2022
DOI: 10.1016/j.fsi.2022.02.051
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Molecular cloning, expression analysis of the IgT gene and detection of IgT+ B cells in the half-smooth tongue sole (Cynoglossus semilaevis)

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Cited by 7 publications
(3 citation statements)
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“…Te highest expression levels of pl-IgM and pl-pIgR were observed both in the mucosal-associated tissues and systemic immune tissues, including the intestine, spleen, kidney, gill, liver, and skin. Te present result is consistent with the previous studies on Japanese founder, turbot, and half-smooth tongue sole [13,24,30]. Te expression levels of IgM and pIgR were afected in fsh under infection with bacteria, parasites, and viruses.…”
Section: Discussionsupporting
confidence: 93%
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“…Te highest expression levels of pl-IgM and pl-pIgR were observed both in the mucosal-associated tissues and systemic immune tissues, including the intestine, spleen, kidney, gill, liver, and skin. Te present result is consistent with the previous studies on Japanese founder, turbot, and half-smooth tongue sole [13,24,30]. Te expression levels of IgM and pIgR were afected in fsh under infection with bacteria, parasites, and viruses.…”
Section: Discussionsupporting
confidence: 93%
“…SC is free or bound to polymeric IgM (or IgA) and contributes as a microbial scavenger to protect the epithelial surface [19,20]. Previous studies reported the gene sequences of pIgR in fugu (Takifugu rubripes) [21], common carp [17], orange-spotted grouper (Epinephelus coioides) [22], tlantic salmon (Salmo salar) [23], olive founder [24], turbot [25], sea bass (Lateolabrax japonicus) [26], crucian carp (Carassius auratus) [27], dojo loach (Misgurnus anguillicaudatus) [28], grass carp (Ctenopharyngodon idellus) [29], half-smooth tongue sole (Cynoglossus semilaevis) [30], and largemouth bass (Micropterus salmoides) [31]. Previously written articles demonstrated that the pIgR transported tetrameric IgM into the skin mucus in fugu and oliver founder [18,21].…”
Section: Introductionmentioning
confidence: 99%
“…Detection of IgT expression in teleost mucosal tissues has previously been established through either immunofluorescence staining or in-situ hybridization ( 7 , 22 , 24 , 26 , 27 ). Previous use of immunofluorescence staining has identified IgT + B cells in the epithelium of gill filaments and within the intestinal epithelium and lamina propria of the intestine in multiple teleost species ( 22 , 24 , 26 ). In this study, IgT-expressing cells were similarly located in the lamina propria of the intestine and primary lamellae (PL) of the gills of the ASB.…”
Section: Discussionmentioning
confidence: 99%