- Open Access
Endometrial beta3 Integrin profile reflects endometrial receptivity defects in women with unexplained recurrent pregnancy loss
© Germeyer et al.; licensee BioMed Central Ltd. 2014
- Received: 10 March 2014
- Accepted: 10 June 2014
- Published: 20 June 2014
The pathophysiology of recurrent pregnancy loss (RPL) is still unknown in 50% of the cases. Herein we measure the expression of beta3 integrin subunit, a well-known implantation marker, in women with or without RPL and correlate it with the histological dating of the endometrial tissue.
LH-timed endometrial biopsies were obtained from cases (RPL; n = 21, age 33.9+/-4.7) and healthy controls (n = 29; age 29.8+/-4.1) during the mid-secretory phase (post ovulatory day: 8 to 10). Endometrial samples were timed histologically according to Noyes’ criteria and underwent immunohistochemical staining for beta3 integrin expression. For statistical analysis the semi-quantitative HSCORE was assessed. Type I (beta3 negative in an out-of-phase endometrium) and Type II defect (beta3 negative in an in-phase endometrium) were also analysed. Statistical analysis was done with Student t-test, Mann Whitney U test, ANCOVA and chi square for trend. Significance was set as P < 0.05.
The mean (SD) age in controls was lower compared to cases [(29.8 (4.1) vs. 33.9 (4.7) – P = 0.001; Student t-test)]. The median (range) expression of beta3 integrin in controls and cases was 1.94 (0 to 3.5) vs. 0.82 (0 to 3.6), respectively (P = 0.001; Mann Whitney U test). Significance was still significant after adjusting for age (P = 0.03;ANCOVA). The normal positive staining > =0.7 of beta3 integrin subunit and in-phase endometrium was seen in 24 out of 29 (82.8%) controls, but in only 6 out of 21 (28.6%) of cases with RPL; Type I and II defects were seen in 10.3 and 6.9% of controls, while present in 52.4 and 19.1% of cases, respectively (P = 0.0005; chi-square).
Women with unexplained RPL had significantly reduced integrin expression compared to controls. Our findings underline the need for further molecular analysis of endometrial tissue in affected women.
- Beta3 integrin
- Recurrent pregnancy loss
- Endometrial dating
Recurrent pregnancy loss (RPL), determined as two or more consecutive abortions by some authors, are seen in 1-3% of couples; an underlying cause, however, is only found in up to 50% . These include embryonic factors, like poor quality embryos with or without karyotype abnormalities, as well as maternal factors, such as uterine malformations, general maternal infections, as well as local inflammation , hormonal abnormalities, immunogenic abnormalities (like thyroid antibodies, cardiolipin antibodies or antinuclear antibodies), genetic imbalances and thrombophilic diseases .
However, when none of these factors are evident, the recurrent pregnancy losses are classified as idiopathic, because the underlying mechanisms are not well understood. The functional expression of endometrial genes and proteins have been examined, because they compromise the endometrial microenviroment and may therefore contribute to an abnormal foetal-maternal interaction, resulting in pregnancy failure . Furthermore synchronisation between embryonic development and endometrial decidualisation is found to be essential for adequate implantation . Many authors have studied the embryo-endometrium interface in order to elucidate the pregnancy failure [6, 7]. Global gene expression analysis [8, 9] has determined the adequate endometrial gene and protein expression during the short endometrial receptive stage in the mid-secretory phase, the so-called window of implantation (WOI) . One of these proteins is the αvβ3 integrin . The combined integrin αvβ3 acts as an adhesion promoter via cell-cell interactions and it has been very well characterized within the human endometrium . The αvβ3 integrin is expressed in the glandular epithelium during the window of implantation and translocates into endometrial stroma, if pregnancy occurs . Reduced expression of αvβ3 has been related to unexplained infertility  and in women with endometriosis . Xu et al., in a recent publication, did not find any difference in β3 integrin expression in women with RPL compared to normal fertile women . However, these authors analysed the expression of β3 integrin in formalin fixed paraffin embedded (FFPE) samples. It is known that β3 integrin expression in FFPE produces artefacts and should be avoided . In order to find a more accurate expression of β3 integrin subunit in cases with RPL, would be necessary to use frozen sections of endometrial biopsies, instead of FFPE. Other authors reported the expression of avβ3 integrin in endometrial-frozen section and did not find any difference between groups [17, 18]. Contrary, other authors found a reduction of αvβ3 integrin during the implantation window in patients with recurrent pregnancy loss, compared to controls, either in frozen sections , or in microarray studies . Possible discrepancies among studies could be related to technical differences. Our group has been using the SSA6 antibody to identify the β3 integrin subunit, and the expertise developed in our group to evaluate β3 immunostaining has been validated using NIH software image analysis . This study has two objectives: a) to examine the expression of the αvβ3 integrin in women with RPL compared to healthy controls, b) to compare integrin expression with morphologic dating of the endometrium, which has been widely used to judge the endometrial development and receptivity.
