2015•Basic & Clinical MedicineRequires access

The quantity and phenotype change of regulatory T cell in the model of mice liver transplantation

Guofen Chen

Open publisher page 0 citations

Abstract

Objective To research immune graft rejection,the quantity and function of regulatory T cells in the model of liver transplantation. Methods Transplantation liver samples were collected at 3,7,14,28 d after allogeneic or syngeneic mice liver transplantation( n = 4 for each group at one time point). Graft rejection score was given with HE staining. T and B lymphocytes and change of regulatory T cells were identified with IHC staining. The change of Foxp3 mRNA and CLAT-4 on surface of regulatory T cells were detected by real-time PCR and IFC respectively. Results Allogeneic graft was rejected during 2 weeks after transplantation,and the ejection receded generally after 2 weeks. Inflammatory cells intra-graft was mainly T lymphocytes. Foxp3 positive cells and mRNA of Foxp3 in allogeneic graft group was significantly higher than these in isogeneic graft group( 15. 0 ± 1. 3vs. 2. 7 ± 1. 0,P 0. 05). Meanwhile,expression of CLAT-4 on regulatory T cells also was higher in allogeneic graft group compared with isogeneic graft group( 53 % ± 3 % vs. 13 % ± 2 %,P 0. 05). Conclusions The immunity rejection after allogeneic liver transplantation achieved negative regulation and achieved immune tolerance by regulatory T cells.

About this research paper

What this paper is about

Objective To research immune graft rejection,the quantity and function of regulatory T cells in the model of liver transplantation. Methods Transplantation liver samples were collected at 3,7,14,28 d after allogeneic or syngeneic mice liver transplantation( n = 4 for each group at one time point). Graft rejection score was given with HE staining. T and B lymphocytes and change of regulatory T cells were identified with IHC staining. The change of Foxp3 mRNA and CLAT-4 on surface of regulatory T cells were detected by real-time PCR and IFC respectively. Results Allogeneic graft was rejected during 2 weeks after transplantation,and the ejection receded generally after 2 weeks. Inflammatory cells intra-graft was mainly T lymphocytes. Foxp3 positive cells and mRNA of Foxp3 in allogeneic graft group was significantly higher than these in isogeneic graft group( 15. 0 ± 1. 3vs. 2. 7 ± 1. 0,P 0. 05). Meanwhile,expression of CLAT-4 on regulatory T cells also was higher in allogeneic graft group compared with isogeneic graft group( 53 % ± 3 % vs. 13 % ± 2 %,P 0. 05). Conclusions The immunity rejection after allogeneic liver transplantation achieved negative regulation and achieved immune tolerance by regulatory T cells.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To research immune graft rejection,the quantity and function of regulatory T cells in the model of liver transplantation. Methods Transplantation liver samples were collected at 3,7,14,28 d after allogeneic or syngeneic mice liver transplantation( n = 4 for each group at one time point). Graft rejection score was given with HE staining. T and B lymphocytes and change of regulatory T cells were identified with IHC staining. The change of Foxp3 mRNA and CLAT-4 on surface of regulatory T cells were detected by real-time PCR and IFC respectively. Results Allogeneic graft was rejected during 2 weeks after transplantation,and the ejection receded generally after 2 weeks. Inflammatory cells intra-graft was mainly T lymphocytes. Foxp3 positive cells and mRNA of Foxp3 in allogeneic graft group was significantly higher than these in isogeneic graft group( 15. 0 ± 1. 3vs. 2. 7 ± 1. 0,P 0. 05). Meanwhile,expression of CLAT-4 on regulatory T cells also was higher in allogeneic graft group compared with isogeneic graft group( 53 % ± 3 % vs. 13 % ± 2 %,P 0. 05). Conclusions The immunity rejection after allogeneic liver transplantation achieved negative regulation and achieved immune tolerance by regulatory T cells.

Key concepts: FOXP3, Transplantation, Liver transplantation, Regulatory T cell, Immune system, IL-2 receptor, Andrology, Immune tolerance

Related papers

Back to paper searchBrowse research topicsOriginal source
The quantity and phenotype change of regulatory T cell in the model of mice liver transplantation — Research Paper | ScholarLens