IR@PKUHSC  > 北京大学第二临床医学院  > 肝胆外科
学科主题临床医学
PD-1/PD-L1 Costimulatory Pathway-induced Mouse Islet Transplantation Immune Tolerance
Li, T.1; Ma, R.2; Zhu, J. Y.1; Wang, F. S.1; Huang, L.1; Leng, X. S.1
刊名TRANSPLANTATION PROCEEDINGS
2015
DOI10.1016/j.transproceed.2014.10.043
47期:1页:165-170
收录类别SCI
文章类型Article
WOS标题词Science & Technology
类目[WOS]Immunology ; Surgery ; Transplantation
研究领域[WOS]Immunology ; Surgery ; Transplantation
关键词[WOS]T-CELL-ACTIVATION ; EXPRESSION ; PD-L1
英文摘要

Background. Programmed death-1/PD-1 ligand-1 (PD-1/PD-L1) costimulatory signals may play an important role in T-cell induced immune response. The aim of this study is to investigate the role of the PD-1/PD-L1 costimulatory pathway on immunotolerance induction in mouse pancreatic islet transplantation.

Methods. Full-length mouse PD-L1 cDNA was subcloned into pShuttle-GFP-CMV(-) shuttle plasmid. The product was cut by certain restriction endonuclease and ligated with pAdxsi vector. The adenovirus bone plasmid was transformed into DH5 alpha-competent bacteria. After linearization, the recombined adenovirus DNA was transfected into 293 cells for package and amplification. Streptozotocin was injected intraperitoneally into C57BL/6 (H-2(b)) mouse to induce diabetic model recipient. Recipients were randomly divided into 3 groups. Group A was the control. Group B and group C were injected with Ad-EGFP and Ad-PD-L1 through the tail vein, respectively, 1 day before islet transplantation. The 300 to 400 islets of DBA/2 (H-2(d)) were transplanted into the renal subcapsular space of the diabetic model recipient. We monitored and analyzed the blood glucose levels and the survival time of grafts after transplantation.

Results. Recombinant adenovirus Ad-PD-L1 had high efficiency expression of PD-L1 in recipient mouse. The blood glucose concentration of mice in the Ad-PD-L1 gene treatment group was obviously lower than that of the control and Ad-EGFP treatment groups and was stable and kept within the normal range at post-transplant 21 days. The survival time of grafts in the Ad-PD-L1 group (27.6 +/- 3.5 days) was significantly longer than in the control (7.8 +/- 0.33 days) and Ad-EGFP groups (7.6 +/- 0.59 days), P < .01. Mixed lymphocyte response showed a specific decrease reaction of recipient lymphocyte vs donor lymphocyte. Flow cytometry detection showed that unsplit cells occupied 90% of recipient mouse lymphocytes, but unsplit cells among normal C57BL/6 mouse lymphocytes without Ad-PD-L1 gene treatment were Si in the control group. The differences between them were significant (P < .01).

Conclusion. Recombinant adenovirus Ad-PD-L1 has been successfully constructed. In mouse pancreatic islet transplantation, it can suppress the activation of recipient T lymphocyte through the PD-1/PD-L1 costimulatory pathway, and significantly prolong the survival time of grafts.

语种英语
WOS记录号WOS:000349499800045
Citation statistics
Cited Times:4[WOS]   [WOS Record]     [Related Records in WOS]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/60506
Collection北京大学第二临床医学院_肝胆外科
作者单位1.Peking Univ, Peoples Hosp, Dept Hepatobiliary Surg, Beijing 100044, Peoples R China
2.Peking Univ, Peoples Hosp, Surg Intens Care Unit, Beijing 100044, Peoples R China
Recommended Citation
GB/T 7714
Li, T.,Ma, R.,Zhu, J. Y.,et al. PD-1/PD-L1 Costimulatory Pathway-induced Mouse Islet Transplantation Immune Tolerance[J]. TRANSPLANTATION PROCEEDINGS,2015,47(1):165-170.
APA Li, T.,Ma, R.,Zhu, J. Y.,Wang, F. S.,Huang, L.,&Leng, X. S..(2015).PD-1/PD-L1 Costimulatory Pathway-induced Mouse Islet Transplantation Immune Tolerance.TRANSPLANTATION PROCEEDINGS,47(1),165-170.
MLA Li, T.,et al."PD-1/PD-L1 Costimulatory Pathway-induced Mouse Islet Transplantation Immune Tolerance".TRANSPLANTATION PROCEEDINGS 47.1(2015):165-170.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
谷歌学术
谷歌学术Similar articles in
[Li, T.]'s Articles
[Ma, R.]'s Articles
[Zhu, J. Y.]'s Articles
百度学术
百度学术Similar articles in
[Li, T.]'s Articles
[Ma, R.]'s Articles
[Zhu, J. Y.]'s Articles
必应学术
必应学术Similar articles in
[Li, T.]'s Articles
[Ma, R.]'s Articles
[Zhu, J. Y.]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.