Obtaining fast screening information on molecular composition of a tissue sample is of great importance for a disease biomarkers search and for online surgery control. In this study, high resolution mass spectrometry analysis of eutopic and ectopic endometrium tissues (90 samples) is done using direct tissue spray mass spectrometry in both positive and negative ion modes. The most abundant peaks in the both ion modes are those corresponding to lipids. Species of three lipid classes are observed, phosphatidylcholines (PC), sphingomyelins (SM) and phosphoethanolamines (PE). Direct tissue analysis gives mainly information on PC and SM lipids (29 species) in positive ion mode and PC, SM and PE lipids (50 species) in negative ion mode which gives complementary data for endometriosis foci differentiation. The biggest differences were found for phospholipids with polyunsaturated acyls and alkils. Although, tissue spray shows itself as appropriate tool for tissue investigation, caution should be paid to the interpretation of mass spectra because of their higher complexity with more possible adducts formation and multiple interferences must be taken into account. The present work extends the application of direct tissue analysis for the rapid differentiation between endometriotic tissues of different foci.
Endometriosis is an abundant gynecological pathology of poorly understood pathogenesis affecting 10% of women1. It is characterized by the extrauterine presence of endometrial glands and stroma. The disease affects mostly women in their reproductive age and can cause wide set of non-specific symptoms including infertility, dysmenorrhea, dyspareunia, and non-cyclic pelvic pain. The only reliable way to diagnose the pathology is surgical laparoscopy for the moment. Many efforts have been applied to find biomarkers of endometriosis and to develop less invasive methods to reveal the presence of early stages2. Such investigations were mainly devoted to body fluids screening3,4,5,6,7. Lack of the information about molecular composition of eutopic (inside uterine) and ectopic (extrauterine) endometrium is observed. There are hypotheses about alteration in composition of ectopic and eutopic endometrial tissues and in surrounding tissue which allows eutopic endometrium survival. Therefore, tissue investigation can shed some light on mechanisms of the disease and be used for validation of biomarkers found in fluids in low-invasive way. Data on eutopic and ectopic endometrium composition is also important for the development of the online surgery control to determine volume of an operation. This necessitates development of method for fast screening of big amount of tissue samples. Wide variety of approaches for tissue composition analysis are present nowadays8: matrix-assisted laser desorption/ionization imaging, desorption electrospray ionization, etc. One of the ambient methods for a sample analysis with minimal pretreatment is suggested by Cooks’ group and named “leaf-spray”9. This method was further extrapolated for fast tissue analysis and turned into different variations of tissue spray10,11,12,13,14,15. The method has been applied to the analysis of brain tissues and various cancer tumors10, 13.
The present work extends the application of direct tissue analysis for the rapid differentiation between endometriotic tissues of different foci. Features of different tissues are identified by conventional lipidomic approach including lipid extraction and following analysis by hydrophilic interaction liquid chromatography with electrospray ionization mass spectrometry (HILIC-LC/ESI-MS)16, 17.
The design of MS analysis of tissue samples and the ion source scheme are presented in Fig. 1. The following settings are varied until obtaining stable TIC in both positive and negative ion modes: distance from tissue tip to the mass spectrometer inlet is varied in the range 5–50 mm; applied potential in the range 2–5 kV, extracting solvent flow rate in the range 5–50 µL/min. Figure S1 shows extracted positive ion chromatograms of some ions obtained with optimized settings. Relative standard deviation of a peak intensity is within 5% for the same tissue piece and about 5–10% for neighboring pieces. Then the scheme of an analysis for every tissue sample is as follows. A piece of tissue of approximate size 2 × 1 × 1 mm is cut from a frozen sample, thawed and fixed on a needle. After that, an MS analysis starts. The suggested construction gives better tissue fixation and control.
