The Effect of Copper on Endometrial Receptivity and Induction of Apoptosis on Decidualized Human Endometrial Stromal Cells

article OA: closed CC0 ⤵ 2 in-corpus citations
AI-generated summary by gemini-2.5-flash-lite+body, 2026-06-09

Copper exposure altered gene expression related to endometrial receptivity and immune response in decidualized human endometrial stromal cells without increasing apoptosis.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-09 · read from full text

This study examined whether copper added to in vitro decidualized human endometrial stromal cells (derived from five fertile women) affects endometrial receptivity and apoptosis, using camptothecin as a positive apoptosis control. Copper did not increase apoptosis or necrosis induced by decidualization, but it caused an order-of-magnitude change in the expression of 49/192 receptivity/immune-related genes (42 upregulated, 9 downregulated), including genes implicated in endometriosis pathology and other gynecologic disorders. Major limitations include the small sample size (five per group) and that the work was conducted in vitro on decidualized stromal cells rather than in vivo endometrium. This paper does directly relate to endometriosis — it reports copper-induced changes in a decidualization gene signature that includes genes involved in endometriosis pathology.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Intrauterine devices (IUDs) have been widely used to prevent pregnancies with great efficacy during decades. It has been demonstrated that IUD alters the endometrial gene expression, but there is no scientific data about how copper, a metal commonly used in these devices, by itself, is able to influence the processes of endometrial receptivity and apoptosis in decidualized human endometrial stromal cells. Five endometrial samples were obtained from fertile women and processed by a standard protocol to obtain human endometrial stromal cells for in vitro studies. Stromal cells were cultured in vitro and decidualized for 8 days. At day 6, copper was added to the treatment group or camptothecin as positive control for apoptosis until day 8. Five endometrial samples were used in each group. The aim of this study was to analyze the effect of copper in apoptosis and necrosis by flow cytometry, to visualize the apoptotic microtubule network during apoptosis by immunofluorescence, and finally to determine the gene expression profile of a panel of 192 genes related to endometrial receptivity and immune system by quantitative reverse transcription PCR (RT-qPCR). Copper, compared to the decidualized group, induced changes in the gene expression by an order of magnitude in 49 genes (42 up- and 9 downregulated). This alteration in the decidualization gene signature by copper includes 19 genes involved in the endometriosis pathology and others related to other gynecological disorders such as preeclampsia and infertility. Our results indicate that copper does not increase the apoptosis level induced by the decidualization treatment. However, copper alters the gene expression of some biomarkers of endometrial receptivity and immune response.
Full text 11,896 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Abstract

Intrauterine devices (IUDs) have been widely used to prevent pregnancies with great efficacy during decades. It has been demonstrated that IUD alters the endometrial gene expression, but there is no scientific data about how copper, a metal commonly used in these devices, by itself, is able to influence the processes of endometrial receptivity and apoptosis in decidualized human endometrial stromal cells. Five endometrial samples were obtained from fertile women and processed by a standard protocol to obtain human endometrial stromal cells for in vitro studies. Stromal cells were cultured in vitro and decidualized for 8 days. At day 6, copper was added to the treatment group or camptothecin as positive control for apoptosis until day 8. Five endometrial samples were used in each group. The aim of this study was to analyze the effect of copper in apoptosis and necrosis by flow cytometry, to visualize the apoptotic microtubule network during apoptosis by immunofluorescence, and finally to determine the gene expression profile of a panel of 192 genes related to endometrial receptivity and immune system by quantitative reverse transcription PCR (RT-qPCR). Copper, compared to the decidualized group, induced changes in the gene expression by an order of magnitude in 49 genes (42 upand 9 downregulated). This alteration in the decidualization gene signature by copper includes 19 genes involved in the endometriosis pathology and others related to other gynecological disorders such as preeclampsia and infertility. Our results indicate that copper does not increase the apoptosis level induced by the decidualization treatment. However, copper alters the gene expression of some biomarkers of endometrial receptivity and immune response. Similar content being viewed by others

