| Literature DB >> 25339675 |
Luz M Reyes1, Jose L Estrada1, Zheng Yu Wang1, Rachel J Blosser1, Rashod F Smith1, Richard A Sidner1, Leela L Paris1, Ross L Blankenship1, Caitlin N Ray1, Aaron C Miner1, Matthew Tector2, A Joseph Tector3.
Abstract
Pigs are emerging as important large animal models for biomedical research, and they may represent a source of organs for xenotransplantation. The MHC is pivotal to the function of the immune system in health and disease, and it is particularly important in infection and transplant rejection. Pigs deficient in class I MHC could serve as important reagents to study viral immunity as well as allograft and xenograft rejection. In this study, we report the creation and characterization of class I MHC knockout pigs using the Cas9 nuclease and guide RNAs. Pig fetal fibroblasts were genetically engineered using Cas9 and guide RNAs, and class I MHC(-) cells were then used as nuclear donors for somatic cell nuclear transfer. We produced three piglets devoid of all cell surface class I proteins. Although these animals have reduced levels of CD4(-)CD8(+) T cells in peripheral blood, the pigs appear healthy and are developing normally. These pigs are a promising reagent for immunological research.Entities:
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Year: 2014 PMID: 25339675 PMCID: PMC5922270 DOI: 10.4049/jimmunol.1402059
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422