Elevated Peritoneal Expression and Estrogen Regulation of Nociceptive Ion Channels in Endometriosis

Erin Greaves, Grieve K, Kelsey Grieve, Kelsey M. Grieve, Andrew W. Horne, Philippa T. K. Saunders
The Journal of clinical endocrinology and metabolism · 2014 · vol. 99(9) , pp. E1738–E1743 · doi:10.1210/jc.2014-2282 · PMID:25029427 · PMC4207935 · W2120171409
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This study found elevated expression of nociceptive ion channels TRPV1, TRPA1, and SCN11A in the peritoneum of women with endometriosis and demonstrated that estrogen increases TRPV1 expression in sensory neurons.

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This study compared peritoneal biopsies and endometriosis lesions from women with confirmed pelvic endometriosis, women with chronic pelvic pain (CPP) without endometriosis, and women without CPP or endometriosis, measuring mRNA levels of nociceptive markers by qPCR and distinguishing lesion-specific from peritoneum-wide changes. The authors found that TAC1 and SCN9A were elevated specifically in endometriosis lesions, while P2RX3 was increased in CPP peritoneum regardless of endometriosis status; additionally, peritoneum and lesions from women with endometriosis showed increased TRPA1 and TRPV1 mRNAs, with SCN11A higher in CPP patients with endometriosis than in CPP without it. In an ES-cell-derived human sensory neuron model, differentiation increased nociceptor-like markers and capsaicin-evoked calcium flux, and estrogen receptor signaling modulated some channels (notably TRPV1 via ER-dependent effects, and TAC1/P2RX3/SCN9A via ERβ agonist DPN), with a stated caveat of small, cross-sectional tissue sample sizes and in vitro reliance on a differentiation model rather than direct tissue causality. This paper is centrally about endometriosis — it identifies estrogen-regulated nociceptive ion channel and neuropeptide mRNA changes in endometriosis lesions and adjacent peritoneum.

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Abstract

CONTEXT: Ovarian suppression is a common treatment for endometriosis-associated pelvic pain. Its exact mechanism of action is poorly understood, although it is assumed to reflect reduced production/action of estrogens. OBJECTIVE: The objective of the study was to measure the expression of mRNAs encoded by nociceptive genes in the peritoneum of women with chronic pelvic pain (CPP) with or without endometriosis and to investigate whether estrogens alter nociceptive gene expression in human sensory neurons. DESIGN: The study was performed using human tissue analysis and cell culture. SETTING: The study was conducted at a university research institute. PATIENTS: Peritoneal biopsies were obtained from women with CPP and endometriosis (n = 12), CPP and no endometriosis (n = 10), and no pain or endometriosis (n = 5). Endometriosis lesions were obtained from women with endometriosis (n = 18). MAIN OUTCOME MEASURES: mRNAs encoding ion channels (P2RX3, SCN9A, SCN11A, TRPA1, TRPV1) and the neurotransmitter TAC1 were measured in human tissue samples and in human embryonic stem cell-derived sensory neurons treated with estrogens. RESULTS: TRPV1, TRPA1, and SCN11A mRNAs were significantly higher in the peritoneum from women with endometriosis (P < .001, P < .01). TRPV1, SCN9A, and TAC1 were elevated in endometriosis lesions (P < .05). P2RX3 mRNA was increased in the peritoneum of women with CPP, with and without endometriosis (P < .05). Incubation of sensory neurons with 17β-estradiol increased TRPV1 mRNA (P < .01). The estrogen receptor-β-selective agonist 2,3-bis(4-hydroxy-phenyl)-propionitrile increased concentrations of TRPV1, P2RX3, SCN9A, and TAC1 mRNAs. CONCLUSIONS: Estrogen-dependent expression of TRPV1 in sensory neurons may explain why ovarian suppression can reduce endometriosis-associated pain. Strategies directly targeting ion channels may offer an alternative option for the management of CPP.
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Results

