Cite

Kulus M, Kranc W, Sujka-Kordowska P, Mozdziak P, Jankowski M, Konwerska A, Kulus J, Bukowska D, Skowroński M, Piotrowska-Kempisty H, Nowicki M, Kempisty B, Antosik P. The processes of cellular growth, aging, and programmed cell death are involved in lifespan of ovarian granulosa cells during short-term IVC – Study based on animal model. Theriogenology. 2020;148:76–88; DOI:10.1016/j.theriogenology.2020.02.044.KulusMKrancWSujka-KordowskaPMozdziakPJankowskiMKonwerskaAKulusJBukowskaDSkowrońskiMPiotrowska-KempistyHNowickiMKempistyBAntosikPThe processes of cellular growth, aging, and programmed cell death are involved in lifespan of ovarian granulosa cells during short-term IVC – Study based on animal modelTheriogenology2020148768810.1016/j.theriogenology.2020.02.044Open DOISearch in Google Scholar

Dompe C, Kranc W, Jopek K, Kowalska K, Ciesiółka S, Chermuła B, Bryja A, Jankowski M, Perek J, Józkowiak M, Moncrieff L, Hutchings G, Janowicz K, Pawelczyk L, Bruska M, Petitte J, Mozdziak P, Kulus M, Piotrowska-Kempisty H, Spaczyński R, Nowicki M, Kempisty B. Muscle Cell Morphogenesis, Structure, Development and Differentiation Processes Are Significantly Regulated during Human Ovarian Granulosa Cells In Vitro Cultivation. J Clin Med. 2020;9:2006; DOI:10.3390/jcm9062006.DompeCKrancWJopekKKowalskaKCiesiółkaSChermułaBBryjaAJankowskiMPerekJJózkowiakMMoncrieffLHutchingsGJanowiczKPawelczykLBruskaMPetitteJMozdziakPKulusMPiotrowska-KempistyHSpaczyńskiRNowickiMKempistyBMuscle Cell Morphogenesis, Structure, Development and Differentiation Processes Are Significantly Regulated during Human Ovarian Granulosa Cells In Vitro CultivationJ Clin Med20209200610.3390/jcm9062006Open DOISearch in Google Scholar

Brązert M, Kranc W, Celichowski P, Jankowski M, Piotrowska-Kempisty H, Pawelczyk L, Bruska M, Zabel M, Nowicki M, Kempisty B. Expression of genes involved in neurogenesis, and neuronal precursor cell proliferation and development: Novel pathways of human ovarian granulosa cell differentiation and transdifferentiation capability in vitro. Mol Med Rep. 2020;21:1749–60; DOI:10.3892/mmr.2020.10972.BrązertMKrancWCelichowskiPJankowskiMPiotrowska-KempistyHPawelczykLBruskaMZabelMNowickiMKempistyB.Expression of genes involved in neurogenesis, and neuronal precursor cell proliferation and development: Novel pathways of human ovarian granulosa cell differentiation and transdifferentiation capability in vitroMol Med Rep20202117496010.3892/mmr.2020.10972Open DOISearch in Google Scholar

Brązert M, Kranc W, Celichowski P, Ożegowska K, Budna-Tukan J, Jeseta M, Pawelczyk L, Bruska M, Zabel M, Nowicki M, Kempisty B. Novel markers of human ovarian granulosa cell differentiation toward osteoblast lineage: A microarray approach. Mol Med Rep. 2019;20:4403–14; DOI:10.3892/mmr.2019.10709.BrązertMKrancWCelichowskiPOżegowskaKBudna-TukanJJesetaMPawelczykLBruskaMZabelMNowickiMKempistyB.Novel markers of human ovarian granulosa cell differentiation toward osteoblast lineage: A microarray approachMol Med Rep20192044031410.3892/mmr.2019.10709Open DOISearch in Google Scholar

