{"paper_id":"568b7acc-47b0-455b-8a35-cda2e4182b96","body_text":"1 Center of Reproduction and Genetics Integrated Traditional Chinese and Western Medicine, The Hospital Affiliated to Shandong University of Traditional Chinese Medicine, 250014 Jinan, Shandong, China\n2 Department of Gynecology of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, 250014 Jinan, Shandong, China\nAbstract\nBackground: Dysregulated migration and invasion of endometrial stromal cells is\nimplicated in the pathogenesis of endometriosis. Hypoxia functions as critical\nmicroenvironmental factor that results in promotion of endometrial stromal cells\nmigration and invasion through up-regulation of autophagy. Paeonol functioned as\na tumor suppressor in human ovarian cancer and promoted cytoprotective autophagy.\nHowever, the role of paeonol in hypoxia-induced autophagy in endometriosis\nremains unknown. Methods: Stromal cells were isolated from endometriotic patients by enzymatic\ndigestion of ectopic endometrial tissues, and then characterized by\nimmunohistochemical analysis of cytoskeleton 19 (CK19) and vimentin. Cellular\nmorphology was evaluated under microscope. Cell viability, proliferation and\napoptosis of stromal cells were assessed by Cell Counting Kit-8, EdU labeling and\nflow cytometry, respectively. Wound healing and transwell assays were performed\nto detect metastasis of the stromal cells. Hypoxia-induced autophagy was\nevaluated through immunohistochemistry and western blot. Results: Paeonol treatment dosage dependently decreased cell proliferation and\nmetastasis of the ectopic endometrial stromal cells (ecESCs), while promoted the\ncell apoptosis. Hypoxia-induced autophagy in the ecESCs was repressed by paeonol\nthrough down-regulation of LC3-II/LC3-I and Beclin-1, while up-regulation of p62.\nHypoxia-inducible factor-1\nKeywords\n- Paeonol\n- Metastasis\n- Endometrial stromal cells\n- HIF-1α\n- Autophagy\n- Endometriosis\nEndometriosis is an estrogen-dependent benign chronic disease [1], and affects 2–10% of premenopausal women as a major cause of infertility and chronic pelvic pain [2]. Endometriosis is generally characterized by the presence of endometrial glands and extracellular matrix, and defined as extra-growth of the endometrial tissues [3]. The pathogenesis of endometriosis is still unclear, and the most widely accepted theory is the implantation theory in which endometrial tissue is implanted outside the uterus through an open fallopian tube during the menstrual cycle [4]. Meanwhile, the enhanced proliferation, adhesion, migration and invasion of endometrial cells, including stromal and epithelial cells, facilitated the ectopic implantation of the endometrial tissues and development of endometriotic lesions [5]. The suppression of endometrial stromal cells metastasis contributed to amelioration of endometriosis [5].\nAutophagy is an evolutionary conservative mechanism that eliminates and circulates non-essential cytoplasmic components to maintain homeostasis [6]. Dysregulated autophagy in the eutopic or ectopic endometrium retarded cell apoptosis and promoted hyperplasia of stromal cells and endometriotic tissues, thus contributing to the pathogenesis of endometriosis [7]. The level of autophagy is relatively high in the ectopic endometrium of patients with ovarian endometriosis [8], and autophagy could promote the migration and invasion of endometrial stromal cells under the condition of hypoxia [9]. Inhibition of autophagy inhibited the angiogenesis of endometriosis and attenuated the ectopic endometriotic lesions [10]. Therefore, regulation of autophagy might be helpful for the suppression of endometrial stromal cells metastasis.\nPaeonol (4-methoxy-2-hydroxyacetophenone), an active compound extracted from traditional chinese medicine, demonstrated antioxidant, anti-tumor, anti-inflammatory and immunomodulatory effects [11]. For example, paeonol promoted colorectal cancer cell apoptosis [12], and retarded non-small-cell lung cancer motility [13]. Moreover, paeonol decreased vascular endothelial growth factor to enhance radiotherapy-induced apoptosis of ovarian cancer [14]. However, whether paeonol has an effect on endometriosis has not been studied yet. Paeonol activated autophagy flux in ovarian cancer [15], and promoted autophagy to demonstrate anti-atherosclerotic in vascular smooth muscle cell [16]. Additionally, oxidized low-density lipoprotein-induced vascular endothelial cell autophagy was suppressed by paeonol [17]. The detailed role of paeonol on autophagy in endometriosis needs further research.\nThis study aimed to investigate roles of paeonol on migration and invasion of isolated ectopic endometrial stromal cells (ecESCs), as well as endometriotic lesion in rats. Specifically, whether autophagy was implicated in paeonol-mediated progression of endometriosis was also determined.\nPatients (N = 7; age of 18 to 50) with ovarian endometriosis were recruited at\nThe Hospital Affiliated to Shandong University of Traditional Chinese Medicine.