A novel follicle culture system markedly increases follicle volume, cell number and oestradiol secretion
Wycherley, G Downey, D Kane, M T Hynes, A C
Wycherley, G
Downey, D
Kane, M T
Hynes, A C
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Publication Date
2004-06-01
Type
Article
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Citation
Wycherley, G; Downey, D; Kane, M T; Hynes, A C (2004). A novel follicle culture system markedly increases follicle volume, cell number and oestradiol secretion. Reproduction 127 (6), 669-677
Abstract
This study reports a novel, simple method for culture of mouse follicles which results in follicles with cell numbers similar to in vivo fully grown follicles. Using this method, follicles (1180-240 mum in diameter) were cultured in a 100 mul inverted drop of medium without oil and compared with culture in upright drops with and without a mineral oil overlay. Follicles, isolated from C57BL/6 x CBA/ca crossbred and MF1 inbred mice, were cultured individually at 37degreesC in 96-well round-bottomed suspension cell tissue culture plates for 6 days. Follicles grown in the inverted drop culture system reached a markedly higher final diameter (means+/- S.E.M.; 471 +/- 6.0 mum) as compared with the upright with oil (363 +/- 2.7 mum) and without oil (358 +/- 4.0) systems. There was no significant effect of mouse strain on follicle diameter. Follicular secretion of oestradiol and lactate into the medium was measured on days 2, 4 and 6 of culture. Secretion of oestradiol per follicle on day 6 was 2.49 +/- 0.45 ng in the inverted and 0.90 +/- 0.17 ng in the upright without oil system (P < 0.001). Follicular secretion of lactate on a per unit of follicle volume basis remained constant in the inverted system over days 2, 4 and 6 and was less (P < 0.001) than secretion in both the upright with and without oil systems. Follicle cell proliferation was markedly increased in the inverted as compared with the upright with oil system; the increases in cell numbers were significant on day 3 (P < 0.01) and on all subsequent days (P < 0.001). These results are discussed in relation to the supply of oxygen to the follicle in culture.
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Publisher
BioScientifica
Publisher DOI
10.1530/rep.1.00040
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland