References
- 1. Monniaux D, Cadoret V, Clément F, Dalbies-Tran R, Elis S, Fabre S, Maillard V, Monget P, Uzbekova S. Folliculogenesis. Encycl Endocr Dis. 2019;377–98; DOI:10.1016/B978-0-12-801238-3.64550-6.10.1016/B978-0-12-801238-3.64550-6
- 2. Adashi EY, Serono Symposia U, International Symposium on Ovulation (1998 : Salt Lake City U. Ovulation : evolving scientific and clinical concepts 2000;335.10.1007/978-0-387-21508-2
- 3. Baker TG. A quantitative and cytological study of germ cells in human ovaries. Proc R Soc London Ser B, Biol Sci. 1963;158:417–33; DOI:10.1098/RSPB.1963.0055.10.1098/rspb.1963.005514070052
- 4. Gougeon A. Regulation of ovarian follicular development in primates: facts and hypotheses. Endocr Rev. 1996;17(2):121–55; DOI:10.1210/EDRV-17-2-121.10.1210/edrv-17-2-1218706629
- 5. Findlay JK, Kerr JB, Britt K, Liew SH, Simpson ER, Rosairo D, Drummond A. Ovarian physiology: follicle development, oocyte and hormone relationships. Anim Reprod, V. n.d.;6(1):16–9.
- 6. McGee EA, Hsueh AJW. Initial and cyclic recruitment of ovarian follicles. Endocr Rev. 2000;21(2):200–14; DOI:10.1210/EDRV.21.2.0394.10.1210/edrv.21.2.039410782364
- 7. Da Silva-Buttkus P, Jayasooriya GS, Mora JM, Mobberley M, Ryder TA, Baithun M, Stark J, Franks S, Hardy K. Effect of cell shape and packing density on granulosa cell proliferation and formation of multiple layers during early follicle development in the ovary. J Cell Sci. 2008;121(Pt 23):3890–900; DOI:10.1242/JCS.036400.10.1242/jcs.03640019001500
- 8. Findlay JK. Folliculogenesis. Encycl Horm. 2003;653–6; DOI:10.1016/B0-12-341103-3/00141-8.10.1016/B0-12-341103-3/00141-8
- 9. Rimon-Dahari N, Yerushalmi-Heinemann L, Alyagor L, Dekel N. Ovarian Folliculogenesis. Results Probl Cell Differ. 2016;58:167–90; DOI:10.1007/978-3-319-31973-5_7.10.1007/978-3-319-31973-5_727300179
- 10. Vidal JD, Dixon D. Ovary. Boorman’s Pathol Rat. 2018;523–36; DOI:10.1016/B978-0-12-391448-4.00026-5.10.1016/B978-0-12-391448-4.00026-5
- 11. Griffin J, Emery BR, Huang I, Peterson CM, Carrell DT. Comparative analysis of follicle morphology and oocyte diameter in four mammalian species (mouse, hamster, pig, and human). J Exp Clin Assist Reprod. 2006;3:2; DOI:10.1186/1743-1050-3-2.10.1186/1743-1050-3-2141354816509981
- 12. Kossowska-Tomaszczuk K, De Geyter C. Cells with stem cell characteristics in somatic compartments of the ovary. Biomed Res Int. 2013;2013; DOI:10.1155/2013/310859.10.1155/2013/310859359121723484108
- 13. Uyar A, Torrealday S, Seli E. Cumulus and granulosa cell markers of oocyte and embryo quality. Fertil Steril. 2013;99(4):979–97; DOI:10.1016/J.FERTNSTERT.2013.01.129.10.1016/j.fertnstert.2013.01.129386613123498999
- 14. Rodgers RJ, Irving-Rodgers HF. Formation of the ovarian follicular antrum and follicular fluid. Biol Reprod. 2010;82(6):1021–9; DOI:10.1095/BIOLREPROD.109.082941.10.1095/biolreprod.109.08294120164441
- 15. Young JM, McNeilly AS. Theca: the forgotten cell of the ovarian follicle. Reproduction. 2010;140(4):489–504; DOI:10.1530/REP-10-0094.10.1530/REP-10-009420628033
- 16. Pan B, Li J. The art of oocyte meiotic arrest regulation. Reprod Biol Endocrinol 2019 171. 2019;17(1):1–12; DOI:10.1186/S12958-018-0445-8.10.1186/s12958-018-0445-8632060630611263
- 17. Cooper GM. The cell: a molecular approach. 2nd ed. Sinauer: Sunder-land; 2000. 625 p.