Samples collection and processing
Characteristics of the population
Control n = 29
Recurrent pregnancy loss n = 21
Age (y) mean (SD)
N. of miscarriage mean (SEM)
Defect type c n (%)
In phase with β3 +
Immunostaining for β3 integrin subunit was performed on endometrial biopsies on 7 μm cryosections using the Vectastain Elite ABC kits (Vector Laboratories, Burlingame, CA) simultaneously in cases and controls in a same batch. Diaminobenzidine (Sigma, St. Louis, MO) was used as chromogen. All procedures were done simultaneously Tissue sections were fixed in 4% paraformaldehyde for 15 minutes. Following a rinse in PBS, pH 7.4, endogenous peroxidase activity was quenched upon incubation for 30 minutes with 0.3% H2O2 in absolute methanol, followed by a 6-minute rehydration in phosphate buffered saline (PBS). Slides were then incubated with 0.4% Triton-x 100 for 10 minutes. After incubation with blocking serum for 30 minutes at room temperature (4% normal goat serum), sections were incubated with SSA6, a mouse monoclonal antibody against human β3 integrin subunit (1:2000). The specificity of this antibody has been shown and confirmed by other authors [12, 21]. Negative controls were analysed on adjacent sections incubated without primary antibody. A PBS rinse was followed by treatment with a secondary antibody consisting of biotinylated goat anti-mouse IgG antibody for 30 minutes (Vector Laboratories). After this incubation, sections were washed and incubated with avidin:biotinylated horseradish peroxidase macromolecular complex for 60 minutes. Diaminobenzidine (DAB) was added and incubated for 8 minutes to complete the reaction and to visualize the immunostaining. As a final step, sections were counterstained with hematoxylin for 5 minutes, dehydrated in a graded series of ethanols, and cleared with xylene. A coverslip was placed over Permount for evaluation by light microscopy. Negative external controls were obtained by withholding the primary antibody and positive internal controls were verified by the endometrial blood vessel staining. The resulting staining was evaluated using a Nikon microscope (Tokyo, Japan), by a single blinded observer (B.A.L.) without knowledge of the subject’s group. Board certified pathologists of both institutions performed the endometrial dating according to Noyes’s criteria . Endometrial dating was considered as out-of-phase, when a discrepancy of 3 days or more was seen between endometrial dating and date of the menstrual cycle.
Assessment of staining intensity and distribution in endometrial glands was made using the semi-quantitative histologic score (HSCORE) system. HSCORE was calculated using the following equation: HSCORE = ∑Pi (i + 1)/100, where i = intensity of staining with a value of 1, 2, or 3, (weak, moderate or strong, respectively) and Pi = the percentage of stained endometrial epithelial cells for each intensity, varying from 0-100%. Low intra-observer (r = 0.983; P < 0.0001) and inter-observer (r = 0.994; P < 0.0001) differences for HSCORE in uterine tissues have been previously reported using this technique . The numerical cut-off for a negative result for the αvβ3 integrin was a HSCORE of ≤ 0.7, based on previous ROC analysis . Based on histological dating, in-phase or out-of-phase, and β3 integrin expression, positive/negative, we proposed two types of defects: Type I defect is an out-of-phase endometrium with negative β3 integrin subunit expression, and Type II defect is an “in-phase” endometrium with negative β3 integrin subunit expression .
Sample size was calculated using the same parameters as previously published ; briefly, it was considered an α and β error of 0.05 and 0.2, respectively; variance of the expression of β3 integrin was considered as 0.79, and a minimal difference of HSCORE between groups was 1.4, i.e., the double of the 0.7 cut-off. These figures yielded, at least, 7 cases per group. Gaussian distribution was confirmed with D'Agostino & Pearson omnibus normality test. If Gaussian distribution was confirmed, unpaired t-test was used; otherwise, it was used Mann–Whitney U test. ANCOVA was used for adjusting HSCORE between groups, since age in controls and cases (recurrent pregnancy loss) was significantly different. ANCOVA online calculator (http://vassarstats.net/ancova2L.html) and GraphPad Prism 6.0 (GraphPad Software, San Diego, CA) were used for statistical analysis.
