[Study on human leukocyte antigen G1 reducing xeno-cell-rejection by transfecting porcine endothelial cells]

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2005 Jun;19(6):486-9.
[Article in Chinese]

Abstract

Objective: To study whether the porcine endothelial cells (PECs) lines transfected by HLA-G1 can alter the lysis mediated by human peripheral blood mononuclear cell (PBMC) and natural killer cell 92 (NK-92).

Methods: By use of liposomes pack, the pcDNA3. 0 eukaryotic expression vector carrying HLA-G1 was transfected into PECs. Using indirect immunofluorescence and RT-PCR assays, the HLA-G1 expression in PECs was detected. The alteration of the lysis mediated by PBMC and NK-92 was detected by 51Cr-release assays.

Results: HLA-G1 expression could be detected in PECs after transfection of HLA-G1 at the levels of protein and RNA. It also could be found that the survival rate of transfected PECs was much higher than that of non-transfected PECs, when both of them faced the lysis mediated by human PBMC and NK-92. After transfecting the expression of HLA-G1 could be found in the transfected PECs and the lysis mediated by PBMC and NK-92 to PECs decreased obviously (P<0.05).

Conclusion: The PECs transfected by HLA-G1 can decrease the NK lysis, so that it may provide us a new thought to inhibit the xeno-cell-rejection.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Endothelial Cells / immunology*
  • Endothelial Cells / metabolism
  • Endothelial Cells / transplantation*
  • Fluorescent Antibody Technique, Indirect
  • Genetic Vectors
  • Graft Rejection / immunology
  • HLA Antigens / genetics*
  • HLA Antigens / immunology
  • HLA-G Antigens
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Killer Cells, Natural / immunology
  • Monocytes / immunology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swine
  • Transfection / methods*
  • Transplantation, Heterologous

Substances

  • HLA Antigens
  • HLA-G Antigens
  • Histocompatibility Antigens Class I