Skip to main content
Log in

Progesterone Receptor or Cytoskeletal Protein?

  • Original Articles
  • Published:
Reproductive Sciences Aims and scope Submit manuscript

Abstract

Immunoblotting is used to characterize the various nuclear progesterone receptor (nPR) isoforms present in tissues; however, the success of this technique is dependent on the specificity of the primary nPR antibody. The authors investigate the specificity of a frequently used nPR antibody, sc-538, in total protein from human myometrium and a myometrial cell line (PHM1-31). Using immunoblotting, 2 sc-538 immunoreactive bands at 100 and 55 kDa were detected. The bands were extracted and identified by 1-dimensional liquid chromatography mass spectrometry. The predominant protein in the 100-kDa band was α -actinin. The dominant proteins in the smaller band were vimentin (57 kDa) and desmin (53 kDa). Myometrial lysate was immunoprecipitated with sc-538, and immunoblotting of the immunoprecipitate with antibodies to α -actinin, desmin, and vimentin confirmed the presence of these proteins. The sc-538 nPR antibody therefore cross-reacts with cytoskeletal proteins that could be misinterpreted as nPR isoforms. Such misinterpretation has confused the progesterone response literature.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  1. Conneely OM, Lydon JP, De Mayo F, O’Malley BW. Reproductive functions of the progesterone receptor. J Soc Gynecol Investig. 2000;7(1 suppl):S25–S32.

    Article  CAS  PubMed  Google Scholar 

  2. Leonhardt SA, Edwards DP. Mechanism of action of progesterone antagonists. Exp Biol Med (Maywood). 2002;227:969–980.

    Article  CAS  Google Scholar 

  3. Kastner P, Krust A, Turcotte B, et al. Two distinct estrogen-regulated promoters generate transcripts encoding the two functionally different human progesterone receptor forms A and B. EMBO J. 1990; 9: 1603–1614.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Giangrande PH, McDonnell DP. The A and B isoforms of the human progesterone receptor: two functionally different transcription factors encoded by a single gene. Recent Prog Horm Res. 1999;54:291–313.

    CAS  PubMed  Google Scholar 

  5. Giangrande PH, Kimbrel EA, Edwards DP, McDonnell DP. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding. Mol Cell Biol. 2000;20:3102–3115.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Vegeto E, Shahbaz MM, Wen DX, Goldman ME, O’Malley BW, McDonnell DP. Human progesterone receptor A form is a cell- and promoter-specific repressor of human progesterone receptor B function. Mol Endocrinol. 1993;7:1244–1255.

    CAS  PubMed  Google Scholar 

  7. Tung L, Mohamed MK, Hoeffler JP, Takimoto GS, Horwitz KB. Antagonist-occupied human progesterone B-receptors activate transcription without binding to progesterone response elements and are dominantly inhibited by A-receptors. Mol Endocrinol. 1993;7:1256–1265.

    CAS  PubMed  Google Scholar 

  8. Condon JC, Hardy DB, Kovaric K, Mendelson CR. Up-regulation of the progesterone receptor (PR)-C isoform in laboring myometrium by activation of nuclear factor-kappaB may contribute to the onset of labor through inhibition of PR function. Mol Endocrinol. 2006;20:764–775.

    Article  CAS  PubMed  Google Scholar 

  9. Taylor AH, McParland PC, Taylor DJ, Bell SC. The progesterone receptor in human term amniochorion and placenta is isoform C. Endocrinology. 2006;147:687–693.

    Article  CAS  PubMed  Google Scholar 

  10. Wei LL, Hawkins P, Baker C, Norris B, Sheridan PL, Quinn PG. An amino-terminal truncated progesterone receptor isoform, PRc, enhances progestin-induced transcriptional activity. Mol Endocrinol. 1996;10:1379–1387.