Karagouni EE, Chryssikopoulos A, Mantzavinos T, Kanakas N, Dotsika EN. Interleukin-1β and interleukin-1α may affect the implantation rate of patients undergoing in vitro fertilization-embryo transfer. Fertil Steril. 1998;70:553–9; DOI:10.1016/S0015-0282(98)00243-X.KaragouniEEChryssikopoulosAMantzavinosTKanakasNDotsikaENInterleukin-1β and interleukin-1α may affect the implantation rate of patients undergoing in vitro fertilization-embryo transferFertil Steril199870553910.1016/S0015-0282(98)00243-XOpen DOISearch in Google Scholar

Pelzer ES, Allan JA, Cunningham K, Mengersen K, Allan JM, Launchbury T, Beagley K, Knox CL. Microbial colonization of follicular fluid: Alterations in cytokine expression and adverse assisted reproduction technology outcomes. Hum Reprod. 2011;26:1799–812; DOI:10.1093/humrep/der108.PelzerESAllanJACunninghamKMengersenKAllanJMLaunchburyTBeagleyKKnoxCLMicrobial colonization of follicular fluid: Alterations in cytokine expression and adverse assisted reproduction technology outcomesHum Reprod201126179981210.1093/humrep/der108Open DOISearch in Google Scholar

Richards JS, Sharma SC, Falender AE, Lo YH. Expression of FKHR, FKHRL1, and AFX genes in the rodent ovary: Evidence for regulation by IGF-I, estrogen, and the gonadotropins. Mol Endocrinol. 2002;16:580–99; DOI:10.1210/mend.16.3.0806.RichardsJSSharmaSCFalenderAELoYHExpression of FKHR, FKHRL1, and AFX genes in the rodent ovary: Evidence for regulation by IGF-I, estrogen, and the gonadotropinsMol Endocrinol2002165809910.1210/mend.16.3.0806Open DOISearch in Google Scholar

Vujisić S, Lepej SŽ, Emedi I, Bauman R, Remenar A, Tiljak MK. Ovarian follicular concentration of IL-12, IL-15, IL-18 and p40 subunit of IL-12 and IL-23. Hum Reprod. 2006;21:2650–5; DOI:10.1093/humrep/del217.VujisićSLepejEmediIBaumanRRemenarATiljakMK.Ovarian follicular concentration of IL-12, IL-15, IL-18 and p40 subunit of IL-12 and IL-23Hum Reprod2006212650510.1093/humrep/del217Open DOISearch in Google Scholar

Yan K, Zhu W, Yu L, Li N, Zhang X, Liu P, Chen Q, Chen Y, Han D. Toll-like receptor 3 and RIG-I-like receptor activation induces innate antiviral responses in mouse ovarian granulosa cells. Mol Cell Endocrinol. 2013;372:73–85; DOI:10.1016/j.mce.2013.03.027.YanKZhuWYuLLiNZhangXLiuPChenQChenYHanDToll-like receptor 3 and RIG-I-like receptor activation induces innate antiviral responses in mouse ovarian granulosa cellsMol Cell Endocrinol2013372738510.1016/j.mce.2013.03.027Open DOISearch in Google Scholar

Onnureddy K, Ravinder, Onteru SK, Singh D. IGF-1 attenuates LPS induced pro-inflammatory cytokines expression in buffalo (Bubalus bubalis) granulosa cells. Mol Immunol. 2015;64:136–43; DOI:10.1016/j.molimm.2014.11.008.OnnureddyKRavinderOnteru SKSinghD.IGF-1 attenuates LPS induced pro-inflammatory cytokines expression in buffalo (Bubalus bubalis) granulosa cellsMol Immunol2015641364310.1016/j.molimm.2014.11.008Open DOISearch in Google Scholar

