Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii
Lamprey is considered to be an excellent model for studying the origin of adaptive immunity. In the present study, three up-regulated and ten down-regulated proteins were identified in the lipopolysaccharide (LPS) induced liver proteome of Lampetra morii. Quantitative real-time PCR (qPCR) was used t...
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2016-12-01
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doaj-86f401d7802c41049b5884d9ae7a56cc2021-02-02T00:06:19ZengKeAi Communications Co., Ltd.Aquaculture and Fisheries2468-550X2016-12-011C91410.1016/j.aaf.2016.09.002Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra moriiYingying LiWenfang XieQingwei LiLamprey is considered to be an excellent model for studying the origin of adaptive immunity. In the present study, three up-regulated and ten down-regulated proteins were identified in the lipopolysaccharide (LPS) induced liver proteome of Lampetra morii. Quantitative real-time PCR (qPCR) was used to characterize in the liver the abundance of transcripts encoding the differentially expressed proteins. The abundance of transcripts and the corresponding differentially expressed proteins revealed that expression of cystathionase and Zgc:112210-201 was not correlated with protein expression level. Polyl 4-hydroxylase, serum lectin, Zgc:112210-201, and cofilin 1 mRNA expression was significantly upregulated in liver tissue after treatment with LPS. Transcript abundance of differentially expressed proteins in the gill, kidney, heart, intestine, liver, and supraneural body was determined. Transcripts of Zgc:112210-201 were almost undetectable in the tissues while polyl 4-hydroxylase, protein disulfide isomerase family A (member 4), cystathionase, and serum lectin were low abundance unlike the protein which was easily detected. This study represents the first attempt at understanding the LPS induced liver proteome of L. morii and our findings contribute to the identification of novel immune genes in lamprey.http://www.sciencedirect.com/science/article/pii/S2468550X16300223Liver proteomeLipopolysaccharideImmune geneLampetra morii |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yingying Li Wenfang Xie Qingwei Li |
spellingShingle |
Yingying Li Wenfang Xie Qingwei Li Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii Aquaculture and Fisheries Liver proteome Lipopolysaccharide Immune gene Lampetra morii |
author_facet |
Yingying Li Wenfang Xie Qingwei Li |
author_sort |
Yingying Li |
title |
Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii |
title_short |
Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii |
title_full |
Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii |
title_fullStr |
Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii |
title_full_unstemmed |
Understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in Lampetra morii |
title_sort |
understanding the lipopolysaccharide induced liver proteome changes and identification of immune genes in lampetra morii |
publisher |
KeAi Communications Co., Ltd. |
series |
Aquaculture and Fisheries |
issn |
2468-550X |
publishDate |
2016-12-01 |
description |
Lamprey is considered to be an excellent model for studying the origin of adaptive immunity. In the present study, three up-regulated and ten down-regulated proteins were identified in the lipopolysaccharide (LPS) induced liver proteome of Lampetra morii. Quantitative real-time PCR (qPCR) was used to characterize in the liver the abundance of transcripts encoding the differentially expressed proteins. The abundance of transcripts and the corresponding differentially expressed proteins revealed that expression of cystathionase and Zgc:112210-201 was not correlated with protein expression level. Polyl 4-hydroxylase, serum lectin, Zgc:112210-201, and cofilin 1 mRNA expression was significantly upregulated in liver tissue after treatment with LPS. Transcript abundance of differentially expressed proteins in the gill, kidney, heart, intestine, liver, and supraneural body was determined. Transcripts of Zgc:112210-201 were almost undetectable in the tissues while polyl 4-hydroxylase, protein disulfide isomerase family A (member 4), cystathionase, and serum lectin were low abundance unlike the protein which was easily detected. This study represents the first attempt at understanding the LPS induced liver proteome of L. morii and our findings contribute to the identification of novel immune genes in lamprey. |
topic |
Liver proteome Lipopolysaccharide Immune gene Lampetra morii |
url |
http://www.sciencedirect.com/science/article/pii/S2468550X16300223 |
work_keys_str_mv |
AT yingyingli understandingthelipopolysaccharideinducedliverproteomechangesandidentificationofimmunegenesinlampetramorii AT wenfangxie understandingthelipopolysaccharideinducedliverproteomechangesandidentificationofimmunegenesinlampetramorii AT qingweili understandingthelipopolysaccharideinducedliverproteomechangesandidentificationofimmunegenesinlampetramorii |
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1724314509372293120 |