Morphological dating and comparison with integrin staining
Compared to controls (n = 29), women with RPL (n = 21) showed more out-of-phase endometrium, i.e., histological delay in maturation. Only 10 out of 21 cases (47.6 - 95 CI: 28.3 to 67.6%) were dated in-phase in RPL samples. In contrast, 26 out 29 controls were in-phase (89.7% - 95 CI: 73.6 to 96.4%). Likewise, positive expression of β3 integrin subunit followed the same pattern in controls. Therefore positive expression of β3 integrin subunit and an in-phase endometrium were present in 24 out of 29 controls (82.8% - 95 CI: 65.5 to 92.4%), while only 6 out of 21 RPL (28.6% -95 CI: 13.8 to 50.0%) samples could be considered “normal”. While a type II defect, determined as in phase endometrium but negative staining for β3 integrin subunit, was found in 6.9% of control samples (CI: 1.9 to 22.0%), 19.1% of RPL samples (CI: 7.7 to 40.0%) were affected (Table 1). The most frequent defect seen in RPL samples (P = 0.0005) however was a type I defect with 11 of 21 RPL samples (52.4% - 95 CI: 32.4 to 71.6%) compared to only 3 out of 29 controls (10.3% - 95CI: 3.6 to 26.4%) (Table 1).
The conflicting data on β3 integrin subunit expression in endometrium of women with RPL led us to conduct the present study. Our data indicate that women with unexplained RPL have significantly reduced integrin expression compared to controls. Our results differ from those published from Xu et al.  and Tuckerman . The probable cause for this discrepancy is the methodology. As it is known, integrin is a membrane adhesion protein and the use of FFPE technique yield artefacts , or the variability between observers . We have shown that inexperienced observers in HSCORE tend to give higher HSCOREs .
Despite the majority of cases from the RPL group (0.52 – 95 CI: 0.32 to 0.71) demonstrated an out-of-phase endometrium and a negative expression of integrin β3 subunit (Type I defect), an additional 4 cases [0.19 (95 CI:0.07 to 0.4)] presented a type II defect, where integrin expression is negative in an “in-phase” endometrium. These findings demonstrate the need for further molecular analysis, besides the histological assessment of endometrial tissue. This finding is not new. Coutifaris et al. suggested that morphological criteria do not differ between fertile and infertile women . Possible causes for this type II defect can be related to the presence of endometriosis . As endometriosis is associated with reduced integrin expression , a high-unknown incidence of endometriosis in women with recurrent abortions might be present, and the reduced expression of integrin could be the first clue. This hypothesis is supported by the findings that anti-lamin-1 antibody is reduced in women with endometriosis and with recurrent pregnancy loss . In light of recent evidence linking endometriosis to progesterone resistance , these findings support a possible connection between occult or undiagnosed gynaecologic pathology and a loss of normal endometrial receptivity. The fact that integrin expression is reduced in RPL highlights the importance of this adhesion protein for implantation. This reduction is in accordance with other conditions related to infertility. For instance, low integrin expression was seen in women with different degrees of hydrosalpinges [24, 29]. After removal of hydrosalpinges, levels of αvb3 integrin increase , as well as pregnancies rates .
The low expression of integrin in endometrium of women with RPL supports the role of this adhesion molecule in the feto-maternal communication during implantation. In patients with RPL, this reduction of integrin expression may be due to the fact that HOXA10, another implantation marker, regulates the expression of β3 integrin . HOXA10 has been shown to be a modulator of integrin β3, and could be deregulated in endometrium of women with RPL, as suggested by animal studies .
There are a few weaknesses in this study. Laparoscopy was not routinely performed in these patients to investigate peritoneal causes such as endometriosis. Likewise, karyotyping was not performed, mainly because it has a low yield for abnormalities (1 to 2%).
The appropriate statistical care, sample size and the appropriate immunohistochemical analysis with a well-established antibody are strengths of this study and corroborate to the accuracy of the results.
In conclusion, we demonstrate that women with RPL present an endometrial defect during the window of implantation, more specifically, a reduced expression of β3 integrin subunit. Such defects comprised both “in-phase” and “out-of-phase” histology. Further prospective studies are needed to better determine the cause and treatment of these types of endometrial receptivity defects in women with otherwise unexplained RPL. If this correlation remains to be seen, women with unexplained RPL may benefit from additional laparoscopic examination in order to discover potential gynaecological conditions.
We would like to acknowledge the assistance with data entry by Lauren Nelson and Ashley Graham. Furthermore, we acknowledge financial support by Deutsche Forschungsgemeinschaft and Ruprecht-Karls-Universität Heidelberg within the funding programme Open Access Publishing.