LEI L, GE J, ZHAO H, WANG X, YANG L. Role of endoplasmic reticulum stress in lipopolysaccharide-inhibited mouse granulosa cell estradiol production. J Reprod Dev. 2019;65:459–65; DOI:10.1262/jrd.2019-052.LEILGEJZHAOHWANGXYANGL.Role of endoplasmic reticulum stress in lipopolysaccharide-inhibited mouse granulosa cell estradiol productionJ Reprod Dev2019654596510.1262/jrd.2019-052Open DOISearch in Google Scholar

Neuvians TP, Schams D, Berisha B, Pfaffl MW. Involvement of Pro-Inflammatory Cytokines, Mediators of Inflammation, and Basic Fibroblast Growth Factor in Prostaglandin F2α-Induced Luteolysis in Bovine Corpus Luteum. Biol Reprod. 2004;70:473–80; DOI:10.1095/biolreprod.103.016154.NeuviansTPSchamsDBerishaBPfafflMWInvolvement of Pro-Inflammatory Cytokines, Mediators of Inflammation, and Basic Fibroblast Growth Factor in Prostaglandin F2α-Induced Luteolysis in Bovine Corpus LuteumBiol Reprod2004704738010.1095/biolreprod.103.016154Open DOISearch in Google Scholar

Jasper M, Norman RJ. Endocrinology: Immunoactive interleukin-1β and tumour necrosis factor-α in thecal, stromal and granulosa cell cultures from normal and polycystic ovaries. Hum Reprod. 1995;10:1352–4; DOI:10.1093/HUMREP/10.6.1352.JasperMNormanRJEndocrinology: Immunoactive interleukin-1β and tumour necrosis factor-α in thecal, stromal and granulosa cell cultures from normal and polycystic ovariesHum Reprod1995101352410.1093/HUMREP/10.6.1352Open DOISearch in Google Scholar

Yasuda K, Fukuoka M, Fujiwara H, Mori T. Effects of Interferon on the Steroidogenic Functions and Proliferation of Immature Porcine Granulosa Cells in Culture. Biol Reprod. 1992;47:931–6; DOI:10.1095/biolreprod47.6.931.YasudaKFukuokaMFujiwaraHMoriTEffects of Interferon on the Steroidogenic Functions and Proliferation of Immature Porcine Granulosa Cells in CultureBiol Reprod199247931610.1095/biolreprod47.6.931Open DOISearch in Google Scholar

Ghizzoni L, Mastorakos G, Vottero A, Barreca A, Furlini M, Cesarone A, Ferrari B, Chrousos GP, Bernasconi S. Corticotropin-releasing hormone (CRH) inhibits steroid biosynthesis by cultured human granulosa-lutein cells in a CRH and interleukin-1 receptor- mediated fashion. Endocrinology. 1997;138:4806–11; DOI:10.1210/endo.138.11.5474.GhizzoniLMastorakosGVotteroABarrecaAFurliniMCesaroneAFerrariBChrousosGPBernasconiSCorticotropin-releasing hormone (CRH) inhibits steroid biosynthesis by cultured human granulosa-lutein cells in a CRH and interleukin-1 receptor- mediated fashionEndocrinology199713848061110.1210/endo.138.11.5474Open DOISearch in Google Scholar

Woolery KT, Kruk PA. Ovarian Epithelial-Stromal Interactions: Role of Interleukins 1 and 6. Obstet Gynecol Int. 2011;2011:1–9; DOI:10.1155/2011/358493.WooleryKTKrukPAOvarian Epithelial-Stromal Interactions: Role of Interleukins 1 and 6Obstet Gynecol Int201120111910.1155/2011/358493Open DOISearch in Google Scholar

Martoriati A, Gérard N. Interleukin-1 (IL-1) system gene expression in granulosa cells: Kinetics during terminal preovulatory follicle maturation in the mare. Reprod Biol Endocrinol. 2003;1:42; DOI:10.1186/1477-7827-1-42.MartoriatiAGérardN.Interleukin-1 (IL-1) system gene expression in granulosa cells: Kinetics during terminal preovulatory follicle maturation in the mareReprod Biol Endocrinol200314210.1186/1477-7827-1-42Open DOISearch in Google Scholar

