Demonstration of membrane estrogen binding proteins in rat brain by ligand blotting using a 17β-estradiol-[125I]bovine serum albumin conjugate

Journal of Steroid Biochemistry and Molecular Biology

Volumn 62, Issue 4, 1997, Pages 327-336

  Zheng, Jianbiao ^a   Ramirez, Victor D ^a,b  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ESTRADIOL; ESTROGEN BINDING PROTEIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; BRAIN; CELL FRACTIONATION; CONTROLLED STUDY; FEMALE; HISTOCHEMISTRY; IMMUNOBLOTTING; MEMBRANE BINDING; MICROSOME; NONHUMAN; RAT;

ANIMALS; BRAIN; CARRIER PROTEINS; ESTRADIOL; ESTROGENS, CONJUGATED (USP); FEMALE; IODINE RADIOISOTOPES; MEMBRANE PROTEINS; RATS; RATS, SPRAGUE-DAWLEY; SERUM ALBUMIN, BOVINE; SUBCELLULAR FRACTIONS;

ANIMALIA; BOVINAE;

EID: 0030733918     PISSN: 09600760     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-0760(97)00037-X     Document Type: Article

References (56)

1. Szego C. M. and Pietras R. J., Membrane recognition and effector sites in steroid hormone action. In Biochemical Actions of Hormones, Vol. VIII, ed G. Litwack. Academic Press, New York, 1981, pp. 308-463.
2. Baulieu E. M., Steroid-membrane adenylate cyclase interactions during Xenopus laevis oocyte meiosis reinitiation. In Progesterone and Progestins, ed. E. Milgrom and P. Mauvais-Jarvis. Raven Press, New York, 1983, pp. 91-105.
3. Duval D., Durant S. and Homo-Delarche F., Non-genomic effects of steroids: interactions of steroid molecules with membrane structures and functions. Biochem. Biophys. Acta 737 (1983) 409-442.
4. Schumacher K., Rapid membrane effects of steroid hormones: an emerging concept in neuroendocrinology. Trends Neurosci. 13 (1990) 359-362.
5. McEwen B. S., Non-genomic and genomic effects of steroids on neural activity. Trends Pharmacol. Sci. 12 (1991) 141-147.
6. Nemere I., Zhou L.-X. and Norman A. W., Nontranscriptional effects of steroid hormones. Receptor 3 (1993) 277-291.
7. Wehling M., Genomic and non-genomic effects of aldosterone. CRC Press, Boca Raton, Florida, 1995.
8. Ramirez V. D. and Zheng J., Membrane sex-steroid receptors in the brain. Frontiers Neuroendocrinol. 17 (1996) 402-439.
9. Evans R. M., The steroid and thyroid hormone receptor super-family. Science 240 (1988) 889-895.
10. Beato M., Gene regulation by steroid hormones. Cell 56 (1989) 335-344.
11. Pietras R. J. and Szego C. M., Estrogen receptors in uterine plasma membrane. J. Steroid Biochem. 11 (1979) 1471-1483.
12. Pietras R. J. and Szego C. M., Partial purification and characterization of oestrogen receptors in subfractions of hepatocyte plasma membranes. Biochem. J. 191 (1980) 743-760.
13. Hernandez-Perez O., Ballesteros L. M. and Rosado A., Binding of 17β-estradiol to the outer surface and nucleus of human spermatozoa. Arch. Androl. 3 (1979) 23-29.
14. Towle A. C. and Sze P. Y., Steroid binding to synaptic plasma membrane: differential binding of glucocorticoids and gonadal steroids. J. Steroid Biochem. 18 (1983) 135-143.
15. Horvat A., Nikezic G. and Martinovic J. V., Estradiol binding to synaptosomal plasma membranes of rat brain regions. Experientia 51 (1995) 11-15.
16. Bression D., Michard M., Le Dafniet M., Pagesy P. and Peillon F., Evidence for a specific estradiol binding site on rat pituitary membranes. Endocrinology 119 (1986) 1048-1051.
17. Blackmore P. F., Neulen J., Lattanzio F. and Beebe S. J., Cell surface-binding sites for progesterone mediate calcium uptake in human sperm. J. Biol. Chem. 266 (1991) 18655-18659.