Positive ion mode
Representative mass spectra of three kinds of endometriotic tissue from one patient collected in positive ion mode are shown in Fig. 2. A total of 1159 ions in sample tissues in positive ion mode are detected over threshold of 200 counts in different tissue types. The most abundant m/z correspond to lipid species. The identification is done in the following way illustrated for m/z 782.5685. An accurate mass of a compound which abundance exceeds a threshold in 200 counts is found from the mass spectrum. Tentative assignment of the compound is done based on LIPID MAPS data18 within 10 ppm mass accuracy. For the considered m/z it can be either protonated species of PC 36:4, PE 39:4 or sodiated species of PC 34:1, PE 37:1. MS/MS information about the fragmentation pattern of the considered m/z is used for better assignment (Figure S2a). Peaks with m/z 147 and 184 are observed in the tandem mass spectra. These peaks are characteristic for fragmentation of sodiated and protonated phosphatidylcholine, correspondingly, and originate from its polar head group19, 20. This fact leads to a conclusion that m/z 782 precursor ion corresponds to interfered protonated PC 36:4 and sodiated PC 34:1. Such peak overlapping is known problem upon lipids study in positive ion mode19, 21, 22. Identified lipid species are listed in Table 1 and some of them are marked with opened circles in Fig. 2. Additional lipids validation is done by HILIC-LC/MS analysis of tissue’s lipid extract using methods described earlier16, 17. Figure S3 represents resulting TIC from HILIC-LC/MS analysis of the lipid extract. Annotated chromatographic peaks correspond to lipid species observed in tissue spray experiments. Retention time of the observed lipids (Table S2) correlates with literature data16, 17 and confirms identification provided in Tables 1 and 2.
Series of peaks denoted with closed circles are worth of consideration (Fig. 2). Their profile is similar to that of the opened circle peaks. The difference between these two groups is 16 Da which can evidence about oxidation of lipids during direct tissue analysis. Such effect has been observed in another ambient method, DESI23. This conclusion is supported by the presence of m/z 163 peak in tandem mass spectra of m/z 799 (Figure S2b). It is also 16 Da bigger then the characteristic fragment of polar head group of sodiated PC. Another explanation of this series can be potassium cation attachment to the initial lipid molecules.
The supervised OPLS-DA model is used to separate different tissue types and find the differentially produced metabolites. As shown in Fig. 3, the OPLS-DA model can separate eutopic endometrium from ectopic one, while two types of endometriotic foci are not clustered demonstrating higher similarity compared to eutopic endometrium (Fig. 3c). R2 values representing explained variance of the data are extracted from the models and listed in Table S3. Predictive capability of the models is estimated by Q2. This parameter is obtained with Leave-one-out cross-validation (LOOCV) and the resulting values are presented in Table S3. All models show a reasonable predictive ability.
Negative ion mode
Figure 4 demonstrates characteristic mass spectra of tissue samples in negative ion mode. 307 peaks in the mass range 400–1000 are detected over 20 counts threshold. Identification in negative ion mode is done in the same way as in the positive one. It is done according to accurate mass within 10 ppm and tandem mass spectra. The principal difference between tandem mass spectra of lipids in positive and negative ion modes is that in positive ion mode product ions which characteristic for lipid class are generated, while in negative ion mode the most probable products are those of fatty acids. So different algorithms for tandem mass spectra processing are used. The list of identified lipids is in the Table 2. Lipids of three classes are found in the mass spectra. Namely, phosphatidylcholines, sphingomyelins and ethanolamines. PC and SM are registered as adducts with chloride ion and PE are in the form of deprotonated molecules. It is worth noting that negative ion mode allows registration of the PE species in contrast to positive ion mode where they undergone signal suppression by choline-containing lipids.
The OPLS-DA score plots are shown in Fig. 5. Eutopic endometrium tissues are also clearly separated from ectopic but the models for negative ions are characterized by somewhat worth parameters (Table S4).
Comaprative lipid profile analysis for endometriotic foci differentiation
Variable influence on projection (VIP) is used in the study to find m/z’s the most contributed to the OPLS-DA models. The highest VIP values belong mainly to lipid species. The comparison box-and-whisker plots for these lipids are shown in Fig. 6. First 30 features with the highest VIP score are selected in positive ion mode data, and from that 30, 12 unique features identified as lipids are presented in the box-and-whisker plot (Fig. 6a). PC, PE and SM lipids are present among first 30 features with highest VIP according to negative ion data. Figure 6b demonstrates levels of the most significant PE measured in negative ion mode. Similar PC and SM species can be found among most significant features in both positive and negative ion mode but they are omitted in Fig. 6b to mark up additional information provided by PE which does not suffer from suppression effect from choline-containing compounds in negative ion mode. Abundances of most lipids are similar for ovarian and pelvic endometriosis and differ from eutopic endometrium.
