Development of In Vitro Bioassay for Detection of Estrogenic Activity of Xenobiotics : Monolayer Culture of Hepatocytes using Fish Serum

내분비 장애물질 검출을 위한 In Vitro Bioassay 개발 : 어류 혈청을 이용한 간세포 단층배양

  • Kwon, Hyuk-Chu (Dept. of Aquatic Life Medical Science, Sun Moon University) ;
  • Maeng, Joon-Ho (Dept. of Aquatic Life Medical Science, Sun Moon University) ;
  • Kim, Eun-Hee (Dept. of Aquatic Life Medical Science, Sun Moon University) ;
  • Choi, Seong-Hee (Dept. of Food Science, Sun Moon University)
  • 권혁추 (선문대학교 수산생명의학과) ;
  • 맹준호 (선문대학교 수산생명의학과) ;
  • 김은희 (선문대학교 수산생명의학과) ;
  • 최성희 (선문대학교 식품과학과)
  • Published : 2009.12.31

Abstract

Effects of sera from several fish species on monolayer formation, viability and functions of catfish hepatocytes were investigated to establish a primary hepatocyte culture system for screening endocrine disruptors. Hepatocytes of Korean catfish (Silurus asotus) were attached and formed monolayer using the media supplemented with their own serum or sera from eel and tilapia, but not with fetal bovine serum (FBS). The amount of fish sera (0.5~3%) for monolayer culture of the catfish hepatocytes was less than 1/10 of FBS (5~20%) that is commonly used for primary culture of hepatocytes of other species. The results indicate that FBS can be replaced with sera from some fish species and the fish sera are more effective than FBS in maintaining the shape and functions of the hepatocytes. The primary culture of catfish hepatocytes was maintained monolayer with fish sera for at least 10 days, which makes possible to be used for screening the activities of endocrine disruptors. In conclusion, the primary culture system of hepatocytes with fish sera in the present study could be a useful tool for screening and studying endocrine disruptors.

본 연구는 내분비 장애물질의 검출을 위하여 간세포의 단층 형성, 생존 및 기능에 미치는 어류 혈청의 영향에 대해 검토하였다. 한국산 메기의 간세포는 자신의 혈청 및 뱀장어, 틸라피아 등 타어종의 혈청에 의해 부착 및 단층이 형성되었으나, FBS는 메기 간세포의 단층을 형성시키지 못했다. 0.5에서 3%의 어류 혈청으로 메기 간세포의 단층을 형성 시킬 수 있는데, 이것은 FBS(5~20%) 사용의 1/10 이하로 적은 양이며, 어류 혈청이 FBS를 대체할 수 있고, FBS보다 간세포의 형태 및 기능 유지에 효과적인 것으로 나타났다. 어류 혈청이 첨가된 배양액에서 메기 간세포는 적어도 10일 이상 단층 형성을 유지할 수 있어, 내분비 장애물질 연구에 이용될 수 있을 것이다. 결론적으로 본 연구에서 개발된 어류 혈청을 사용한 메기 간세포 배양시스템과 효소면역측정법(ELISA)은 bisphenol A 등의 내분비 장애물질의 검출 및 연구를 위한 유용한 도구로서 이용될 수 있다고 생각된다.