Measurement of mRNAs encoded by TAC1 and nociceptive ion channels revealed differences between tissue samples; TAC1 was elevated only in endometriosis lesions ( Figure 1 A; P < .05), and P2RX3 was increased in the peritoneum of women with CPP, regardless of whether they were diagnosed with endometriosis compared with the peritoneum of healthy women ( Figure 1 B; P < .05). SCN9A (Nav1.7) was elevated in lesions from women with endometriosis ( Figure 1 C; P < .05), whereas SCN11A was significantly higher in the peritoneum of women with CPP and endometriosis compared with the peritoneum of women with CPP alone ( Figure 1 D; P < .001). mRNA encoded by TRPA1 was significantly increased in the peritoneum of women with endometriosis compared with the peritoneum of healthy women and those with CPP alone ( Figure 1 E; P < .001). TRPV1 was elevated in peritoneum ( P < .01) and in lesions ( P < .05) of women with endometriosis compared with the peritoneum of healthy women ( Figure 1 F). The neuropeptide TAC1 and nociceptive ion channels are differentially expressed in CPP and in endometriosis. A–F, mRNA concentrations of the neuropeptide TAC1 (A) and the nociceptive ion channels P2RX3 (B), SCN9A (C), SCN11A (D), TRPA1 (E), and TRPV1 (F) were analyzed using QPCR. Concentrations of mRNAs were measured in the peritoneum of women with no pain (control; n = 5), compared with the peritoneum of women with CPP but no obvious underlying pathology (PP; n = 10), and the peritoneum (EP; n = 12) and peritoneal lesions (EL; n = 18) of women with confirmed endometriosis. RQ, relative quantification. Statistical analysis was performed using a one-way ANOVA combined with a Newman Keuls post hoc test. *, P < .05; **, P < .01; ***, P < .001. Asterisks denote statistical significance compared with control, and lines and asterisks denote significance between specific groups. Sensory neurons immunopositive for neurofilament were generated in vitro ( 15 ) ( Figure 2 , A–C). Differentiation was accompanied by a reduction in octamer transcription factor-4 mRNA concentrations and an increase in TAC1, SCN9A , and SCN11A ( Figure 2 D), consistent with differentiation of sensory neurons with a nociceptor-like phenotype. When the differentiated cells were incubated with capsaicin (activates TRPV1), an intracellular calcium flux was detected ( Figure 2 E). The expression of ER subtypes changed during differentiation; ER α mRNA concentrations decreased and ER β mRNAs increased ( Figure 2 F). Stimulation of sensory neurons with the estrogen ligands E2, DPN, and PPT revealed ER-dependent regulation of nociceptive ion channels. TAC1 and P2RX3 mRNAs were increased after the incubation with DPN compared with cells incubated with DPN in the presence of ICI ( Figure 2 G; P < .001) or vehicle control (DMSO; Figure 2 H; P < .05), respectively. TAC1 was also elevated by PPT compared with PPT + ICI ( Figure 2 G; P < .01). Although SCN9A increased with DPN ( P < .05), this was not blocked by the addition of ICI ( Figure 2 I), and the expression of SCN11A ( Figure 2 J) and TRPA1 ( Figure 2 K) did not appear to be ER dependent. In contrast, TRPV1 mRNA concentrations were elevated by both E2 ( P < .05) and DPN ( Figure 2 I; P < .01), and this effect was abrogated by ICI. mRNA concentrations of nociceptive markers are regulated by estrogens in an in vitro model of human sensory neurons with a nociceptor-like phenotype derived from ES cells. A, Human ES cells were differentiated into sensory neurons with a nociceptor-like phenotype using combined small molecule inhibitors. Sensory neurons developed projections (B) and stained positively for neurofilament using immunocytochemistry (C). Scale bar, 200 μM. D, During the differentiation method, RNA was extracted from cells at different time points: pluripotent stem cells (d −7, n = 3), day 1 (n = 4), day 3 (n = 4), day 5 (n = 6), day 7 (n = 4), day 9 (n = 3), day 11 (n = 3), day 17 (n = 3), and day 21 (n = 3). QPCR analysis revealed that mRNA concentrations of the pluripotency marker octamer transcription factor-4 ( Oct4 ) declined as the differentiation procedure progressed. The nociceptive markers TAC1, SCN9A , and SCN11A increased. E, Sensory neuron functionality was determined by stimulating cells with 4 nM capsaicin and recording calcium flux. F, During differentiation from ES cells to mature sensory neurons, ER α mRNAs declined, whereas ER β inclined. G–L, Mature sensory neurons were incubated with DMSO (vehicle), E2, DPN, or PPT, with or without ICI, and RNA was extracted after 24h. G–I, Using QPCR TAC1 mRNAs were elevated by DPN and PPT compared to DPN + ICI and PPT + ICI. P2RX3 and SCN9A mRNAs were elevated by DPN compared with vehicle control (DMSO). J and K, No significant differences were detected in SCN11A and TRPA1 . L, TRPV1 mRNAs were elevated by E2 and DPN. RQ, relative quantification. Statistical analysis was performed using a one-way ANOVA and Newman Keuls post hoc test. *, P < .05; **, P < .01; ***, P < .001. Asterisks denote statistical significance compared with vehicle control (DMSO), and lines and asterisks denote significance between specific treatment groups.

