PRONUCLEAR SYNCHRONIZATION AND NUCLEAR MORPHOLOGY OF MATURE AND IN VITRO MATURED OOCYTES IN THE RAT: AN ULTRASTRUCTURAL STUDY

2005 ◽  
Vol 41 (8) ◽  
pp. 272 ◽  
Author(s):  
M. CINCIK ◽  
B. BAYKAL ◽  
S. ZETEROGLU ◽  
G. ONALAN ◽  
S. T. CEYHAN ◽  
...  
2010 ◽  
Vol 106 (6) ◽  
pp. 1465-1469 ◽  
Author(s):  
Juliana Quero Reimão ◽  
Noemi Nosomi Taniwaki ◽  
André Gustavo Tempone

Parasitology ◽  
1981 ◽  
Vol 82 (1) ◽  
pp. 55-62 ◽  
Author(s):  
M. A. Ouaissi ◽  
A. Haque ◽  
A. Capron

SUMMARYThe in vitro interaction between rat peritoneal macrophages and Dipetalonema viteae microfilariae in the presence of amicrofilaraemic rat immune serum was studied by transmission electron microscopy. The probable sequence of events leading to the killing of D. viteae microfilaria by macrophages is as follows. (a) Rat peritoneal macrophages in the presence of amicrofilaraemic rat immune serum adhere to the parasite surface, (b) the macrophages extend their pseudopodia around the parasite, (c) the ‘lysosome-like’ granules discharge their contents on to the parasite surface, (d) the lytic activity of these products begins at the parasite surface and (e) subsequent breaking of the microfilarial cuticle occurs, exposing the parasite intracellular material.


2003 ◽  
Vol 98 (7) ◽  
pp. 905-908 ◽  
Author(s):  
Wolfan Araque ◽  
Emilia E Barrios ◽  
Pedro Rodríguez ◽  
Víctor S Delgado ◽  
Héctor J Finol

In Vitro ◽  
1984 ◽  
Vol 20 (3) ◽  
pp. 216-228 ◽  
Author(s):  
Frederick B. Merk ◽  
Paul W. L. Kwan ◽  
Stanley Spilman ◽  
Louis Terracio ◽  
William H. J. Douglas

Cancer ◽  
1976 ◽  
Vol 37 (1) ◽  
pp. 327-337 ◽  
Author(s):  
William R. Markesbery ◽  
William H. Brooks ◽  
Larry Milsow ◽  
Richard H. Mortara

1986 ◽  
Vol 31 (10) ◽  
pp. 703-706 ◽  
Author(s):  
T. Takahashi ◽  
N. Kurihara ◽  
K. Takahashi ◽  
M. Kumegawa

Bone ◽  
1985 ◽  
Vol 6 (6) ◽  
pp. 484-485
Author(s):  
H.C. Tenenbaum ◽  
D. Holmyard ◽  
K. Palangio ◽  
K.P.H. Pritzker

2003 ◽  
Vol 15 (4) ◽  
pp. 223 ◽  
Author(s):  
Muhammad Rizwan Yousaf ◽  
Kazim Raza Chohan

The nuclear morphology, diameter and in vitro meiotic competence of buffalo oocytes was compared relative to follicle size. Cumulus–oocyte complexes (COCs) were collected from 1–<2, 2–<3, 3–<4, 4–<6 and 6–<8 mm follicles from abattoir ovaries. Cumulus cells were removed using 3 mg mL−1 hyaluronidase in saline and repeated pipetting. Denuded oocytes were measured, fixed in 3% glutaraldehyde, stained with 4,6-diamidoino-2-phenylindole and evaluated for nuclear morphology, namely the stage of germinal vesicle (GV) development before in vitro maturation (IVM). The COCs from >2-mm follicles were matured in vitro in their respective size groups for 24 h in Medium 199 supplemented with 10 μg mL−1 follicle-stimulating hormone, 10 μg mL−1 luteinizing hormone, 1.5 μg mL−1 oestradiol, 75 μg mL−1 streptomycin, 100 IU mL−1 penicillin, 10 mM HEPES and 10% fetal bovine serum. Matured oocytes were fixed, stained and evaluated for GV status and meiotic development. The number of oocytes collected from follicles 1–<8 mm in diameter averaged 1.82 per ovary. Oocytes from follicles 1–<2 mm (107.7 ± 1.6 μm), 2–<3 mm (108 ± 1.1 μm) and 3–<4 mm (114.6 ± 1.3 μm) in diameter were smaller in diameter (P < 0.05) than oocytes from follicles 4–<6 mm (124.4 ± 1.3 μm) and 6–<8 mm (131.9 ± 1.4 μm) in diameter. A majority of oocytes (P < 0.05) from <4-mm follicles was at the initial stages of GV development (GV-I, II and III), whereas oocytes from 4–<6- and 6–<8-mm follicles were at the final stages of GV-IV (35.0 and 21.6% respectively) and GV-V (49.1 and 67.5% respectively). Poor IVM rates of 32.0% and 32.7% to metaphase (M)-II were observed for oocytes isolated from 2–<3- and 3–<4-mm follicles, respectively, whereas significantly (P < 0.05) more oocytes from 4–<6- and 6–<8-mm follicles reached M-II (67.1% and 79.1% respectively). In conclusion, buffalo oocytes displayed a size-dependent ability to undergo meiotic maturation and we suggest that oocytes from >4-mm follicles should be considered in buffalo in vitro fertilization systems for better results.


Sign in / Sign up

Export Citation Format

Share Document