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Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation

OBJECTIVE: Cell proliferation is known to be controlled by many networks of regulatory proteins. These multiple and complicated mechanisms of control are still being investigated. The aim of the present study is to determine the different properties of adult rat brain thermostable protein complex (T...

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Autores principales: Dzidziguri, Diana, Modebadze, Irina, Bakuradze, Ekaterine, Mosidze, Giorgi, Berulava, Manana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672093/
https://www.ncbi.nlm.nih.gov/pubmed/29105389
http://dx.doi.org/10.22074/cellj.2018.4835
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author Dzidziguri, Diana
Modebadze, Irina
Bakuradze, Ekaterine
Mosidze, Giorgi
Berulava, Manana
author_facet Dzidziguri, Diana
Modebadze, Irina
Bakuradze, Ekaterine
Mosidze, Giorgi
Berulava, Manana
author_sort Dzidziguri, Diana
collection PubMed
description OBJECTIVE: Cell proliferation is known to be controlled by many networks of regulatory proteins. These multiple and complicated mechanisms of control are still being investigated. The aim of the present study is to determine the different properties of adult rat brain thermostable protein complex (TPC) which affect cell proliferation. MATERIALS AND METHODS: This experimental study used brain, kidney and liver tissue from adult (150-170 g) and adolescent (7, 10, 21, 28 days) white rats, adult pigeons and mice. Brain TPC was isolated by alcohol extraction, and primary antibodies Ki67 and GAD65/67 were used for immunohistochemistry, evaluation of transcriptional activity of the tissues and determination of the mitotic index. RESULTS: The results show that brain TPC from rats reversibly decreases cell proliferation by inhibiting transcription. The evidence suggests that TPC is not species-specific, but expresses tissue specificity with regards to terminally differentiated cells. Rat brain TPC inhibits mitotic activity of the progenitor cells in the dentate gyrus of adolescent rats, and corresponding with this decrease in the mitotic index the number of Ki67 positive cells increases. Simultaneously, the number of GAD65/67-positive cells in the hippocampus decreases by approximately threefold. CONCLUSION: These results indicate that rat brain TPC causes the reversible suppression of cell proliferation through the inhibition of transcription. Inhibitory effects of rat brain TPC leads to an increase the number of cells in the cell cycle, in tissues of adolescent rats.
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spelling pubmed-56720932018-01-01 Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation Dzidziguri, Diana Modebadze, Irina Bakuradze, Ekaterine Mosidze, Giorgi Berulava, Manana Cell J Original Article OBJECTIVE: Cell proliferation is known to be controlled by many networks of regulatory proteins. These multiple and complicated mechanisms of control are still being investigated. The aim of the present study is to determine the different properties of adult rat brain thermostable protein complex (TPC) which affect cell proliferation. MATERIALS AND METHODS: This experimental study used brain, kidney and liver tissue from adult (150-170 g) and adolescent (7, 10, 21, 28 days) white rats, adult pigeons and mice. Brain TPC was isolated by alcohol extraction, and primary antibodies Ki67 and GAD65/67 were used for immunohistochemistry, evaluation of transcriptional activity of the tissues and determination of the mitotic index. RESULTS: The results show that brain TPC from rats reversibly decreases cell proliferation by inhibiting transcription. The evidence suggests that TPC is not species-specific, but expresses tissue specificity with regards to terminally differentiated cells. Rat brain TPC inhibits mitotic activity of the progenitor cells in the dentate gyrus of adolescent rats, and corresponding with this decrease in the mitotic index the number of Ki67 positive cells increases. Simultaneously, the number of GAD65/67-positive cells in the hippocampus decreases by approximately threefold. CONCLUSION: These results indicate that rat brain TPC causes the reversible suppression of cell proliferation through the inhibition of transcription. Inhibitory effects of rat brain TPC leads to an increase the number of cells in the cell cycle, in tissues of adolescent rats. Royan Institute 2018 2017-11-04 /pmc/articles/PMC5672093/ /pubmed/29105389 http://dx.doi.org/10.22074/cellj.2018.4835 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited.
spellingShingle Original Article
Dzidziguri, Diana
Modebadze, Irina
Bakuradze, Ekaterine
Mosidze, Giorgi
Berulava, Manana
Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title_full Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title_fullStr Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title_full_unstemmed Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title_short Determination of The Properties of Rat Brain Thermostable Protein Complex which Inhibit Cell Proliferation
title_sort determination of the properties of rat brain thermostable protein complex which inhibit cell proliferation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672093/
https://www.ncbi.nlm.nih.gov/pubmed/29105389
http://dx.doi.org/10.22074/cellj.2018.4835
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