Ayumi,
Alvares Eliana Parisi,
Gama Patrícia
Publication year - 2003
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.10320
Subject(s) - biology , autocrine signalling , paracrine signalling , medicine , epithelium , endocrinology , receptor , gastric glands , stomach , gastric mucosa , immunohistochemistry , gastric chief cell , transforming growth factor , growth factor , immunology , biochemistry , genetics
The stomach of the rat undergoes extensive changes during the formation and maturation of gastric glands. The presence of transforming growth factor beta (TGFβ) in rat milk and in the gastrointestinal tract of pups may suggest its role in this process. The current study evaluated the in vivo dynamic expression and distribution of TGFβ1, β2, β3 and their receptors TβRI and TβRII in the gastric epithelium of 20‐day fetal rats and 1‐, 14‐, 21‐, and 30‐day‐old pups. Immunohistochemistry was used to detect the proteins, and staining was classified according to intensity and cell type. The results showed that the gastric epithelium expresses TGFβ isoforms and receptors throughout development. We found that immunoreactivity paralleled the appearance of differentiated cells, such that surface mucous cells were the first to be immunostained and chief cells were the last. The intensity of reactions followed this same pattern, showing that the expression of TGFβ isoforms spread along the gland with growth. Of interest, the highest apparent activity of TGFβ was observed from 21 days onward, a period that is concomitant with weaning and maturation of most gastric cell types. In addition, surface mucous cells were strongly labeled at the basal cytoplasm at 14 days, suggesting an interaction with the connective tissue. In conclusion, the dynamic expression of TGFβ1, β2, β3, and TβRI and TβRII through stomach development suggests significant paracrine and autocrine roles for this growth factor. We propose that temporal and spatial differences may be regulated by dietary changes, which in turn control cell proliferation and differentiation in the gastric epithelium. Developmental Dynamics 227:450–457, 2003. © 2003 Wiley‐Liss, Inc.