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Effect of rapamycin treatment during post‐activation and/or in vitro culture on embryonic development after parthenogenesis and in vitro fertilization in pigs

Reproduction in domestic animals : Zuchthygiene, v.52 no.5, 2017년, pp.741 - 748  

Elahi, F (Laboratory of Theriogenology, College of Veterinary Medicine, Kangwon National University, Chuncheon, Korea) ,  Lee, H (Laboratory of Theriogenology, College of Veterinary Medicine, Kangwon National University, Chuncheon, Korea) ,  Lee, J (Laboratory of Theriogenology, College of Veterinary Medicine, Kangwon National University, Chuncheon, Korea) ,  Lee, ST (Division of Applied Animal Science, College of Animal Life Science, Kangwon National University, Chuncheon, Korea) ,  Park, CK (Division of Applied Animal Science, College of Animal Life Science, Kangwon National University, Chuncheon, Korea) ,  Hyun, S‐H (Laboratory of Veterinary Embryology and Biotechnology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Korea) ,  Lee, E (Laboratory of Theriogenology, College of Veterinary Medicine, Kangwon Natio)

Abstract AI-Helper 아이콘AI-Helper

ContentsThis study investigated the effects of early induction of autophagy on embryonic development in pigs. For this, oocytes or embryos were treated with an autophagy inducer, rapamycin (RP), during post‐activation (Pa), in vitro fertilization (IVF) and/or in vitro culture (IVC). When parth...

주제어

참고문헌 (38)

  1. Abeydeera, L.R.. In vitro production of embryos in swine. Theriogenology, vol.57, no.1, 257-273.

  2. Alizadeh, Zohreh, Kageyama, Shun-Ichiro, Aoki, Fugaku. Degradation of maternal mRNA in mouse embryos: Selective degradation of specific mRNAs after fertilization. Molecular reproduction and development, vol.72, no.3, 281-290.

  3. Baehrecke, E H. Autophagic programmed cell death in Drosophila. Cell death and differentiation, vol.10, no.9, 940-945.

  4. Betthauser, Jeff, Forsberg, Erik, Augenstein, Monica, Childs, Lynette, Eilertsen, Kenneth, Enos, Joellyn, Forsythe, Todd, Golueke, Paul, Jurgella, Gail, Koppang, Richard, Lesmeister, Tiffany, Mallon, Kelly, Mell, Greg, Misica, Pavla, Pace, Marvin, Pfister-Genskow, Martha, Strelchenko, Nikolai, Voelker, Gary, Watt, Steven, Thompson, Simon, Bishop, Michael. Production of cloned pigs from in vitro systems. Nature biotechnology, vol.18, no.10, 1055-1059.

  5. Chan, Leo Li-Ying, Shen, Dee, Wilkinson, Alisha R., Patton, Wayne, Lai, Ning, Chan, Eric, Kuksin, Dmitry, Lin, Bo, Qiu, Jean. A novel image-based cytometry method for autophagy detection in living cells. Autophagy, vol.8, no.9, 1371-1382.

  6. DeRenzo, Cynthia, Seydoux, Geraldine. A clean start: degradation of maternal proteins at the oocyte-to-embryo transition. Trends in cell biology, vol.14, no.8, 420-426.

  7. Ferraro, Elisabetta, Cecconi, Francesco. Autophagic and apoptotic response to stress signals in mammalian cells. Archives of biochemistry and biophysics, vol.462, no.2, 210-219.

  8. Fingar, Diane C., Richardson, Celeste J., Tee, Andrew R., Cheatham, Lynn, Tsou, Christina, Blenis, John. mTOR Controls Cell Cycle Progression through Its Cell Growth Effectors S6K1 and 4E-BP1/Eukaryotic Translation Initiation Factor 4E. Molecular and cellular biology, vol.24, no.1, 200-216.

  9. Foster, Kathryn G., Fingar, Diane C.. Mammalian Target of Rapamycin (mTOR): Conducting the Cellular Signaling Symphony. The Journal of biological chemistry, vol.285, no.19, 14071-14077.

  10. Hong, J., Lee, E.. Intrafollicular amino acid concentration and the effect of amino acids in a defined maturation medium on porcine oocyte maturation, fertilization, and preimplantation development. Theriogenology, vol.68, no.5, 728-735.

  11. Kawamura, Nobuyuki, Sun-Wada, Ge-Hong, Aoyama, Minako, Harada, Akihiro, Takasuga, Shunsuke, Sasaki, Takehiko, Wada, Yoh. Delivery of endosomes to lysosomes via microautophagy in the visceral endoderm of mouse embryos. Nature communications, vol.3, 1071-.