Hurwitz A, Ricciarelli E, Botero L, Rohan RM, Hernandez ER, Adashi EY. Endocrine-and autocrine-mediated regulation of rat ovarian (Theca-interstitial) interleukin-1ß gene expression: Gonadotropin-dependent preovulatory acquisition. Endocrinology. 1991;129:3427–9; DOI:10.1210/endo-129-6-3427.HurwitzARicciarelliEBoteroLRohanRMHernandezERAdashiEYEndocrine-and autocrine-mediated regulation of rat ovarian (Theca-interstitial) interleukin-1ß gene expression: Gonadotropin-dependent preovulatory acquisitionEndocrinology19911293427910.1210/endo-129-6-3427Open DOISearch in Google Scholar

Machelon V, Nome F, Durand-gasselin I, Emilie D. Macrophage and granulosa interleukin-1β mRNA in human ovulatory follicles. Hum Reprod. 1995;10:2198–203; DOI:10.1093/oxfordjournals.humrep.a136268.MachelonVNomeFDurand-gasselinIEmilieDMacrophage and granulosa interleukin-1β mRNA in human ovulatory folliclesHum Reprod199510219820310.1093/oxfordjournals.humrep.a136268Open DOISearch in Google Scholar

Gérard N, Caillaud M, Martoriati A, Goudet G, Lalmanach AC. The interleuking-1 system and female reproduction. J Endocrinol. 2004;180:203–12; DOI:10.1677/joe.0.1800203.GérardNCaillaudMMartoriatiAGoudetGLalmanachAC.The interleuking-1 system and female reproductionJ Endocrinol20041802031210.1677/joe.0.1800203Open DOISearch in Google Scholar

Best CL, Hill JA. Interleukin-1α and -β modulation of luteinized human granulosa cell oestrogen and progesterone biosynthesis. Hum Reprod. 1995;10:3206–10; DOI:10.1093/oxfordjournals.humrep.a135889.BestCLHillJAInterleukin-1α and -β modulation of luteinized human granulosa cell oestrogen and progesterone biosynthesisHum Reprod19951032061010.1093/oxfordjournals.humrep.a135889Open DOISearch in Google Scholar

Santana P, Llanes L, Hernandez I, Gonzalez-Robayna I, Tabraue C, Gonzalez-Reyes J, Quintana J, Estevez F, Ruiz De Galarreta CM, Fanjul LF. Interleukin-1β stimulates sphingomyelin hydrolysis in cultured granulosa cells: Evidence for a regulatory role of ceramide on progesterone and prostaglandin biosynthesis. Endocrinology. 1996;137:2480–9; DOI:10.1210/endo.137.6.8641202.SantanaPLlanesLHernandezIGonzalez-RobaynaITabraueCGonzalez-ReyesJQuintanaJEstevezFRuizDe Galarreta CMFanjulLF.Interleukin-1β stimulates sphingomyelin hydrolysis in cultured granulosa cells: Evidence for a regulatory role of ceramide on progesterone and prostaglandin biosynthesisEndocrinology19961372480910.1210/endo.137.6.8641202Open DOISearch in Google Scholar

CHEN H-F, CHAO K-H, CHANG L-J, HO H-N, YANG Y-S, SHEW J-Y. Luteinizing Hormone Up-Regulates the Expression of Interleukin-1beta mRNA in Human Granulosa-Luteal Cells. Am J Reprod Immunol. 2000;43:125–33; DOI:10.1111/j.8755-8920.2000.430301.x.CHENH-FCHAOK-HCHANGL-JHOH-NYANGY-SSHEWJ-Y.Luteinizing Hormone Up-Regulates the Expression of Interleukin-1beta mRNA in Human Granulosa-Luteal CellsAm J Reprod Immunol2000431253310.1111/j.8755-8920.2000.430301.xOpen DOISearch in Google Scholar

