Characterization of Mouse Interferon-Induced Transmembrane Protein-1 Expression in Mouse Testis

  • Lee, Ran (Department of Animal & Food Bioscience, College of Natural Science, Konkuk University) ;
  • Park, Hyun Jung (Department of Animal & Food Bioscience, College of Natural Science, Konkuk University) ;
  • Lee, Won Young (Department of Animal & Food Bioscience, College of Natural Science, Konkuk University) ;
  • Kim, Ji Hyuk (National Institute of Animal Science, RDA) ;
  • Kim, In Chul (National Institute of Animal Science, RDA) ;
  • Kim, Dong Woon (National Institute of Animal Science, RDA) ;
  • Lee, Sung Dae (National Institute of Animal Science, RDA) ;
  • Jung, Hyun Jung (National Institute of Animal Science, RDA) ;
  • Kim, Jong Moon (Department of Rehabilitation, School of Medicine, Konkuk University) ;
  • Yoon, Hyung Moon (Department of Orthopaedic Surgery, School of Medicine, Konkuk University) ;
  • Kwon, Hyuk Jung (Department of Family Medicine, School of Medicine, Konkuk University) ;
  • Song, Hyuk (Department of Animal & Food Bioscience, College of Natural Science, Konkuk University)
  • Received : 2012.09.14
  • Accepted : 2012.09.25
  • Published : 2012.09.30

Abstract

Interferon induced transmembrane protein-1 (Ifitm-1) has been reported to have an important role in primordial germ cell formation, and it has expressed in female reproductive organ. In the present study, Ifitm-1 gene expression was identified in testes and all part of epididymis using western immunoblot and immunohistochemistry. Interestingly, Ifitm-1 expression was observed on the head of spermatozoa. To investigate the role of Ifitm-1 gene expression in behavior of spermatozoa after acrosome reaction, fresh sperm was incubated with calcium ionophore to induce acrosome reaction, whereas the expression of Ifitm-1 was not altered after the acrosome reaction. Then to identify the effect of Ifitm-1 in sperm motility and other seminal parameters, different concentration of Ifitm-1 antibody was incubated with spermatozoa, and seminal parameters were assessed using computer-assisted semen analysis (CASA). Interestingly, motility, progressive, and VAP were increased in the sperm with Ifitm-1 antibody treated compared to rabbit serum, however other parameters such as straightness were not changed. In order to identify the functional significance of Ifitm-1 in fertilization, capacitated spermatozoa were pre-incubated with anti-Ifitm-1 antibody and subsequently examined the ability to adhere to mouse oocytes. However, any defection or alteration in sperm-egg fusion was not found, Ifitm-1 antibody treated or non-treated spermatozoa showed a normal penetration. Although the precise role of Ifitm-1 in sperm motility and following fertilization need to be elucidated, this study suggests that the activation of Ifitm-1 on the sperm may enhance the motility of spermatozoa in mice.