  12. Kim, Young June, Ahn, Kwang Sung, Kim, Minjeong, Shim, Hosup. Comparison of potency between histone deacetylase inhibitors trichostatin A and valproic acid on enhancing in vitro development of porcine somatic cell nuclear transfer embryos. In vitro cellular & developmental biology. Animal, vol.47, no.4, 283-289.

  13. Journal of Animal Science Krisher R. L. 14 82 2004 The effect of oocyte quality on development 

  14. Lai, Liangxue, Kolber-Simonds, Donna, Park, Kwang-Wook, Cheong, Hee-Tae, Greenstein, Julia L., Im, Gi-Sun, Samuel, Melissa, Bonk, Aaron, Rieke, August, Day, Billy N., Murphy, Clifton N., Carter, David B., Hawley, Robert J., Prather, Randall S.. Production of α-1,3-Galactosyltransferase Knockout Pigs by Nuclear Transfer Cloning. Science, vol.295, no.5557, 1089-1092.

  15. Lee, Y., Lee, H., Park, B., Elahi, F., Lee, J., Lee, S. T., Park, C. K., Hyun, S. H., Lee, E.. Alpha-linolenic acid treatment during oocyte maturation enhances embryonic development by influencing mitogen-activated protein kinase activity and intraoocyte glutathione content in pigs1. Journal of animal science, vol.94, no.8, 3255-3263.

  16. Lee, Joohyeong, Park, Jong-Im, Yun, Jung Im, Lee, Yongjin, Yong, Hwanyul, Lee, Seung Tae, Park, Choon-Keun, Hyun, Sang-Hwan, Lee, Geun-Shik, Lee, Eunsong. Rapamycin treatment during in vitro maturation of oocytes improves embryonic development after parthenogenesis and somatic cell nuclear transfer in pigs. Journal of veterinary science, vol.16, no.3, 373-380.

  17. Levine, Beth, Klionsky, Daniel J. Development by Self-Digestion : Molecular Mechanisms and Biological Functions of Autophagy. Developmental cell, vol.6, no.4, 463-477.

  18. Li, L., Lu, X., Dean, J.. The maternal to zygotic transition in mammals. Molecular aspects of medicine, vol.34, no.5, 919-938.

  19. Luo, Shi-Ming, Ge, Zhao-Jia, Wang, Zhong-Wei, Jiang, Zong-Zhe, Wang, Zhen-Bo, Ouyang, Ying-Chun, Hou, Yi, Schatten, Heide, Sun, Qing-Yuan. Unique insights into maternal mitochondrial inheritance in mice. Proceedings of the National Academy of Sciences of the United States of America, vol.110, no.32, 13038-13043.

  20. 10.4161/cc.10.21.18128 

  21. Mizushima, Noboru, Komatsu, Masaaki. Autophagy: Renovation of Cells and Tissues. Cell, vol.147, no.4, 728-741.

  22. Othman, Ekhlas Qaid Gazem, Kaur, Gurjeet, Mutee, Ahmad Faisal, Tengku Muhammad, Tengku Sifzizul, Tan, Mei Lan. Immunohistochemical expression of MAP1LC3A and MAP1LC3B protein in breast carcinoma tissues. Journal of clinical laboratory analysis, vol.23, no.4, 249-258.

  23. Paffoni, A., Brevini, T.A.L., Gandolfi, F., Ragni, G.. Parthenogenetic Activation: Biology and Applications in the ART Laboratory. Placenta, vol.29, no.suppl2, 121-125.

  24. Pyo, Jong-Ok, Yoo, Seung-Min, Ahn, Hye-Hyun, Nah, Jihoon, Hong, Se-Hoon, Kam, Tae-In, Jung, Sunmin, Jung, Yong-Keun. Overexpression of Atg5 in mice activates autophagy and extends lifespan. Nature communications, vol.4, 2300-.

  25. Qu, Xueping, Zou, Zhongju, Sun, Qihua, Luby-Phelps, Kate, Cheng, Pengfei, Hogan, Robert N., Gilpin, Christopher, Levine, Beth. Autophagy Gene-Dependent Clearance of Apoptotic Cells during Embryonic Development. Cell, vol.128, no.5, 931-946.

