Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1997 Mar 15;322(Pt 3):777–783. doi: 10.1042/bj3220777

Differential expression of ryanodine receptor RyR2 mRNA in the non-pregnant and pregnant human myometrium.

S S Awad 1, H K Lamb 1, J M Morgan 1, W Dunlop 1, J I Gillespie 1
PMCID: PMC1218255  PMID: 9148749

Abstract

We describe here the expression of the ryanodine receptor isoforms RyR2 and RyR3 in human non-pregnant and pregnant (non-labouring) myometrium, and in isolated cultured myometrial cells. The mRNA encoding the RyR3 isoform was found in both non-pregnant and pregnant myometrial tissue samples; however, the mRNA for RyR2 was found only in pregnant samples. It can be speculated that the appearance of this additional isoform in the pregnant myometrium may increase the ability of this tissue to contract at term. Control of expression of the RyR2 gene may therefore be another example of an up-regulated signalling system in pregnancy. Although the mRNA for RyR3 was expressed in cultured myometrial cells, the mRNA for RyR2 could not be detected. Thus cultured myometrial cells appear to be similar to the non-pregnant myometrium. The cytokine transforming growth factor beta (TGF-beta) has been reported to alter RyR mRNA expression in many cell types. After treatment with TGF-beta, both RyR2 and RyR3 mRNAs could be detected in cultured myometrial cells. These observations support the idea that the expression of the RyR2 isoform is up-regulated both in pregnancy and in TGF-beta-treated cultured myometrial cells. Using measurements of 45Ca2+ release, we have further demonstrated that cultured human myometrial cells show a significant augmentation of both the Ca2+-induced Ca2+ release (CICR) mechanism and ryanodine-induced Ca2+ release after treatment with TGF-beta. Additionally, caffeine was able to induce Ca2+ release and sensitize the CICR mechanism to ryanodine. Thus we suggest that the appearance of RyR2 mRNA leads to the expression of this receptor/channel protein with identifiable pharmacological characteristics. These results are discussed in the context of the potential role of gene activation in the process of maturation of the human myometrium during pregnancy.

Full Text

The Full Text of this article is available as a PDF (355.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Airey J. A., Baring M. D., Sutko J. L. Ryanodine receptor protein is expressed during differentiation in the muscle cell lines BC3H1 and C2C12. Dev Biol. 1991 Nov;148(1):365–374. doi: 10.1016/0012-1606(91)90344-3. [DOI] [PubMed] [Google Scholar]
  2. Balducci J., Risek B., Gilula N. B., Hand A., Egan J. F., Vintzileos A. M. Gap junction formation in human myometrium: a key to preterm labor? Am J Obstet Gynecol. 1993 May;168(5):1609–1615. doi: 10.1016/s0002-9378(11)90806-0. [DOI] [PubMed] [Google Scholar]
  3. Berridge M. J. Inositol trisphosphate and calcium signalling. Nature. 1993 Jan 28;361(6410):315–325. doi: 10.1038/361315a0. [DOI] [PubMed] [Google Scholar]
  4. Birnboim H. C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523. doi: 10.1093/nar/7.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  6. Cathala G., Savouret J. F., Mendez B., West B. L., Karin M., Martial J. A., Baxter J. D. A method for isolation of intact, translationally active ribonucleic acid. DNA. 1983;2(4):329–335. doi: 10.1089/dna.1983.2.329. [DOI] [PubMed] [Google Scholar]
