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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546981/ https://www.ncbi.nlm.nih.gov/pubmed/23342159 http://dx.doi.org/10.1371/journal.pone.0054437 |
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author | Okada, Masayoshi Matsuda, Hiroko Okimura, Yasuhiko |
author_facet | Okada, Masayoshi Matsuda, Hiroko Okimura, Yasuhiko |
author_sort | Okada, Masayoshi |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-3546981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35469812013-01-22 Lentiviral and Moloney Retroviral Expression of Green Fluorescent Protein in Somatotrophs In Vivo Okada, Masayoshi Matsuda, Hiroko Okimura, Yasuhiko PLoS One Research Article 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. Public Library of Science 2013-01-16 /pmc/articles/PMC3546981/ /pubmed/23342159 http://dx.doi.org/10.1371/journal.pone.0054437 Text en © 2013 Okada et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Okada, Masayoshi Matsuda, Hiroko Okimura, Yasuhiko Lentiviral and Moloney Retroviral Expression of Green Fluorescent Protein in Somatotrophs In Vivo |
title | Lentiviral and Moloney Retroviral Expression of Green Fluorescent Protein in Somatotrophs In Vivo
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title_full | Lentiviral and Moloney Retroviral Expression of Green Fluorescent Protein in Somatotrophs In Vivo
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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
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title_short | Lentiviral and Moloney Retroviral Expression of Green Fluorescent Protein in Somatotrophs In Vivo
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title_sort | lentiviral and moloney retroviral expression of green fluorescent protein in somatotrophs in vivo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546981/ https://www.ncbi.nlm.nih.gov/pubmed/23342159 http://dx.doi.org/10.1371/journal.pone.0054437 |
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