Cellular and Dynamic Aspects of Oocyte Growth in Teleosts

1981 ◽  
Vol 21 (2) ◽  
pp. 325-343 ◽  
Author(s):  
ROBIN A. WALLACE ◽  
KELLY SELMAN
Keyword(s):  
2014 ◽  
Author(s):  
Akihiko Sakashita ◽  
Yosuke Iseki ◽  
Mei Nakajima ◽  
Takuya Wakai ◽  
Hisato Kobayashi ◽  
...  

Zygote ◽  
2008 ◽  
Vol 16 (3) ◽  
pp. 239-247 ◽  
Author(s):  
T. Metoki ◽  
H. Iwata ◽  
M. Itoh ◽  
M. Kasai ◽  
A. Takajyo ◽  
...  

SummaryWe examined the effect of supplementing the culture medium with follicular fluid (FF) on the growth of porcine preantral follicles and oocytes. Firstly, preantral follicles were retrieved from ovaries and then FF was collected from all antral follicles that were 2–7 mm in diameter (AFF), which included large follicles of 4–7 mm in diameter (LFF) and small follicles of 2–3 mm in diameter (SFF). When preantral follicles with a diameter of 250 μm were cultured in medium containing AFF, the growth of follicles and oocytes was greater than when follicles were cultured in medium containing fetal calf serum (FCS). When this growth-promoting effect in AFF was compared for LFF and SFF, the LFF were shown to be significantly more effective than SFF. This LFF effect was lost, however, when the concentration of LFF in the medium was decreased from 5% to 0.5% or when LFF were heat treated (60 °C for 30 min) or trypsin was added. In contrast, a decrease in SFF concentration from 5% to 0.5% and heat treatment of the SFF enhanced preantral follicle growth. Furthermore, proteins obtained from LFF that had molecular weights greater than 10 kDa (LFF > 10 kDa) had similar, but relatively reduced, growth-promoting properties. The remaining three LFF protein fractions (<10 kDa or <100 kDa or >100 kDa), however, did not have these growth-promoting properties. In conclusion, the supplementation of medium with LFF, rather than serum, enhanced preantral follicle and oocyte growth. Factors that enhanced follicle development in LFF and factors that suppressed follicle development in SFF were proteins and these LFF factors ranged in size from 10 kDa to over 100 kDa.


Development ◽  
1991 ◽  
Vol 112 (1) ◽  
pp. 317-326
Author(s):  
M. Caizergues-Ferrer ◽  
C. Mathieu ◽  
P. Mariottini ◽  
F. Amalric ◽  
F. Amaldi

Fibrillarin is one of the protein components that together with U3 snRNA constitute the U3 snRNP, a small nuclear ribonucleoprotein particle involved in ribosomal RNA processing in eucaryotic cells. Using an antifibrillarin antiserum for protein detection and a fibrillarin cDNA and a synthetic oligonucleotide complementary to U3 snRNA as hybridization probes, the expression of these two components has been studied during Xenopus development. Fibrillarin mRNA is accumulated early in oogenesis, like many other messengers, and translated during oocyte growth. Fibrillarin protein is thus progressively accumulated throughout oogenesis to be assembled with U3 snRNA and used for ribosome production in the amplified nucleoli. After fertilization, the amount of U3 snRNA decreases while the maternally accumulated fibrillarin mRNA is maintained and utilized to produce more protein. After the mid-blastula transition, stored fibrillarin is assembled with newly synthesized U3 snRNA and becomes localized in the prenucleolar bodies and reforming nucleoli.


1994 ◽  
Vol 161 (1) ◽  
pp. 194-205 ◽  
Author(s):  
Alan I. Packer ◽  
Ying Chang Hsu ◽  
Peter Besmer ◽  
Rosemary F. Bachvarova
Keyword(s):  

Author(s):  
Fabio Castaño Rivera ◽  
Julián Botero Arango

Two groups of adult Mutton snapper fish Lutjanus analis captured in the wild, each one of three females and four males, were kept during eight months under controlled temperature and photoperiod conditions in the lab in order to stimulate their sexual maturation which was in a state of latency because of the effects of confinement. The first group was maintained under an artificial cycle with temperature manipulation and the second under a control cycle, in which this parameter was left at natural conditions. Every two months blood samples from all females were taken for the analysis of plasma testosterone (T) and oestradiol (E2) levels, taking ovarian biopsies simultaneously to register the mean diameter of the oocytes. After six months, a significative increase in the mean diameter of the oocytes of the three females of the artificial cycle was observed, with coincidence and statistic relationship with the increase in the T and E2 (r = 0.62 y 0.82 respectively). No oocyte growth was observed in the females under the control cycle. In both, artificial and control cycles, T and E2 levels showed a close relationship with photoperiod (r = 0.84 y r = 0.61) while temperature showed a lower or non significant relationship (r = 0.40 y r = 0.20). Statistical differences (P<0.1) were found between the condition factors of the two groups, while the sexual steroids didn’t show any differences between them. The present work constitutes the first report on the analysis of sexual steroid levels during the gonadal maturation process in fish of the Family Lutjanidae kept under an artificial conditioning cycle.


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