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

被引:10
作者
Terayama, Hayato [1 ,2 ]
Hirai, Shuichi [2 ,3 ]
Naito, Munekazu [2 ,3 ]
Qu, Ning [2 ]
Katagiri, Chiaki [4 ]
Nagahori, Kenta [2 ]
Hayashi, Shogo [2 ]
Sasaki, Hiraku [5 ]
Moriya, Shota [6 ]
Hiramoto, Masaki [6 ]
Miyazawa, Keisuke [6 ]
Hatayama, Naoyuki [2 ,3 ]
Li, Zhong-Lian [2 ]
Sakabe, Kou [1 ]
Matsushita, Masayuki [4 ]
Itoh, Masahiro [2 ]
机构
[1] Tokai Univ, Sch Med, Div Basic Med Sci, Dept Anat, Hiratsuka, Kanagawa 25912, Japan
[2] Tokyo Med Univ, Dept Anat, Tokyo, Japan
[3] Aichi Med Univ, Dept Anat, Nagakute, Aichi, Japan
[4] Univ Ryukyus, Grad Sch Med, Dept Mol & Cellular Physiol, Nishihara, Okinawa 90301, Japan
[5] Juntendo Univ, Sch Hlth & Sports Sci, Dept Hlth Sci, Chiba, Japan
[6] Tokyo Med Univ, Dept Biochem, Tokyo, Japan
基金
日本学术振兴会;
关键词
CANCER-TESTIS ANTIGENS; BINDING-PROTEIN; AUTOIMMUNE ORCHITIS; CANCER/TESTIS ANTIGENS; SEMINIFEROUS EPITHELIUM; EXPRESSION PATTERNS; PROTEOMIC ANALYSIS; POTENTIAL TARGETS; UP-REGULATION; MURINE MODEL;
D O I
10.1038/srep35599
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:16
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