References

d’Arcangues C. Worldwide use of intrauterine devices for contraception. Contraception. 2007;75(suppl 6):S2–S7. UNDP/UNFPA/WHO/World Bank Special Programme of Development and Research Training in Human Reproduction. Long term safety and effectiveness of copper-releasing intrauterine devices: a case study. Retrieved from http://whqlibdoc.who.int/ hq/2008/WHO_RHR_HRP_08.08_eng.pdf. (accessed May 10, 2017). Hatcher RA, Trussell J, Nelson AL, Cates W, Stewart FH. Contraceptive Technology. 19th ed. New York, NY: Ardent Media; 2007. Brahmi D, Steenland MW, Renner RM, Gaffield ME, Curtis KM. Pregnancy outcomes with an IUD in situ: a systematic review. Contraception. 2012;85(2):131–139. Ortiz ME, Croxatto HB. Copper-T intrauterine device and levonorgestrel intrauterine system: biological bases of their mechanism of action. Contraception. 2007;75(suppl 6):S16–S30. World Health Organization Scientific Group. Mechanism of Action, Safety and Efficacy of Intrauterine Devices. Geneva, Switzerland: World Health Organization; 1987. Technical report series No: 753. Speroff L, Darney PD. A Clinical Guide for Contraception. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2001. Hatcher RA, Robert A. Contraceptive Technology. 20th ed. New York, NY: Ardent Media; 2011. Gemzell-Danielsson K, Lalitkumar PG, Berger C. Emergency contraception—mechanisms of action. Contraception. 2013; 88(4):581–582. Stanford JB, Mikolajczyk RT. Mechanisms of action of intrauterine devices: update and estimation of postfertilization effects. Am J Obstet Gynecol. 2002;187(6):1699–1708. Horcajadas JA, Sharkey AM, Catalano RD, et al. Effect of an intrauterine device on the gene expression profile of the endometrium. J Clin Endocrinol Metab. 2006;91(8):3199–3207. Tetrault AM, Richman SM, Fei X, Taylor HS. Decreased endometrial HOXA10 expression associated with use of the copper intrauterine device. Fertil Steril. 2009;92(6):1820–1824. Du H, Taylor HS. Molecular regulation of mullerian development by Hox genes. Ann N Y Acad Sci. 2004;1034:152–165. Filomeni G, Piccirillo S, Graziani I, et al. The isatin-Schiff base copper(II) complex Cu(isaepy)2 acts as delocalized lipophilic cation, yields widespread mitochondrial oxidative damage and induces AMP-activated protein kinase-dependent apoptosis. Carcinogenesis. 2009;30(7):1115–1124. Reinprayoon D. Intrauterine contraception. Curr Opin Obstet Gynecol. 1992;4(4):527–530. Ylikorkala O. Prostaglandin synthesis inhibitors in menorrhagia, intrauterine contraceptive device-induced side effects and endometriosis. Pharmacol Toxicol. 1994;75(2):86–88. Oruc S, Vatansever HS, Karaer O, Eskicioglu F, Narlikuyu B. Changes in distribution patterns of integrins in endometrium in copper T380 intrauterine device users. Acta Histochem. 2005; 107(2):95–103. Grillo CA, Reigosa MA, de Mele MA. Does over-exposure to copper ions released from metallic copper induce cytotoxic and genotoxic effects on mammalian cells? Contraception. 2010; 81(4):343–349. Sanchez-Alcazar JA, Rodriguez-Hernandez A, Cordero MD, et al. The apoptotic microtubule network preserves plasma membrane integrity during the execution phase of apoptosis. Apoptosis. 2007;12(7):1195–1208. Simón C, Mercader A, Garcia-Velasco J, et al. Coculture of human embryos with autologous human endometrial epithelial cells in patients with implantation failure. J Clin Endocrinol Metab. 1999;84(8):2638–2646. Kasahara K, Takakura K, Takebayashi K, Kimura F, Nakanishi K, Noda Y. The role of human chorionic gonadotropin on decidualization of endometrial stromal cells in vitro. J Clin Endocrinol Metab. 