Dang X, Zhu Q, He Y, Wang Y, Lu Y, Li X, Qi J, Wu H, Sun Y. Il-1b upregulates star and progesterone production through the erk1/2-and p38-mediated creb signaling pathways in human granulosa-lutein cells. Endocrinology. 2017;158:3281–91; DOI:10.1210/en.2017-00029.DangXZhuQHeYWangYLuYLiXQiJWuHSunYIl-1b upregulates star and progesterone production through the erk1/2-and p38-mediated creb signaling pathways in human granulosa-lutein cellsEndocrinology201715832819110.1210/en.2017-00029Open DOISearch in Google Scholar

Van Der Zee AGJ, De Bruijn HWA, Krans M, De Cuyper EMJ, Hollema H, Limburg PC, Bijzet J, De Vries EGE. Higher levels of interleukin‐6 in cystic fluids from patients with malignant versus benign ovarian tumors correlate with decreased hemoglobin levels and increased platelet counts. Cancer. 1995;75:1004–9; DOI:10.1002/10970142(19950215)75:4<1004::AID-CNCR2820750416>3.0.CO;2-G.VanDer Zee AGJDeBruijn HWAKransMDeCuyper EMJHollemaHLimburgPCBijzetJDeVries EGE.Higher levels of interleukin‐6 in cystic fluids from patients with malignant versus benign ovarian tumors correlate with decreased hemoglobin levels and increased platelet countsCancer1995751004910.1002/10970142(19950215)75:4<1004::AID-CNCR2820750416>3.0.CO;2-GOpen DOISearch in Google Scholar

Wang Y, Niu XL, Qu Y, Wu J, Zhu YQ, Sun WJ, Li LZ. Autocrine production of interleukin-6 confers cisplatin and paclitaxel resistance in ovarian cancer cells. Cancer Lett. 2010;295:110–23; DOI:10.1016/j.canlet.2010.02.019.WangYNiuXLQuYWuJZhuYQSunWJLiLZAutocrine production of interleukin-6 confers cisplatin and paclitaxel resistance in ovarian cancer cellsCancer Lett20102951102310.1016/j.canlet.2010.02.019Open DOISearch in Google Scholar

Gorospe WC, Spangelo BL. Interleukin-6 production by rat granulosa cells in vitro: Effects of cytokines, follicle-stimulating hormone, and cyclic 3’,5’-adenosine monophosphate. Biol Reprod. 1993;48:538–43; DOI:10.1095/biolreprod48.3.538.GorospeWCSpangeloBLInterleukin-6 production by rat granulosa cells in vitro: Effects of cytokines, follicle-stimulating hormone, and cyclic 3’,5’-adenosine monophosphateBiol Reprod1993485384310.1095/biolreprod48.3.538Open DOISearch in Google Scholar

Kuang H, Duan Y, Li D, Xu Y, Ai W, Li W, Wang Y, Liu S, Li M, Liu X, Shao M. The role of serum inflammatory cytokines and berberine in the insulin signaling pathway among women with polycystic ovary syndrome. PLoS One. 2020;15:e0235404; DOI:10.1371/journal.pone.0235404.KuangHDuanYLiDXuYAiWLiWWangYLiuSLiMLiuXShaoMThe role of serum inflammatory cytokines and berberine in the insulin signaling pathway among women with polycystic ovary syndromePLoS One202015e023540410.1371/journal.pone.0235404Open DOISearch in Google Scholar

Nakayama M, Manabe N, Inoue N, Matsui T, Miyamoto H. Changes in the expression of tumor necrosis factor (TNF) α, TNFα receptor (TNFR) 2, and TNFR-associated factor 2 in granulosa cells during atresia in pig ovaries. Biol Reprod. 2003;68:530–5; DOI:10.1095/biolreprod.102.004820.NakayamaMManabeNInoueNMatsuiTMiyamotoHChanges in the expression of tumor necrosis factor (TNF) α, TNFα receptor (TNFR) 2, and TNFR-associated factor 2 in granulosa cells during atresia in pig ovariesBiol Reprod200368530510.1095/biolreprod.102.004820Open DOISearch in Google Scholar