- 18. Dzafic E, Stimpfel M, Virant-Klun I. Plasticity of granulosa cells: on the crossroad of stemness and transdifferentiation potential. J Assist Re-prod Genet. 2013;30(10):1255–61; DOI:10.1007/s10815-013-0068-0.10.1007/s10815-013-0068-0382486223893266
- 19. Kossowska-Tomaszczuk K, De Geyter C, De Geyter M, Martin I, Holzgreve W, Scherberich A, Zhang H. The multipotency of luteinizing granulosa cells collected from mature ovarian follicles. Stem Cells. 2009;27(1):210–9; DOI:10.1634/STEMCELLS.2008-0233.10.1634/stemcells.2008-023319224509
- 20. Stefańska K, Sibiak R, Hutchings G, Dompe C, Moncrieff L, Janowicz K, Jeseta M, Kempisty B, Machatkova M, Mozdziak P. Evidence for existence of molecular stemness markers in porcine ovarian follicular granulosa cells. Med J Cell Biol. 2019; DOI:10.2478/acb-2019-0025.10.2478/acb-2019-0025
- 21. Madkour A, Bouamoud N, Kaarouch I, Louanjli N, Saadani B, Assou S, Aboulmaouahib S, Sefrioui O, Amzazi S, Copin H, Benkhalifa M. Follicular fluid and supernatant from cultured cumulus-granulosa cells improve in vitro maturation in patients with polycystic ovarian syndrome. Fertil Steril. 2018;110(4):710–9; DOI:10.1016/J.FERTNSTERT.2018.04.038.10.1016/j.fertnstert.2018.04.03830196968
- 22. Bruckova L, Soukup T, Visek B, Moos J, Moosova M, Pavelkova J, Rezabek K, Kucerova L, Micuda S, Brcakova E, Mokry J. Proliferative potential and phenotypic analysis of long-term cultivated human granulosa cells initiated by addition of follicular fluid n.d.; DOI:10.1007/s10815-011-9617-6.10.1007/s10815-011-9617-6322043421822582
- 23. Vireque AA, Campos JR, Dentillo DB, Bernuci MP, Campos CO, Silva-De-Sá MF, Ferriani RA, Nunes AA, Rosa-E-Silva ACJDS. Driving Human Granulosa-Luteal Cells Recovered From In Vitro Fertilization Cycles Toward the Follicular Phase Phenotype. Reprod Sci. 2015;22(8):1015–27; DOI:10.1177/1933719115570909.10.1177/193371911557090925701839
- 24. Oki Y, Ono H, Motohashi T, Sugiura N, Nobusue H, Kano K. Dedifferentiated follicular granulosa cells derived from pig ovary can transdifferentiate into osteoblasts. Biochem J. 2012;447(2):239–48; DOI:10.1042/BJ20120172.10.1042/BJ20120172345922222839299
- 25. Sadat Tahajjodi S, Farashahi Yazd E, Agha-Rahimi A, Aflatoonian R, Ali Khalili M, Mohammadi M, Aflatoonian B. Biological and physiological characteristics of human cumulus cells in adherent culture condition. Int J Reprod Biomed. 2019;18(1):1–10; DOI:10.18502/ijrm.v18i1.6189.10.18502/ijrm.v18i1.6189699612232043066
- 26. Orisaka M, Tajima K, Mizutani T, Miyamoto K, Tsang BK, Fukuda S, Yoshida Y, Kotsuji F. Granulosa cells promote differentiation of cortical stromal cells into theca cells in the bovine ovary. Biol Reprod. 2006;75(5):734–40; DOI:10.1095/BIOLREPROD.105.050344.10.1095/biolreprod.105.05034416914692
- 27. Ding T, Luo A, Yang S, Lai Z, Wang Y, Shen W, Jiang J, Lu Y, Ma D, Wang S. Effects of basal media and supplements on diethylstilbestrol-treated immature mouse primary granulosa cell growth and regulation of steroidogenesis in vitro. Reprod Domest Anim. 2012;47(3):355–64; DOI:10.1111/J.1439-0531.2011.01879.X.10.1111/j.1439-0531.2011.01879.x21999365