18. Meizel S. and Turner K. O., Progesterone acts at the plasma membrane of human sperm. Mol. Cell. Endocrinol. 11 (1991) R1-R5.
19. Ke F.-C. and Ramirez V. D., Membrane mechanism mediates progesterone stimulatory effect on LHRH release from super-fused rat hypothalami in vitro. Neuroendocrinology 45 (1987) 514-517.
20. Dluzen D. E. and Ramirez V. D., Progesterone effects upon dopamine release from the corpus striatum of female rats. II. Evidence for a membrane site of action and the role of albumin. Brain Res. 476 (1989) 338-344.
21. Nenci T., Marchetti E., Marzola A. and Fabris G., Affinity cytochemistry visualizes specific estrogen binding sites on the plasma membrane of breast cancer cells. J. Steroid Biochem. 14 (1981) 1139-1146.
22. Berthois Y., Pourreau-Schneider N., Gandilhon P., Mittre H., Tubiana N. and Martin P. M., Estradiol membrane binding sites on human breast cancer cell lines: use of a fluorescent estradiol conjugate to demonstrate plasma membrane binding systems. J. Steroid Biochem. 25 (1986) 963-972.
23. Pappas T. C., Gametchu B. and Watson C. S., Membrane estrogen receptors identified by multiple antibody labeling and impeded-ligand binding. FASEB J. 9 (1995) 404-410.
24. 125-bovine serum albumin as a ligand. J. Neurochem. 54 (1990) 467-472.
25. Zheng J., Ali A. and Ramirez V. D., Steroids conjugated to bovine serum albumin as tools to demonstrate specific steroid neuronal membrane binding sites. J. Psychiatr. Neurosci. 21 (1996) 187-197.
26. Ramirez V. D., Zheng J. and Khawar M. S., Membrane receptors for estrogen, progesterone and testosterone in the rat brain; fantasy or reality?. Mol. Cell. Neurobiol. 16 (1996) 175-198.
27. Soutar A. K. and Wade D. P., Ligand blotting. In Protein Function: a Practical Approach, ed T. E. Creighton. IRL Press, Oxford, 1989, pp. 55-76.
28. Lieberherr M., Grosse B., Kachkache M. and Balsan S., Cell signalling and estrogens in female rat osteoblasts: a possible involvement of unconventional nonnuclear receptors. J. Bone Min. Res. 8 (1993) 1365-1376.
29. Tesarik J. and Mendoza C., Nongenomic effects of 17β-estra-diol on maturing human oocytes: relationship to oocyte developmental potential. J. Clin. Endocrinol. Metab. 80 (1995) 1438-1443.
30. Mermelstein P. G., Becker J. B. and Surmeier D. J., Estradiol reduces calcium currents in rat neostriatal neurons via a membrane receptor. J. Neurosci. 16 (1996) 595-604.
31. Rothe G. M. and Maurer W. D., One-dimensional PAA-gel eletrophoretic techniques to separate functional and denatured proteins. In Gel Eleltrophoresis of Proteins, ed. M. J. Dunn. IOP Publishing Ltd, Bristol, 1986, pp. 37-140.
32. Hossenlopp P. and Binoux M., Use of peptide ligands for the detection of binding proteins by Western blotting. In Protein Blotting: A practical Approach, ed B. S. Dunbar. IRL Press, Oxford, 1994, pp. 169-188.
33. Gershoni J. M., Hawrot E. and Lentz T. L., Binding of α-bun-garotoxin to isolated α-subunit of the acetylcholine receptor of Torpedo californica: quantitative analysis with protein blots. Proc. Natl. Acad. Sci. U.S.A. 80 (1983) 4973-4977.
34. Hossenlopp P., Seurin D., Segovia-Quinson B., Hardouin S. Binoux M., Analysis of serum insulin-like growth factor binding proteins using western blotting: use of the method of titration of the binding proteins and competitive binding studies. Analyt. Biochem. 154 (1986) 138-143.
