Pituitary corticotroph ontogeny and regulation in transgenic zebrafish.

We characterized zebrafish proopiomelanocortin (POMC) gene promoter, and sequence analysis revealed that the promoter contains regulatory elements conserved among vertebrate species. To monitor the ontogeny of the pituitary POMC lineage in living vertebrates, we generated transgenic zebrafish expressing green fluorescent protein (GFP) driven by the POMC promoter. Zebrafish POMC-GFP is first expressed asymmetrically as two bilateral groups of cells most anterior to the neural ridge midline at 18-20 h post fertilization (hpf). POMC-GFP-positive cells then fuse into a single-cell mass within the pituitary anlage after 24 hpf and subsequently organize as distinct anterior and posterior domains between 48 and 64 hpf. Immunohistochemical studies with ACTH and alphaMSH antisera showed that POMC-GFP was mainly targeted to both anterior and posterior pituitary corticotrophs, whereas posterior pituitary region melanotrophs did not express GFP. To determine in vivo zebrafish corticotroph responses, dexamethasone (10(-5) m) was added to live embryos, which selectively suppressed POMC-GFP expression in the anterior group of corticotrophs, suggesting a distinct domain that is responsive to glucocorticoid feedback. Transgenic zebrafish with specific POMC-GFP expression in pituitary corticotrophs offers a powerful genetic system for in vivo study of vertebrate corticotroph lineage development.

[1]  A. Hori,et al.  Proliferation of adenohypophyseal cells into posterior lobe , 2005, Acta Neurochirurgica.

[2]  H. Ikeda,et al.  The development and morphogenesis of the human pituitary gland , 2004, Anatomy and Embryology.

[3]  Z. Lele,et al.  Adenohypophysis formation in the zebrafish and its dependence on sonic hedgehog. , 2003, Developmental biology.

[4]  Z. Gong,et al.  Expressed sequence tag analysis of expression profiles of zebrafish testis and ovary. , 2002, Gene.

[5]  T. Maures,et al.  Structure, developmental expression, and physiological regulation of zebrafish IGF binding protein-1. , 2002, Endocrinology.

[6]  T. Maures,et al.  Structural, biochemical, and expression analysis of two distinct insulin-like growth factor I receptors and their ligands in zebrafish. , 2002, Endocrinology.

[7]  G. Martens,et al.  Transgene‐driven protein expression specific to the intermediate pituitary melanotrope cells of Xenopus laevis , 2002, FEBS letters.

[8]  Kathleen M. Scully,et al.  Pituitary Development: Regulatory Codes in Mammalian Organogenesis , 2002, Science.

[9]  S. Melmed,et al.  The central role of SOCS-3 in integrating the neuro-immunoendocrine interface. , 2001, The Journal of clinical investigation.

[10]  S. Melmed The immuno-neuroendocrine interface , 2001 .

[11]  S. Melmed Series Introduction: The immuno-neuroendocrine interface , 2001 .

[12]  K. Karalis,et al.  Corticotropin-releasing hormone regulates IL-6 expression during inflammation. , 2001, The Journal of clinical investigation.

[13]  M. Rosenfeld,et al.  Tbx19, a tissue-selective regulator of POMC gene expression , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. Pack,et al.  Zebrafish pdx1 morphant displays defects in pancreas development and digestive organ chirality, and potentially identifies a multipotent pancreas progenitor cell , 2001, Genesis.

[15]  Haigen Huang,et al.  Analysis of pancreatic development in living transgenic zebrafish embryos , 2001, Molecular and Cellular Endocrinology.

[16]  L. Muglia,et al.  The physiology of corticotropin-releasing hormone deficiency in mice , 2001, Peptides.

[17]  J. Drouin,et al.  A Pituitary Cell-Restricted T Box Factor, Tpit, Activates POMC Transcription in Cooperation with Pitx Homeoproteins , 2001, Cell.

[18]  E. Linney,et al.  Retinoic acid-mediated gene expression in transgenic reporter zebrafish. , 2001, Developmental biology.

[19]  S. Melmed,et al.  Direct regulation of pituitary proopiomelanocortin by STAT3 provides a novel mechanism for immuno-neuroendocrine interfacing. , 2000, The Journal of clinical investigation.

[20]  G. Poulin,et al.  Specific Protein-Protein Interaction between Basic Helix-Loop-Helix Transcription Factors and Homeoproteins of the Pitx Family , 2000, Molecular and Cellular Biology.

[21]  S. Melmed,et al.  Critical Role for STAT3 in Murine Pituitary Adrenocorticotropin Hormone Leukemia Inhibitory Factor Signaling* , 1999, The Journal of Biological Chemistry.

