Your browser doesn't support javascript.
loading
In vitro maturation using porcine follicular fluid-derived exosomes as an alternative to the conventional method.
No, Jingu; Kim, Seokho; Lee, Haesun; Kwak, Taeuk; Lim, Jihyeon; Lee, Poongyeon; Oh, Keonbong; Lee, Seunghoon.
Afiliación
  • No J; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Kim S; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Lee H; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Kwak T; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Lim J; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Lee P; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Oh K; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea.
  • Lee S; National Institute of Animal Science, Wanju, Jeonbuk, 55365, Republic of Korea. Electronic address: sage@korea.kr.
Theriogenology ; 230: 37-45, 2024 Aug 29.
Article en En | MEDLINE | ID: mdl-39243630
ABSTRACT
Extracellular vesicles, also known as exosomes, influence numerous cellular functions by regulating different signaling pathways. However, their role in animal reproduction remains understudied. This study aimed to evaluate the effects of porcine follicular fluid-derived exosomes (pff-Exos) on porcine oocyte in vitro maturation and parthenogenetic embryo development. We obtained pff-Exos through mixed-method ultracentrifugation and size-exclusion chromatography. Transmission electron microscopy revealed an increase in the expression of exosome markers in the first four of thirteen fractions. The number of pff-Exo was 2.2 × 106 particles per microliter. The highest maturation rate of porcine oocytes treated with pff-Exo was observed with 1.1 × 107 particles of pff-Exo in the absence of porcine follicular fluid (pFF) culture conditions. Moreover, increased expression of Gdf9 and Bmp15 was observed. The developmental rate was the highest upon treatment with 1.1 × 107 particles of pff-Exo, which increased the total cell number in blastocysts. Embryonic development to the 2-cell stage was similar between the control and pff-Exo groups; however, development to the 4-cell stage and blastocyst was significantly increased in the pff-Exo group (61.6 ± 6.08 % and 29.72 ± 1.41 %, respectively; P < 0.05) compared with that in the control group (42.0 ± 5.19 % and 18.14 ± 1.78 %, respectively). The expression levels of Oct4, Sox2, Bcl2, Elf4, and Gcn5 significantly increased at the pff-Exo 2-cell stage, whereas those of Bax, Hdac1, Hdac6, and Sirt6 decreased. Specifically, the Oct4, Sox2, Elf4, Gcn5, and Hdac6 levels remained stable in pff-Exo 4-cell embryos, whereas those of p53 and Hat1 were reduced and increased, respectively. Treatment with pffExos significantly increased H3K9 and H3K14 acetylation levels. These results demonstrate that pff-Exo affects the in vitro maturation of porcine oocytes and early embryonic development by regulating gene expression.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Theriogenology Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Theriogenology Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos