Suppr超能文献

鉴定蛋白酪氨酸磷酸酶受体γ胞外域(可溶性PTPRG)为血浆中的一种天然可溶性蛋白。

Identification of protein tyrosine phosphatase receptor gamma extracellular domain (sPTPRG) as a natural soluble protein in plasma.

作者信息

Moratti Elisabetta, Vezzalini Marzia, Tomasello Luisa, Giavarina Davide, Sorio Claudio

机构信息

Department of Pathology and Diagnostics, University of Verona, Verona, Italy.

Clinical Chemistry and Hematology Laboratory St. Bortolo Hospital, Vicenza, Italy.

出版信息

PLoS One. 2015 Mar 16;10(3):e0119110. doi: 10.1371/journal.pone.0119110. eCollection 2015.

Abstract

BACKGROUND

PTPRG is a widely expressed protein tyrosine phosphatase present in various isoforms. Peptides from its extracellular domain have been detected in plasma by proteomic techniques. We aim at characterizing the plasmatic PTPRG (sPTPRG) form and to identify its source.

METHODOLOGY/PRINCIPAL FINDINGS: The expression of sPTPRG was evaluated in human plasma and murine plasma and tissues by immunoprecipitation and Western blotting. The polypeptides identified have an apparent Mr of about 120 kDa (major band) and 90 kDa (minor band) respectively. Full length PTPRG was identified in the 100.000×g pelleted plasma fraction, suggesting that it was present associated to cell-derived vesicles (exosomes). The release of sPTPRG by HepG2 human hepatocellular carcinoma cell line was induced by ethanol and sensitive to metalloproteinase and not to Furin inhibitors. Finally, increased levels of the plasmatic ∼120 kDa isoform were associated with the occurrence of liver damage.

CONCLUSIONS

These results demonstrate that sPTPRG represent a novel candidate protein biomarker in plasma whose increased expression is associated to hepatocyte damage. This observation could open a new avenue of investigation in this challenging field.

摘要

背景

PTPRG是一种广泛表达的蛋白质酪氨酸磷酸酶,存在多种异构体。通过蛋白质组学技术已在血浆中检测到其细胞外结构域的肽段。我们旨在表征血浆中的PTPRG(sPTPRG)形式并确定其来源。

方法/主要发现:通过免疫沉淀和蛋白质印迹法评估人血浆、小鼠血浆和组织中sPTPRG的表达。鉴定出的多肽表观分子量分别约为120 kDa(主要条带)和90 kDa(次要条带)。在100,000×g沉淀的血浆组分中鉴定出全长PTPRG,表明它与细胞来源的囊泡(外泌体)相关。乙醇诱导人肝癌细胞系HepG2释放sPTPRG,且其对金属蛋白酶敏感,对弗林蛋白酶抑制剂不敏感。最后,血浆中约120 kDa异构体水平升高与肝损伤的发生有关。

结论

这些结果表明,sPTPRG是血浆中一种新型候选蛋白质生物标志物,其表达增加与肝细胞损伤有关。这一观察结果可能为这一具有挑战性的领域开辟一条新的研究途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7fb/4361625/9edc92396903/pone.0119110.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验