The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas

Integrins are an important family of cell receptors that can bind foreign particles and promote cell phagocytosis after they are activated. In the present study, a novel beta integrin was identified from pacific oyster Crassostrea gigas with an extracellular domain, a single transmembrane segment, a...

Full description

Bibliographic Details
Published in:Fish & Shellfish Immunology
Main Authors: Lv, Zhao, Qiu, Limei, Jia, Zhihao, Wang, Weilin, Liu, Zhaoqun, Wang, Lingling, Song, Linsheng
Format: Report
Language:English
Published: ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD 2019
Subjects:
Online Access:http://ir.qdio.ac.cn/handle/337002/161137
http://ir.qdio.ac.cn/handle/337002/161138
https://doi.org/10.1016/j.fsi.2019.01.047
id ftchinacasciocas:oai:ir.qdio.ac.cn:337002/161138
record_format openpolar
spelling ftchinacasciocas:oai:ir.qdio.ac.cn:337002/161138 2023-05-15T15:58:32+02:00 The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas Lv, Zhao Qiu, Limei Jia, Zhihao Wang, Weilin Liu, Zhaoqun Wang, Lingling Song, Linsheng 2019-04-01 http://ir.qdio.ac.cn/handle/337002/161137 http://ir.qdio.ac.cn/handle/337002/161138 https://doi.org/10.1016/j.fsi.2019.01.047 英语 eng ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD FISH & SHELLFISH IMMUNOLOGY http://ir.qdio.ac.cn/handle/337002/161137 http://ir.qdio.ac.cn/handle/337002/161138 doi:10.1016/j.fsi.2019.01.047 C. gigas RGD-Binding Integrin activation Integrin-mediated phagocytosis Fisheries Immunology Marine & Freshwater Biology Veterinary Sciences 期刊论文 2019 ftchinacasciocas https://doi.org/10.1016/j.fsi.2019.01.047 2022-07-29T12:11:37Z Integrins are an important family of cell receptors that can bind foreign particles and promote cell phagocytosis after they are activated. In the present study, a novel beta integrin was identified from pacific oyster Crassostrea gigas with an extracellular domain, a single transmembrane segment, and a short cytoplasmic domain. It was phylogenetically clustered with phagocytosis-related insecta beta V, and designated as Cg beta V. Cg beta V shared a conserved NPX[Y/F] motif related to integrin activation with other phagocytosis-related beta integrins. The mRNA transcripts of Cg beta V were widely detected in oyster tissues including hemocytes, gonad, adductor muscle, mantle, gill, and hepatopancreas, and the expression level in hemocytes was significantly up-regulated at 12 h after lipopolysaccharide (LPS) stimulation (p < 0.05), which was 2.29-fold higher than that in the control group. Cg beta V proteins were mainly observed on the hemocytes surface. The oyster hemocytes were found to bind fluorescein isothiocyanate (FITC)-labeled Arg-Gly-Asp-containing peptides (RGDCPs), and the binding capability was significantly up-regulated with the peak percentage of 37.6% at 12 h post LPS stimulation, which was higher than that in the control group (8.8%, p < 0.05), suggesting the activation of RGD-binding integrins on oyster hemocytes surface. The label-free RGDCPs and anti-Cg beta V antibody inhibited the binding capability of hemocytes towards FITC-labeled RGDCPs, which were significant lower in RGD blocking group (7.4%, p < 0.05) and anti-Cg beta V blocking group (22.1%, p < 0.05) than that in the control group (37.6%), indicating that Cg beta V could be a RGD-binding integrin. Phagocytosis assay demonstrated that LPS could enhance the phagocytosis of hemocytes towards Escherichia cob and fluorescent beads with the phagocytic rate (PR) of 18.3% and 17.4%, and phagocytic index (PI) of 5.29 and 37.71, respectively, which were significant higher than that in the control group (11.0% and 3.65 for E. coli, ... Report Crassostrea gigas Pacific oyster Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR Pacific Fish & Shellfish Immunology 87 638 649
institution Open Polar
collection Institute of Oceanology, Chinese Academy of Sciences: IOCAS-IR
op_collection_id ftchinacasciocas
language English
topic C. gigas
RGD-Binding