Keywords

References

  1. Bon E, Barbe U, Nunez Rodriguez J, Cuisset B, Pelissero C, Sumpter JP, Le Menn F (1997) Plasma vitellogenin levels during the annual reproductive cycle of the female rainbow trout (Oncorhynchus mykiss): establishment and validation fo an ELISA. Comp Biochem Physiol 117B:75-84.
  2. Burki R, Vermeirssen ELM, Koerner O, Joris C, Burkhardt- Holm P, Seger H (2006) Assessment of estrogenic exposure in brown trout (Salmo trutta) in a Swiss midland river: integrated analysis of passive samplers, wild and caged fish, and vitellogenin mRNA and protein. Environ Toxicol Chem 25:2077-2086. https://doi.org/10.1897/05-545R.1
  3. Fossi MC, Casini S, Marsili L, Neri G, Mori G, Ancora S (2002) Biomarkers for endocrine disruptors in three species of Mediterranean large pelagic fish. Mar Environ Res 54:667-671. https://doi.org/10.1016/S0141-1136(02)00149-6
  4. Guillette LJ, Gross TS, Masson GR, Matter JM, Percival HF, Woodward AR (1999) Developmental abnormalities of the gonad and abnormal sex hormone concentrations in juvenile alligators from contaminated and control lakes in Florida. Environ Health Perspect 102:680-688. https://doi.org/10.2307/3432198
  5. Hyashi S, Ooshiro Z (1975) Gluconeogenesis and glycolysis in isolated perfused liver of the eel. Bull Jap Soc Fish 41:201-208. https://doi.org/10.2331/suisan.41.201
  6. Jobling S, Nolan M, Tyler C, Brighty G, Sumpter JP (1998) Widespread sexual disruption in wild fish. Environ Sci Technol 32:2498-2506. https://doi.org/10.1021/es9710870
  7. Kim BH, Takemura A (2003) Culture conditions affect induction of vitellogenin synthesis by estradiol-17${\beta}$ in primary cultures of tilapia hepatocytes. Comp Biochem Physiol 135B:231-239.
  8. Kordes C, Rieberb EP, Gutzeita HO (2002) An in vitro vitellogenin bioassay for oestrogenic substances in the medaka (Oryzias latipes). Aquat Toxicol 58:151-164. https://doi.org/10.1016/S0166-445X(01)00227-2
  9. Kwon HC, Hara A, Mugiya Y, Yamada Y (1990) Enzyme linked immunosorbent assay of vitellogenin in white spotted charr. Bull Fac Fish Hokkaido Univ 41:162- 180.
  10. Kwon HC, Hayashi S, Mugiya Y (1993) Vitellogenin inducton by estradiol-17 in primary hepatocyte culture in the rainbow trout, Oncorhynchus mykiss. Comp Biochem Physiol 104B:381-386.
  11. Kwon HC, Mugiya Y (1994) Involvement of growth hormone and prolactinthe induction of vitellogenin synthesis in primary hepatocyte culture in the Anguilla japonica. Gen Comp Endocrinol 93:51-60. https://doi.org/10.1006/gcen.1994.1007
  12. Kwon HC, Choi SH, Kim EH, Han DW, Kwon JY (2006) Effect of fish serum on the primary monolayer culture of catfish hepatocytes. J Kor Fish Soc 39:23-26.
  13. Marin MG, Matozzo V (2004) Vitellogenin induction as a biomarker of exposure to estrogenic compounds in aquatic environments. Marine Pollution Bulletin 48:835-839. https://doi.org/10.1016/j.marpolbul.2004.02.037
  14. Mommsen TP, Moon TW, Walsh PJ (1994) Hepatocytes: isolation maintenance and utilization. In: Hochachka PW, Mommsen TP, eds. Biochemistry and Molecular Biology of Fishes, Analytical Techniques, vol. 3. p355- 372, Amsterdam, Elsevier.
  15. Nakari T, Pessala P (2005) In vitro estrogenicity of polybrominated flame retardants. Aquatic Toxicology 74: 272-279. https://doi.org/10.1016/j.aquatox.2005.06.004
  16. Navas JM, Segner H (2006) Vitellogenin synthesis in primary cultures of fish liver cells as endpoint for in vitro screening of the (anti) estrogenic activity of chemical substances. Aquatic Toxicology 80:1-22. https://doi.org/10.1016/j.aquatox.2006.07.013
  17. Rutishauser BV, Pesonen M, Escher BI, Ackermann GE, Aerni HR, Suter MJ, Eggen RI (2004) Comparative analysis of estrogenic activity in sewage treatment plant effluents involving three in vitro assays and chemical analysis of steroids. Environ Toxicol Chem 23:857- 864. https://doi.org/10.1897/03-286
  18. Segner H (1998) Isolation and primary culture of teleost hepatocytes. Comp Biochem Physiol 120:71-81. https://doi.org/10.1016/S1095-6433(98)10012-0
  19. Sole M, Porte C, Barcelo D (2000) Vitellogenin induction and other biochemical responses in Carp, Cyprinus carpio, after experimental injection with 17${\alpha}$-ethynlestradiol. Arch Environ Contam Toxicol 38:494-500. https://doi.org/10.1007/s002449910065
  20. Tyler CR, Jobling S, Sumpter JP (1998) Endocrine disrupion in wildlife: a critical review of evidence. Crit Rev Toxicol 28:319-361. https://doi.org/10.1080/10408449891344236
  21. Vaillant C, Le Guellec C, Pakdel F, Valotaire Y (1998) Vitellogenin gene expression in primary culture of male rainbow trout hepatocytes. Gen Comp Endocrinol 70:284-290. https://doi.org/10.1016/0016-6480(88)90148-7