Literature DB >> 7895669

Corticotropin-releasing hormone and epidermal growth factor: mitogens for anterior pituitary corticotropes.

G V Childs1, D Rougeau, G Unabia.   

Abstract

Anterior pituitary corticotropes increase in number after stimulation by adrenalectomy or corticotropin-releasing hormone (CRH). However, is this brought about by mitoses? Furthermore, as epidermal growth factor (EGF) is a potent secretagogue for corticotropes, is it also a mitogen? To address these questions, populations of corticotropes enriched to 88-97% by counterflow centrifugation were studied after growth in 0-10 nM CRH with and without 0.1-10 ng/ml EGF. Three types of assays were used to detect changes in mitotic cells or cell number. An enzyme immunoassay for bromodeoxyuridine uptake during DNA synthesis [bromodeoxyuridine (BrDU) uptake] detected a 3-fold increase in optical density readings in the presence of 0.5 nM CRH or EGF. Together the peptides increased the optical density to 4.8-fold basal levels. No further increases in BrDU uptake were seen with higher concentrations of CRH or EGF. Cytochemical detection of BrDU uptake by immunolabeled corticotropes showed BrDU in 18 +/- 2% of 3- to 5-day ACTH cells. In the presence of 0.5 nM CRH or 0.5 ng/ml EGF, this value increased to 37 +/- 3% or 34 +/- 2% of ACTH cells, respectively. Together CRH and EGF stimulated increases in mitotic activity so that 47 +/- 4% of the ACTH cells were labeled for BrDU after a 1-h exposure. Cell growth/cell death assays in 3-(4,5-dimethyltiazol-2-yl)2,5- diphenyl tetrazolium bromide were also used to detect changes in overall cell number or cell survival in the same groups of enriched corticotrope cultures. Both 0.5 nM CRH and 0.5 ng/ml EGF caused increases to 1.5- to 1.7-fold basal readings. However, higher concentrations did not stimulate increases in number, and their combined effects were not additive. These studies show that CRH and EGF can be mitogens for ACTH-bearing corticotropes, in a limited dose range. In a higher dose range, their differentiating effects may eliminate dividing cells and retard further growth of the population.

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Year:  1995        PMID: 7895669     DOI: 10.1210/endo.136.4.7895669

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  20 in total

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Journal:  Pituitary       Date:  1999-05       Impact factor: 4.107

Review 2.  Endocrine/paracrine control of pituitary cell proliferation and its involvement in pituitary tumorigenesis.

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Journal:  Pituitary       Date:  1999-05       Impact factor: 4.107

3.  Expression of IGFBP7 mRNA in corticotrophs in the anterior pituitary of adrenalectomized rats.

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Review 4.  Paracrinicity: the story of 30 years of cellular pituitary crosstalk.

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5.  Rat prolactinoma cell growth regulation by epidermal growth factor receptor ligands.

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Review 6.  Growth factors in the pathogenesis of prolactin-secreting tumors.

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Review 7.  Expression and function of ErbB receptors and ligands in the pituitary.

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8.  Anterior pituitary corticotropes of adrenalectomized, leptin-administered rats.

Authors:  L K Malendowicz; A Ziólkowska; M Trejter
Journal:  Pituitary       Date:  2001 Jan-Apr       Impact factor: 4.107

9.  Lack of annexin 1 results in an increase in corticotroph number in male but not female mice.

Authors:  J F Morris; S Omer; E Davies; E Wang; C John; T Afzal; S Wain; J C Buckingham; R J Flower; H C Christian
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10.  A Sex-Dependent, Tropic Role for Leptin in the Somatotrope as a Regulator of POU1F1 and POU1F1-Dependent Hormones.

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Journal:  Endocrinology       Date:  2016-08-29       Impact factor: 4.736

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