- Ford HB, Schust DJ: Recurrent pregnancy loss: etiology, diagnosis, and therapy. Rev Obstet Gynecol. 2009, 2: 76-83.PubMed CentralPubMedGoogle Scholar
- Kwak-Kim J, Bao S, Lee SK, Kim JW, Gilman-Sachs A: Immunological modes of pregnancy loss: inflammation, immune effectors, and stress. Am J Reprod Immunol. 2014, doi:10.1111/aji.12234. [Epub ahead of print]Google Scholar
- Larsen EC, Christiansen OB, Kolte AM, Macklon N: New insights into mechanisms behind miscarriage. BMC Med. 2013, 11: 154-PubMed CentralView ArticlePubMedGoogle Scholar
- Wilcox AJ, Baird DD, Weinberg CR: Time of implantation of the conceptus and loss of pregnancy. N Engl J Med. 1999, 340: 1796-1799.View ArticlePubMedGoogle Scholar
- Navot D, Scott RT, Droesch K, Veeck LL, Liu HC, Rosenwaks Z: The window of embryo transfer and the efficiency of human conception in vitro. Fertil Steril. 1991, 55: 114-118.PubMedGoogle Scholar
- Serle E, Aplin JD, Li TC, Warren MA, Graham RA, Seif MW, Cooke ID: Endometrial differentiation in the peri-implantation phase of women with recurrent miscarriage: a morphological and immunohistochemical study. Fertil Steril. 1994, 62: 989-996.PubMedGoogle Scholar
- Othman R, Omar MH, Shan LP, Shafiee MN, Jamal R, Mokhtar NM: Microarray profiling of secretory-phase endometrium from patients with recurrent miscarriage. Reprod Biol. 2012, 12: 183-199.View ArticlePubMedGoogle Scholar
- Kao LC, Tulac S, Lobo S, Imani B, Yang JP, Germeyer A, Osteen K, Taylor RN, Lessey BA, Giudice LC: Global gene profiling in human endometrium during the window of implantation. Endocrinology. 2002, 143: 2119-2138.View ArticlePubMedGoogle Scholar
- Najwa AR, Sengupta J, Ghosh D: A systems biology approach towards understanding the process of blastocyst implantation. Indian J Physiol Pharmacol. 2009, 53: 197-208.PubMedGoogle Scholar
- Talbi S, Hamilton AE, Vo KC, Tulac S, Overgaard MT, Dosiou C, Le Shay N, Nezhat CN, Kempson R, Lessey BA, Nayak NR, Giudice LC: Molecular phenotyping of human endometrium distinguishes menstrual cycle phases and underlying biological processes in normo-ovulatory women. Endocrinology. 2006, 147: 1097-1121.View ArticlePubMedGoogle Scholar
- Lessey BA, Castelbaum AJ, Sawin SW, Sun J: Integrins as markers of uterine receptivity in women with primary unexplained infertility. Fertil Steril. 1995, 63: 535-542.PubMedGoogle Scholar
- Lessey BA, Damjanovich L, Coutifaris C, Castelbaum A, Albelda SM, Buck CA: Integrin adhesion molecules in the human endometrium. Correlation with the normal and abnormal menstrual cycle. J Clin Invest. 1992, 90: 188-195.PubMed CentralView ArticlePubMedGoogle Scholar
- Lessey BA, Castelbaum AJ, Buck CA, Lei Y, Yowell CW, Sun J: Further characterization of endometrial integrins during the menstrual cycle and in pregnancy. Fertil Steril. 1994, 62: 497-506.PubMedGoogle Scholar
- Lessey BA: Implantation defects in infertile women with endometriosis. Ann N Y Acad Sci. 2002, 955: 265-280. discussion 293–5, 396–406View ArticlePubMedGoogle Scholar
- Xu B, Sun X, Li L, Wu L, Zhang A, Feng Y: Pinopodes, leukemia inhibitory factor, integrin-beta3, and mucin-1 expression in the peri-implantation endometrium of women with unexplained recurrent pregnancy loss. Fertil Steril. 2012, 98: 389-395.View ArticlePubMedGoogle Scholar
- Lessey BA, Castelbaum AJ: Integrins and endometriosis: fact or artefact?. Hum Reprod. 1998, 13: 3578-3580.View ArticlePubMedGoogle Scholar
- Tuckerman EM, Laird SM, Prakash A, Li TC: Expression of integrins in the endometrium of women with recurrent miscarriage. Fertil Steril. 2006, 86: 755-757.View ArticlePubMedGoogle Scholar
