Literature DB >> 8299592

Cells that express luteinizing hormone (LH) and follicle-stimulating hormone (FSH) beta-subunit messenger ribonucleic acids during the estrous cycle: the major contributors contain LH beta, FSH beta, and/or growth hormone.

G V Childs1, G Unabia, D Rougeau.   

Abstract

There is a 2-fold increase in the percentage of gonadotropes bearing LH beta or FSH beta mRNAs or antigens as the cells approach proestrus. The purpose of this study was to identify the source of these cells with dual labeling techniques. The first hypothesis was that they stemmed from small monohormonal gonadotropes (containing only LH or FSH) that were driven to transcribe and translate the other gonadotropin. Alternatively, they may stem from other pituitary cell types. We detected the LH beta or FSH beta mRNAs by in situ hybridization (biotinylated oligonucleotide probes were detected by peroxidase-labeled avidin). Second, immunolabeling protocols localized the pituitary hormones. The percentages of cells with LH beta antigens and FSH beta mRNA increased to 81% of the LH beta antigen-bearing cells by the time of peak expression of FSH beta mRNA. Similarly, FSH beta antigen-bearing cells increased their expression of LH beta mRNA to 40% of such cells by the morning of proestrus. During the peak period of expression (the evening of proestrus), LH antigen-bearing cells had increased their expression of LH beta mRNA to 93%. Furthermore, 81% of the same cells expressed FSH beta mRNA. Thus, at least 80% of cells with LH antigens became bihormonal as the cells approached proestrus. This partially supports the first hypothesis for the origin of the new gonadotropes. However, the dual labeling studies also showed that 47% or 60% of cells with GH antigens expressed LH beta or FSH beta mRNAs, respectively, during peak expression (14% of pituitary cells contained gonadotropin mRNAs and GH antigens). Expression by cells with other antigens was low or absent (< 5% of pituitary cells). Perhaps a subset of somatotropes expresses gonadotropin mRNAs. Alternatively, the labeling could signify the presence of GH bound to GH receptors in gonadotropes. In either case, it appears that GH cells may be somehow linked to gonadotrope function as the cells approach proestrus.

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Year:  1994        PMID: 8299592     DOI: 10.1210/endo.134.2.8299592

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


  15 in total

1.  Bipotential effects of estrogen on growth hormone synthesis and storage in vitro.

Authors:  Gwen V Childs; Mary Iruthayanathan; Noor Akhter; Geda Unabia; Brandy Whitehead-Johnson
Journal:  Endocrinology       Date:  2004-12-23       Impact factor: 4.736

2.  Anterior pituitary leptin expression changes in different reproductive states: in vitro stimulation by gonadotropin-releasing hormone.

Authors:  Noor Akhter; Brandy W Johnson; Christopher Crane; Mary Iruthayanathan; Yi-Hong Zhou; Akihiko Kudo; Gwen V Childs
Journal:  J Histochem Cytochem       Date:  2006-10-16       Impact factor: 2.479

3.  The somatotrope as a metabolic sensor: deletion of leptin receptors causes obesity.

Authors:  Gwen V Childs; Noor Akhter; Anessa Haney; Mohsin Syed; Angela Odle; Michael Cozart; Zachary Brodrick; Dana Gaddy; Larry J Suva; Nisreen Akel; Christopher Crane; Helen Benes; Amanda Charlesworth; Raul Luque; Streamson Chua; Rhonda D Kineman
Journal:  Endocrinology       Date:  2010-11-17       Impact factor: 4.736

4.  Plurihormonality in pituitary adenomas associated with acromegaly.

Authors:  Fateme Salehi; Sandra Cohen; Luis V Syro; Humberto Uribe; Eva Horvath; Kalman Kovacs; Sylvia L Asa
Journal:  Endocr Pathol       Date:  2006       Impact factor: 3.943

5.  A Sex-Dependent, Tropic Role for Leptin in the Somatotrope as a Regulator of POU1F1 and POU1F1-Dependent Hormones.

Authors:  Angela K Odle; Melody L Allensworth-James; Noor Akhter; Mohsin Syed; Anessa C Haney; Melanie MacNicol; Angus M MacNicol; Gwen V Childs
Journal:  Endocrinology       Date:  2016-08-29       Impact factor: 4.736

Review 6.  Effects of gonadotrophin-releasing hormone outside the hypothalamic-pituitary-reproductive axis.

Authors:  D C Skinner; A J Albertson; A Navratil; A Smith; M Mignot; H Talbott; N Scanlan-Blake
Journal:  J Neuroendocrinol       Date:  2009-03       Impact factor: 3.627

7.  Atrazine binds to the growth hormone-releasing hormone receptor and affects growth hormone gene expression.

Authors:  Walid D Fakhouri; Joseph L Nuñez; Frances Trail
Journal:  Environ Health Perspect       Date:  2010-06-08       Impact factor: 9.031

8.  Selective deletion of leptin receptors in gonadotropes reveals activin and GnRH-binding sites as leptin targets in support of fertility.

Authors:  Noor Akhter; Tyler CarlLee; Mohsin M Syed; Angela K Odle; Michael A Cozart; Anessa C Haney; Melody L Allensworth-James; Helen Beneš; Gwen V Childs
Journal:  Endocrinology       Date:  2014-07-24       Impact factor: 4.736

9.  Fasting and glucose effects on pituitary leptin expression: is leptin a local signal for nutrient status?

Authors:  Christopher Crane; Noor Akhter; Brandy W Johnson; Mary Iruthayanathan; Farhan Syed; Akihiko Kudo; Yi-Hong Zhou; Gwen V Childs
Journal:  J Histochem Cytochem       Date:  2007-06-26       Impact factor: 2.479

10.  Diethylstilbestrol increases the density of prolactin cells in male mouse pituitary by inducing proliferation of prolactin cells and transdifferentiation of gonadotropic cells.

Authors:  Keiko Shukuwa; Shin-Ichi Izumi; Yoshitaka Hishikawa; Kuniaki Ejima; Satoshi Inoue; Masami Muramatsu; Yasuyoshi Ouchi; Takashi Kitaoka; Takehiko Koji
Journal:  Histochem Cell Biol       Date:  2006-02-09       Impact factor: 4.304

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