- 28. Zırh S, Erol S, Zırh EB, Sokmensuer LK, Bozdag G, Muftuoglu SF. A new isolation and culture method for granulosa cells. Cell Tissue Bank. 2021;22(4):719–26; DOI:10.1007/S10561-021-09929-5.10.1007/s10561-021-09929-533914204
- 29. Barano JLS, Hammond JM. Serum-free medium enhances growth and differentiation of cultured pig granulosa cells. Endocrinology. 1985;116(1):51–8; DOI:10.1210/ENDO-116-1-51.10.1210/endo-116-1-513917254
- 30. Hensen K, Pook M, Sikut A, Org T, Maimets T, Salumets A, Kurg A. Utilising FGF2, IGF2 and FSH in serum-free protocol for long-term in vitro cultivation of primary human granulosa cells. Mol Cell Endocrinol. 2020;510; DOI:10.1016/J.MCE.2020.110816.10.1016/j.mce.2020.11081632294491
- 31. Figenschau Y, Sundsfjord JA, Yousef MI, Fuskevåg OM, Sveinbjörnsson B, Bertheussen K. A simplified serum-free method for preparation and cultivation of human granulosa-luteal cells. Hum Reprod. 1997;12(3):523–31; DOI:10.1093/HUMREP/12.3.523.10.1093/humrep/12.3.5239130754
- 32. Lane CA, Pax RA, Bennett JL. L-glutamine: an amino acid required for maintenance of the tegumental membrane potential of Schistosoma mansoni. Parasitology. 1987;94(Pt 2)(2):233–42; DOI:10.1017/S0031182000053919.10.1017/S0031182000053919
- 33. Asadi E, Najafi A, Moeini A, Pirjani R, Hassanzadeh G, Mikaeili S, Sale-hi E, Adutwum E, Soleimani M, Khosravi F, Barati M, Abolhassani F. Ovarian tissue culture in the presence of VEGF and fetuin stimulates follicle growth and steroidogenesis. J Endocrinol. 2017;232(2):205–19; DOI:10.1530/JOE-16-0368.10.1530/JOE-16-0368
- 34. Max MC, Bizarro-Silva C, Búfalo I, González SM, Lindquist AG, Gomes RG, Barreiros TRR, Lisboa LA, Morotti F, Seneda MM. In vitro culture supplementation of EGF for improving the survival of equine preantral follicles. In Vitro Cell Dev Biol Anim. 2018;54(10):687–91; DOI:10.1007/S11626-018-0296-9.10.1007/s11626-018-0296-9
- 35. Palmerini MG, Nottola SA, Tunjung WAS, Kadowaki A, Bianchi S, Cecconi S, Sato E, Macchiarelli G. EGF-FSH supplementation reduces apoptosis of pig granulosa cells in co-culture with cumulus-oocyte complexes. Biochem Biophys Res Commun. 2016;481(1–2):159–64; DOI:10.1016/J.BBRC.2016.10.151.10.1016/j.bbrc.2016.10.151
- 36. Nilsson EE, Kezele P, Skinner MK. Leukemia inhibitory factor (LIF) promotes the primordial to primary follicle transition in rat ovaries. Mol Cell Endocrinol. 2002;188(1–2):65–73; DOI:10.1016/S0303-7207(01)00746-8.10.1016/S0303-7207(01)00746-8
- 37. Bauer S, Patterson PH. Leukemia inhibitory factor promotes neural stem cell self-renewal in the adult brain. J Neurosci. 2006;26(46):12089–99; DOI:10.1523/JNEUROSCI.3047-06.2006.10.1523/JNEUROSCI.3047-06.2006
- 38. He Z, Li JJ, Zhen CH, Feng LY, Ding XY. Effect of leukemia inhibitory factor on embryonic stem cell differentiation: implications for supporting neuronal differentiation 2006;27(1):80–90.
- 39. Komatsu K, Koya T, Wang J, Yamashita M, Kikkawa F, Iwase A. Analysis of the effect of leukemia inhibitory factor on follicular growth in cultured murine ovarian tissue. Biol Reprod. 2015;93(1):1–8; DOI:10.1095/BIOLREPROD.115.128421/2434200.
