The cytological observation of immune adherence of porcine erythrocyte.

Q2 Biochemistry, Genetics and Molecular Biology
Cell Communication and Adhesion Pub Date : 2012-10-01 Epub Date: 2012-11-14 DOI:10.3109/15419061.2012.743999
Yao-Gui Sun, Wei Yin, Xin-Feng Fan, Kuo-Hai Fan, Jun-Bing Jiang, Hong-Quan Li
{"title":"The cytological observation of immune adherence of porcine erythrocyte.","authors":"Yao-Gui Sun,&nbsp;Wei Yin,&nbsp;Xin-Feng Fan,&nbsp;Kuo-Hai Fan,&nbsp;Jun-Bing Jiang,&nbsp;Hong-Quan Li","doi":"10.3109/15419061.2012.743999","DOIUrl":null,"url":null,"abstract":"<p><p>The immune adherence (IA) between the porcine erythrocytes and the opsonized Escherichia coli carried green fluorescent protein gene (GFP-E.coli) were detected by the fluorescence microscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) with an attempt to verify the existence of IA between the porcine erythrocytes and complemented-opsonized microbes. Under fluorescence microscopy, GFP-E.coli opsonized by fresh rabbit serum complement adhered to the erythrocytes and could not be detached by PBS washing, and no IA was observed between the erythrocytes and nonopsonized GFP-E.coli after co-incubation. SEM and TEM also revealed the existence of IA between the serum complement-opsonized GFP-E.coli membrane and the erythrocyte membrane. The partial complement receptor type 1 (CR1)-like gene from porcine was generated by RT-PCR and rapid amplification of cDNA 3' end (3' RACE) (157bp and 578bp), both of which have high similarity with published mammal's CR1 gene. The sequences were spliced based on homology comparison and submitted to GenBank (GenBank Accession No. JX033989). These results indicated that the porcine erythrocytes were able to bind to the opsonized microorganisms. Furthermore, the sequencing results confirmed that the CR1-like gene exists in porcine.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"19 5-6","pages":"79-84"},"PeriodicalIF":0.0000,"publicationDate":"2012-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2012.743999","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Communication and Adhesion","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/15419061.2012.743999","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/11/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 5

Abstract

The immune adherence (IA) between the porcine erythrocytes and the opsonized Escherichia coli carried green fluorescent protein gene (GFP-E.coli) were detected by the fluorescence microscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) with an attempt to verify the existence of IA between the porcine erythrocytes and complemented-opsonized microbes. Under fluorescence microscopy, GFP-E.coli opsonized by fresh rabbit serum complement adhered to the erythrocytes and could not be detached by PBS washing, and no IA was observed between the erythrocytes and nonopsonized GFP-E.coli after co-incubation. SEM and TEM also revealed the existence of IA between the serum complement-opsonized GFP-E.coli membrane and the erythrocyte membrane. The partial complement receptor type 1 (CR1)-like gene from porcine was generated by RT-PCR and rapid amplification of cDNA 3' end (3' RACE) (157bp and 578bp), both of which have high similarity with published mammal's CR1 gene. The sequences were spliced based on homology comparison and submitted to GenBank (GenBank Accession No. JX033989). These results indicated that the porcine erythrocytes were able to bind to the opsonized microorganisms. Furthermore, the sequencing results confirmed that the CR1-like gene exists in porcine.

猪红细胞免疫粘附的细胞学观察。
采用荧光显微镜、扫描电镜(SEM)和透射电镜(TEM)检测了猪红细胞与携带绿色荧光蛋白基因(GFP-E.coli)的增效大肠杆菌之间的免疫粘附(IA),试图验证猪红细胞与增效增效微生物之间存在IA。荧光显微镜下,GFP-E。经新鲜兔血清补体调理的大肠杆菌粘附在红细胞上,PBS洗涤不能分离,红细胞与未调理的GFP-E之间未观察到IA。大肠杆菌共孵育后。扫描电镜(SEM)和透射电镜(TEM)也显示血清补体活化GFP-E之间存在IA。大肠杆菌膜和红细胞膜。通过RT-PCR和快速扩增cDNA 3′端(3′RACE) (157bp和578bp),从猪中分离得到与已发表的哺乳动物CR1基因高度相似的部分补体受体1 (CR1)样基因。经同源性比较,将序列拼接后提交GenBank (GenBank登录号:JX033989)。这些结果表明,猪红细胞能够与调理过的微生物结合。此外,测序结果证实了猪中存在cr1样基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信