  7. Centrella M., McCarthy T. L., Canalis E. Parathyroid hormone modulates transforming growth factor beta activity and binding in osteoblast-enriched cell cultures from fetal rat parietal bone. Proc Natl Acad Sci U S A. 1988 Aug;85(16):5889–5893. doi: 10.1073/pnas.85.16.5889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chegini N., Flanders K. C. Presence of transforming growth factor-beta and their selective cellular localization in human ovarian tissue of various reproductive stages. Endocrinology. 1992 Mar;130(3):1707–1715. doi: 10.1210/endo.130.3.1537318. [DOI] [PubMed] [Google Scholar]
  9. Chegini N., Zhao Y., Williams R. S., Flanders K. C. Human uterine tissue throughout the menstrual cycle expresses transforming growth factor-beta 1 (TGF beta 1), TGF beta 2, TGF beta 3, and TGF beta type II receptor messenger ribonucleic acid and protein and contains [125I]TGF beta 1-binding sites. Endocrinology. 1994 Jul;135(1):439–449. doi: 10.1210/endo.135.1.8013382. [DOI] [PubMed] [Google Scholar]
  10. Cochet C., Feige J. J., Chambaz E. M. Bovine adrenocortical cells exhibit high affinity transforming growth factor-beta receptors which are regulated by adrenocorticotropin. J Biol Chem. 1988 Apr 25;263(12):5707–5713. [PubMed] [Google Scholar]
  11. Europe-Finner G. N., Phaneuf S., Tolkovsky A. M., Watson S. P., López Bernal A. Down-regulation of G alpha s in human myometrium in term and preterm labor: a mechanism for parturition. J Clin Endocrinol Metab. 1994 Dec;79(6):1835–1839. doi: 10.1210/jcem.79.6.7989491. [DOI] [PubMed] [Google Scholar]
  12. Europe-Finner G. N., Phaneuf S., Watson S. P., López Bernal A. Identification and expression of G-proteins in human myometrium: up-regulation of G alpha s in pregnancy. Endocrinology. 1993 Jun;132(6):2484–2490. doi: 10.1210/endo.132.6.8504751. [DOI] [PubMed] [Google Scholar]
  13. Fabiato A. Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum. Am J Physiol. 1983 Jul;245(1):C1–14. doi: 10.1152/ajpcell.1983.245.1.C1. [DOI] [PubMed] [Google Scholar]
  14. Giannini G., Clementi E., Ceci R., Marziali G., Sorrentino V. Expression of a ryanodine receptor-Ca2+ channel that is regulated by TGF-beta. Science. 1992 Jul 3;257(5066):91–94. doi: 10.1126/science.1320290. [DOI] [PubMed] [Google Scholar]
  15. Giannini G., Sorrentino V. Molecular structure and tissue distribution of ryanodine receptors calcium channels. Med Res Rev. 1995 Jul;15(4):313–323. doi: 10.1002/med.2610150405. [DOI] [PubMed] [Google Scholar]
  16. Izumi H., Garfield R. E., Morishita F., Shirakawa K. Some mechanical properties of skinned fibres of pregnant human myometrium. Eur J Obstet Gynecol Reprod Biol. 1994 Jul;56(1):55–62. doi: 10.1016/0028-2243(94)90154-6. [DOI] [PubMed] [Google Scholar]
  17. Kanmura Y., Missiaen L., Casteels R. Properties of intracellular calcium stores in pregnant rat myometrium. Br J Pharmacol. 1988 Sep;95(1):284–290. doi: 10.1111/j.1476-5381.1988.tb16575.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Khan R. N., Smith S. K., Morrison J. J., Ashford M. L. Properties of large-conductance K+ channels in human myometrium during pregnancy and labour. Proc Biol Sci. 1993 Jan 22;251(1330):9–15. doi: 10.1098/rspb.1993.0002. [DOI] [PubMed] [Google Scholar]
  19. Kimura T., Takemura M., Nomura S., Nobunaga T., Kubota Y., Inoue T., Hashimoto K., Kumazawa I., Ito Y., Ohashi K. Expression of oxytocin receptor in human pregnant myometrium. Endocrinology. 1996 Feb;137(2):780–785. doi: 10.1210/endo.137.2.8593830. [DOI] [PubMed] [Google Scholar]