\nThe presence of endometriosis was confirmed by pathological examination and\nlaparoscopy. The pathological examination was performed by an experienced\nfertility specialist based on the criteria of Noyes. The study was approved by\nthe Center of Reproduction and Genetics, The Hospital Affiliated to Shandong\nUniversity of Traditional Chinese Medicine and the patients signed written\ninformed consents. Laparoscopy was performed to isolate the ectopic endometrial\ntissues, and the normal endometrial tissues were also isolated from regularly\ncycling women without endometriosis. The tissues were digested with collagenase A\nand DNase (Sigma Aldrich, St. Louis, MO, USA) for 2 hours. The cells were then\ncultured in DMEM medium (Lonza, Basel, Switzerland) containing 10% fetal bovine\nserum (Lonza) at 37\nThe isolated ecESCs were formalin-fixed and soaked in 0.3% Triton X-100.\nFollowing incubation with 3% H\npcDNA-mediated over-expression of HIF-1\nThe ecESCs with indicated transfection and treatment, as well as normal\nendometrial stromal cells and IOSE80 cells, were plated and incubated with Cell\nCounting Kit-8 solution (Dojindo, Tokyo, Japan) for 2 hours. Absorbance at 450 nm\nwas determined by Microplate Autoreader (Thermo Fisher Scientific). For EdU\nstaining, cells were incubated with diluted EdU solution (1:1000, Sigma\nAldrich, St. Louis, MO, USA) for 2 hours, and then fixed in 4% paraformaldehyde.\nCells were incubated with 100\nThe ecESCs with indicated transfection and treatment were stained using an Annexin V-fluorescein isothiocyanate apoptosis detection kit (Beyotime, Beijing China). The proportion of apoptotic cells was determined via flow cytometer (Attune, Life Technologies, Darmstadt, Germany).\nThe ecESCs with indicated transfection and treatment were plated and scratched by a plastic tips. Forty-eight hours later, the wound was calculated under microscope (Olympus). For transwell assay, cells in serum-free medium were seeded in the upper Matrigel-coated Transwell chamber, and medium with 20% fetal bovine serum was added into the bottom chamber. Forty-eight hours later, the invasive cells in the bottom chamber were fixed with paraformaldehyde and stained with 0.1% crystal violet before measurement under microscope (Olympus).\nThe ecESCs with indicated transfection and treatment were fixed with 4% paraformaldehyde before incubation with 5% bovine serum albumin for 1 hour. Specific antibody against LC3B (1:300; Abcam, Cambridge, MA, USA) was applied to incubated the cells overnight. Following incubation with FITC-conjugated secondary antibody (1:100; Abcam, Cambridge, MA, USA), DAPI was used to stain cell nucleus before measurement under fluorescence microscope (Olympus).\nTotal RNAs extracted from ecESCs by TRIzol Reagent (Sigma Aldrich) were reversed\ninto cDNAs under cDNA synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA).\nSYBR Green Master (Roche, Mannheim, Germany) was applied to determined mRNA\nexpression of HIF-1\nExperiments were performed according to National Institutes of Health Laboratory\nAnimal Care and Use Guidelines. and approved by The Hospital Affiliated to\nShandong University of Traditional Chinese Medicine. Female SD rats (6–8 weeks\nold, 200–220 g) were purchased from Envigo (Indianapolis, IN, USA), and housed\nin cages with 12:12 h light and dark cycles and controlled environment (24\nRats were sacrificed by carbon dioxide inhalation, the serum samples were\ncollected, and then performed with commercial ELISA kits (Krishgen Biosystem,\nMumbai, India) to determine levels of IL-1\nThe endometriotic lesions were surgically removed from the rats, and fixed in\nformalin. The paraffin-embedded tissues were cut into 5\nProteins extracted from ecESCs or endometriotic lesions were separated by\nSDS-PAGE, and then transferred to PVDF membranes (Sigma Aldrich). The membrane\nwas blocked in 5% bovine serum albumin before incubation with primary antibodies\nagainst HIF-1\nData with at least three times repeat were presented as mean\nTo explore the effects of paeonol on endometriosis, ecESCs were isolated and\ncharacterized under microscope. The cells showed spindle shape (Fig. 1A).\nMoreover, immunohistochemical analysis demonstrated negative staining of CK19 and\npositive staining of vimentin (Fig. 1A), indicating that endometrial stromal\ncells were successful isolated. The ecESCs under hypoxia treatment were applied\nto paeonol condition. Results showed that paeonol condition dosage dependently\nreduced cell viability of ecESCs (Fig. 1B), while dosage dependently promoted\ncell apoptosis of ecESCs (Fig. 1C). However, paeonol 100\nPaeonol repressed cell proliferation of ecESCs.(A) Isolated ecESCs showed spindle shape, negative staining of CK19 and positive\nstaining of vimentin. Scale bar: 100\nThe role of paeonol on metastasis of endometriosis was then investigated. Data from wound healing (Fig. 2A) and transwell (Fig. 2B) assays demonstrated that cell migration and invasion of ecESCs were dosage dependently repressed by paeonol treatment, suggesting the anti-invasive role of paeonol on ecESCs.\nPaeonol repressed cell migration and invasion of ecESCs.