Specific autoantigens identified by sera obtained from mice that are immunized with testicular germ cells alone

Sci Rep. 2016 Oct 18:6:35599. doi: 10.1038/srep35599.

Abstract

There are various autoimmunogenic antigens (AIs) in testicular germ cells (TGCs) recognized as foreign by the body's immune system. However, there is little information of TGC-specific AIs being available. The aim of this study is to identify TGC-specific AIs. We have previously established that immunization using viable syngeneic TGC can also induce murine experimental autoimmune orchitis (EAO) without using any adjuvant. This study is to identify TGC-specific AIs by TGC liquid chromatography-tandem mass spectrometry analysis, followed by two-dimensional gel electrophoresis that reacted with serum IgG from EAO mice. In this study, we identified 11 TGC-specific AIs that reacted with serum from EAO mice. Real-time RT-PCR analysis showed that the mRNA expressions of seven TGC-specific AIs were significantly higher in only mature testis compared to other organs. Moreover, the recombinant proteins of identified 10 (except unnamed protein) TGC-specific AIs were created by using human embryonic kidney 293 (HEK293) cells and these antigencities were reconfirmed by Western blot using EAO serum reaction. These results indicated Atp6v1a, Hsc70t, Fbp1 and Dazap1 were candidates for TGC-specific AIs. Identification of these AIs will facilitate new approaches for understanding infertility and cancer pathogenesis and may provide a basis for the development of novel therapies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantibodies / blood
  • Autoantigens / blood*
  • Autoimmune Diseases / blood
  • Autoimmune Diseases / immunology
  • Epididymis / metabolism
  • Gene Expression Regulation
  • Germ Cells / cytology*
  • HEK293 Cells
  • Humans
  • Immunization*
  • Immunoglobulin G / metabolism
  • Male
  • Mice
  • Orchitis / blood
  • Orchitis / immunology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction
  • Reproducibility of Results
  • Spermatozoa / metabolism
  • Testis / cytology*

Substances

  • Autoantibodies
  • Autoantigens
  • Immunoglobulin G
  • RNA, Messenger