Use of anti-inhibin monoclonal antibody for increasing the litter size of mouse strains and its application to in vivo-genome editing technology†.


Journal

Biology of reproduction
ISSN: 1529-7268
Titre abrégé: Biol Reprod
Pays: United States
ID NLM: 0207224

Informations de publication

Date de publication:
09 08 2022
Historique:
received: 21 01 2022
revised: 08 03 2022
accepted: 25 03 2022
pubmed: 4 4 2022
medline: 19 8 2022
entrez: 3 4 2022
Statut: ppublish

Résumé

The litter size of mouse strains is determined by the number of oocytes naturally ovulated. Many attempts have been made to increase litter sizes by conventional superovulation regimens (e.g., using equine or human gonadotropins, eCG/hCG but had limited success because of unexpected decreases in the numbers of embryos surviving to term. Here, we examined whether rat-derived anti-inhibin monoclonal antibodies (AIMAs) could be used for this purpose. When C57BL/6 female mice were treated with an AIMA and mated, the number of healthy offspring per mouse increased by 1.4-fold (11.9 vs. 8.6 in controls). By contrast, treatment with eCG/hCG or anti-inhibin serum resulted in fewer offspring than in nontreated controls. The overall efficiency of production based on all females treated (including nonpregnant ones) was improved 2.4 times with AIMA compared with nontreated controls. The AIMA treatment was also effective in ICR mice, increasing the litter size from 15.3 to 21.2 pups. We then applied this technique to an in vivo genome-editing method (improved genome-editing via oviductal nucleic acid delivery, i-GONAD) to produce C57BL/6 mice deficient for tyrosinase. The mean litter size following i-GONAD increased from 4.8 to 7.3 after the AIMA treatment and genetic modifications were confirmed in 80/88 (91%) of the offspring. Thus, AIMA treatment is a promising method for increasing the litter size of mice and may be applied for the easy proliferation of mouse colonies as well as in vivo genetic manipulation, especially when the mouse strains are sensitive to handling.

Identifiants

pubmed: 35368067
pii: 6562767
doi: 10.1093/biolre/ioac068
pmc: PMC9382380
doi:

Substances chimiques

Antibodies, Monoclonal 0
Chorionic Gonadotropin 0
Inhibins 57285-09-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

605-618

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Ayumi Hasegawa (A)

RIKEN BioResource Research Center, Tsukuba, Ibaraki, Japan.

Keiji Mochida (K)

RIKEN BioResource Research Center, Tsukuba, Ibaraki, Japan.

Ayaka Nakamura (A)

Support Center for Medical Research and Education, Tokai University, Kanagawa, Japan.

Rico Miyagasako (R)

Division of Basic Medical Science and Molecular Medicine, School of Medicine, Tokai University, Kanagawa Japan.

Masato Ohtsuka (M)

Division of Basic Medical Science and Molecular Medicine, School of Medicine, Tokai University, Kanagawa Japan.
The Institute of Medical Sciences, Tokai University, Kanagawa, Japan.

Masahiko Hatakeyama (M)

Yaotsu Breeding Facility, CLEA Japan Inc., Gifu, Japan.

Atsuo Ogura (A)

RIKEN BioResource Research Center, Tsukuba, Ibaraki, Japan.
Graduate School of Life and Environmental Science, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo, Bunkyo-ku, Tokyo, Japan.
RIKEN Cluster for Pioneering Research, Wako, Saitama, Japan.

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Classifications MeSH