  20. Ledbetter M. W., Preiner J. K., Louis C. F., Mickelson J. R. Tissue distribution of ryanodine receptor isoforms and alleles determined by reverse transcription polymerase chain reaction. J Biol Chem. 1994 Dec 16;269(50):31544–31551. [PubMed] [Google Scholar]
  21. Lynn S., Morgan J. M., Lamb H. K., Meissner G., Gillespie J. I. Isolation and partial cloning of ryanodine-sensitive Ca2+ release channel protein isoforms from human myometrial smooth muscle. FEBS Lett. 1995 Sep 18;372(1):6–12. doi: 10.1016/0014-5793(95)00924-x. [DOI] [PubMed] [Google Scholar]
  22. López Bernal A., Rivera J., Europe-Finner G. N., Phaneuf S., Asbóth G. Parturition: activation of stimulatory pathways or loss of uterine quiescence? Adv Exp Med Biol. 1995;395:435–451. [PubMed] [Google Scholar]
  23. Marks A. R., Taubman M. B., Saito A., Dai Y., Fleischer S. The ryanodine receptor/junctional channel complex is regulated by growth factors in a myogenic cell line. J Cell Biol. 1991 Jul;114(2):303–312. doi: 10.1083/jcb.114.2.303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. McPherson P. S., Campbell K. P. The ryanodine receptor/Ca2+ release channel. J Biol Chem. 1993 Jul 5;268(19):13765–13768. [PubMed] [Google Scholar]
  25. Meissner G. Ryanodine receptor/Ca2+ release channels and their regulation by endogenous effectors. Annu Rev Physiol. 1994;56:485–508. doi: 10.1146/annurev.ph.56.030194.002413. [DOI] [PubMed] [Google Scholar]
  26. Mershon J. L., Mikala G., Schwartz A. Changes in the expression of the L-type voltage-dependent calcium channel during pregnancy and parturition in the rat. Biol Reprod. 1994 Nov;51(5):993–999. doi: 10.1095/biolreprod51.5.993. [DOI] [PubMed] [Google Scholar]
  27. Morgan J. M., Gillespie J. I. The modulation and characterisation of the Ca(2+)-induced Ca2+ release mechanism in cultured human myometrial smooth muscle cells. FEBS Lett. 1995 Aug 7;369(2-3):295–300. doi: 10.1016/0014-5793(95)00771-z. [DOI] [PubMed] [Google Scholar]
  28. Morgan J. M., Lynn S., Gillespie J. I., Greenwell J. R. The induction of intracellular calcium activity in cultured human myometrial smooth muscle cells. Biochim Biophys Acta. 1993 Aug 20;1158(1):98–102. doi: 10.1016/0304-4165(93)90102-e. [DOI] [PubMed] [Google Scholar]
  29. Murayama T., Ogawa Y. Properties of Ryr3 ryanodine receptor isoform in mammalian brain. J Biol Chem. 1996 Mar 1;271(9):5079–5084. doi: 10.1074/jbc.271.9.5079. [DOI] [PubMed] [Google Scholar]
  30. Neylon C. B., Bryant S. M., Little P. J., Bobik A. Transforming growth factor-beta 1 regulates the expression of ryanodine-sensitive Ca2+ oscillations in cardiac myocytes. Biochem Biophys Res Commun. 1994 Oct 28;204(2):678–684. doi: 10.1006/bbrc.1994.2513. [DOI] [PubMed] [Google Scholar]
  31. Otsu K., Willard H. F., Khanna V. K., Zorzato F., Green N. M., MacLennan D. H. Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. J Biol Chem. 1990 Aug 15;265(23):13472–13483. [PubMed] [Google Scholar]
  32. Phaneuf S., Europe-Finner G. N., Varney M., MacKenzie I. Z., Watson S. P., López Bernal A. Oxytocin-stimulated phosphoinositide hydrolysis in human myometrial cells: involvement of pertussis toxin-sensitive and -insensitive G-proteins. J Endocrinol. 1993 Mar;136(3):497–509. doi: 10.1677/joe.0.1360497. [DOI] [PubMed] [Google Scholar]
  33. Pérez G., Toro L. Differential modulation of large-conductance KCa channels by PKA in pregnant and nonpregnant myometrium. Am J Physiol. 1994 May;266(5 Pt 1):C1459–C1463. doi: 10.1152/ajpcell.1994.266.5.C1459. [DOI] [PubMed] [Google Scholar]
