The challenge of ovarian tissue culture: 2D versus 3D culture

被引:15
作者
Pais, Ana Sofia [1 ,2 ,3 ,4 ,5 ]
Reis, Sandra [1 ,6 ,7 ]
Laranjo, Mafalda [3 ,4 ,5 ]
Caramelo, Francisco [3 ,4 ,5 ]
Silva, Fatima [8 ]
Botelho, Maria Filomena [3 ,4 ,5 ]
Almeida-Santos, Teresa [1 ,5 ,6 ,9 ]
机构
[1] Ctr Hosp & Univ Coimbra CHUC, Reprod Med Unit, EPE, Coimbra, Portugal
[2] Univ Coimbra, Fac Med, Obstet Dept, Coimbra, Portugal
[3] Univ Coimbra, Coimbra Inst Clin & Biomed Res iCBR, Area Environm Genet & Oncobiol CIMAGO, Biophys Inst,Fac Med, Coimbra, Portugal
[4] Univ Coimbra, Ctr Innovat Biomed & Biotechnol CIBB, Coimbra, Portugal
[5] Clin Acad Ctr Coimbra CACC, Coimbra, Portugal
[6] Univ Coimbra, Ctr Neurosci & Cell Biol CNC, CIBB, Azinhaga Santa Comba,Celas, Coimbra, Portugal
[7] Univ Coimbra, PhD Programme Expt Biol & Biomed, IIIUC Inst Interdisciplinary Res, Coimbra, Portugal
[8] Ctr Hosp & Univ Coimbra CHUC, Pathol Unit, EPE, Coimbra, Portugal
[9] Univ Coimbra, Fac Med, Coimbra, Portugal
关键词
Alginate; Ovary; Fertility preservation; Tissue culture techniques; PRE-ANTRAL FOLLICLES; IN-VITRO CULTURE; CELL-DEATH; ALGINATE; GROWTH; SURVIVAL; CRYOPRESERVATION; TRANSPLANTATION; EXPRESSION; VIABILITY;
D O I
10.1186/s13048-021-00892-z
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Cryopreservation of ovarian tissue is a powerful technique for preserving female fertility, as it can restore fertility and endocrine function. To increase the longevity of the transplant and decrease the risk of reimplantation of neoplastic cells, several studies have been carried out with culture of ovarian tissue. The aim of this study was to compare a conventional (2D) culture with an alginate matrix three-dimensional (3D) model for ovarian tissue culture. Results The ovarian tissue culture within the alginate matrix (3D) was similar to 2D culture, regarding follicular density and cell apoptosis in follicles and stroma. The proliferation rate remained stable in both models for follicles, but for stromal cell proliferation it decreased only in 3D culture (p = 0.001). At 24 h of culture, cytotoxicity was lower in the 3D model (p = 0.006). As culture time increased, cytotoxicity seemed similar. Degradation of the tissue was suggested by the histological score analysis of tissue morphology after 72 h of culture. Tissue injury was greater (p = 0.01) in 3D culture due to higher interstitial oedema (p = 0.017) and tissue necrosis (p = 0.035). Conclusion According to our results, 3D culture of ovarian tissue has no advantage over 2Dculture; it is more time consuming and difficult to perform and has worse reproducibility.
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页数:12
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