Literature DB >> 26711701

The base medium affects ultrastructure and survival of bovine preantral follicles cultured in vitro.

Carolina Rodriguez Jimenez1, Valdevane Rocha Araújo2, Jurandy Mauro Penitente-Filho3, Jovana Luiza de Azevedo3, Renata Gomes Silveira3, Ciro Alexandre Alves Torres3.   

Abstract

The aim of this study was to determine the effectiveness of minimum essential medium alpha modification (α-MEM), tissue culture medium 199 (TCM-199), and McCoy's medium (McCoy's) on IVC of preantral follicles included in the bovine ovarian cortex (in situ). Bovine ovarian fragments were cultured in α-MEM, TCM-199, or McCoy supplemented ((+)) with glutamine, insulin, transferrin, selenium, ascorbic acid, BSA, penicillin, streptomycin, and HEPES buffer in 24-well plates, at 37 °C and 5% CO2 for 1 or 7 days. The morphology of follicles, normal, primordial and development (primary and secondary), as well as viability and morphometric variables of follicles and oocytes were assessed. The morphology and morphometry of preantral follicles were analyzed by ANOVA followed by the Tukey and Dunnett tests, and viability variables were determined by the chi-square test. The results showed that TCM-199(+) reduced significantly (P < 0.05) the percentage of morphologically normal and viable follicles after 7 days of culture compared to the control. Similar results were observed in McCoy(+), in which the percentage of viable follicles after 7 days of culture was significantly lower (P < 0.05) than in the control. However, it was similar (P > 0.05) between α-MEM(+) and TCM-199(+). Moreover, follicular diameters in McCoy(+) and TCM-199(+) were significantly smaller (P < 0.05) than in control and α-MEM(+) after 7 days of culture. In addition, the ultrastructure of preantral follicles was similar between the control and α-MEM(+) after 7 days of culture. In conclusion, α-MEM(+) showed to be the most effective medium to preserve morphology, morphometry and ultrastructure of bovine preantral follicles, ensuring their viability and growth after in situ culture.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Folliculogenesis; In situ; McCoy; Minimum essential medium alpha modification; Oocyte; Tissue culture medium 199

Mesh:

Substances:

Year:  2015        PMID: 26711701     DOI: 10.1016/j.theriogenology.2015.11.007

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  5 in total

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Authors:  Marilu Constantino Max; Camila Bizarro-Silva; Isabela Búfalo; Suellen Miguez González; Andressa Guidugli Lindquist; Roberta Garbelini Gomes; Thales Ricardo Rigo Barreiros; Lívia Aires Lisboa; Fábio Morotti; Marcelo Marcondes Seneda
Journal:  In Vitro Cell Dev Biol Anim       Date:  2018-10-03       Impact factor: 2.416

2.  Advances in in vitro folliculogenesis in domestic ruminants.

Authors:  José Ricardo de Figueiredo; Jesús Cadenas; Laritza Ferreira de Lima; Regiane Rodrigues Santos
Journal:  Anim Reprod       Date:  2020-05-22       Impact factor: 1.807

3.  Analysing culture methods of frozen human ovarian tissue to improve follicle survival.

Authors:  Briet D Bjarkadottir; Charlotte A Walker; Muhammad Fatum; Sheila Lane; Suzannah A Williams
Journal:  Reprod Fertil       Date:  2021-03-23

4.  Follicle-stimulating hormone mediates the consumption of serum-derived glycogen by bovine cumulus-oocyte complexes during in vitro maturation.

Authors:  Ludymila F Cantanhêde; Cristiane T Santos-Silva; Marcelo T Moura; José C Ferreira-Silva; Júnior M B Oliveira; Daniel N A Gonçalves; Álvaro A C Teixeira; Valéria Wanderley-Teixeira; Marcos A L Oliveira
Journal:  Vet World       Date:  2021-09-24

5.  Control of growth and development of preantral follicle: insights from in vitro culture.

Authors:  José Ricardo de Figueiredo; Laritza Ferreira de Lima; José Roberto Viana Silva; Regiane Rodrigues Santos
Journal:  Anim Reprod       Date:  2018-08-03       Impact factor: 1.810

  5 in total

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