Sasson R, Winder N, Kees S, Amsterdam A. Induction of apoptosis in granulosa cells by TNFα and its attenuation by glucocorticoids involve modulation of Bcl-2. Biochem Biophys Res Commun. 2002;294:51–9; DOI:10.1016/S0006-291X(02)00431-X.SassonRWinderNKeesSAmsterdamAInduction of apoptosis in granulosa cells by TNFα and its attenuation by glucocorticoids involve modulation of Bcl-2Biochem Biophys Res Commun200229451910.1016/S0006-291X(02)00431-XOpen DOISearch in Google Scholar

Nakao K, Kishi H, Imai F, Suwa H, Hirakawa T, Minegishi T. TNF-α suppressed FSH-induced LH receptor expression through transcriptional regulation in rat granulosa cells. Endocrinology. 2015;156:3192–202; DOI:10.1210/EN.2015-1238.NakaoKKishiHImaiFSuwaHHirakawaTMinegishiTTNF-α suppressed FSH-induced LH receptor expression through transcriptional regulation in rat granulosa cellsEndocrinology2015156319220210.1210/EN.2015-1238Open DOISearch in Google Scholar

Yamada-Nomoto K, Yoshino O, Akiyama I, Iwase A, Ono Y, Nakamura T, Harada M, Nakashima A, Shima T, Ushijima A, Osuga Y, Chang RJ, Shimasaki S, Saito S. PAI-1 in granulosa cells is suppressed directly by statin and indirectly by suppressing TGF-β and TNF-α in mononuclear cells by insulin-sensitizing drugs. Am J Reprod Immunol. 2017;78; DOI:10.1111/aji.12669.Yamada-NomotoKYoshinoOAkiyamaIIwaseAOnoYNakamuraTHaradaMNakashimaAShimaTUshijimaAOsugaYChangRJShimasakiSSaitoS.PAI-1 in granulosa cells is suppressed directly by statin and indirectly by suppressing TGF-β and TNF-α in mononuclear cells by insulin-sensitizing drugsAm J Reprod Immunol20177810.1111/aji.12669Open DOISearch in Google Scholar

Yan K, Liang J, Zhang X, Deng L, Feng D, Ling B. Polyinosinic-polycytidylic acid induces innate immune responses via Toll-like receptor 3 in human ovarian granulosa cells. Immunol Cell Biol. 2019;97:753–65; DOI:10.1111/imcb.12269.YanKLiangJZhangXDengLFengDLingBPolyinosinic-polycytidylic acid induces innate immune responses via Toll-like receptor 3 in human ovarian granulosa cellsImmunol Cell Biol2019977536510.1111/imcb.12269Open DOISearch in Google Scholar

Wang Q, Wu H, Cheng L, Yan K, Shi L, Zhao X, Jiang Q, Wang F, Chen Y, Li Q, Han D. Mumps virus induces innate immune responses in mouse ovarian granulosa cells through the activation of Toll-like receptor 2 and retinoic acid-inducible gene I. Mol Cell Endocrinol. 2016;436:183–94; DOI:10.1016/j.mce.2016.07.033.WangQWuHChengLYanKShiLZhaoXJiangQWangFChenYLiQHanDMumps virus induces innate immune responses in mouse ovarian granulosa cells through the activation of Toll-like receptor 2 and retinoic acid-inducible gene IMol Cell Endocrinol20164361839410.1016/j.mce.2016.07.033Open DOISearch in Google Scholar

eISSN:
2544-3577
Language:
English
Publication timeframe:
4 times per year
Journal Subjects:
Life Sciences, Molecular Biology, Biochemistry