- Coughlan C, Sinagra M, Ledger W, Li TC, Laird S: Endometrial integrin expression in women with recurrent implantation failure after in vitro fertilization and its relationship to pregnancy outcome. Fertil Steril. 2013, 100: 825-830.View ArticlePubMedGoogle Scholar
- Quenby S, Anim-Somuah M, Kalumbi C, Farquharson R, Aplin JD: Different types of recurrent miscarriage are associated with varying patterns of adhesion molecule expression in endometrium. Reprod Biomed Online. 2007, 14: 224-234.View ArticlePubMedGoogle Scholar
- Fuhrich DG, Lessey BA, Savaris RE: Comparison of HSCORE assessment of endometrial beta3 integrin subunit expression with digital HSCORE using computerized image analysis (ImageJ). Anal Quant Cytol Histol. 2013, 35: 210-216.Google Scholar
- Lessey BA, Castelbaum AJ, Sawin SW, Buck CA, Schinnar R, Bilker W, Strom BL: Aberrant integrin expression in the endometrium of women with endometriosis. J Clin Endocrinol Metab. 1994, 79: 643-649.PubMedGoogle Scholar
- Noyes RW, Hertig AT, Rock J: Dating the endometrial biopsy. Fertil Steril. 1950, 1: 3-25.Google Scholar
- Budwit-Novotny DA, McCarty KS, Cox EB, Soper JT, Mutch DG, Creasman WT, Flowers JL, McCarty KSJ: Immunohistochemical analyses of estrogen receptor in endometrial adenocarcinoma using a monoclonal antibody. Cancer Res. 1986, 46: 5419-5425.PubMedGoogle Scholar
- Savaris RF, Pedrini JL, Flores R, Fabris G, Zettler CG: Expression of alpha 1 and beta 3 integrins subunits in the endometrium of patients with tubal phimosis or hydrosalpinx. Fertil Steril. 2006, 85: 188-192.View ArticlePubMedGoogle Scholar
- Coutifaris C, Myers ER, Guzick DS, Diamond MP, Carson SA, Legro RS, McGovern PG, Schlaff WD, Carr BR, Steinkampf MP, Silva S, Vogel DL, Leppert PC: Histological dating of timed endometrial biopsy tissue is not related to fertility status. Fertil Steril. 2004, 82: 1264-1272.View ArticlePubMedGoogle Scholar
- Lessey BA, Young SL: Integrins and other cell adhesion molecules in endometrium and endometriosis. Semin Reprod Endocrinol. 1997, 15: 291-299.View ArticlePubMedGoogle Scholar
- Inagaki J, Kondo A, Lopez LR, Shoenfeld Y, Matsuura E: Pregnancy loss and endometriosis: pathogenic role of anti-laminin-1 autoantibodies. Ann N Y Acad Sci. 2005, 1051: 174-184.View ArticlePubMedGoogle Scholar
- Aghajanova L, Velarde MC, Giudice LC: Altered gene expression profiling in endometrium: evidence for progesterone resistance. Semin Reprod Med. 2010, 28: 51-58.View ArticlePubMedGoogle Scholar
- Meyer WR, Castelbaum AJ, Somkuti S, Sagoskin AW, Doyle M, Harris JE, Lessey BA: Hydrosalpinges adversely affect markers of endometrial receptivity. Hum Reprod. 1997, 12: 1393-1398.View ArticlePubMedGoogle Scholar
- Bildirici I, Bukulmez O, Ensari A, Yarali H, Gurgan T: A prospective evaluation of the effect of salpingectomy on endometrial receptivity in cases of women with communicating hydrosalpinges. Hum Reprod. 2001, 16: 2422-2426.PubMedGoogle Scholar
- Sagoskin AW, Lessey BA, Mottla GL, Richter KS, Chetkowski RJ, Chang AS, Levy MJ, Stillman RJ: Salpingectomy or proximal tubal occlusion of unilateral hydrosalpinx increases the potential for spontaneous pregnancy. Hum Reprod. 2003, 18: 2634-2637.View ArticlePubMedGoogle Scholar
- Daftary GS, Troy PJ, Bagot CN, Young SL, Taylor HS: Direct regulation of beta3-integrin subunit gene expression by HOXA10 in endometrial cells. Mol Endocrinol. 2002, 16: 571-579.PubMedGoogle Scholar
- Yao MW, Lim H, Schust DJ, Choe SE, Farago A, Ding Y, Michaud S, Church GM, Maas RL: Gene expression profiling reveals progesterone-mediated cell cycle and immunoregulatory roles of Hoxa-10 in the preimplantation uterus. Mol Endocrinol. 2003, 17: 610-627.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.