Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time

The role of heat shock protein in reproduction is widely known as a molecular chaperone in aiding and repairing protein formation when stress occurred. The present objectives were to evaluate the effect of different thawing temperature and time on the expression of HSP70 gene expression and the capa...

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Published in:Sains Malaysiana
Main Author: Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
Format: Article
Language:English
Published: Penerbit Universiti Kebangsaan Malaysia 2018
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051025696&doi=10.17576%2fjsm-2018-4706-04&partnerID=40&md5=0f61d43e9dc1a3ace980bbc4d128407d
id 2-s2.0-85051025696
spelling 2-s2.0-85051025696
Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
2018
Sains Malaysiana
47
6
10.17576/jsm-2018-4706-04
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051025696&doi=10.17576%2fjsm-2018-4706-04&partnerID=40&md5=0f61d43e9dc1a3ace980bbc4d128407d
The role of heat shock protein in reproduction is widely known as a molecular chaperone in aiding and repairing protein formation when stress occurred. The present objectives were to evaluate the effect of different thawing temperature and time on the expression of HSP70 gene expression and the capacitation status in cryopreserved bovine spermatozoa. Briefly, fresh ejaculates were obtained from three different adult bulls. The semen then underwent a sperm washing technique known as Magnetic Activated Cell Sorting System (MACS) and later on, cryopreserved. The sperm-containing straws were then thawed at five different thawing temperatures and time post-cryostorage; 20°C for 13 s, 37°C for 30 s, 40°C for 7 s, 60°C for 6 s and 80°C for 5 s. The RNA was extracted from each of the sperm’s pellets and converted to cDNA prior to the qPCR process. Capacitation status was then determined by means of CTC assay. The results showed that after the process of amplification, there is a significant different of HSP70 gene expression in MACS process samples when the thawing process was performed at 37°C for 30 s, with p<0.05. Furthermore, the CTC assay also showed that thawing at the same temperature gave less capacitated spermatozoa with p<0.05. As a conclusion, MACS yield spermatozoa with a better expression of HSP70 gene and less capacitated spermatozoa when thawing was done at 37°C for 30 s. © 2018 Penerbit Universiti Kebangsaan Malaysia. All rights reserved.
Penerbit Universiti Kebangsaan Malaysia
1266039
English
Article
All Open Access; Gold Open Access
author Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
spellingShingle Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
author_facet Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
author_sort Mohamad S.F.S.; Ibrahim S.F.; Ismail N.H.; Osman K.; Jaafar F.H.F.; Nang C.F.; Zuraina F.; Yusof M.
title Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
title_short Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
title_full Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
title_fullStr Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
title_full_unstemmed Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
title_sort Quantification of HSP70 gene expression and determination of capacitation status of magnetically separated cryopreserved bovine spermatozoa at different thawing temperature and time
publishDate 2018
container_title Sains Malaysiana
container_volume 47
container_issue 6
doi_str_mv 10.17576/jsm-2018-4706-04
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85051025696&doi=10.17576%2fjsm-2018-4706-04&partnerID=40&md5=0f61d43e9dc1a3ace980bbc4d128407d
description The role of heat shock protein in reproduction is widely known as a molecular chaperone in aiding and repairing protein formation when stress occurred. The present objectives were to evaluate the effect of different thawing temperature and time on the expression of HSP70 gene expression and the capacitation status in cryopreserved bovine spermatozoa. Briefly, fresh ejaculates were obtained from three different adult bulls. The semen then underwent a sperm washing technique known as Magnetic Activated Cell Sorting System (MACS) and later on, cryopreserved. The sperm-containing straws were then thawed at five different thawing temperatures and time post-cryostorage; 20°C for 13 s, 37°C for 30 s, 40°C for 7 s, 60°C for 6 s and 80°C for 5 s. The RNA was extracted from each of the sperm’s pellets and converted to cDNA prior to the qPCR process. Capacitation status was then determined by means of CTC assay. The results showed that after the process of amplification, there is a significant different of HSP70 gene expression in MACS process samples when the thawing process was performed at 37°C for 30 s, with p<0.05. Furthermore, the CTC assay also showed that thawing at the same temperature gave less capacitated spermatozoa with p<0.05. As a conclusion, MACS yield spermatozoa with a better expression of HSP70 gene and less capacitated spermatozoa when thawing was done at 37°C for 30 s. © 2018 Penerbit Universiti Kebangsaan Malaysia. All rights reserved.
publisher Penerbit Universiti Kebangsaan Malaysia
issn 1266039
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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