Confirmation of differentiation clusters’ and endoglin markers preset in porcine buccal mucosa cells

Q4 Biochemistry, Genetics and Molecular Biology Medical Journal of Cell Biology Pub Date : 2020-12-30 DOI:10.2478/acb-2020-0015
B. Borowiec, Rut Bryl, A. Bryja, P. Mozdziak, M. Dyszkiewicz-Konwińska
{"title":"Confirmation of differentiation clusters’ and endoglin markers preset in porcine buccal mucosa cells","authors":"B. Borowiec, Rut Bryl, A. Bryja, P. Mozdziak, M. Dyszkiewicz-Konwińska","doi":"10.2478/acb-2020-0015","DOIUrl":null,"url":null,"abstract":"Abstract Several genes, namely CD44, CD90, CD105 and PCNA may be important in differentiation of porcine mucosa cell cultures. These genes are, inter alia, responsible for cell adhesion to extracellular matrix and its constituent secretion, cytoskeleton organization, epithelial to mesenchymal transition or proper course of DNA replication. A total of 20 pubertal crossbred Landrace gilts bred on commercial farms were used to produce buccal mucosa cultures, which were harvested on the 7th, 15th and 30th day after initiation of the culture. Expression levels of CD44, CD90, CD105 and PCNA were evaluated employing Real-Time Quantitative Polymerase Chain Reaction. CD44, CD90 and PCNA showed an unchanged expression pattern. Expression of CD44 on day 7 was the highest of all factors measured. The greatest difference between the measurement on 7th and 30th day was found in the PCNA gene. These results broaden the understanding of the transcriptome changes in porcine buccal mucosa cells for the duration of in vitro cultivation. Nevertheless, it is very important to consider that the in vitro conditions do not fully reflect the changes taking place in the living organism. It appears that tissues of the oral cavity possess high regenerative potential, and constitute suitable model for wound healing investigation. Running title: Confirmation of differentiation clusters’ and endoglin markers preset in porcine buccal mucosa cells","PeriodicalId":18329,"journal":{"name":"Medical Journal of Cell Biology","volume":"8 1","pages":"118 - 123"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Journal of Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/acb-2020-0015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Several genes, namely CD44, CD90, CD105 and PCNA may be important in differentiation of porcine mucosa cell cultures. These genes are, inter alia, responsible for cell adhesion to extracellular matrix and its constituent secretion, cytoskeleton organization, epithelial to mesenchymal transition or proper course of DNA replication. A total of 20 pubertal crossbred Landrace gilts bred on commercial farms were used to produce buccal mucosa cultures, which were harvested on the 7th, 15th and 30th day after initiation of the culture. Expression levels of CD44, CD90, CD105 and PCNA were evaluated employing Real-Time Quantitative Polymerase Chain Reaction. CD44, CD90 and PCNA showed an unchanged expression pattern. Expression of CD44 on day 7 was the highest of all factors measured. The greatest difference between the measurement on 7th and 30th day was found in the PCNA gene. These results broaden the understanding of the transcriptome changes in porcine buccal mucosa cells for the duration of in vitro cultivation. Nevertheless, it is very important to consider that the in vitro conditions do not fully reflect the changes taking place in the living organism. It appears that tissues of the oral cavity possess high regenerative potential, and constitute suitable model for wound healing investigation. Running title: Confirmation of differentiation clusters’ and endoglin markers preset in porcine buccal mucosa cells
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
猪口腔黏膜细胞分化簇和内啡肽标记物的初步确定
CD44、CD90、CD105和PCNA等基因可能在猪粘膜细胞的分化过程中起重要作用。除其他外,这些基因负责细胞与细胞外基质的粘附及其成分的分泌、细胞骨架组织、上皮细胞向间质细胞的转化或DNA复制的适当过程。选用20只在商品养殖场饲养的青春期杂交长白母猪进行口腔黏膜培养,培养开始后第7、15和30天收获。采用实时定量聚合酶链反应(Real-Time Quantitative Polymerase Chain Reaction)检测CD44、CD90、CD105和PCNA的表达水平。CD44、CD90和PCNA表达模式不变。CD44在第7天的表达是所有因子中最高的。第7天与第30天的测量差异最大的是PCNA基因。这些结果拓宽了对猪口腔黏膜细胞在体外培养期间转录组变化的理解。然而,考虑到体外条件并不能完全反映生物体中发生的变化是非常重要的。口腔组织具有较高的再生潜力,是研究口腔创面愈合的合适模型。标题:猪口腔黏膜细胞分化簇和内啡肽标记物的确定
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 去求助
来源期刊
Medical Journal of Cell Biology
Medical Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
0.00%
发文量
15
期刊最新文献
The negative effect on human health due to disruption of circadian rhythm in modern times Understanding endometriosis: a threat to fertility Glioblastoma: A molecular insight into current discoveries and treatment directions Neuromolecular analysis of post-traumatic stress disorder – the dysregulation in neuronal and signalling pathways Molecular and metabolic changes in neurological manifestations of Post-COVID conditions with special consideration of spectroscopy MR analysis
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1