[22]  C. Readhead,et al.  Pituitary-directed leukemia inhibitory factor transgene causes Cushing's syndrome: neuro-immune-endocrine modulation of pituitary development. , 1998, Molecular endocrinology.

[23]  Juan I. Young,et al.  Authentic Cell-Specific and Developmentally Regulated Expression of Pro-Opiomelanocortin Genomic Fragments in Hypothalamic and Hindbrain Neurons of Transgenic Mice , 1998, The Journal of Neuroscience.

[24]  A. McMahon,et al.  Multistep signaling requirements for pituitary organogenesis in vivo. , 1998, Genes & development.

[25]  T. Jessell,et al.  Integrated FGF and BMP signaling controls the progression of progenitor cell differentiation and the emergence of pattern in the embryonic anterior pituitary. , 1998, Development.

[26]  I. Dawid,et al.  Neuronal and neuroendocrine expression of lim3, a LIM class homeobox gene, is altered in mutant zebrafish with axial signaling defects. , 1997, Developmental biology.

[27]  G. Poulin,et al.  NeuroD1/beta2 contributes to cell-specific transcription of the proopiomelanocortin gene , 1997, Molecular and cellular biology.

[28]  M. Farrell,et al.  GATA-1 expression pattern can be recapitulated in living transgenic zebrafish using GFP reporter gene. , 1997, Development.

[29]  J. Drouin,et al.  Novel dimeric Nur77 signaling mechanism in endocrine and lymphoid cells , 1997, Molecular and cellular biology.

[30]  S. Melmed,et al.  Leukemia inhibitory factor (LIF) induces acute adrenocorticotrophic hormone (ACTH) secretion in fetal rhesus macaque primates: a novel dynamic test of pituitary function. , 1996, The Journal of clinical endocrinology and metabolism.

[31]  M. Therrien,et al.  Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene. , 1996, Genes & development.

[32]  J. Pintar,et al.  Ontogeny of basal and regulated secretion from POMC cells of the developing anterior lobe of the rat pituitary gland. , 1996, Developmental Biology.

[33]  C. Kimmel,et al.  Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[34]  P. Dubois,et al.  Embryology of the pituitary gland , 1995, Trends in Endocrinology & Metabolism.

[35]  M. Mortrud,et al.  Identification of DNA elements cooperatively activating proopiomelanocortin gene expression in the pituitary glands of transgenic mice , 1992, Molecular and cellular biology.

[36]  A. Hori,et al.  Proliferation of adenohypophyseal cells into posterior lobe : their normal anatomical condition and possible neoplastic potentiality , 1990 .

[37]  B. Jenks,et al.  The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis. , 1986, Journal of embryology and experimental morphology.

[38]  I. Doniach Histopathology of the pituitary. , 1985, Clinics in endocrinology and metabolism.

[39]  N. L. Le Douarin,et al.  Mapping of the early neural primordium in quail-chick chimeras. I. Developmental relationships between placodes, facial ectoderm, and prosencephalon. , 1985, Developmental biology.

[40]  P. Leroux,et al.  Radioautographic study of binding and internalization of corticotropin-releasing factor by rat anterior pituitary corticotrophs. , 1984, Endocrinology.

[41]  J. Vaughan,et al.  Effects of synthetic ovine corticotropin-releasing factor, glucocorticoids, catecholamines, neurohypophysial peptides, and other substances on cultured corticotropic cells. , 1983, Endocrinology.

[42]  W. Nicholson,et al.  Equine Cushing's disease: plasma immunoreactive proopiolipomelanocortin peptide and cortisol levels basally and in response to diagnostic tests. , 1982, Endocrinology.

[43]  W. Nicholson,et al.  Proopiolipomelanocortin peptides in normal pituitary, pituitary tumor, and plasma of normal and Cushing's horses. , 1982, Endocrinology.

[44]  S. Lamberts,et al.  Adrenocorticotropin-secreting pituitary adenomas originate from the anterior or the intermediate lobe in Cushing's disease: differences in the regulation of hormone secretion. , 1982, The Journal of clinical endocrinology and metabolism.

[45]  M. Brownstein,et al.  In vivo corticotropin-releasing factor-induced secretion of adrenocorticotropin, beta-endorphin, and corticosterone. , 1982, Endocrinology.

[46]  D. Krieger,et al.  Pituitary intermediate lobe in dog: two cell types and high bioactive adrenocorticotropin content. , 1981, Science.

[47]  S. Daikoku,et al.  An immunohistochemical study on the cytogenesis of adenohypophysial cells in fetal rats. , 1979, Developmental biology.

[48]  Mohamad Maghniea,et al.  The Pituitary , 1919, The Indian Medical Gazette.