  26. Rogers, Christopher S., Stoltz, David A., Meyerholz, David K., Ostedgaard, Lynda S., Rokhlina, Tatiana, Taft, Peter J., Rogan, Mark P., Pezzulo, Alejandro A., Karp, Philip H., Itani, Omar A., Kabel, Amanda C., Wohlford-Lenane, Christine L., Davis, Greg J., Hanfland, Robert A., Smith, Tony L., Samuel, Melissa, Wax, David, Murphy, Clifton N., Rieke, August, Whitworth, Kristin, Uc, Aliye, Starner, Timothy D., Brogden, Kim A., Shilyansky, Joel, McCray Jr., Paul B., Zabner, Joseph, Prather, Randall S., Welsh, Michael J.. Disruption of the CFTR Gene Produces a Model of Cystic Fibrosis in Newborn Pigs. Science, vol.321, no.5897, 1837-1841.

  27. SAKATANI, Miki, SUDA, Ikuo, OKI, Tomoyuki, KOBAYASHI, Shu-ichi, KOBAYASHI, Shuji, TAKAHASHI, Masashi. Effects of Purple Sweet Potato Anthocyanins on Development and Intracellular Redox Status of Bovine Preimplantation Embryos Exposed to Heat Shock. The Journal of reproduction and development, vol.53, no.3, 605-614.

  28. Shen, XingHui, Zhang, Na, Wang, ZhenDong, Bai, GuangYu, Zheng, Zhong, Gu, YanLi, Wu, YanShuang, Liu, Hui, Zhou, DongJie, Lei, Lei. Induction of autophagy improves embryo viability in cloned mouse embryos. Scientific reports, vol.5, 17829-.

  29. Shimada, Y., Kobayashi, H., Kawagoe, S., Aoki, K., Kaneshiro, E., Shimizu, H., Eto, Y., Ida, H., Ohashi, T.. Endoplasmic reticulum stress induces autophagy through activation of p38 MAPK in fibroblasts from Pompe disease patients carrying c.546G>T mutation. Molecular genetics and metabolism, vol.104, no.4, 566-573.

  30. Song, Bong-Seok, Kim, Ji-Su, Kim, Young-Hyun, Sim, Bo-Woong, Yoon, Seung-Bin, Cha, Jae-Jin, Choi, Seon-A, Yang, Hae-Jun, Mun, Seong-Eun, Park, Young-Ho, Jeong, Kang-Jin, Huh, Jae-Won, Lee, Sang-Rae, Kim, Sang-Hyun, Kim, Sun-Uk, Chang, Kyu-Tae. Induction of autophagy during in vitro maturation improves the nuclear and cytoplasmic maturation of porcine oocytes. Reproduction, fertility, and development, vol.26, no.7, 974-.

  31. Biology of Reproduction Song B. S. 1 87 8 2012 Induction of autophagy promotes preattachment development of bovine embryos by reducing endoplasmic reticulum stress 

  32. Sully, K, Akinduro, O, Philpott, M P, Naeem, A S, Harwood, C A, Reeve, V E, O'Shaughnessy, R F, Byrne, C. The mTOR inhibitor rapamycin opposes carcinogenic changes to epidermal Akt1/PKBα isoform signaling. Oncogene, vol.32, no.27, 3254-3262.

  33. Tseng, J.K., Tang, P.C., Ju, J.C.. In vitro thermal stress induces apoptosis and reduces development of porcine parthenotes. Theriogenology, vol.66, no.5, 1073-1082.

  34. Tsukamoto, Satoshi, Kuma, Akiko, Mizushima, Noboru. The role of autophagy during the oocyte-to-embryo transition. Autophagy, vol.4, no.8, 1076-1078.

  35. Tsukamoto, Satoshi, Kuma, Akiko, Murakami, Mirei, Kishi, Chieko, Yamamoto, Akitsugu, Mizushima, Noboru. Autophagy Is Essential for Preimplantation Development of Mouse Embryos. Science, vol.321, no.5885, 117-120.

  36. XU, Yong-Nan, SHEN, Xing-Hui, LEE, Seung-Eun, KWON, Jung-Suk, KIM, Deuk-Joong, HEO, Young-Tae, CUI, Xiang-Shun, KIM, Nam-Hyung. Autophagy Influences Maternal mRNA Degradation and Apoptosis in Porcine Parthenotes Developing In Vitro. The Journal of reproduction and development, vol.58, no.5, 576-584.

  37. Biology of Reproduction Yamamoto A. 1 91 7 2014 Fertilization‐induced autophagy in mouse embryos is independent of mTORC1 

  38. You, J., Kim, J., Lim, J., Lee, E.. Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species. Theriogenology, vol.74, no.5, 777-785.

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