(A) Paeonol dosage dependently reduced cell migration of hypoxia-induced ecESCs. N =\n3. Scale bar: 100\nTo explore role of paeonol in autophagy of ecESCs, indicators of autophagy, including LC3B, Beclin and p62, were examined. As shown in Fig. 3A, paeonol treatment dosage dependently induced decrease in LC3-II and Beclin, and increase in p62, suggesting that paeonol repressed autophagy of ecESCs. Moreover, there was a gradual decrease in the immunofluorescence of LC3 in ecESCs (Fig. 3B), further confirming that paeonol could induce suppression of autophagic flux in ecESCs.\nPaeonol repressed autophagy of ecESCs.(A) Paeonol dosage dependently reduced LC3-II and Beclin, while increase of p62 in\nhypoxia-induced ecESCs. N = 3.(B) Paeonol dosage dependently reduced LC3 through immunofluorescence analysis. N =\n3. * p\nHypoxia-induced HIF-1\nPaeonol repressed HIF-1\nThe ecESCs transfected with pcDNA-mediated HIF-1\nPaeonol repressed autophagy of ecESCs through down-regulation of\nHIF-1\nThe ecESCs transfected with pcDNA-mediated HIF-1\nPaeonol repressed migration and invasion of ecESCs through\nsuppression of autophagy.(A) Over-expression of HIF-1\nTo investigate role of paeonol in in vivo endometriosis, endometriotic\nrats were established through transplantation of uterine tissue towards intestine\nmesentry. Histopathological analysis by H&E staining showed hallmarks of\nendometriosis in the endometriotic rats, as demonstrated by perforation of\nstroma, increased number of glands and thickening walls of endometrial glands\ncompared with the sham group (Fig. 7A). In addition, the number and thickened\nwalls of glands were reduced by paeonol (Fig. 7A). Serum levels of IL-1\nPaeonol ameliorated endometriotic lesions of rats in a\nHIF-1\nPrevious study has shown that the dysregulation of endometrial stromal cells leads to endometriotic lesions during the development of endometriosis [5]. Endometriosis was found to be related to increased risk of clear-cell carcinoma and other malignancies [18]. Impaired autophagy was found to be closely associated with stage and prognosis of endometriosis, and mediated the cell proliferation, apoptosis, migration and invasion of endometrial cells [19]. Inhibition of autophagy contributed to suppression of endometrial cell migration and invasion [20]. Since paeonol promoted cytoprotective autophagy in ovarian cancer cells [15], and suppressed the oxidized low-density lipoprotein-induced vascular endothelial cell autophagy [17], the functional role of paeonol in autophagy, migration and invasion of endometrial stromal cells was investigated in this study.\nThe increase in endometrial stromal cell migration and invasion contributed to epithelial-to-mesenchymal transition in endometriosis [21]. Suppression of endometrial stromal cell migration and invasion could ameliorate endometriotic lesions [22]. Results in this study indicated that paeonol treatment decreased cell viability, proliferation, migration and invasion of ecESCs, and promoted the cell apoptosis. In vivo endometriosis showed that paeonol ameliorated hallmarks of endometriosis in the endometriotic rats, suggesting that paeonol might ameliorate endometriotic lesions during the development of endometriosis. Since epithelial-to-mesenchymal transition was considered as the original establishment of endometriotic lesions [23], the effects of paeonol on epithelial-to-mesenchymal transition of ecESCs should be investigated in the further study.\nAutophagy was found to be promoted in ovarian endometriosis [8], and the\ninduction of autophagy resulted in abnormal apoptosis during development of\nendometriosis [24]. Expression of HIF-1\nHIF-1\nIn general, our results showed that paeonol repressed migration and invasion of\necESCs through attenuation of hypoxia-triggered autophagy, and ameliorated\nhistopathological changes and inflammatory response of endometriotic rats in a\nHIF-1\nCP and ZW designed the study, supervised the data collection, XX analyzed the data, interpreted the data, WY, XW and YQ prepared the manuscript for publication and reviewed the draft of the manuscript. All authors have read and approved the manuscript.\nWritten informed consent was obtained from a legally authorized representative(s) for anonymized patient information to be published in this article. All animal care and treatments were done as approved by Animal Care Committee, the Hospital Affiliated to Shandong University of Traditional Chinese Medicine.\nThanks to all the peer reviewers for their opinions and suggestions.\nThis work was supported by the Project of Shandong Traditional Chinese Medicine Administration (Grant No. 2019-0116) and National Natural Science Foundation of China (Grant No. 81774355).\nThe authors declare no conflict of interest.\nAll data generated or analyzed during this study are included in this published article.\nSupplementary material associated with this article can be found, in the online version, at https://www.fbscience.com/Landmark/articles/10.52586/4961.\nCK19, cytoskeleton 19; ecESCs, ectopic endometrial stromal cells;\nHIF-1","source_license":"CC0","license_restricted":false}