- 40. De Matos DG, Miller K, Scott R, Tran CA, Kagan D, Nataraja SG, Clark A, Palmer S. Leukemia inhibitory factor induces cumulus expansion in immature human and mouse oocytes and improves mouse two-cell rate and delivery rates when it is present during mouse in vitro oocyte maturation. Fertil Steril. 2008;90(6):2367–75; DOI:10.1016/J.FERTNSTERT.2007.10.061.10.1016/j.fertnstert.2007.10.061
- 41. Xu J, Lawson MS, Yeoman RR, Molskness TA, Ting AY, Stouffer RL, Zelinski MB. Fibrin promotes development and function of macaque primary follicles during encapsulated three-dimensional culture. Hum Reprod. 2013;28(8):2187–200; DOI:10.1093/humrep/det093.10.1093/humrep/det093
- 42. Telfer EE, Zelinski MB. Ovarian follicle culture: advances and challenges for human and nonhuman primates. Fertil Steril. 2013;99(6):1523–33; DOI:10.1016/J.FERTNSTERT.2013.03.043.10.1016/j.fertnstert.2013.03.043
- 43. He X, Toth TL. In vitro culture of ovarian follicles from Peromyscus. Semin Cell Dev Biol. 2017;61:140–9; DOI:10.1016/j.semcdb.2016.07.006.10.1016/j.semcdb.2016.07.006
- 44. Zareifard N, Soleimani A, Talaei-Khozani T, Bahmanpour S. Improved BALB/c mice granulosa cell functions using purified alginate scaffold. Iran J Vet Res. 2018;19(3):182.
- 45. Jeon MJ, Choi YS, Kim ID, Criswell T, Atala A, Yoo JJ, Jackson JD. Engineering Functional Rat Ovarian Spheroids Using Granulosa and Theca Cells 2021;28(6):1697–708.
- 46. Azhar S, Tsai L, Maffe W, Reaven E. Cultivation of rat granulosa cells in a serum-free chemically defined medium-a useful model to study lipoprotein metabolism. Biochim Biophys Acta. 1988;963(2):139–50; DOI:10.1016/0005-2760(88)90275-5.10.1016/0005-2760(88)90275-5
- 47. Kulus J, Kulus M, Kranc W, Jopek K, Zdun M, Józkowiak M, Jaśkowski JM, Piotrowska-Kempisty H, Bukowska D, Antosik P, Mozdziak P, Kempisty B. Transcriptomic profile of new gene markers encoding proteins responsible for structure of porcine ovarian granulosa cells. Biology (Basel). 2021;10(11):1214; DOI:10.3390/biology10111214.10.3390/biology10111214
- 48. Mohammed BT, Donadeu FX. Bovine granulosa cell culture. Methods Mol Biol. 2018;1817:79–87; DOI:10.1007/978-1-4939-8600-2_8.10.1007/978-1-4939-8600-2_8
- 49. Beker ARCL, Colenbrander B, Bevers MM. Effect of 17 β-estradiol on the in vitro maturation of bovine oocytes. Theriogenology. 2002;58(9):1663–73; DOI:10.1016/S0093-691X(02)01082-8.10.1016/S0093-691X(02)01082-8
- 50. Antonino D de C, Soares MM, Júnior J de M, de Alvarenga PB, Mohallem R de FF, Rocha CD, Vieira LA, de Souza AG, Beletti ME, Alves BG, Jacomini JO, Goulart LR, Alves KA. Three-dimensional levitation culture improves in-vitro growth of secondary follicles in bovine model. Reprod Biomed Online. 2019;38(3):300–11; DOI:10.1016/J.RBMO.2018.11.013.10.1016/j.rbmo.2018.11.013
- 51. Ikeda H. Serum-free medium conditions for steroidogenesis of bovine follicular thecal cells cultured on collagen gel matrix. In Vitro Cell Dev Biol. 1990;26(2):193–200; DOI:10.1007/BF02624112.10.1007/BF02624112
- 52. Zhang J, Deng Y, Li J, Zi Y, Shi D, Lu F. Theca cell-conditioned medium enhances steroidogenesis competence of buffalo (Bubalus bubalis) granulosa cells. Reprod Domest Anim. 2021;56(2):254–62; DOI:10.1111/RDA.13792.10.1111/rda.13792
- 53. Gupta PSP, Nandi S, Ravindranatha BM, Sarma P V. In vitro culture of buffalo (Bubalus bubalis) preantral follicles. Theriogenology. 2002;57(7):1839–54; DOI:10.1016/S0093-691X(02)00694-5.10.1016/S0093-691X(02)00694-5
