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Fish Physiol Biochem. 2005 Apr;31(2):209-14. doi: 10.1007/s10695-006-0026-1.

Gonadotropins and their paracrine signaling network in the zebrafish ovary.

Fish physiology and biochemistry

Wei Ge

Affiliations

  1. Department of Biology, The Chinese University of Hong Kong, Shatin, Hong Kong, New Territories, China, [email protected].

PMID: 20035460 DOI: 10.1007/s10695-006-0026-1

Abstract

Pituitary gonadotropins, follicle-stimulating hormone (FSH) and luteinizing hormone (LH), play fundamental roles in vertebrate ovarian development and function. However, there has been an increasing body of evidence that the actions of FSH and LH are mediated or modulated by a variety of locally produced peptide or protein factors, which form an intimate regulatory network within and between the ovarian follicles. In the past few years, a variety of growth factors have been identified and characterized in the zebrafish ovary including activin and epidermal growth factor (EGF), which are important components of the intraovarian communication network. To understand how this local network interacts with the gonadotropins from the pituitary, we have recently cloned and characterized all the subunits of zebrafish FSH and LH from the pituitary as well as their receptors (FSHR and LHR) from the ovary. Using the Chinese hamster ovary (CHO) cells as the bioreactor, we have produced recombinant zebrafish FSH and LH with biological activities. With the recombinant hormones available, the functions of zebrafish FSH and LH in the ovary and their interactions with the local factors will be an important issue to address in the future. This review briefly summarizes some recent work from our laboratory and others on both gonadotropins and their potential intraovarian signaling factors in the zebrafish.

References

  1. Gen Comp Endocrinol. 1988 Sep;71(3):459-67 - PubMed
  2. Endocrinology. 2005 Jan;146(1):77-84 - PubMed
  3. Endocrinology. 2002 Jan;143(1):47-54 - PubMed
  4. Gen Comp Endocrinol. 2003 Dec;134(3):308-15 - PubMed
  5. Biol Reprod. 2005 Jun;72(6):1382-96 - PubMed
  6. Gen Comp Endocrinol. 1998 Apr;110(1):46-57 - PubMed
  7. Endocr Rev. 1990 Feb;11(1):177-99 - PubMed
  8. Gen Comp Endocrinol. 1988 Aug;71(2):292-301 - PubMed
  9. Eur J Morphol. 2000 Jul;38(3):145-52 - PubMed
  10. Gen Comp Endocrinol. 1988 Aug;71(2):302-6 - PubMed
  11. Biol Reprod. 2004 Sep;71(3):749-60 - PubMed
  12. Gen Comp Endocrinol. 1999 Oct;116(1):81-9 - PubMed
  13. Endocr Rev. 1994 Jun;15(3):310-25 - PubMed
  14. Mech Dev. 2003 Jul;120(7):811-22 - PubMed
  15. Am J Physiol. 1996 May;270(5 Pt 2):R1065-72 - PubMed
  16. Exp Cell Res. 2003 Mar 10;284(1):2-13 - PubMed
  17. Biol Reprod. 1999 Oct;61(4):987-92 - PubMed
  18. Biol Reprod. 2000 May;62(5):1262-9 - PubMed
  19. Biol Reprod. 2002 Feb;66(2):259-65 - PubMed
  20. J Reprod Fertil. 1996 Jan;106(1):117-24 - PubMed
  21. Biol Reprod. 2005 Jun;72(6):1370-81 - PubMed
  22. Mol Cell Endocrinol. 2002 Feb 25;188(1-2):195-205 - PubMed
  23. Gen Comp Endocrinol. 1997 Feb;105(2):186-93 - PubMed
  24. J Biol Chem. 1990 May 15;265(14):7709-12 - PubMed
  25. Science. 2004 Jan 30;303(5658):682-4 - PubMed
  26. Gen Comp Endocrinol. 1997 Mar;105(3):379-89 - PubMed
  27. Gen Comp Endocrinol. 1995 Dec;100(3):397-403 - PubMed
  28. Biol Reprod. 2000 Jun;62(6):1585-92 - PubMed
  29. J Endocrinol. 1998 Mar;156(3):529-42 - PubMed
  30. Front Neuroendocrinol. 1998 Oct;19(4):287-322 - PubMed
  31. Gen Comp Endocrinol. 1991 Nov;84(2):291-9 - PubMed
  32. Biochem Pharmacol. 1998 Apr 1;55(7):953-63 - PubMed
  33. Gen Comp Endocrinol. 1992 Feb;85(2):217-29 - PubMed
  34. Endocrinology. 2003 Feb;144(2):491-9 - PubMed
  35. Trends Endocrinol Metab. 2000 Oct;11(8):309-14 - PubMed
  36. Biol Reprod. 2003 Dec;69(6):1998-2006 - PubMed

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