2001;86(3):1281–1286. Huang da W, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res. 2009;37(1):1–13. Szklarczyk D, Franceschini A, Wyder S, et al. STRING v10: protein-protein interaction networks, integrated over the tree of life. Nucleic Acids Res. 2015;43(Database issue): D447–D452. Gellersen B, Brosens JJ. Cyclic decidualization of the human endometrium in reproductive health and failure. Endocr Rev. 2014;35(6):851–905. Arancibia V, Peña C, Allen HE, Lagos G. Characterization of copper in uterine fluids of patients who use copper T-380-A intrauterine device. Clin Chim Acta. 2003;332(1-2):69–78. Boeddeker SJ, Baston-Buest DM, Fehm T, Kruessel J, Hess A. Decidualization and syndecan-1 knock down sensitize endometrial stromal cells to apoptosis induced by embryonic stimuli. PLoS One. 2015;10(4):e0121103. Moulton BC. Transforming growth factor-beta stimulates endometrial stromal apoptosis in vitro. Endocrinol. 1994;134(3): 1055–1060. Shikone T, Kokawa K, Yamoto M, Nakano R. Apoptosis of human ovary and uterine endometrium during the menstrual cycle. Horm Res. 1997;48(3):27–34. Dowd DR, Miesfeld RL. Evidence that glucocorticoid- and cyclic AMP-induced apoptotic pathways in lymphocytes share distal events. Mol Cell Biol. 1992;12(8):3600–3608. Bøe R, Gjertsen BT, Døskeland SO, Vintermyr OK. 8-ChlorocAMP induces apoptotic cell death in a human mammary carcinoma cell (MCF-7) line. Br J Cancer. 1995;72(5):1151–1159. Leno-Duran E, Ruiz-Magana MJ, Munoz-Fernandez R, Requena F, Olivares EG, Ruiz-Ruiz C. Human decidual stromal cells secrete soluble pro-apoptotic factors during decidualization in a cAMP-dependent manner. Hum Reprod. 2014;29(10):2269–2277. Jasinska A, Strakova Z, Szmidt M, Fazleabas AT. Human chorionic gonadotropin and decidualization in vitro inhibits cytochalasin-D-induced apoptosis in cultured endometrial stromal fibroblasts. Endocrinol. 2006;147(9):4112–4121. Kayisli UA, Selam B, Guzeloglu-Kayisli O, Demir R, Arici A. Human chorionic gonadotropin contributes to maternal immunotolerance and endometrial apoptosis by regulating Fas-Fas ligand system. J Immunol. 2003;171(5):2305–2313. Li HY, Chang SP, Yuan CC, Chao HT, Ng HT, Sung YJ. Induction of p38 mitogen-activated protein kinase-mediated apoptosis is involved in outgrowth of trophoblast cells on endometrial epithelial cells in a model of human trophoblast-endometrial interactions. Biol Reprod. 2003;69(5):1515–1524. Carson DD, Lagow E, Thathiah A, et al. Changes in gene expression during the early to mid-luteal (receptive phase) transition in human endometrium detected by high-density microarray screening. Mol Hum Reprod. 2002;8(9):871–879. Kao LC, Tulac S, Lobo S, et al. Global gene profiling in human endometrium during the window of implantation. Endocrinol. 2002;143(6):2119–2138. Borthwick JM, Charnock-Jones DS, Tom BD, et al. Determination of the transcript profile of human endometrium. Mol Hum Reprod. 2003;9(1):19–33. Riesewijk A, Martin J, van Os R, et al. Gene expression profiling of human endometrial receptivity on days LHþ2 versus LHþ7 by microarray technology. Mol Hum Reprod. 2003;9(5):253–264. Mirkin S, Nikas G, Hsiu JG, Diaz J, Oehninger S. Gene expression profiles and structural/functional features of the peri-implantation endometrium in natural and gonadotropinstimulated cycles. J Clin Endocrinol Metab. 