Integrin activation
Integrin-mediated phagocytosis
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
spellingShingle C. gigas
RGD-Binding
Integrin activation
Integrin-mediated phagocytosis
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
Lv, Zhao
Qiu, Limei
Jia, Zhihao
Wang, Weilin
Liu, Zhaoqun
Wang, Lingling
Song, Linsheng
The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
topic_facet C. gigas
RGD-Binding
Integrin activation
Integrin-mediated phagocytosis
Fisheries
Immunology
Marine & Freshwater Biology
Veterinary Sciences
description Integrins are an important family of cell receptors that can bind foreign particles and promote cell phagocytosis after they are activated. In the present study, a novel beta integrin was identified from pacific oyster Crassostrea gigas with an extracellular domain, a single transmembrane segment, and a short cytoplasmic domain. It was phylogenetically clustered with phagocytosis-related insecta beta V, and designated as Cg beta V. Cg beta V shared a conserved NPX[Y/F] motif related to integrin activation with other phagocytosis-related beta integrins. The mRNA transcripts of Cg beta V were widely detected in oyster tissues including hemocytes, gonad, adductor muscle, mantle, gill, and hepatopancreas, and the expression level in hemocytes was significantly up-regulated at 12 h after lipopolysaccharide (LPS) stimulation (p < 0.05), which was 2.29-fold higher than that in the control group. Cg beta V proteins were mainly observed on the hemocytes surface. The oyster hemocytes were found to bind fluorescein isothiocyanate (FITC)-labeled Arg-Gly-Asp-containing peptides (RGDCPs), and the binding capability was significantly up-regulated with the peak percentage of 37.6% at 12 h post LPS stimulation, which was higher than that in the control group (8.8%, p < 0.05), suggesting the activation of RGD-binding integrins on oyster hemocytes surface. The label-free RGDCPs and anti-Cg beta V antibody inhibited the binding capability of hemocytes towards FITC-labeled RGDCPs, which were significant lower in RGD blocking group (7.4%, p < 0.05) and anti-Cg beta V blocking group (22.1%, p < 0.05) than that in the control group (37.6%), indicating that Cg beta V could be a RGD-binding integrin. Phagocytosis assay demonstrated that LPS could enhance the phagocytosis of hemocytes towards Escherichia cob and fluorescent beads with the phagocytic rate (PR) of 18.3% and 17.4%, and phagocytic index (PI) of 5.29 and 37.71, respectively, which were significant higher than that in the control group (11.0% and 3.65 for E. coli, ...
format Report
author Lv, Zhao
Qiu, Limei
Jia, Zhihao
Wang, Weilin
Liu, Zhaoqun
Wang, Lingling
Song, Linsheng
author_facet Lv, Zhao
Qiu, Limei
Jia, Zhihao
Wang, Weilin
Liu, Zhaoqun
Wang, Lingling
Song, Linsheng
author_sort Lv, Zhao
title The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
title_short The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
title_full The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
title_fullStr The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
title_full_unstemmed The activated beta-integrin (Cg beta V) enhances RGD-binding and phagocytic capabilities of hemocytes in Crassostrea gigas
title_sort activated beta-integrin (cg beta v) enhances rgd-binding and phagocytic capabilities of hemocytes in crassostrea gigas
publisher ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
publishDate 2019
url http://ir.qdio.ac.cn/handle/337002/161137
http://ir.qdio.ac.cn/handle/337002/161138
https://doi.org/10.1016/j.fsi.2019.01.047
geographic Pacific
geographic_facet Pacific
genre Crassostrea gigas
Pacific oyster
genre_facet Crassostrea gigas
Pacific oyster
op_relation FISH & SHELLFISH IMMUNOLOGY
http://ir.qdio.ac.cn/handle/337002/161137
http://ir.qdio.ac.cn/handle/337002/161138
doi:10.1016/j.fsi.2019.01.047
op_doi https://doi.org/10.1016/j.fsi.2019.01.047
container_title Fish & Shellfish Immunology
container_volume 87
container_start_page 638
op_container_end_page 649
_version_ 1766394292428865536