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生成胰岛素样生长因子1受体基因敲除猪作为种间器官发生的潜在系统。

Generation of insulin-like growth factor 1 receptor-knockout pigs as a potential system for interspecies organogenesis.

作者信息

Nagaya Masaki, Uchikura Ayuko, Nakano Kazuaki, Watanabe Masahito, Matsunari Hitomi, Umeyama Kazuhiro, Mizuno Naoaki, Nishimura Toshiya, Nakauchi Hiromitsu, Nagashima Hiroshi

机构信息

Meiji University International Institute for Bio-Resource Research, 1-1-1 Higashimita, Tama-ku, Kawasaki 214-8571, Japan.

PorMedTec Co. Ltd., 2-3227 Mita, Tama-ku, Kawasaki, Kanagawa, 214-0034, Japan.

出版信息

Regen Ther. 2024 Sep 11;26:783-791. doi: 10.1016/j.reth.2024.08.025. eCollection 2024 Jun.

DOI:10.1016/j.reth.2024.08.025
PMID:39309395
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11416208/
Abstract

BACKGROUND

To overcome organ shortage during transplantation, interspecies organ generation via blastocyst complementation has been proposed, although not yet in evolutionarily distant species. To establish high levels of chimerism, low chimerism is required early in development, followed by high chimerism, to effectively complement the organ niche. Very few human cells are expected to contribute to chimerism in heterologous animals. Previous studies had demonstrated increased donor chimerism in both intra- and interspecies chimeras in rodents, using () knockout (KO) mice; deletion of the gene in the mouse host embryo created a cell-competitive niche. The current study aimed to generate KO pigs and evaluate whether they have the same phenotype as -KO mice.

METHODS

To generate KO pigs, genome-editing molecules were injected into the cytoplasm of pig zygotes. The fetuses were evaluated at 104 days of gestation.

RESULTS

-KO pigs were generated successfully. Their phenotypes were almost identical to those of -KO mice, including small lungs and enlarged endodermal organs in fetuses, and they were highly reproducible.

CONCLUSIONS

Pigs may allow the generation of organs using blastocyst complementation with developmentally-compatible xenogeneic pluripotent stem cells over a large evolutionary distance.

摘要

背景

为了克服移植过程中的器官短缺问题,人们提出了通过囊胚互补来生成种间器官的方法,尽管在进化距离较远的物种中尚未实现。为了建立高水平的嵌合体,在发育早期需要低嵌合体,随后是高嵌合体,以有效地补充器官微环境。预计在异源动物中,很少有人类细胞会对嵌合体产生贡献。先前的研究表明,使用()基因敲除(KO)小鼠,啮齿动物的种内和种间嵌合体中的供体嵌合率均有所提高;在小鼠宿主胚胎中删除该基因可创造一个细胞竞争微环境。本研究旨在培育基因敲除猪,并评估它们是否具有与基因敲除小鼠相同的表型。

方法

为了培育基因敲除猪,将基因组编辑分子注入猪受精卵的细胞质中。在妊娠104天时对胎儿进行评估。

结果

成功培育出了基因敲除猪。它们的表型与基因敲除小鼠几乎相同,包括胎儿的肺小和内胚层器官增大,并且具有高度的可重复性。

结论

猪可能允许利用囊胚互补与发育兼容的异种多能干细胞在较大的进化距离上生成器官。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/b27e1a44b28c/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/5988b400f213/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/9c2528b508af/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/cddaa6c1d26b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/0834ab7e3ce8/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/a8d505ffeb7c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/b27e1a44b28c/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/5988b400f213/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/9c2528b508af/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/cddaa6c1d26b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/0834ab7e3ce8/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/a8d505ffeb7c/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f107/11416208/b27e1a44b28c/figs1.jpg

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