Generation of rat offspring from ovarian oocytes by xenotransplantation.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
29 Aug 2024
Historique:
received: 08 03 2024
accepted: 23 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: epublish

Résumé

The idea of utilizing unused oocytes present in the ovaries has been tested in various ways to produce offspring. However, only a limited number of studies succeeded in offspring generation. They include transplantation of ovaries into autologous or allogeneic animals, and acquisition of pups from oocytes obtained by transplanting mouse ovaries into immunodeficient rats. Here we report successful production of rat oocytes by transplanting rat ovaries under the kidney capsule of immunodeficient mice with addition of hormone administration to the mice. In addition, these oocytes were developed by in vitro fertilization, and transplanted into the oviducts of pseudopregnant rats, resulting in successful delivery of pups. The modified gene of the donor rat was confirmed to be correctly inherited to the pups. These results show that xenotransplantation of ovarian tissue makes it possible to leave offspring, beginning a new phase in developmental engineering.

Identifiants

pubmed: 39209914
doi: 10.1038/s41598-024-71030-0
pii: 10.1038/s41598-024-71030-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20109

Subventions

Organisme : JST SPRING Grant
ID : JPMJSP2145
Organisme : Japan Agency for Medical Research and Development
ID : JP23dm0207091h0005
Organisme : Japan Society for the Promotion of Science
ID : JP16H06276

Informations de copyright

© 2024. The Author(s).