  34. Rhoads D. D., Dixit A., Roufa D. J. Primary structure of human ribosomal protein S14 and the gene that encodes it. Mol Cell Biol. 1986 Aug;6(8):2774–2783. doi: 10.1128/mcb.6.8.2774. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Roberts A. B., Roche N. S., Winokur T. S., Burmester J. K., Sporn M. B. Role of transforming growth factor-beta in maintenance of function of cultured neonatal cardiac myocytes. Autocrine action and reversal of damaging effects of interleukin-1. J Clin Invest. 1992 Nov;90(5):2056–2062. doi: 10.1172/JCI116087. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Roy S. K., Kole A. R. Transforming growth factor-beta receptor type II expression in the hamster ovary: cellular site(s), biochemical properties, and hormonal regulation. Endocrinology. 1995 Oct;136(10):4610–4620. doi: 10.1210/endo.136.10.7664681. [DOI] [PubMed] [Google Scholar]
  37. Sakai N., Tabb T., Garfield R. E. Modulation of cell-to-cell coupling between myometrial cells of the human uterus during pregnancy. Am J Obstet Gynecol. 1992 Aug;167(2):472–480. doi: 10.1016/s0002-9378(11)91432-x. [DOI] [PubMed] [Google Scholar]
  38. Sorrentino V., Giannini G., Malzac P., Mattei M. G. Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization. Genomics. 1993 Oct;18(1):163–165. doi: 10.1006/geno.1993.1446. [DOI] [PubMed] [Google Scholar]
  39. Tamada H., McMaster M. T., Flanders K. C., Andrews G. K., Dey S. K. Cell type-specific expression of transforming growth factor-beta 1 in the mouse uterus during the periimplantation period. Mol Endocrinol. 1990 Jul;4(7):965–972. doi: 10.1210/mend-4-7-965. [DOI] [PubMed] [Google Scholar]
  40. Tang X. M., Zhao Y., Rossi M. J., Abu-Rustum R. S., Ksander G. A., Chegini N. Expression of transforming growth factor-beta (TGF beta) isoforms and TGF beta type II receptor messenger ribonucleic acid and protein, and the effect of TGF beta s on endometrial stromal cell growth and protein degradation in vitro. Endocrinology. 1994 Jul;135(1):450–459. doi: 10.1210/endo.135.1.8013384. [DOI] [PubMed] [Google Scholar]
  41. Tunwell R. E., Wickenden C., Bertrand B. M., Shevchenko V. I., Walsh M. B., Allen P. D., Lai F. A. The human cardiac muscle ryanodine receptor-calcium release channel: identification, primary structure and topological analysis. Biochem J. 1996 Sep 1;318(Pt 2):477–487. doi: 10.1042/bj3180477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Wray S. Uterine contraction and physiological mechanisms of modulation. Am J Physiol. 1993 Jan;264(1 Pt 1):C1–18. doi: 10.1152/ajpcell.1993.264.1.C1. [DOI] [PubMed] [Google Scholar]
  43. Zhao Y., Chegini N., Flanders K. C. Human fallopian tube expresses transforming growth factor (TGF beta) isoforms, TGF beta type I-III receptor messenger ribonucleic acid and protein, and contains [125I]TGF beta-binding sites. J Clin Endocrinol Metab. 1994 Oct;79(4):1177–1184. doi: 10.1210/jcem.79.4.7962292. [DOI] [PubMed] [Google Scholar]
  44. Zorzato F., Fujii J., Otsu K., Phillips M., Green N. M., Lai F. A., Meissner G., MacLennan D. H. Molecular cloning of cDNA encoding human and rabbit forms of the Ca2+ release channel (ryanodine receptor) of skeletal muscle sarcoplasmic reticulum. J Biol Chem. 1990 Feb 5;265(4):2244–2256. [PubMed] [Google Scholar]
  45. Zumbihl R., Breuiller-Fouché M., Carrette J., Dufour M. N., Ferré F., Bockaert J., Rouot B. Up-regulation in late pregnancy of both Go1 alpha and Go2 alpha isoforms in human myometrium. Eur J Pharmacol. 1994 Dec 15;288(1):9–15. doi: 10.1016/0922-4106(94)90004-3. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES