Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.

Previous studies have shown that the locus control region (LCR) and the promoter of the growth hormone (GH) gene can control the expression of GH. Therefore, lenti- and retro-viral vectors with these elements might be useful to monitor the activation of the GH gene and the development of newborn som...

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Main Authors: Masayoshi Okada, Hiroko Matsuda, Yasuhiko Okimura
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3546981?pdf=render
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spelling doaj-4383e79f7c2f4236b4afa356caf64c3b2020-11-25T02:32:46ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5443710.1371/journal.pone.0054437Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.Masayoshi OkadaHiroko MatsudaYasuhiko OkimuraPrevious studies have shown that the locus control region (LCR) and the promoter of the growth hormone (GH) gene can control the expression of GH. Therefore, lenti- and retro-viral vectors with these elements might be useful to monitor the activation of the GH gene and the development of newborn somatotrophs. To test this, we first constructed a lentiviral vector, which expresses green fluorescent protein (GFP) under the control of these elements, and injected them into rat pituitaries in situ and in vivo. The lentiviral vector expressed GFP specifically in the anterior lobe, and nearly all GFP-positive cells were anti-GH immunoreactive. The GFP expression was upregulated by the administration of growth hormone releasing hormone and an IGF-1 receptor blocker. Furthermore, the social isolation stress, which was shown to decrease the GH secretion, decreased the GFP expression. Second, we injected the retroviral vector into neonatal rat pituitaries in vivo. At 30 days postinjection (DPI), almost all GFP-positive cells were anti-GH positive and anti-prolactin negative as the lentiviral expression. However, GFP was transiently expressed by developing lactotrophs at 8 and 16 DPI, suggesting that our vector lacks an element(s) which suppresses the expression. Meanwhile, the retrovirally labeled cells tended to cluster with the cells of same type. An analysis of cell numbers in each cluster revealed some features of cell proliferation. These viral vectors are shown to be useful tools to monitor the activation of the GH gene and the development of somatotrophs.http://europepmc.org/articles/PMC3546981?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Masayoshi Okada
Hiroko Matsuda
Yasuhiko Okimura
spellingShingle Masayoshi Okada
Hiroko Matsuda
Yasuhiko Okimura
Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
PLoS ONE
author_facet Masayoshi Okada
Hiroko Matsuda
Yasuhiko Okimura
author_sort Masayoshi Okada
title Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
title_short Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
title_full Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
title_fullStr Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
title_full_unstemmed Lentiviral and Moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
title_sort lentiviral and moloney retroviral expression of green fluorescent protein in somatotrophs in vivo.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Previous studies have shown that the locus control region (LCR) and the promoter of the growth hormone (GH) gene can control the expression of GH. Therefore, lenti- and retro-viral vectors with these elements might be useful to monitor the activation of the GH gene and the development of newborn somatotrophs. To test this, we first constructed a lentiviral vector, which expresses green fluorescent protein (GFP) under the control of these elements, and injected them into rat pituitaries in situ and in vivo. The lentiviral vector expressed GFP specifically in the anterior lobe, and nearly all GFP-positive cells were anti-GH immunoreactive. The GFP expression was upregulated by the administration of growth hormone releasing hormone and an IGF-1 receptor blocker. Furthermore, the social isolation stress, which was shown to decrease the GH secretion, decreased the GFP expression. Second, we injected the retroviral vector into neonatal rat pituitaries in vivo. At 30 days postinjection (DPI), almost all GFP-positive cells were anti-GH positive and anti-prolactin negative as the lentiviral expression. However, GFP was transiently expressed by developing lactotrophs at 8 and 16 DPI, suggesting that our vector lacks an element(s) which suppresses the expression. Meanwhile, the retrovirally labeled cells tended to cluster with the cells of same type. An analysis of cell numbers in each cluster revealed some features of cell proliferation. These viral vectors are shown to be useful tools to monitor the activation of the GH gene and the development of somatotrophs.
url http://europepmc.org/articles/PMC3546981?pdf=render
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