Correlation Engine 2.0
Clear Search sequence regions


Sizes of these terms reflect their relevance to your search.

Previously, we performed gene knockout (KO) of interleukin-2 receptor gamma (IL2RG) in porcine fetal fibroblasts using zinc finger nuclease-encoding mRNAs, subsequently generating IL2RG KO pigs using these cells through somatic cell nuclear transfer. The IL2RG KO pigs lacked a thymus and were deficient in T lymphocytes and natural killer cells, similar to human X-linked severe combined immunodeficiency (SCID) patients. The present study aimed to evaluate whether pigs can support the growth of xenografted human cells and have the potential to be an effective animal model. The IL2RG XKOY pigs used in this study were obtained by mating IL2RG XKOX females with wild-type boars. This permitted the routine production of IL2RG KO pigs via natural breeding without complicated somatic cell cloning procedures; therefore, a sufficient number of pigs could be prepared. We transplanted human HeLa S3 cells expressing the tandem dimer tomato into the ears and pancreas of IL2RG KO pigs. Additionally, a newly developed method for the aseptic rearing of SCID pigs was used in case of necessity. Tumors from the transplanted cells quickly developed in all pigs and were verified by histology and immunohistochemistry. We also transplanted these cells into the pancreas of designated pathogen-free pigs housed in novel biocontainment facilities, and large tumors were confirmed. IL2RG KO pigs have the potential to become useful animal models in a variety of translational biology fields. © 2022 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V.

Citation

Koki Hasegawa, Kazuaki Nakano, Masaki Nagaya, Masahito Watanabe, Ayuko Uchikura, Hitomi Matsunari, Kazuhiro Umeyama, Eiji Kobayashi, Hiroshi Nagashima. Transplantation of human cells into Interleukin-2 receptor gamma gene knockout pigs under several conditions. Regenerative therapy. 2022 Dec;21:62-72


PMID: 35765545

View Full Text