Références

Petrich, B. G. et al. c-Jun N-terminal kinase activation mediates downregulation of connexin43 in cardiomyocytes. Circ. Res. 91, 640–647 (2002).
doi: 10.1161/01.RES.0000035854.11082.01 pubmed: 12364393
Raja, M. A., Maldonado, M., Chen, J., Zhong, Y. & Gu, J. Development and evaluation of curcumin encapsulated self-assembled nanoparticles as potential remedial treatment for PCOS in a female rat model. Int. J. Nanomed. 16, 6231–6247 (2021).
doi: 10.2147/IJN.S302161
Kaneko, T. Reproductive technologies for the generation and maintenance of valuable animal strains. J. Reprod. Dev. 64, 209–215 (2018).
doi: 10.1262/jrd.2018-035 pubmed: 29657233 pmcid: 6021608
Lee, D. M. et al. Live birth after ovarian tissue transplant. Nature 428, 137–138 (2004).
doi: 10.1038/428137a pubmed: 15014485
Youm, H. W. et al. Transplantation of mouse ovarian tissue: Comparison of the transplantation sites. Theriogenology 83, 854–861 (2015).
doi: 10.1016/j.theriogenology.2014.11.026 pubmed: 25533928
Gunasena, K. T., Villines, P. M., Critser, E. S. & Critser, J. K. Live births after autologous transplant of cryopreserved mouse ovaries. Hum. Reprod. Oxf. Engl. 12, 101–106 (1997).
doi: 10.1093/humrep/12.1.101
Meirow, D. et al. Monitoring the ovaries after autotransplantation of cryopreserved ovarian tissue: Endocrine studies, in vitro fertilization cycles, and live birth. Fertil. Steril. 87(418), e7-418.e15 (2007).
Snow, M., Cox, S.-L., Jenkin, G., Trounson, A. & Shaw, J. Generation of live young from xenografted mouse ovaries. Science 297, 2227–2227 (2002).
doi: 10.1126/science.1073693 pubmed: 12351780
Agca, C., Lucy, M. C. & Agca, Y. Gene expression profile of rat ovarian tissue following xenotransplantation into immune-deficient mice. Reprod. Camb. Engl. 137, 957–967 (2009).
doi: 10.1530/REP-09-0048
Hirayama, R. et al. Production of marmoset eggs and embryos from xenotransplanted ovary tissues. Sci. Rep. 13, 18196 (2023).
doi: 10.1038/s41598-023-45224-x pubmed: 37875516 pmcid: 10598121
Noyes, R. W. Fertilization of follicular ova. Fertil. Steril. 3, 1–12 (1952).
doi: 10.1016/S0015-0282(16)30780-4 pubmed: 14906378
Yamazaki, W., Takahashi, M. & Kawahara, M. Restricted development of mouse triploid fetuses with disorganized expression of imprinted genes. Zygote 23, 874–884 (2015).
doi: 10.1017/S0967199414000550 pubmed: 25318586
Matzuk, M. M., Burns, K. H., Viveiros, M. M. & Eppig, J. J. Intercellular communication in the mammalian ovary: Oocytes carry the conversation. Science 296, 2178–2180 (2002).
doi: 10.1126/science.1071965 pubmed: 12077402
Hamazaki, N. et al. Reconstitution of the oocyte transcriptional network with transcription factors. Nature 589, 264–269 (2021).
doi: 10.1038/s41586-020-3027-9 pubmed: 33328630
Hunzicker-Dunn, M. & Maizels, E. T. FSH signaling pathways in immature granulosa cells that regulate target gene expression: Branching out from protein kinase A. Cell. Signal. 18, 1351–1359 (2006).
doi: 10.1016/j.cellsig.2006.02.011 pubmed: 16616457 pmcid: 1564187
Sela-Abramovich, S., Chorev, E., Galiani, D. & Dekel, N. Mitogen-activated protein kinase mediates luteinizing hormone-induced breakdown of communication and oocyte maturation in rat ovarian follicles. Endocrinology 146, 1236–1244 (2005).
doi: 10.1210/en.2004-1006 pubmed: 15576461
Sen, A. & Caiazza, F. Oocyte maturation: A story of arrest and release. Front. Biosci. Sch. Ed. 5, 451–477 (2013).
doi: 10.2741/S383
Shimamoto, S. et al. Hypoxia induces the dormant state in oocytes through expression of Foxo3. Proc. Natl. Acad. Sci. U.S.A. 116, 12321–12326 (2019).
doi: 10.1073/pnas.1817223116 pubmed: 31147464 pmcid: 7056940
Cross, P. C. & Brinster, R. L. In vitro development of mouse oocytes. Biol. Reprod. 3, 298–307 (1970).
doi: 10.1093/biolreprod/3.3.298 pubmed: 5522859
Eppig, J. J. & Schroeder, A. C. Capacity of mouse oocytes from preantral follicles to undergo embryogenesis and development to live young after growth, maturation, and fertilization in vitro. Biol. Reprod. 41, 268–276 (1989).
doi: 10.1095/biolreprod41.2.268 pubmed: 2508774
Eppig, J. J. & O’Brien, M. J. Development in vitro of mouse oocytes from primordial follicles. Biol. Reprod. 54, 197–207 (1996).
doi: 10.1095/biolreprod54.1.197 pubmed: 8838017
Hikabe, O. et al. Reconstitution in vitro of the entire cycle of the mouse female germ line. Nature 539, 299–303 (2016).
doi: 10.1038/nature20104 pubmed: 27750280
Ito, T., Suzuki, A., Imai, E., Okabe, M. & Hori, M. Bone marrow is a reservoir of repopulating mesangial cells during glomerular remodeling. J. Am. Soc. Nephrol. JASN 12, 2625–2635 (2001).
doi: 10.1681/ASN.V12122625 pubmed: 11729231
Kanda, Y. Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics. Bone Marrow Transplant. 48, 452–458 (2013).
doi: 10.1038/bmt.2012.244 pubmed: 23208313

Auteurs

Hiroaki Taketsuru (H)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Department of Comparative and Experimental Medicine, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Division of Animal Genetics, Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.

Runa Hirayama (R)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Department of Behavioral Physiology, Graduate School of Innovative Life Science, University of Toyama, Toyama, 930-0194, Japan.

Ena Nakatsukasa (E)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.

Rie Natsume (R)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.

Keizo Takao (K)

Department of Behavioral Physiology, Graduate School of Innovative Life Science, University of Toyama, Toyama, 930-0194, Japan.
Department of Behavioral Physiology, Faculty of Medicine, University of Toyama, Toyama, 930-0194, Japan.
Research Center for Idling Brain Science, University of Toyama, Toyama, 930-0194, Japan.

Manabu Abe (M)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan. manabu@bri.niigata-u.ac.jp.

Kenji Sakimura (K)

Department of Animal Model Development, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan. sakimura@bri.niigata-u.ac.jp.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH