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Original Article

Heat stress disrupts mitochondrial dynamics and ATF5 expression during porcine oocyte maturation

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  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Journal of Animal Reproduction and Biotechnology 바로가기
  • 통권
    Volume. 40 No. 4 (2025.12)바로가기
  • 페이지
    pp.207-219
  • 저자
    Seul-Gi Yang, Hyo-Jin Park, Hun-Wook Ha, Deog-Bon Koo
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A479683

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초록

영어
Background: In mammals, DRP1 is a key regulator of mitochondrial fission during mitochondrial dynamics, whereas ATF5 promotes the mitochondrial unfolded protein response (UPRmt). Both pathways are essential for maintaining cellular homeostasis and protecting oocytes and embryos from external stressors. However, the relationship between ATF5 expression and DRP1 under heat stress conditions during porcine oocyte maturation remains unclear. Methods: In this study, we investigated the mitochondrial dynamics and ATF5 expression in porcine oocytes exposed to heat stress during in vitro maturation (IVM). Protein and gene expression levels were assessed using immunofluorescence staining, Western blotting, and quantitative PCR. Results: During IVM, both DRP1 and ATF5 expression were increased (p < 0.01) significantly. In contrast, heat stress markedly impaired (p < 0.05) meiotic progression and cumulus cell expansion. Mitochondrial dynamics were disrupted (p < 0.05), as fission and fusion markers displayed reciprocal changes relative to those in controls. Concomitantly, the expression of ATF proteins was significantly reduced (p < 0.01) under heat stress. Heat-stressed oocytes also exhibited decreased (p < 0.05) expression of genes involved in antioxidant defense and NAD metabolism, whereas autophagy- and apoptosis-related transcripts were significantly upregulated (p < 0.05). At the blastocyst stage, embryos derived from heat-stressed oocytes exhibited nuclear localization of the UPR-associated transcription factors ATF4, CHOP, and ATF5. Conclusions: Collectively, our findings suggest that heat stress disrupts mitochondrial dynamics and ATF5 expression during porcine oocyte maturation while the UPRmt pathway remains active during early embryonic development to mitigate heat-induced cellular damage.

목차

ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
Chemicals and animals
Oocyte collection and in vitro maturation (IVM)
In vitro fertilization and culture (IVF and IVC)
Orcein staining and assessment of cumulus cell expansion
Immunofluorescence (IF) staining
Western blotting
Quantitative PCR (qPCR) analysis
Statistical analysis
RESULTS
DRP1 and ATF5 expression during IVM of porcine oocytes and heat-stress effects on meiotic progression and cumulus cell expansion
Changes in the expression of mitochondrial-related proteins and genes under heat stress
Localization of UPRmt-related proteins in blastocysts derived from heat-stressed oocytes
DISCUSSION
CONCLUSION
REFERENCES

저자

  • Seul-Gi Yang [ Department of Companion Animal Industry, Daegu University/DU Center for Infertility, Daegu University, Gyeongsan 38453, Korea ]
  • Hyo-Jin Park [ DU Center for Infertility, Daegu University/Department of Biotechnology, Daegu University, Gyeongsan 38453, Korea ]
  • Hun-Wook Ha [ DU Center for Infertility, Daegu University/Department of Biotechnology, Daegu University, Gyeongsan 38453, Korea ]
  • Deog-Bon Koo [ Department of Companion Animal Industry, Daegu University/ DU Center for Infertility, Daegu University/ Department of Biotechnology, Daegu University, Gyeongsan 38453, Korea ] Corresponding Author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국동물생명공학회(구 한국동물번식학회) [The Korean Society of Animal Reproduction and Biotechnology]
  • 설립연도
    1976
  • 분야
    농수해양>축산학
  • 소개
    동물번식생리학, 동물생명공학, 수의학, 인공수정 및 수정란이식을 이용한 동물개량에 관한 이론과 기술의 발전을 통해 학계, 연구계, 산업계 및 양축가 상호간의 협력을 도모함으로써 동물과학발전 및 사회일반의 이익에 기여 한다는 목적을 위해 노력해 나가겠습니다.

간행물

  • 간행물명
    Journal of Animal Reproduction and Biotechnology
  • 간기
    계간
  • pISSN
    2671-4639
  • eISSN
    2671-4663
  • 수록기간
    2019~2026
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / Journal of Animal Reproduction and Biotechnology Volume. 40 No. 4

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