    CAS  PubMed  Google Scholar 

  11. Welter BH, Hansen EL, Saner KJ, Wei Y, Price TM. Membrane-bound progesterone receptor expression in human aortic endothelial cells. J Histochem Cytochem. 2003;51:1049–1055.

    Article  CAS  PubMed  Google Scholar 

  12. O’Brien SN, Welter BH, Mantzke KA, Price TM. Identification of progesterone receptor in human subcutaneous adipose tissue. J Clin Endocrinol Metab. 1998;83:509–513.

    Article  PubMed  Google Scholar 

  13. Mesiano S, Chan EC, Fitter JT, Kwek K, Yeo G, Smith R. Progesterone withdrawal and estrogen activation in human parturition are coordinated by progesterone receptor A expression in the myometrium. J Clin Endocrinol Metab. 2002; 87:2924–2930.

    Article  CAS  PubMed  Google Scholar 

  14. Madsen G, Zakar T, Ku CY, Sanborn BM, Smith R, Mesiano S. Prostaglandins differentially modulate progesterone receptor-A and -B expression in human myometrial cells: evidence for prostaglandin-induced functional progesterone withdrawl. J Clin Endocrinol Metab. 2004;89:1010–1013.

    Article  CAS  PubMed  Google Scholar 

  15. Scheer JM, Ryan CA. A method for the quantitative recovery of proteins from polyacrylamide gels. Anal Biochem. 2001;298: 130–132.

    Article  CAS  PubMed  Google Scholar 

  16. Osborn M, Debus E, Weber K. Monoclonal antibodies specific for vimentin. Eur J Cell Biol. 1984;34:137–143.

    CAS  PubMed  Google Scholar 

  17. Pollock L, Rampling D, Greenwald SE, Malone M. Desmin expression in rhabdomyosarcoma: influence of the desmin clone and immunohistochemical method. J Clin Pathol. 1995;48: 535–538.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Feramisco JR, Blose SH. Distribution of fluorescently labeled alpha-actinin in living and fixed fibroblasts. J Cell Biol. 1980; 86:608–615.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Brown AG, Leite RS, Strauss JF III. Mechanisms underlying “functional” progesterone withdrawal at parturition. Ann N Y Acad Sci. 2004;1034:36–49.

    Article  CAS  PubMed  Google Scholar 

  20. Mesiano S. Myometrial progesterone responsiveness and the control of human parturition. J Soc Gynecol Investig. 2004;11: 193–202.

    Article  CAS  PubMed  Google Scholar 

  21. Pieber D, Allport VC, Hills F, Johnson M, Bennett PR. Interactions between progesterone receptor isoforms in myometrial cells in human labour. Mol Hum Reprod. 2001; 7:875–879.

    Article  CAS  PubMed  Google Scholar 

  22. Merlino AA, Welsh TN, Tan H, et al. Nuclear progesterone receptors in the human pregnancy myometrium: evidence that parturition involves functional progesterone withdrawal mediated by increased expression of PR-A. J Clin Endocrinol Metab. Epub ahead of print March 6, 2007.

  23. Yu JT, Lopez Bernal A. The cytoskeleton of human myometrial cells. J Reprod Fertil. 1998;112:185–198.

    Article  CAS  PubMed  Google Scholar 

  24. Wilkins MR, Lindskog I, Gasteiger E, et al. Detailed peptide characterization using PEPTIDEMASS—a World-Wide-Web— accessible tool. Electrophoresis. 1997;18:403–408.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gemma Madsen MSc.

Additional information

This research has been facilitated by access to the Australian Proteome Analysis Facility established under the Australian government’s Major National Research Facilities Program. SM is supported by the March of Dimes Birth Defects Foundation.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Madsen, G., MacIntyre, D.A., Mesiano, S. et al. Progesterone Receptor or Cytoskeletal Protein?. Reprod. Sci. 14, 217–222 (2007). https://doi.org/10.1177/1933719107302380

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1177/1933719107302380

Key words