Rapid, nongenomic steroid actions initiated at the cell surface: Lessons from studies with fish

Fish Physiology and Biochemistry

Volumn 28, Issue 1-4, 2003, Pages 3-12

  Thomas, Peter ^a  

^a The University of Texas at Austin   (United States)

Author keywords

Endocrine disruption; Hormonal regulation steroid membrane receptors; Nongenomic steroid actions; Oocyte maturation; Progestin membrane receptors; Sperm motility; Steroid membrane receptors

Indexed keywords

CELL NUCLEUS RECEPTOR; COMPLEMENTARY DNA; G PROTEIN COUPLED RECEPTOR; GESTAGEN; MEMBRANE RECEPTOR; PROGESTERONE RECEPTOR; STEROID; STEROID RECEPTOR;

AMPHIBIA; ANIMAL CELL; ARTICLE; BINDING AFFINITY; CELL SURFACE; CHEMICAL STRUCTURE; CONTROLLED STUDY; FEMALE; FISH; GENE IDENTIFICATION; GONAD; HORMONAL REGULATION; HORMONE ACTION; MALE; NONHUMAN; OOCYTE MATURATION; OVARY; POLLUTANT; RECEPTOR BINDING; SPERM; TELEOST; TROUT; VERTEBRATE; WESTERN BLOTTING;

AMPHIBIA; CYNOSCION NEBULOSUS; PISCES; TELEOSTEI; VERTEBRATA;

EID: 3543021743     PISSN: 09201742     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:FISH.0000030461.35242.57     Document Type: Article

References (33)

1. Blackmore, P.F., Neulen, J., Lattanzio, F. and Beebe, S.J. 1991. Cell-surface binding sites for progesterone mediate calcium uptake in human sperm. J. Biol. Chem. 266: 18655-18659.
2. Braun A. and Thomas, P. 2003. Androgens inhibit estradiol-17β synthesis in Atlantic croaker (Micropogonias undulatus) ovaries by a nongenomic mechanism initiated at the cell surface. Biol. Reprod. 69: 1642-1650.
3. Das, S. and Thomas, P. 1999. Pesticides interfere with the nongenomic action of a progestogen on meiotic maturation by binding to its plasma membrane receptor on fish oocytes. Endocrinology 140: 1953-1956.
4. Detweiler, C. and Thomas, P. 1998. Role of ions and ion channels in the regulation of Atlantic croaker sperm motility. J. Exp. Zool. 281: 139-148.
5. Ghosh, S. and Thomas, P. 1995. Antagonistic effects of xenobiotics on steroid-induced final maturation of Atlantic croaker oocytes in vitro. Mar. Environ. Res. 39: 159-163.
6. Hammes, S.R. 2003. The further redefining of steroid-mediated signaling. Proc. Natl. Acad. Sci. USA 100: 2168-2170.
7. King, V,W., Ghosh, S., Thomas, P. and Sullivan, C.V. 1997. A receptor for the oocyte maturation-inducing hormone, 17, 20β, 21-trihydroxy-4-pregnen-3-one on ovarian membranes of striped bass. Biol. Reprod. 56: 266-271.
8. Loomis, A.K. and Thomas, P. 2000. Effects of estrogens and xenoestrogens on androgen production by Atlantic croaker testes in vitro: Evidence for a nongenomic action mediated by an estrogen membrane receptor. Biol. Reprod. 62: 995-1004.
9. Maller, J.L. 1998. Recurring themes in oocyte maturation. Biology of the Cell 90: 453-460.
10. Maller, J.L. 2003. Fishing at the cell surface. Science 300: 594-595.
11. Miura, T.K., Yamauchi, K., Takahashi, H. and Nagahama, Y. 1992. The role of hormones in the acquisition of sperm motility in salmonid fish. J. Exp. Zool. 126: 89-96.
12. Nadal, A., Ropero, A.B., Laribi, O., Maillet, M., Fuentes, E. and Soria, B. 2000. Nongenomic actions of estrogens and xenoestrogens by binding at a plasma membrane receptor unrelated to estrogen receptor alpha and estrogen receptor beta. Proc. Natl. Acad. Sci. USA 97: 11603-11608.
13. Nagahama, Y., Yoshikuni, M., Yamashita, M. And Tanaka, M. 1994 Regulation of oocyte maturation in fish. Pp. 393-439. In: Sherwood N.M, Hew C.L, editors. Fish Physiology Vol. XIII. San Diego, Academic Press.
14. Patiño, R. and Thomas, P. 1990 Characterization of membrane receptor activity for 17β, 20β, 21-trihydroxy-4-pregnen-3-one in ovaries of spotted seatrout (Cynoscion nebulosus). Gen. Comp. Endocrinol. 78: 204-217.
15. Pickford, D.B. and Morris, I.D. 1999. Effects of endocrine-disrupting contaminants on amphibian oogenesis: Methoxychlor inhibits progesterone-induced maturation of Xenopus laevis oocytes in vitro. Environ, Hlth. Perspect. 107: 285-92.
16. Rahman, M., Ohta, K., Yoshikuni, M., Nagahama, Y., Chuda, H. and Matsuyama, M. 2002. Characterization of ovarian membrane receptor for 17, 20β-dihydroxy-4-pregnen-3-one, a maturation-inducing hormone in yellowtail, Seriola quinqueradiata. Gen Comp Endocrinol. 127: 71-79.
17. Revelli, A., Massobrio, M. and Tesarik, J. 1998. Nongenomic actions of steroid hormones in reproductive tissues. Endocr. Rev. 19: 3-17.
18. Ruehlmann, D.O., Steinert, J.R., Valverde, M.A., Jacob, R., and Mann, G.E. 1998. Environmental estrogenic pollutants induce acute vascular relaxation by inhibiting L-Type Ca2 channels in smooth muscle cells. FASEB Journal. 12: 613-619.
19. Thomas, P. 1994. Hormonal control of final oocyte maturation in sciaenid fishes. In: K.G., Davey., R.E. Peter, S.S. Tobe, editors. Pp. 619-625. Perspectives in Comparative Endocrinology, Ottawa National Research Council of Canada.
20. Thomas, P. 2000a. Nuclear and membrane steroid receptors and their functions in teleost gonads. In: Proceedings of the Sixth International symposium on the Reproductive Physiology of Fish, Pp. 149-156. Edited by B. Norberg, O.S. Kjesbu, G.L.Taranger, E.Andersson and S.O. Stefansson, Institute of Marine Research and University of Bergen, Bergen, Norway.
21. Thomas, P. 2000b. Chemical interference with the genomic and non-genomic actions of steroids in fishes: Role of receptor binding. Mar. Environ. Res. 50: 127-134.
22. Thomas P., Breckenridge-Miller, D. and Detweiler, C. 1997 Binding characteristics and regulation of the 17β, 20β, 21-trihydroxy-4-pregen-3-one (20β-S) receptor on testicular and sperm membranes of spotted seatrout (Cynocscion nebulosus). Fish Physiol. Biochem. 17: 109-117.
23. Thomas, P., Breckenridge-Miller, D. and Detweiler, C. 1998. The teleost sperm membrane progestogen receptor: Interactions with xenoestrogens. Marine Environmental Research 46: 163-167.
24. Thomas, P., Pinter, J. and Das, S. 2001 Upregulation of the maturation-inducing steroid membrane receptor in spotted seat-rout ovaries by gonadotropin during oocyte maturation and its physiological significance. Biol. Reprod. 64: 21-29.
25. Thomas, P. and Das, S. 1997. Correlation between binding affinities of C21 steroids for the maturation-inducing steroid membrane receptor in spotted seatrout ovaries and their agonist and antagonist activities in an oocyte maturation bioassay. Biol. Reprod. 57: 999-1007.
26. Thomas, P. and Patiño, R. 1991. Changes in 17α, 20β, 21-trihydroxy-4-pregnen-3-one membrane receptor concentrations in ovaries of spotted seatrout during final oocyte maturation. In: A.P. Scott, J. Sumpter, D. Kime, M.S. Rolge, editors. Proceedings of the Fourth International Symposium on the Reproductive Physiology of Fish. Pp. 122-124. Sheffield, UK: University of East Anglia.
27. Thomas, P., Zhu, Y. and Pace, M. 2002. Progestin membrane receptors involved in the meiotic maturation of teleost oocytes: A review with some new findings. Steroids 67: 511-517.
28. Thomas, P., Zhu, Y. and Pang, Y.F. 2003. Current knowledge of the nature of progestin and estrogen membrane receptors in fish gonads. In Identities of Steroid Membrane Receptors, pp. 131-138. Edited by C.S.Watson. Kluwer Academic Publishers, Boston.
29. Watson, C.S. and Gametchu, B. 1999. Membrane-initiated steroid actions and the proteins that mediate them. Proc. Soc. Exp. Biol. Med. 220: 9-19.
30. 3H]17α, 20β-dihydroxy-4-pregnen-3-one to oocyte cortices of rainbow trout (Oncorhynchus mykiss). Fish Physiol. Biochem. 1993; 11: 15-24.
31. Yoshikuni, M. and Nagahama, Y. 1994. Involvement of an inhibitory G-protein in the signal transduction pathway of maturation-inducing hormone (17α, 20β, 21-dihydroxy-4-pregnen-3-one) action in rainbow trout (Oncorhynchus mykiss) oocytes. Dev. Biol. 16: 615-622.
32. Zhu, Y., Rice, C.D., Pang, Y., Pace, M. and Thomas, P. 2003a. Cloning, expression, and characterization of a membrane progestin receptor and evidence it is an intermediary in meiotic maturation of fish oocytes. Proc. Natl. Acad. Sci. USA 100: 2231-2236.
33. Zhu, Y, Bond, J. and Thomas, P. 2003b. Identification, classification, and partial characterization of genes in humans and other vertebrates homologous to a fish membrane progestin receptor. Proc. Natl. Acad. Sci. USA 100: 2237-2242.