Discussion

We believe this is the first study to detect differences in the expression of mRNAs encoded by the ion channels TRPA1 , P2RX3 , SCN9A , and SCN11A in the peritoneum and lesions of women suffering from CPP, some of whom had endometriosis. We believe these insights may be indicative of sensitization of nerves present within the peritoneal lining of women with pain and therefore shed new light on the mechanisms responsible for development of chronic hypersensitivity. In women with active endometriosis, we discovered that the concentrations of mRNAs encoded by SCN11A , TRPA1 , and TRPV1 were all significantly increased in the samples of peritoneum. We believe these novel findings are consistent with nociceptive changes taking place within the peritoneum of women with endometriosis, suggesting an increased sensitization of the peritoneum adjacent to the lesion. We detected significant increases in TRPV1 mRNAs in both the peritoneum and in lesions, confirming and extending a previous study ( 11 ). Notably, P2RX3 mRNAs were significantly elevated in the peritoneum of women with CPP, regardless of whether they had active endometriosis and would be consistent with a neuropathic component to idiopathic CPP. To date, researchers have used rat or chick dorsal root ganglia (DRG) neurons as an in vitro model to investigate the function of sensory neurons. However, because DRG neurons represent a mixed population of somatosensory neurons, the development of a differentiation protocol allowing the generation of a population of human sensory neurons with a nociceptor-like phenotype ( 15 ) is particularly welcome. In the current study, we detected expression of estrogen receptor mRNAs in our ES cell-derived cultures. Treatment of cells with E2 or the ERβ agonist DPN induced a significant increase in TRPV1 mRNAs that was blocked by the addition of the ER antagonist ICI. In addition, P2RX3, SCN9A , and TAC1 mRNAs were all increased when cells were incubated with the ERβ agonist DPN, and TAC1 was also increased by PPT. We have previously demonstrated DPN-dependent changes in gene expression in endometrial endothelial cells and have shown that these were mediated via specificity protein-1 tethered transcription ( 16 ). Bioinformatics revealed the presence of specificity protein-1 transcription factor binding sites in the promoter regions of TRPV1 , P2RX3 , SCN9A , and TAC1 (Match; Biobase international.com). TRPV1 mRNA was the only transcript that was increased in response to E2 treatment and abrogated by the antiestrogen ICI. Notably, bioinformatics detected several estrogen response elements in the promoter region of TRPV1 and throughout the length of the transcript (Dragon estrogen response element locator version 6.0; National Institute of Health) that could facilitate direct binding of E2-activated ER receptor dimers. Further studies are required to validate these findings. Estrogens are reported to have both pro- and antinociceptive properties. Mice exhibit hyperalgesia when estrogens are depleted after ovariectomy ( 17 ), and nociceptive responses are lower in ERβ knockout mice during the early stages of inflammation ( 18 ). The results of our study suggest estrogens may have a direct impact on nociception by up-regulating the expression of ion channels and would be consistent with reports that the expression of Trpv1 and P2x3 proteins are decreased in DRGs from mice with targeted deletions of Esr2 and Esr2 ( 19 ). In summary, the results of this study indicate that therapies targeting P2RX3 may be useful in treating CPP in women with a diverse range of painful etiologies, whereas women with active endometriosis could benefit from treatments targeting TRPV1, TRPA1, SCN9A, or SCN11A. Studies using sensory neurons suggest regulation of TRPV1 by estrogens may provide an explanation for the reduction in pain experienced when ovarian steroids are suppressed and an opportunity for development of novel therapies.

