Recipients withIn UteroInduction of Tolerance Upregulated MHC Class I in the Engrafted Donor Skin

Author:

Chen Jeng-Chang1ORCID,Ou Liang-Shiou2,Yu Hsiu-Yueh3,Kuo Ming-Ling4,Chang Pei-Yeh1,Chang Hsueh-Ling3

Affiliation:

1. Department of Surgery, Chang Gung Children’s Hospital, College of Medicine, Chang Gung University, 5 Fu-Shin Street, Kweishan, Taoyuan 333, Taiwan

2. Department of Allergy, Asthma and Rheumatology, Chang Gung Children’s Hospital, College of Medicine, Chang Gung University, 5 Fu-Shin Street, Kweishan, Taoyuan 333, Taiwan

3. Pediatric Research Center, Chang Gung Children’s Hospital, 5 Fu-Shin Street, Kweishan, Taoyuan 333, Taiwan

4. Department of Microbiology and Immunology, Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, 259 Wen-Hwa 1st Road, Kweishan, Taoyuan 333, Taiwan

Abstract

The alterations in MHC class I expression play a crucial step in immune evasion of cancer or virus-infected cells. This study aimed to examine whether tolerized grafts modified MHC class I expression. FVB/N mice were rendered tolerant of C57BL/6 alloantigens byin uterotransplantation of C57BL/6 marrows. Postnatally, engrafted donor skins and leukocytes were examined for their MHC expression by quantitative real-time PCR and flow cytometry. Engrafted donor skins upregulated their MHC class I related gene transcripts after short-term (1~2 weeks) or long-term (>1 month) engraftment. This biological phenomenon was simultaneously associated with upregulation of TAP1 gene transcripts, suggesting an important role of TAP1 in the regulation of MHC class I pathway. The surface MHC class I molecules of H-2Kbin engrafted donor leukocytes consistently showed overexpression. Conclusively, the induction of allograft tolerance involved biological modifications of donor transplants. The overexpression of MHC class I within engrafted transplants of tolerant mice might be used as the tolerance biomarkers for identifying a state of graft tolerance.

Funder

National Science Council

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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