- 54. Baufeld A, Vanselow J. A tissue culture model of estrogen-producing primary bovine granulosa cells. J Vis Exp. 2018;2018(139); DOI:10.3791/58208.10.3791/58208623510430247464
- 55. Arunakumari G, Shanmugasundaram N, Rao VH. Development of morulae from the oocytes of cultured sheep preantral follicles. Theriogenology. 2010;74(5):884–94; DOI:10.1016/J.THERIOGENOLOGY.2010.04.013.10.1016/j.theriogenology.2010.04.01320615540
- 56. Varnosfaderani SR, Hajian M, Jafarpour F, Zadegan FG, Nasr-Esfahani MH. Granulosa secreted factors improve the developmental competence of cumulus oocyte complexes from small antral follicles in sheep. PLoS One. 2020;15(3); DOI:10.1371/JOURNAL.PONE.0229043.10.1371/journal.pone.0229043707780932182244
- 57. Jing J, Jiang X, Chen J, Yao X, Zhao M, Li P, Pan Y, Ren Y, Liu W, Lyu L. Notch signaling pathway promotes the development of ovine ovarian follicular granulosa cells. Anim Reprod Sci. 2017;181:69–78; DOI:10.1016/J.ANIREPROSCI.2017.03.017.10.1016/j.anireprosci.2017.03.017
- 58. Brito IR, Silva GM, Sales AD, Lobo CH, Rodrigues GQ, Sousa RF, Moura AAA, Calderón CEM, Bertolini M, Campello CC, Smitz J, Figueiredo JR. Fibrin–alginate hydrogel supports steroidogenesis, in vitro maturation of oocytes and parthenotes production from caprine preantral follicles cultured in group. Reprod Domest Anim. 2016;51(6):997–1009; DOI:10.1111/rda.12779.10.1111/rda.12779
- 59. Yao X, Wang Z, El-Samahy MA, Ren C, Liu Z, Wang F, You P. Roles of vitamin D and its receptor in the proliferation and apoptosis of luteinised granulosa cells in the goat. Reprod Fertil Dev. 2020;32(3):335–48; DOI:10.1071/RD18442.10.1071/RD18442
- 60. Boon CH, Cao T, Bested SM, Guo QT, Soon CN. “Waste” follicular aspirate from fertility treatment-a potential source of human germline stem cells? Stem Cells Dev. 2005;14(1):11–4; DOI:10.1089/SCD.2005.14.11.10.1089/scd.2005.14.11
- 61. Ai A, Tang Z, Liu Y, Yu S, Li B, Huang H, Wang X, Cao Y, Zhang W. Characterization and identification of human immortalized granulosa cells derived from ovarian follicular fluid. Exp Ther Med. 2019;18(3):2167–77; DOI:10.3892/etm.2019.7802.10.3892/etm.2019.7802
- 62. Matysiak J, Dereziński P, Klupczyńska A, Hajduk J, S wiatły A, Plewa S, Lemańska A, Jaźwiński P, Banach P, Nowak-Markwitz E, Kokot ZJ. Proteomic and metabolomic strategy of searching for biomarkers of genital cancer diseases using mass spectrometry methods. J Med Sci. 2016;85(4):330–3; DOI:10.20883/JMS.2016.180.10.20883/jms.2016.180
- 63. Hanrieder J, Nyakas A, Naessén T, Bergquist J. Proteomic analysis of human follicular fluid using an alternative bottom-up approach. J Proteome Res. 2008;7(1):443–9; DOI:10.1021/PR070277Z.10.1021/pr070277z
- 64. Yousefi S, Soleimanirad J, Hamdi K, Farzadi L, Ghasemzadeh A, Kazemi M, Mahdipour M, Rahbarghazi R, Nouri M. Distinct effect of fetal bovine serum versus follicular fluid on multipotentiality of human granulosa cells in in vitro condition. Biologicals. 2018;52:44–8; DOI:10.1016/J.BIOLOGICALS.2018.01.002.10.1016/j.biologicals.2018.01.002
- 65. Williams RL, Hilton DJ, Pease S, Willson TA, Stewart CL, Gearing DP, Wagner EF, Metcalf D, Nicola NA, Gough NM. Myeloid leukaemia inhibitory factor maintains the developmental potential of embryonic stem cells. Nat 1988 3366200. 1988;336(6200):684–7; DOI:10.1038/336684a0.10.1038/336684a0
