Literature DB >> 12769229

Growth hormone in the nervous system: autocrine or paracrine roles in retinal function?

S Harvey1, M Kakebeeke, A E Murphy, E J Sanders.   

Abstract

Growth hormone (GH) is primarily produced in the pituitary gland, although GH gene expression also occurs in the central and autonomic nervous systems. GH-immunoreactive proteins are abundant in the brain, spinal cord, and peripheral nerves. The appearance of GH in these tissues occurs prior to the ontogenic differentiation of the pituitary gland and prior to the presence of GH in systemic circulation. Neural GH is also present in neonates, juveniles, and adults and is independent of changes in pituitary GH secretion. Neural GH is therefore likely to have local roles in neural development or neural function, especially as GH receptors (GHRs) are widespread in the nervous system. In recent studies, GH mRNA and GH immunoreactive proteins have been identified in the neural retina of embryonic chicks. GH immunoreactivity is present in the optic cup of chick embryos at embryonic day (ED) 3 of the 21-d incubation period. It is widespread in the neural retina by ED 7 but also present in the nonpigmented retina, choroid, sclera, and cornea. This immunoreactivity is associated with proteins in the neural retina comparable in size with those in the adult pituitary gland, although it is primarily associated with 15-16 kDa moieties rather than with the full-length molecule of approximately 22 kDa. These small GH moieties may reflect proteolytic fragments of "monomer" GH and (or) the presence of different GH gene transcripts, since full-length and truncated GH cDNAs are present in retinal tissue extracts. The GH immunoreactivity in the retina persists throughout embryonic development but is not present in juvenile birds (after 6 weeks of age). This immunoreactivity is also associated with the presence of GH receptor (GHR) immunoreactivity and GHR mRNA in ocular tissues of chick embryos. The retina is thus an extrapituitary site of GH gene expression during early development and is probably an autocrine or paracrine site of GH action. The marked ontogenic pattern of GH immunoreactivity in the retina suggests hitherto unsuspected roles for GH in neurogenesis or ocular development.

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Year:  2003        PMID: 12769229     DOI: 10.1139/y03-034

Source DB:  PubMed          Journal:  Can J Physiol Pharmacol        ISSN: 0008-4212            Impact factor:   2.273


  11 in total

Review 1.  Extrapituitary growth hormone.

Authors:  S Harvey
Journal:  Endocrine       Date:  2010-10-23       Impact factor: 3.633

2.  Corneal properties in children with congenital isolated growth hormone deficiency.

Authors:  Pinar Nalcacioglu-Yuksekkaya; Emine Sen; Ufuk Elgin; Mumin Hocaoglu; Faruk Ozturk; Sebahat Agladıoglu Yilmaz; Havva Nur Kendirci; Semra Cetinkaya; Zehra Aycan
Journal:  Int J Ophthalmol       Date:  2014-04-18       Impact factor: 1.779

3.  Cornea in acromegalic patients as a possible target of growth hormone action.

Authors:  A Ciresi; M C Amato; D Morreale; G Lodato; A Galluzzo; C Giordano
Journal:  J Endocrinol Invest       Date:  2010-07-22       Impact factor: 4.256

4.  Retinal growth hormone in perinatal and adult rats.

Authors:  Steve Harvey; Marie-Laure Baudet; Esmond J Sanders
Journal:  J Mol Neurosci       Date:  2006       Impact factor: 3.444

Review 5.  Neural growth hormone: an update.

Authors:  Steve Harvey; Kerry Hull
Journal:  J Mol Neurosci       Date:  2003-02       Impact factor: 3.444

6.  Ocular findings in Sheehan's syndrome.

Authors:  Murat Atmaca; Esra Kızıldağ; Zehra Candan; Mehmet Fatih Özbay; İsmet Seven
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-01-10       Impact factor: 3.117

7.  Evaluation of central corneal and central retinal thicknesses and intraocular pressure in acromegaly patients.

Authors:  Sefika Burcak Polat; Nagihan Ugurlu; Reyhan Ersoy; Oguzhan Oguz; Necati Duru; Bekir Cakir
Journal:  Pituitary       Date:  2014-08       Impact factor: 4.107

8.  Growth hormone localization in the neural retina and retinal pigmented epithelium of embryonic chicks.

Authors:  Steve Harvey; Mia Kakebeeke; Esmond J Sanders
Journal:  J Mol Neurosci       Date:  2004       Impact factor: 3.444

9.  Prion disease induced alterations in gene expression in spleen and brain prior to clinical symptoms.

Authors:  Hyeon O Kim; Greg P Snyder; Tyler M Blazey; Richard E Race; Bruce Chesebro; Pamela J Skinner
Journal:  Adv Appl Bioinform Chem       Date:  2008-09-07

10.  Comparing acromegalic patients to healthy controls with respect to intraocular pressure, central corneal thickness, and optic disc topography findings.

Authors:  Emine Sen; Yasemin Tutuncu; Ufuk Elgin; Melike Balikoglu-Yilmaz; Dilek Berker; F Nur Aksakal; Faruk Ozturk; Serdar Guler
Journal:  Indian J Ophthalmol       Date:  2014-08       Impact factor: 1.848

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