2004;89(11): 5742–5752. Horcajadas JA, Riesewijk A, Domínguez F, Cervero A, Pellicer A, Simón C. Determinants of endometrial receptivity. Ann N Y Acad Sci. 2004;1034:166–175. Horcajadas JA, Pellicer A, Simón C. Wide genomic analysis of human endometrial receptivity: new times, new opportunities. Hum Reprod Update. 2007;13(1):77–86. Diaz-Gimeno P, Horcajadas JA, Martinez-Conejero JA, et al. A genomic diagnostic tool for human endometrial receptivity based on the transcriptomic signature. Fertil. Steril. 2011;95(1):50–60. Hu S, Yao G, Wang Y, et al. Transcriptomic changes during the pre-receptive to receptive transition in human endometrium detected by RNA-Seq. J Clin Endocrinol Metab. 2014;99(12): 2744–2753. Brar AK, Handwerger S, Kessler CA, Aronow BJ. Gene induction and categorical reprogramming during in vitro human endometrial fibroblast decidualization. Phisiol Genomics. 2001;7(2): 135–148. Germeyer A, Sharkey AM, Prasadajudio M, et al. Paracrine effects of uterine leucocytes on gene expression of human uterine stromal fibroblasts. Mol Hum Reprod. 2009;15(1):39–48. Cloke B, Huhtinen K, Fusi L, et al. The androgen and progesterone receptors regulate distinct gene networks and cellular functions in decidualizing endometrium. Endocrinol. 2008;149(9): 4462-4474 Dimitriadis E, Robb L, Salamonsen LA. Interleukin 11 advances progesterone-induced decidualization of human endometrial stromal cells. Mol Hum Reprod. 2002;8(7):636–643. Takano M, Lu Z, Goto T, et al. Transcriptional cross talk between the forkhead transcription factor forkhead box O1A and the progesterone receptor coordinates cell cycle regulation and differentiation in human endometrial stromal cells. Mol Endocrinol. 2007; 21(10):2334–2349. Kajihara T, Tochigi H, Prechapanich J, et al. Androgen signaling in decidualizing human endometrial stromal cells enhances resistance to oxidative stress. Fertil. Steril. 2012;97(1):185–191. Vasquez YM, Mazur EC, Li X, et al. FOXO1 is required for binding of PR on IRF4, novel transcriptional regulator of endometrial stromal decidualization. Mol Endocrinol. 2015;29(3): 421–433. Hubacher D, Chen PL, Park S. Side effects from the copper IUD: do they decrease over time?. Contraception. 2009;79(5):356–362. Jiménez MF, Passos EP, Fagundes PA, de Freitas FM, Arbo E, Cunha-Filho JS. Effect of the copper-intrauterine device (TCu 380A) on subendometrial vascularization and uterine artery blood flow. Fertil Steril. 2006;86(6):1780–1782. Hubacher D. Copper intrauterine device use by nulliparous women: review of side effects. Contraception. 2007;75(suppl 6):S8–S11. Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Carrascosa, J.P., Cotán, D., Jurado, I. et al. The Effect of Copper on Endometrial Receptivity and Induction of Apoptosis on Decidualized Human Endometrial Stromal Cells. Reprod. Sci. 25, 985–999 (2018). https://doi.org/10.1177/1933719117732165 Published: Version of record: Issue date: DOI: https://doi.org/10.1177/1933719117732165

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

MeSH descriptors

Apoptosis Copper Decidua Endometrium Apoptosis Cells, Cultured Copper Decidua Decidua Embryo Implantation Endometrium Endometrium Endometrium Female Gene Expression Gene Expression Humans Necrosis Necrosis Stromal Cells

Citation neighborhood (sparse)

Too few in-corpus citations on either side for a chart; here are the lists.

Cites (1)

Cited by (2)

References (55)

Cited by (2)

Source provenance

europepmc
last seen: 2026-09-18T06:10:57.818014+00:00
openalex
last seen: 2026-06-04T00:00:01.174412+00:00
pubmed
last seen: 2026-05-13T22:20:13.663096+00:00
unpaywall
last seen: 2026-09-18T06:25:56.777850+00:00
License: CC0 · commercial use OK