Comparative study of normal and pathological tissues is a necessary step of biomarkers discovery and mechanisms of a disease development. Direct tissue analysis allows fast screening of a tissue composition. Mainly lipid constituents can be studied with such method if not to make some additional efforts. Among tissue differentiating compounds PC, SM and PE polyunsaturated lipids are identified. Species of these classes have been found as features of endometriosis in biofluids as well3, 4, 7, 24.
The feasability of endometriotic tissue type differentiation by tissue spray method is demonstrated. The differentiating features are several lipid species from PC, SM, PE classes. There are investigations of endometriosis based on lipid profiling but most of them use plasma, serum or peritoneal fluid as an object4, 7, 24. The same lipid classes were found to be altered in endometriosis patients compared to healthy ones. In the study of Bi-Cheng Yang with coworkers7, PC 38:4 and SM 34:1 are also among featured lipids as well as SM 34:2 in Vouk’s paper24. In Dutta’s work lipids from endometriosis mice serum and liver were profiled4. It was found that PEs were downregulated whereas SMs, PCs, lysoPCs, lysoPEs, and plasmeny-PEs were upregulated in endometriosis mice4. Observed lipids are essential participants of many important pathways. PC is one of the major sources of polyunsaturated fatty acids, which are the precursors of eicosanoids and has numerous biological activities. Abnormal PC metabolism is reported to exist in many disease25, 26. Sphingolipids are a distinctive and highly important class of lipids functioning in different biological processes such as signal transduction and cell fate determination27. Although the role of sphingolipids in endometriosis has not been fully investigated. Sphingolipids are increasingly known to be important bioactive signaling molecules and are involved in a diverse range of cellular processes28. PE is a substrate for numerous phospholipids of membrane cells, primarily phosphatidylcholine29. This may explain the phosphoethanolamine in endometrial tissues as phosphatidylethanolamine is a precursor of phosphatidylcholine30. Phosphoethanolamine is the most widespread lipid on the cytoplasmic membrane that is involved in different cellular activities, e.g. cell cycle, membrane fusion, autophagy and apoptosis29.
Although, tissue spray shows itself as appropriate tool for tissue investigation, caution should be paid to the interpretation of mass spectra because of their higher complexity with more possible adducts formation and multiple interferences must be taken into account. The biggest differences were found for phospholipids with polyunsaturated acyls and alkils. Direct tissue analysis gives mainly information on PC and SM lipids (29 species) in positive ion mode and PC, SM and PE lipids (50 species) in negative ion mode which gives complementary data for endometriotic foci differentiation.
All experimental protocols are approved by the Ethical Committee of the V. Kulakov Research Center for Obstetrics, Gynecology and Perinatology (Moscow, Russia). All clinical investigations are conducted according to the principles expressed in the Declaration of Helsinki.
Methanol, acetonitrile, 2-propanol, chloroform and formic acid of HPLC grade are purchased from Sigma-Aldrich (St. Louis, MO, USA). Deionized water is purchased from Panreac (Barcelona, Spain).
Endometrial tissues (90 samples) of different localization of 30 patients (Table S1) are obtained from the Department of Surgery, V. Kulakov Research Center for Obstetrics, Gynecology and Perinatology (Moscow, Russia). All patients have read and signed Informed consent approved by the Ethical Committee of the V. Kulakov Research Center for Obstetrics, Gynecology and Perinatology (Moscow, Russia). The classification of the American Fertility Society is used in this study31. All patients have stage III–IV of the outer genital endometriosis according to this classification. The mandatory criteria for inclusion of patients into the investigation are as follows: the reproductive age of women, the lack of hormonal and drug therapy for 6 months before surgery, the absence of inflammatory diseases of the pelvic organs and severe somatic pathology. The samples are frozen in liquid nitrogen immediately after surgery and stored under −75 °C until the analysis. For the analysis, a small piece of a sample (approximately 2 × 1 × 1 mm) is cut, thawed and fixed on the needle in the ion source (Fig. 1).