35. Grissom F., Rivero-Grespo F., Lindgren B. and Hall K., Ligand blot analysis: validation of quantitative capabilities and utilization for measurement of truncated insulin-like growth factor regulation of Hep-G2 insulin-like growth factor binding protein-1 production. Analyt. Biochem. 212 (1993) 412-420.
36. Rosemblit N., Ascoli M. and Segaloff D. L., Characterization of an antiserum to the rat luteal luteinizing hormone/chorionic gonadotropin receptor. Endocrinology 123 (1988) 2284-2290.
37. Liu M., Chen T.-Y., Ahamed B., Li J. and Yau K.-W., Calcium-calmodulin modulation of the olfactory cyclic nucleotide-gated cation channel. Science 266 (1994) 1348-1354.
38. Zheng J. and Ramirez V. D., Neural membrane estrogen binding proteins: Western ligand blot studies. Endocrine Soc. Abst. 77 (1995) 218.
39. Darnell J., Lodish H. and Baltimore D., Molecular Cell Biology, 2nd edn. W. H. Freeman and Co., New York, 1990, pp. 109-150.
40. Bradford M. M., A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analyt. Biochem. 72 (1976) 248-254.
41. Tischkau S. A. and Ramirez V. D., A specific membrane binding protein for progesterone in rat brain: sex difference and induction by estrogen. Proc. Natl. Acad. Sci. U.S.A. 90 (1993) 1285-1289.
42. Laemmli U. K., Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685.
43. Towbin H., Staehelin R. and Gordon J., Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets. Proc. Natl. Acad. Sci. U.S.A. 76 (1979) 4350-4354.
44. Dufy B., Partouche C., Poulain D., Dufy-Barbe L. and Vincent J. D., Effects of estrogen on the electrical activity of identified and unidentified hypothalamic units. Neuroendocrinology 22 (1976) 38-47.
45. Moss R. L. and Dudley C. A., Molecular aspects of the interaction between estrogen and the membrane excitability of hypothalamic nerve cells. Prog. Brain Res. 61 (1984) 3-22.
46. Caldwell J. D., Morris M. A., Walker C. H., Carr R. B., Faggin B. M. and Mason G. A., Estradiol conjugated to BSA release oxytocin from synaptosome-containing homogenates from the medial preoptic area-hypothalamus. Hormone Metab. Res. 28 (1996) 119-121.
47. Smith S. S., Waterhouse B. D. and Woodward D. J., Sex steroid effects on extrahypothalamic CNS. I. Estrogen augments neuronal responsiveness to iontophoretically applied glutamate in the cerebellum. Brain Res. 442 (1987) 40-51.
48. Smith S. S., Waterhouse B. D. and Woodward D. J., Locally applied estrogens potentiate glutamate-evoked excitation of cerebellar Purkinje cells. Brain Res. 475 (1988) 272-282.
49. Nebekura J., Oomure Y., Minami T., Mizuno Y. and Fukuda A., Mechanism of the rapid effect of 17β-estradiol on medial amygdala neurons. Science 233 (1986) 226-228.
50. Becker J. B., Direct effect of 17β-estradiol on striatum: sex differences in dopamine release. Synapse 5 (1990) 5157-5164.
51. Wong M. and Moss R. L., Long-term and short-term electro-physiological effects of estrogen on the synaptic properties of hippocampal CA1 neurons. J. Neurosci. 12 (1992) 3217-3225.
52. Korenman S. G., Comparative binding affinity of estrogens and its relation to estrogenic potency. Steroids 13 (1969) 163-177.
53. 125I]BSA as a subunit of the mitochondria F0F1 ATP-synthase/ATPase. (submitted) 1997.
54. Gametchu B., Glucocorticoid receptor-like antigen in lymphoma cell membranes: correlation to cell lysis. Science 236 (1987) 456-461.
55. 125I]iodohistamine) identifies four protein bands in mouse brain membranes. J. Neurochem. 63 (1994) 1434-1438.
56. 125I]iodohistamine) in mouse brain membranes. J. Steroid Biochem. Mol. Biol. 58 (1996) 89-94.