- 66. Abir R, Fisch B, Nitke S, Okon E, Raz A, Ben Rafael Z. Morphological study of fully and partially isolated early human follicles. Fertil Steril. 2001;75(1):141–6; DOI:10.1016/S0015-0282(00)01668-X.10.1016/S0015-0282(00)01668-X
- 67. Shah SM, Saini N, Ashraf S, Singh MK, Manik RS, Singla SK, Palta P, Chauhan MS. Cumulus cell-conditioned medium supports embryonic stem cell differentiation to germ cell-like cells. Reprod Fertil Dev. 2017;29(4):679–93; DOI:10.1071/RD15159.10.1071/RD1515926595369
- 68. Kossowska-Tomaszczuk K, Pelczar P, Güven S, Kowalski J, Volpi E, De Geyter C, Scherberich A. A novel three-dimensional culture system allows prolonged culture of functional human granulosa cells and mimics the ovarian environment. Tissue Eng - Part A. 2010;16(6):2063–73; DOI:10.1089/ten.tea.2009.0684.10.1089/ten.tea.2009.068420109057
- 69. Hummitzsch K, Ricken AM, Kloß D, Erdmann S, Nowicki MS, Rothermel A, Robitzki AA, Spanel-Borowski K. Spheroids of granulosa cells provide an in vitro model for programmed cell death coupled to steroidogenesis. Differentiation. 2009;77(1):60–9; DOI:10.1016/J.DIFF.2008.09.002.10.1016/j.diff.2008.09.00219281765
- 70. Becker J, Walz A, Daube S, Keck C, Pietrowski D. Distinct responses of human granulosa lutein cells after hCG or LH stimulation in a spheroidal cell culture system. Mol Reprod Dev. 2007;74(10):1312–6; DOI:10.1002/MRD.20696.10.1002/mrd.2069617290424
- 71. Yadav M, Agrawal H, Pandey M, Singh D, Onteru SK. Three-dimensional culture of buffalo granulosa cells in hanging drop mimics the preovula-tory follicle stage. J Cell Physiol. 2018;233(3):1959–70; DOI:10.1002/JCP.25909.10.1002/jcp.2590928294325
- 72. Pandey M, Singh S, Yadav M, Singh D, Onteru SK. Transcriptome analysis of buffalo granulosa cells in three dimensional culture systems. Mol Re-prod Dev. 2021;88(4):287–301; DOI:10.1002/mrd.23465.10.1002/mrd.2346533734523
- 73. Green LJ, Shikanov A. In vitro culture methods of preantral follicles. Theriogenology. 2016;86(1):229–38; DOI:10.1016/J.THERIOGENOLOGY.2016.04.036.10.1016/j.theriogenology.2016.04.03627173961
- 74. West ER, Shea LD, Woodruff TK. Engineering the follicle microenvironment. Semin Reprod Med. 2007;25(4):287–99; DOI:10.1055/S-2007-980222.10.1055/s-2007-980222264840217594609
- 75. Adam AAG, Takahashi Y, Katagiri S, Nagano M. In vitro culture of mouse preantral follicles using membrane inserts and developmental competence of in vitro ovulated oocytes. J Reprod Dev. 2004;50(5):579–86; DOI:10.1262/JRD.50.579.10.1262/jrd.50.57915514465
- 76. Choi JK, Agarwal P, He X. In Vitro Culture of Early Secondary Preantral Follicles in Hanging Drop of Ovarian Cell-Conditioned Medium to Obtain MII Oocytes from Outbred Deer Mice. Tissue Eng Part A. 2013;19(23–24):2626; DOI:10.1089/TEN.TEA.2013.0055.10.1089/ten.tea.2013.0055
- 77. Kreeger PK, Deck JW, Woodruff TK, Shea LD. The in vitro regulation of ovarian follicle development using alginate-extracellular matrix gels. Biomaterials. 2006;27(5):714–23; DOI:10.1016/J.BIOMATERIALS.2005.06.016.10.1016/j.biomaterials.2005.06.016
- 78. Woodruff TK, Shea LD. The role of the extracellular matrix in ovarian follicle development. Reprod Sci. 2007;14(8 Suppl):6; DOI:10.1177/1933719107309818.10.1177/1933719107309818
- 79. Jones ASK, Shikanov A. Follicle development as an orchestrated signaling network in a 3D organoid. J Biol Eng. 2019;13(1):1–12; DOI:10.1186/S13036-018-0134-3/FIGURES/4.