Keywords

References

  1. Abou-Haila A, Tulsiani DR (2000): Mammalian sperm acrosome: formation, contents, and function. Arch Biochem Biophys 379:173-182. https://doi.org/10.1006/abbi.2000.1880
  2. Akyerli CB, Beksac M, Holko M, Frevel M, Dalva K, Ozbek U, Soydan E, Ozcan M, Ozet G, Ilhan O, Gürman G, Akan H, Williams BR, Ozcelik T (2005): Expression of IFITM1 in chronic myeloid leukemia patients. Leuk Res 29:283-286. https://doi.org/10.1016/j.leukres.2004.07.007
  3. Boyer A, Hermo L, Paquet M, Robaire B, Boerboom D (2008): Semiferous tuble degeneration and infertility in mice with sustained activation of WNT/CTNNB1 signaling in sertoli cells. Biol Reprod 79:475- 485. https://doi.org/10.1095/biolreprod.108.068627
  4. Bradbury LE, Kansas GS, Levy S, Evans RL, Tedder TF (1992): The CD19/CD21 signal transducing complex of human B lymphocytes includes the target of antiproliferative antibody-1 and Leu-13 molecules. J Immunol 149:2841-2850.
  5. Töpfer-Petersen E, Petrounkina AM, Ekhlasi-Hundrieser M (2000): Oocyte-sperm interactions. Ani reprod sci 60-61:653-662. https://doi.org/10.1016/S0378-4320(00)00128-7
  6. Evans SS, Collea RP, Leasure JA, Lee DB (1993): IFNalpha induces homotypic adhesion and Leu-13 expression in human B lymphoid cells. J Immunol 150:736-747.
  7. Evans SS, Lee DB, Han T, Tomasi TB, Evans RL (1990): Monoclonal antibody to the interferon-inducible protein Leu-13 triggers aggregation and inhibits proliferation of leukemic B cells. Blood 76:2583-2593.
  8. Fumoto S, Shimokuni T, Tanimoto K, Hiyama K, Otani K, Ohtaki M, Hihara J, Yoshida K, Hiyama E, Noguchi T, Nishiyama M (2008): Selection of a novel drug-response predictor in esophageal cancer: a novel screening method using microarray and identification of IFITM1 as a potent marker gene of CDDP response. Int J Oncol 32:413-23.
  9. Hecht NB (1998): Molecular mechanisms of male germ cell differentiation. Bioessays 20:555-561. https://doi.org/10.1002/(SICI)1521-1878(199807)20:7<555::AID-BIES6>3.0.CO;2-J
  10. Lickert H, Cox B, Wehrle C, Taketo MM, Kemler R, Rossant J (2005): Dissecting Wnt/beta-catenin signaling during gastrulation using RNA interference in mouse embryos. Development 132:2599-2609. https://doi.org/10.1242/dev.01842
  11. Lacham-Kaplan O (2004): In vivo and in vitro differentiation of male germ cells in the mouse. Reproduction 128:147-152. https://doi.org/10.1530/rep.1.00220
  12. Park HJ, Kuk IS, Kim JH, Song SJ, Choi BC, Kim B, Kim NH, Song H (2011): Characterisation of mouse interferon-induced transmembrane protein- 1 gene expression in the mouse uterus during the estrous cycle and pregnancy. Reprod Fertil Dev 23: 798-808.
  13. Park HJ (2011): Characterization and gene expression study of mouse interferon-induced transmembrane protein-1. PhD Thesis. Konkuk University.
  14. Pumarola-Sune T, Graus F, Chen YX, Cordon-Cardo C, Evans RL (1986): A monoclonal antibody that induces T cell aggregation reacts with vascular endothelial cells and placental trophoblasts. J Immunol 137:826-829.
  15. Saitou M, Payer B, Lange UC, Erhardt S, Barton SC, Surani MA (2003): Specification of germ cell fate in mice. Philos Trans R Soc Lond B Biol Sci 358:1363- 1370. https://doi.org/10.1098/rstb.2003.1324
  16. Tanaka SS, Matsui Y (2002): Developmentally regulated expression of mil-1 and mil-2, mouse interferon- induced transmembrane protein like genes, during formation and differentiation of primodial germ cells. Gene Expr Patterns 2:297-303 https://doi.org/10.1016/S0925-4773(02)00384-2
  17. Tanaka SS, Yamaguchi YL, Tsoi B, Lickert H, Tam PP (2005): IFITM/Mil/fragilis family proteins IFITM1 and IFITM3 play distinct roles in mouse primodial germ cell homing and repulsion. Dev cell 9:745-756 https://doi.org/10.1016/j.devcel.2005.10.010
  18. Yang G, Xu Y, Chen X, Hu G (2007): IFITM1 plays an essential role in the antiproliferative action of interferon-gamma. Oncogene 26:594-603. https://doi.org/10.1038/sj.onc.1209807
  19. Xu Y, Yang G, Hu G (2009): Binding of IFITM1 enhances the inhibiting effect of caveolin-1 on ERK activation. Acta Biochim Biophys Sin 41:488-494. https://doi.org/10.1093/abbs/gmp034