Ontogeny of the endocrine pancreatic cells of the gilthead sea bream, Sparus aurata (Teleost).

The development of the gilthead sea bream, Sparus aurata, endocrine pancreas was studied from hatching to 114 days, using immunocytochemical techniques. Bonito insulin (INS)-, synthetic somatostatin-14 (SS-14)-, salmon somatostatin-25 (SS-25)-, mammalian somatostatin-28 (1-12) (SS-28)-, porcine glucagon (GLU)-, glucagon-like peptide-1 (1-19) (GLP-1)-, synthetic porcine peptide tyrosine tyrosine (PYY)-, and neuropeptide Y (NPY)-like immunoreactivities were demonstrated. The different types of endocrine cells appear at distinct stages of development and differ in their arrangement.

FSH-, LH-, and TSH-expressing cells during development of Sparus aurata L. (Teleostei). An immunocytochemical study.

Follicle-stimulating hormone-like gonadotropin (FSH), luteinizing hormone-like gonadotropin (LH), and thyrotropin (TSH) cells were detected in adult and developing pituitary gland of gilthead seabream. Antisera obtained against the alpha- and beta-subunits of FSH (anti-My FSH) and the beta-subunit of LH (anti-My LHbeta), respectively, of the teleost Mediterranean yellowtail, and an antiserum against the beta-subunit of human TSH (anti-h TSHbeta), were applied to identify and follow these cells during ontogeny using light microscopy. FSH cells were immunoreactive to anti-My FSH serum, LH cells were immunoreactive to anti-My LHbeta and anti-My FSH sera, and TSH cells were immunoreactive to anti-h TSHbeta and anti-My FSH sera.

Immunocytochemical and ultrastructural characterization of mammosomatotrope-, growth hormone-, and prolactin-cells from the gilthead sea bream (Sparus aurata l., Teleostei): an ontogenic study.

Growth hormone (GH), prolactin (PRL), and mammosomatotrope (MS) cells of gilthead sea bream, Sparus aurata, a teleost fish, were studied in specimens from hatching to 15 months (adults) using conventional electron microscopy and an immunogold method using anti-tilapia GH sera and anti-chum salmon PRL serum. MS cells, immunoreactive to both anti-GH sera and anti-PRL sera, had been first identified in fish in a previous study in newly hatched larvae and in older larvae and juvenile specimens of Sparus aurata by light microscopic immunocytochemistry. In the present work, MS cells reacted positively to immunogold label only in older larvae and juveniles and their secretory granules immunoreacted with both GH and PRL antisera or with only one of them.

Investigation into the duality of gonadotropic cells of Mediterranean yellowtail (Seriola dumerilii, Risso 1810): immunocytochemical and ultrastructural studies.

Two antisera against the follicle-stimulating hormone-like gonadotropin (FSH) of Mediterranean (M.) yellowtail, anti-My FSHa and anti-My FSHb, were obtained. Anti-My FSHa serum specifically recognized FSH cells and did not react with any other pituitary cell type, while anti-My FSHb serum recognized the alpha-subunit of the pituitary glycoprotein hormones and immunostained FSH, luteinizing hormone-like gonadotropin (LH), and thyrotropin (TSH) cells.

Immunocytochemical demonstration of melanotropic and adrenocorticotropic cells from the gilthead sea bream (Sparus aurata L., Teleostei) by light and electron microscopy: an ontogenic study.

In the pituitary of gilthead sea bream, Sparus aurata, melanotropic (MSH) and adrenocorticotropic (ACTH) cells were identified at the light and electron microscopic levels using rabbit anti-synthetic alphaMSH (MSH) and anti-human ACTH (1-24) (ACTH) sera. The distribution of these cell types was followed from hatching to 48 months. The techniques used included the peroxidase anti-peroxidase (PAP) method, conventional electron microscopy, and an immunogold technique.