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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Main Authors: Yingying Li, Wenfang Xie, Qingwei Li
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2016-12-01
Series:Aquaculture and Fisheries
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468550X16300223
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spelling 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
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AT wenfangxie understandingthelipopolysaccharideinducedliverproteomechangesandidentificationofimmunegenesinlampetramorii
AT qingweili understandingthelipopolysaccharideinducedliverproteomechangesandidentificationofimmunegenesinlampetramorii
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