Lipid extracts are prepared according to a modified Folch method32. Briefly, 40 mg of tissue is homogenized in liquid nitrogen, 4 mL of chloroform–methanol (2:1, v/v) mixture is added to the sample and the mixture is incubated for 10 min. The homogenate is filtered using coarse filter paper. 800 µL of 1 mol/L NaCl is added, and the mixture is centrifuged at 3000 rpm for 5 min at the ambient temperature. The organic bottom layer containing lipids is evaporated with a stream of nitrogen and redissolved in acetonitrile-2-propanol (1:1, v/v) mixture for LC/MS analysis.
Tissue spray conditions
MS analysis of tissue samples is performed using in-lab designed ion source (Fig. 1) similar to that described earlier10 but with minor modifications. Constant stream of H2O/methanol 1/9 is supplied to the tissue with flow rate of 1 mL/min by Dionex binary pump. Distance between a sample and MS inlet is about 5–10 mm. Applied potential between tissue and inlet capillary is 4.2 kV. Maxis Impact qTOF (BrukerDaltonics, Bremen, Germany) is used as a mass analyzer. The signal of a tissue is saved during 3 min after total ion current (TIC) equilibration. Analysis schedule is as follows: 3 minutes in positive ion mode, data dependent analysis (DDA) in positive ion mode, 3 minutes in negative ion mode, DDA in negative ion mode. Mass spectra are registered at a 2 Hz frequency resulting in 360 spectra for 3 minutes. The mass range is m/z 400–1000.
Tandem MS is done using DDA with the following characteristics. Three most abundant peaks are chosen after full mass scan and subjected MS/MS analysis with collision induced dissociation applying 35 eV collision energy, mass exclusion time is 1 minute.
Extract of endometriotic tissue is analyzed using a Spherisorb Si column (150 × 2.1 mm, 5 µm; Waters, Milford, MA, USA), a flow rate of 50 µL/min, an injection volume of 3 µL, column temperature of 40 °C and a mobile phase gradient: 0–0.5 min−6% B, 60.5 min−23% B, 61–64 min−6% B where solvent B is 5 mM aqueous ammonium acetate. Solvent A is acetonitrile16, 17. All LC/MS experiments are performed on the Dionex UltiMate 3000 liquid chromatograph (ThermoScientific, Germering, Germany) coupled to the Maxis Impact qTOF analyzer with ESI (Bruker Daltonics, Bremen, Germany).
Maxis Impact qTOF is used in the HILIC-LC/MS method with ESI (Bruker Daltonics, Bremen, Germany). Mass spectra are obtained in positive ion and negative ion modes in the mass range m/z 400–1000 with the following setting of tuning parameters: capillary voltage 4.1 kV in positive ion mode (3.0 kV in negative ion mode), pressure of the nebulizing gas 0.7 bar, drying gas flow rate 6 L/min, and temperature of the drying gas 200 °C.
Obtained mass spectra from each sample is averaged over 3 min and saved in m/z – Intensity tables using DataAnalysis software (BrukerDaltonica, Bremen, Germany). Thus obtained data is processed with scaling on TIC and peak alignment. Multivariate data analyses is performed using orthogonal projections onto latent structures discriminant analysis (OPLS-DA) method33 implemented in ropls package34. Multivariate models are described using R2 and Q2 parameters, where R2 describes fraction of data that the model can explain using the latent variables, and Q2 describes part of data predicted by the model according to the cross validation.
Tentative lipid identification is conducted with in-lab created R code. The code searches a record in LIPID MAPS database18 within 10 ppm from the experimental m/z. More precise identification is done based on the MS/MS data for the peak under consideration, if it undergone MS/MS analysis.
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This work was supported by Ministry of Education and Science of the RussianFederation grant (agreement No. 14.613.21.0059, RFMEFI61316X0059) and International Science & Technology Cooperation Program of China (No. 2015DFA40290), Science and Technology Planning Project at the Ministry of Science and Technology of Jiangxi Province, China (No. 20152ACB21013, 20161BBH80055).