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Histochemistry. 1991;96(5):419-34. doi: 10.1007/BF00316000.

Uptake, distribution and binding of vertebrate and invertebrate steroid hormones and time-dependence of ponasterone A binding in Calliphora vicina. Comparisons among cholesterol, corticosterone, cortisol, dexamethasone, 5 alpha-dihydrotestosterone, 1,25-dihydroxyvitamin D3, ecdysone, estradiol-17 beta, ponasterone A, progesterone, and testosterone.

Histochemistry

H J Bidmon, W E Stumpf

Affiliations

  1. Department of Cell Biology and Anatomy, University of North Carolina, Chapel Hill 27599-7090.

PMID: 1748566 DOI: 10.1007/BF00316000

Abstract

The presence of specific binding sites for radiolabelled vertebrate-type and arthropod-type steroid hormones was investigated in several organs including salivary gland, and central nervous system of third instar Calliphora vicina larvae by thaw-mount autoradiography. Ponasterone A, a 20-hydroxyecdysone agonist and 20-hydroxyecdysone are the only steroids which bind to nuclear high affinity binding sites. These binding sites are DNA associated while nucleoli show no tracer binding. Ecdysone, an endogenous 20-hydroxyecdysone precursor, is taken up by target cells but no significant nuclear binding occurs. 1,25-Dihydroxyvitamin D3 concentrates in cytoplasm only and its uptake is highest compared to all other steroids. Progesterone and testosterone show weak accumulation in the cytoplasm, while for cholesterol, corticosterone, cortisol, dexamethasone, dihydrotestosterone and estradiol-17 beta, no noticeable uptake occurs. For ponasterone A, a clear time dependence of uptake and intracellular distribution is visible, suggesting the existence and involvement of specific ecdysteroid uptake and transport mechanisms. These results suggest the presence of binding sites for various mammalian steroids in insects. Whether vertebrate steroid hormones or metabolites of them play a role in insects or whether the uptake and binding is based on chemical similarities alone without biological significance remains to be further investigated.

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References

  1. Biochem Pharmacol. 1974 Sep 15;23 (18):2495-531 - PubMed
  2. Mol Cell Endocrinol. 1983 Sep;32(1):73-9 - PubMed
  3. Eur J Biochem. 1977 Dec 1;81(2):293-8 - PubMed
  4. Monogr Neural Sci. 1983;9:205-12 - PubMed
  5. Experientia. 1985 Apr 15;41(4):516-9 - PubMed
  6. Science. 1990 Nov 2;250(4981):691-4 - PubMed
  7. J Biol Chem. 1990 Jan 25;265(3):1376-80 - PubMed
  8. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6035-8 - PubMed
  9. Mol Cell Endocrinol. 1981 Feb;21(2):97-108 - PubMed
  10. Prog Histochem Cytochem. 1991;22(4):1-59 - PubMed
  11. Mol Cell Endocrinol. 1983 Jul;31(1):93-104 - PubMed
  12. J Biol Chem. 1983 Oct 25;258(20):12210-4 - PubMed
  13. Gen Comp Endocrinol. 1986 Feb;61(2):214-28 - PubMed
  14. J Neurochem. 1990 Feb;54(2):467-72 - PubMed
  15. Cell Tissue Res. 1991 Jan;263(1):183-94 - PubMed
  16. Exp Cell Res. 1960 Sep;20:623-6 - PubMed
  17. Biochem J. 1989 Dec 1;264(2):539-46 - PubMed
  18. Biochim Biophys Acta. 1983 Aug 11;737(3-4):409-42 - PubMed
  19. Mol Cell Endocrinol. 1987 Jul;52(1-2):81-4 - PubMed
  20. J Insect Physiol. 1976;22(2):227-34 - PubMed
  21. J Steroid Biochem. 1985 Mar;22(3):419-26 - PubMed
  22. Histochemistry. 1987;87(5):393-406 - PubMed
  23. J Neurobiol. 1989 Dec;20(8):681-702 - PubMed
  24. J Steroid Biochem. 1989 Apr;32(4):613-22 - PubMed
  25. Gen Comp Endocrinol. 1984 Jun;54(3):429-32 - PubMed
  26. J Histochem Cytochem. 1981 Jan;29(1A Suppl):201-6 - PubMed
  27. Nat New Biol. 1971 Sep 15;234(50):220-2 - PubMed
  28. J Membr Biol. 1973 Aug 30;13(1):89-96 - PubMed
  29. Biochem Biophys Res Commun. 1969 Jul 23;36(2):251-6 - PubMed
  30. Exp Cell Res. 1989 Apr;181(2):492-504 - PubMed
  31. Endocrinology. 1987 Apr;120(4):1232-42 - PubMed
  32. Reprod Nutr Dev. 1981;21(5A):681-7 - PubMed
  33. Exp Cell Res. 1980 Feb;125(2):490-3 - PubMed

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