- 80. Healy MW, Dolitsky SN, Villancio-Wolter M, Raghavan M, Tillman AR, Morgan NY, Decherney AH, Park S, Wolff EF. Creating an artificial 3-dimensional ovarian follicle culture system using a microfluidic system. Micromachines. 2021;12(3):1–15; DOI:10.3390/MI12030261.10.3390/mi12030261
- 81. Picton HM, Harris SE, Muruvi W, Chambers EL. The in vitro growth and maturation of follicles. Reproduction. 2008;136(6):703-15; DOI:10.1530/REP-08-0290.10.1530/REP-08-0290
- 82. Gomes JE, Correia SC, Gouveia-Oliveira A, Cidadão AJ, Plancha CE. Three-dimensional environments preserve extracellular matrix compartments of ovarian follicles and increase FSH-dependent growth. Mol Reprod Dev. 1999;54(2):163–72; DOI:https://doi.org/10.1002/(SICI)1098-2795(199910)54:2<163::AID-MRD8>3.0.CO;2-4.10.1002/(SICI)1098-2795(199910)54:2<163::AID-MRD8>3.0.CO;2-4
- 83. Smith RM, Woodruff TK, Shea LD. Designing follicle–environment interactions with biomaterials. Cancer Treat Res. 2010;156:11; DOI:10.1007/978-1-4419-6518-9_2.10.1007/978-1-4419-6518-9_2
- 84. Heise M, Koepsel R, Russell AJ, McGee EA. Calcium alginate microencapsulation of ovarian follicles impacts FSH delivery and follicle morphology 2005;3(1):1–8.
- 85. Shikanov A, Xu M, Woodruff TK, Shea LD. Interpenetrating fibrin-alginate matrices for in vitro ovarian follicle development. Biomaterials. 2009;30(29):5476; DOI:10.1016/J.BIOMATERIALS.2009.06.054.10.1016/j.biomaterials.2009.06.054
- 86. Joo S, Oh SH, Sittadjody S, Opara EC, Jackson JD, Lee SJ, Yoo JJ, Atala A. The effect of collagen hydrogel on 3D culture of ovarian follicles 2016;11(6); DOI:10.1088/1748-6041/11/6/065009.10.1088/1748-6041/11/6/065009
- 87. Desai N, Abdelhafez F, Calabro A, Falcone T. Three dimensional culture of fresh and vitrified mouse pre-antral follicles in a hyaluronan-based hydrogel: a preliminary investigation of a novel biomaterial for in vitro follicle maturation. Reprod Biol Endocrinol. 2012;10; DOI:10.1186/1477-7827-10-29.10.1186/1477-7827-10-29
- 88. Zhu J. Bioactive modification of poly(ethylene glycol) hydrogels for tissue engineering. Biomaterials. 2010;31(17):4639–56; DOI:10.1016/J.BIOMATERIALS.2010.02.044.10.1016/j.biomaterials.2010.02.044
- 89. Mendez U, Zhou H, Shikanov A. Synthetic PEG hydrogel for engineering the environment of ovarian follicles. Methods Mol Biol. 2018;1758:115–28; DOI:10.1007/978-1-4939-7741-3_9.10.1007/978-1-4939-7741-3_929679326
- 90. Szczepańska MA, Jagodziński PP, Wender-Ożegowska E. The effect of endometrioma on ovarian reserve. J Med Sci. 2017;86(3):237–9; DOI:10.20883/JMS.2017.201.10.20883/jms.2017.201
- 91. Xu F, Lawson MS, Bean Y, Ting AY, Pejovic T, De Geest K, Moffitt M, Mitalipov SM, Xu J. Matrix-free 3D culture supports human follicular development from the unilaminar to the antral stage in vitro yielding morphologically normal metaphase II oocytes. Hum Reprod. 2021;36(5):1326–38; DOI:10.1093/humrep/deab003.10.1093/humrep/deab003860017633681988
- 92. Ophir L, Yung Y, Maman E, Rubinstein N, Yerushalmi GM, Haas J, Barzilay E, Hourvitz A. Establishment and validation of a model for non-luteinized human mural granulosa cell culture. Mol Cell Endocrinol. 2014;384(1–2):165–74; DOI:10.1016/J.MCE.2014.01.018.10.1016/j.mce.2014.01.01824508664