Materials|Methods

The study was approved by the Lothian Research Ethics Committee (LREC 11/AL/0376). Peritoneal biopsies [∼1.0 × 0.5 cm size: stored in RNAlater (Applied Biosystems) at −20°C] were obtained from 3 groups of women (aged 18–45 y) at the time of surgery with informed consent: 1) women undergoing laparoscopic investigation for CPP with histological evidence of pelvic endometriosis (n = 12); 2) women undergoing laparoscopic investigation for CPP without evidence of endometriosis (n = 10); and 3) women undergoing laparoscopic sterilization without CPP and without evidence of endometriosis (n = 5). Endometriosis lesions were also collected from women with endometriosis (n = 18). Peritoneal biopsies from women without endometriosis were recovered from a site prone to endometriosis (pouch of Douglas) and in women with endometriosis the peritoneal biopsy was recovered from a site adjacent to the endometriosis lesion. None of the women had taken exogenous hormones for at least 3 months at the time of sampling. Human ES cells, strain H9 (WiCell) were cultured on inactivated mouse embryonic fibroblasts maintained in Knockout DMEM/F12 supplemented with 20% knockout serum replacement (Gibco), 1 mM L-glutamine, 100 μM MEM nonessential amino acids, and 0.1 μM β-mercaptoethanol, with 6 ng/mL FGF-2 (R&D Systems). Differentiation of ES cells was induced using a cocktail of small molecule inhibitors as detailed by Chambers et al ( 15 ). RNA was extracted from cells at selected time points for the characterization and verification of phenotype. On day 22 the sensory neurons were trypsinized and reseeded into 12-well plates at equal densities (5 × 10 −5 cells/well). On day 25, the cells were treated for 24 hours with 10 −8 M 17β-estradiol (E2; Sigma), the estrogen receptor (ER)-α selective agonist 4,4′,4′-[4-propyl-(1H)-pyrazole-1,3,5-tryl] trisphenol (PPT), or the ERβ selective agonist 2,3-bis(4-hydroxy-phenyl)-propionitrile (DPN; Tocris) alone or in combination with the antiestrogen fulvestrant (ICI; 10 −7 M; Tocris) dissolved in dimethylsulfoxide (DMSO). Expression of neurofilament protein was detected using neurofilament H chicken antineurofilament H (1:1000; Covance); nuclei were stained with 4′,6′-diamino-2-phenylindole and images captured on an Axiovert microscope (Carl Zeiss Inc). Neurons were stimulated with 4 nM capsaicin (Sigma), and intracellular calcium was measured using a calcium indicator kit (BD Biosciences) with calcium flux captured using a NOVOstar microplate fluorometer (BMG Labtech). RNA was extracted from human tissues by homogenization in TRI reagent, chloroform phase separation and the lysates processed using an RNAeasy kit (QIAGEN). RNA was extracted from cells using RLT (lysis) buffer and an RNAeasy kit. Samples were deoxyribonuclease treated (QIAGEN) and concentration and purity assessed using a NanoDrop ND 1000. cDNA was synthesized using SuperScript VILO enzyme (Invitrogen) with 100 ng starting template in a 20-μL reaction. PCRs (15 μL) were performed using the Roche Universal Probe Library (Roche Applied Science) and Express quantitative PCR supermix (Invitrogen) with primers added at a concentration of 20 μM and thermal cycling performed on a 7900 Fast real-time PCR machine (Applied Biosystems) with 18S selected as the reference gene because we have confirmed this gene is not altered by estrogenic treatments. cDNA was added at 1.5 μL per reaction and duplicate technical replicates performed. Data were analyzed with RQ manager software (Applied Biosystems) using the δδCt method, and samples were normalized to either one laparoscopic sterilization sample (patients) or one vehicle control sample (cells). Primer sequences included the following: TRPA1 , forward, 5′-tggacaccttcttcttgcatt-3′, reverse, 5′-tcatccatttcatgcagcac-3′; TRPV1 , forward, 5′-agagtcacgctggcaacc-3′, reverse, 5′-ggcagagactctccatcacac-3′; SCN9A , forward, 5′-caacttttaagggatggacga-3′, reverse, 5′-tcatatttgggctgcttgtct-3′; SCN11A , forward, 5′-acctgagcctgaacaacagg-3′, reverse, 5′-tttgaactctctggctcgtg-3′; P2RX3 , forward, 5′-ggcctttacttctgtgggagt-3′, reverse, 5′-aaacttcttggctttgtactggtc-3′; TAC1 , forward, 5′-gcctcagcagttctttggat-3′, reverse, 5′-agcctttaacagggccactt-3′; ER α, forward, 5′-ttactgaccaacctggcaga-3′, reverse, 5′-atcatggagggtcaaatcca-3′; and ER β, forward, 5′-atcatggagggtcaaatcca-3′, reverse, 5′-tgggcattcagcatctcc-3′. Quantitative PCR (QPCR) data were analyzed using a one-way ANOVA and a Newman Keuls post hoc multiple comparison test. Statistics were generated using GraphPad Prism 6 software.

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Condition tags

endometriosischronic_pelvic_pain

MeSH descriptors

Endometriosis Ion Channels Nociceptors Pelvic Pain Biopsy Calcium Channels Calcium Channels Cells, Cultured Chronic Pain Chronic Pain Chronic Pain Embryonic Stem Cells Embryonic Stem Cells Endometriosis Endometriosis Endometriosis Estrogens Estrogens Female Humans

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