In vitro steroid production by triploid ovarian follicles

2003 ◽  
Vol 133 (3) ◽  
pp. 279-286 ◽  
Author(s):  
D. Schafhauser-Smith ◽  
T.J. Benfey
1977 ◽  
Vol 73 (1) ◽  
pp. 59-65 ◽  
Author(s):  
E. V. YOUNGLAI

SUMMARY Follicles were isolated from rabbits before and after mating and the effects of LH on steroidogenesis were studied using an incubation technique. Before mating testosterone was the major steroid produced in response to LH. Mating or administration of ovine LH in vivo caused the follicles to produce mainly progesterone and these follicles were refractory to LH in vitro. Up to 72 h after mating, LH would stimulate follicles to produce progesterone. At 96 h after mating, the testosterone response to LH was again manifest. These results suggest that the responsiveness of rabbit follicles to LH is dependent on the endocrine status of the animal when the ovaries were removed.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shauna Kehoe ◽  
Katarina Jewgenow ◽  
Paul R. Johnston ◽  
Susan Mbedi ◽  
Beate C. Braun

AbstractIn vitro growth (IVG) of dormant primordial ovarian follicles aims to produce mature competent oocytes for assisted reproduction. Success is dependent on optimal in vitro conditions complemented with an understanding of oocyte and ovarian follicle development in vivo. Complete IVG has not been achieved in any other mammalian species besides mice. Furthermore, ovarian folliculogenesis remains sparsely understood overall. Here, gene expression patterns were characterised by RNA-sequencing in primordial (PrF), primary (PF), and secondary (SF) ovarian follicles from Felis catus (domestic cat) ovaries. Two major transitions were investigated: PrF-PF and PF-SF. Transcriptional analysis revealed a higher proportion in gene expression changes during the PrF-PF transition. Key influencing factors during this transition included the interaction between the extracellular matrix (ECM) and matrix metalloproteinase (MMPs) along with nuclear components such as, histone HIST1H1T (H1.6). Conserved signalling factors and expression patterns previously described during mammalian ovarian folliculogenesis were observed. Species-specific features during domestic cat ovarian folliculogenesis were also found. The signalling pathway terms “PI3K-Akt”, “transforming growth factor-β receptor”, “ErbB”, and “HIF-1” from the functional annotation analysis were studied. Some results highlighted mechanistic cues potentially involved in PrF development in the domestic cat. Overall, this study provides an insight into regulatory factors and pathways during preantral ovarian folliculogenesis in domestic cat.


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