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Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow?
There is growing interest in the potential neuroprotective properties of gelsolin. In particular, plasma-type gelsolin (pGSN) can ameliorate deleterious inflammatory response by scavenging pro-inflammatory signals such as actin and lipopolysaccharide. In a recent issue of Critical Care, Pan and coll...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056622/ https://www.ncbi.nlm.nih.gov/pubmed/24393331 http://dx.doi.org/10.1186/cc13178 |
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author | Chou, Sherry Hsiang-Yi Lo, Eng H Ning, MingMing |
author_facet | Chou, Sherry Hsiang-Yi Lo, Eng H Ning, MingMing |
author_sort | Chou, Sherry Hsiang-Yi |
collection | PubMed |
description | There is growing interest in the potential neuroprotective properties of gelsolin. In particular, plasma-type gelsolin (pGSN) can ameliorate deleterious inflammatory response by scavenging pro-inflammatory signals such as actin and lipopolysaccharide. In a recent issue of Critical Care, Pan and colleagues report an important association between pGSN and subarachnoid hemorrhage (SAH) disease severity, and found pGSN to be a novel and promising biomarker for SAH clinical outcome. Previous research shows pGSN may be actively degraded by neurovascular proteases such as matrix metalloproteinases in the cerebral spinal fluid of SAH patients. Taken together, these results suggest that pGSN is not only a novel marker of SAH clinical outcome, but may also play an active mechanistic role in SAH, and potentially serve as a future therapeutic target. |
format | Online Article Text |
id | pubmed-4056622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40566222015-01-06 Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? Chou, Sherry Hsiang-Yi Lo, Eng H Ning, MingMing Crit Care Commentary There is growing interest in the potential neuroprotective properties of gelsolin. In particular, plasma-type gelsolin (pGSN) can ameliorate deleterious inflammatory response by scavenging pro-inflammatory signals such as actin and lipopolysaccharide. In a recent issue of Critical Care, Pan and colleagues report an important association between pGSN and subarachnoid hemorrhage (SAH) disease severity, and found pGSN to be a novel and promising biomarker for SAH clinical outcome. Previous research shows pGSN may be actively degraded by neurovascular proteases such as matrix metalloproteinases in the cerebral spinal fluid of SAH patients. Taken together, these results suggest that pGSN is not only a novel marker of SAH clinical outcome, but may also play an active mechanistic role in SAH, and potentially serve as a future therapeutic target. BioMed Central 2014 2014-01-06 /pmc/articles/PMC4056622/ /pubmed/24393331 http://dx.doi.org/10.1186/cc13178 Text en Copyright © 2014 BioMed Central Ltd. |
spellingShingle | Commentary Chou, Sherry Hsiang-Yi Lo, Eng H Ning, MingMing Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title | Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title_full | Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title_fullStr | Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title_full_unstemmed | Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title_short | Plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
title_sort | plasma-type gelsolin in subarachnoid hemorrhage: novel biomarker today, therapeutic target tomorrow? |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056622/ https://www.ncbi.nlm.nih.gov/pubmed/24393331 http://dx.doi.org/10.1186/cc13178 |
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