ONTOGENIC EXPRESSION OF CHROMOGRANIN-A AND ITS DERIVED PEPTIDES, WE-14 AND PANCREASTATIN, IN THE RAT NEUROENDOCRINE SYSTEM

Citation
Sc. Barkatullah et al., ONTOGENIC EXPRESSION OF CHROMOGRANIN-A AND ITS DERIVED PEPTIDES, WE-14 AND PANCREASTATIN, IN THE RAT NEUROENDOCRINE SYSTEM, HISTOCHEM C, 107(3), 1997, pp. 251-257
Citations number
25
Categorie Soggetti
Cell Biology",Microscopy
Journal title
HISTOCHEMISTRY AND CELL BIOLOGY
ISSN journal
09486143 → ACNP
Volume
107
Issue
3
Year of publication
1997
Pages
251 - 257
Database
ISI
SICI code
0948-6143(1997)107:3<251:OEOCAI>2.0.ZU;2-A
Abstract
The ontogenetic expression of chromogranin A (CgA) and its derived pep tides, WE-14 and pancreastatin (PST), was studied in the rat neuroendo crine system employing immunohistochemical analysis of fetal and neona tal specimens from 12.5-day embryos (E12.5), to 42-day postnatal (P42) rats. C(g)A immunostaining was first detected in endocrine cells of t he pancreas, stomach, intestine, adrenal gland and thyroid at E13.5, E 14.5, E15.5, E15.5 and E18.5, respectively. PST-like immunoreactivity was detected in endocrine cells of the pancreas at E13.5, stomach, int estine at E15.5, adrenal gland at E17.5 and thyroid at E18.5. WE-14 im munoreactivity was first observed in the immature pancreas at E15.5, m ucosal cells of the stomach at E15.5, scattered chromaffin cells in th e immature adrenal gland and mucosal cells of the intestine at E17.5 a nd thyroid parafollicular cells at E18.5. These data confirm that the translation of the CgA gene is regulated differentially in various neu roendocrine tissues and, moreover, suggests that the posttranslational processing of the molecule is developmentally controlled.