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Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study

Background  Spinal cord injury (SCI) leads to serious complications involving primary trauma and progressive loss due to inflammation, local ischemia, or infection. Despite a worldwide annual incidence of 15 to 40 cases per million, methylprednisolone is the only treatment available to alleviate neu...

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Autores principales: Boraiah, Vidyasagar, Modgil, Shweta, Sharma, Kaushal, Podder, Vivek, Sivapuram, Madhava Sai, Miranpuri, Gurwattan S., Anand, Akshay, Goni, Vijay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779554/
https://www.ncbi.nlm.nih.gov/pubmed/31595117
http://dx.doi.org/10.1055/s-0039-1697683
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author Boraiah, Vidyasagar
Modgil, Shweta
Sharma, Kaushal
Podder, Vivek
Sivapuram, Madhava Sai
Miranpuri, Gurwattan S.
Anand, Akshay
Goni, Vijay
author_facet Boraiah, Vidyasagar
Modgil, Shweta
Sharma, Kaushal
Podder, Vivek
Sivapuram, Madhava Sai
Miranpuri, Gurwattan S.
Anand, Akshay
Goni, Vijay
author_sort Boraiah, Vidyasagar
collection PubMed
description Background  Spinal cord injury (SCI) leads to serious complications involving primary trauma and progressive loss due to inflammation, local ischemia, or infection. Despite a worldwide annual incidence of 15 to 40 cases per million, methylprednisolone is the only treatment available to alleviate neurologic dysfunction; therefore, research is currently focused on identifying novel targets by biochemical and molecular studies. Purpose  Here, we investigated the expression of various molecular markers at the messenger ribonucleic acid (mRNA) and protein level at day 0 and day 30 post-SCI. Methods  Enzyme-linked immunosorbent assay (ELISA) was performed to determine the expression of CASPASE-3 and heat shock protein-27 (HSP-27) in serum samples. Real-time polymerase chain reaction (RT-PCR) was performed to determine the level of mRNA expression of vascular endothelial growth factor receptor-1 (VEGFR-1), VEGFR-2, HSP-27, monocyte chemoattractant protein-1 (MCP-1), and CASPASE-3. Results  HSP-27 expression at day 30, as compared with day 0, showed significant downregulation. In contrast, there was elevated expression of MCP-1. ELISA analysis showed no significant change in the expression of CASPASE-3 or HSP-27. Conclusion  There may be possible opposing role of HSP-27 and MCP-1 governing SCI. Their association can be studied by designing in vitro studies.
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spelling pubmed-67795542019-10-08 Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study Boraiah, Vidyasagar Modgil, Shweta Sharma, Kaushal Podder, Vivek Sivapuram, Madhava Sai Miranpuri, Gurwattan S. Anand, Akshay Goni, Vijay J Neurosci Rural Pract Background  Spinal cord injury (SCI) leads to serious complications involving primary trauma and progressive loss due to inflammation, local ischemia, or infection. Despite a worldwide annual incidence of 15 to 40 cases per million, methylprednisolone is the only treatment available to alleviate neurologic dysfunction; therefore, research is currently focused on identifying novel targets by biochemical and molecular studies. Purpose  Here, we investigated the expression of various molecular markers at the messenger ribonucleic acid (mRNA) and protein level at day 0 and day 30 post-SCI. Methods  Enzyme-linked immunosorbent assay (ELISA) was performed to determine the expression of CASPASE-3 and heat shock protein-27 (HSP-27) in serum samples. Real-time polymerase chain reaction (RT-PCR) was performed to determine the level of mRNA expression of vascular endothelial growth factor receptor-1 (VEGFR-1), VEGFR-2, HSP-27, monocyte chemoattractant protein-1 (MCP-1), and CASPASE-3. Results  HSP-27 expression at day 30, as compared with day 0, showed significant downregulation. In contrast, there was elevated expression of MCP-1. ELISA analysis showed no significant change in the expression of CASPASE-3 or HSP-27. Conclusion  There may be possible opposing role of HSP-27 and MCP-1 governing SCI. Their association can be studied by designing in vitro studies. Thieme Medical and Scientific Publishers 2019-07 2019-10-07 /pmc/articles/PMC6779554/ /pubmed/31595117 http://dx.doi.org/10.1055/s-0039-1697683 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Boraiah, Vidyasagar
Modgil, Shweta
Sharma, Kaushal
Podder, Vivek
Sivapuram, Madhava Sai
Miranpuri, Gurwattan S.
Anand, Akshay
Goni, Vijay
Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title_full Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title_fullStr Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title_full_unstemmed Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title_short Altered Expression of Heat Shock Protein-27 and Monocyte Chemoattractant Protein-1 after Acute Spinal Cord Injury: A Pilot Study
title_sort altered expression of heat shock protein-27 and monocyte chemoattractant protein-1 after acute spinal cord injury: a pilot study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779554/
https://www.ncbi.nlm.nih.gov/pubmed/31595117
http://dx.doi.org/10.1055/s-0039-1697683
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