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Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology

We investigated potential protein markers of post-mortem interval (PMI) using rat kidney and psoas muscle. Tissue samples were taken at 12 h intervals for up to 96 h after death by suffocation. Expression levels of eight soluble proteins were analyzed by Western blotting. Degradation patterns of sel...

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Autores principales: Lee, Dong-Gi, Yang, Kyeong Eun, Hwang, Jeong Won, Kang, Hwan-Soo, Lee, Seung-Yeul, Choi, Seoyeon, Shin, Joonchul, Jang, Ik-Soon, An, Hyun Joo, Chung, Heesun, Jung, Hyo-Il, Choi, Jong-Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995019/
https://www.ncbi.nlm.nih.gov/pubmed/27552165
http://dx.doi.org/10.1371/journal.pone.0160557
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author Lee, Dong-Gi
Yang, Kyeong Eun
Hwang, Jeong Won
Kang, Hwan-Soo
Lee, Seung-Yeul
Choi, Seoyeon
Shin, Joonchul
Jang, Ik-Soon
An, Hyun Joo
Chung, Heesun
Jung, Hyo-Il
Choi, Jong-Soon
author_facet Lee, Dong-Gi
Yang, Kyeong Eun
Hwang, Jeong Won
Kang, Hwan-Soo
Lee, Seung-Yeul
Choi, Seoyeon
Shin, Joonchul
Jang, Ik-Soon
An, Hyun Joo
Chung, Heesun
Jung, Hyo-Il
Choi, Jong-Soon
author_sort Lee, Dong-Gi
collection PubMed
description We investigated potential protein markers of post-mortem interval (PMI) using rat kidney and psoas muscle. Tissue samples were taken at 12 h intervals for up to 96 h after death by suffocation. Expression levels of eight soluble proteins were analyzed by Western blotting. Degradation patterns of selected proteins were clearly divided into three groups: short-term, mid-term, and long-term PMI markers based on the half maximum intensity of intact protein expression. In kidney, glycogen synthase (GS) and glycogen synthase kinase-3β were degraded completely within 48 h making them short-term PMI markers. AMP-activated protein kinase α, caspase 3 and GS were short-term PMI markers in psoas muscle. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was a mid-term PMI marker in both tissues. Expression levels of the typical long-term PMI markers, p53 and β-catenin, were constant for at least 96 h post-mortem in both tissues. The degradation patterns of GS and caspase-3 were verified by immunohistochemistry in both tissues. GAPDH was chosen as a test PMI protein to perform a lateral flow assay (LFA). The presence of recombinant GAPDH was clearly detected in LFA and quantified in a concentration-dependent manner. These results suggest that LFA might be used to estimate PMI at a crime scene.
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spelling pubmed-49950192016-09-12 Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology Lee, Dong-Gi Yang, Kyeong Eun Hwang, Jeong Won Kang, Hwan-Soo Lee, Seung-Yeul Choi, Seoyeon Shin, Joonchul Jang, Ik-Soon An, Hyun Joo Chung, Heesun Jung, Hyo-Il Choi, Jong-Soon PLoS One Research Article We investigated potential protein markers of post-mortem interval (PMI) using rat kidney and psoas muscle. Tissue samples were taken at 12 h intervals for up to 96 h after death by suffocation. Expression levels of eight soluble proteins were analyzed by Western blotting. Degradation patterns of selected proteins were clearly divided into three groups: short-term, mid-term, and long-term PMI markers based on the half maximum intensity of intact protein expression. In kidney, glycogen synthase (GS) and glycogen synthase kinase-3β were degraded completely within 48 h making them short-term PMI markers. AMP-activated protein kinase α, caspase 3 and GS were short-term PMI markers in psoas muscle. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was a mid-term PMI marker in both tissues. Expression levels of the typical long-term PMI markers, p53 and β-catenin, were constant for at least 96 h post-mortem in both tissues. The degradation patterns of GS and caspase-3 were verified by immunohistochemistry in both tissues. GAPDH was chosen as a test PMI protein to perform a lateral flow assay (LFA). The presence of recombinant GAPDH was clearly detected in LFA and quantified in a concentration-dependent manner. These results suggest that LFA might be used to estimate PMI at a crime scene. Public Library of Science 2016-08-23 /pmc/articles/PMC4995019/ /pubmed/27552165 http://dx.doi.org/10.1371/journal.pone.0160557 Text en © 2016 Lee 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Dong-Gi
Yang, Kyeong Eun
Hwang, Jeong Won
Kang, Hwan-Soo
Lee, Seung-Yeul
Choi, Seoyeon
Shin, Joonchul
Jang, Ik-Soon
An, Hyun Joo
Chung, Heesun
Jung, Hyo-Il
Choi, Jong-Soon
Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title_full Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title_fullStr Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title_full_unstemmed Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title_short Degradation of Kidney and Psoas Muscle Proteins as Indicators of Post-Mortem Interval in a Rat Model, with Use of Lateral Flow Technology
title_sort degradation of kidney and psoas muscle proteins as indicators of post-mortem interval in a rat model, with use of lateral flow technology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995019/
https://www.ncbi.nlm.nih.gov/pubmed/27552165
http://dx.doi.org/10.1371/journal.pone.0160557
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