| Literature DB >> 32095422 |
Heasun Lee1, In-Sul Hwang1, Bala Murali Krishna Vasamsetti1, Harikrishna Reddy Rallabandi1, Mi-Ryung Park1, Sung-June Byun1, Hyeon Yang1, Sun A Ock1, Hwi-Cheul Lee1, Jae-Seok Woo1, Seongsoo Hwang1, Keon Bong Oh1.
Abstract
In this study, we attempted to upgrade GT -MCP/-MCP pig genetically to express MCP at a higher level and additionally thrombomodulin (TBM), which have respective roles as a complement regulatory protein and a coagulation inhibitor. We constructed a dicistronic cassette consisting of codon-optimized MCP (mMCP) and TBM (m-pI2), designed for ubiquitous expression of MCP and endothelium specific expression of TBM. The cassette was confirmed to allow extremely increased MCP expression compared with non-modified MCP, and an endothelial-specific TBM expression. We thus transfected m-pI2 into ear-skin fibroblasts isolated from a GT -MCP/-MCP pig. By twice selection using magnetically activated cell sorting (MACS), and single-cell culture, we were able to obtain clones over 90% expressing MCP. The cells of a clone were provided as a donor for nuclear transfer resulting in the generation of a GT -MCP/-MCP /mMCP/TBM pig, which was confirmed to be carrying cells expressing MCP and functioning as an inhibitor against the cytotoxic effect of normal monkey serum, comparable with donor cells. Collectively, these results demonstrated an effective approach for upgrading transgenic pig, and we assumed that upgraded pig would increase graft survival. © King Abdulaziz City for Science and Technology 2020.Entities:
Keywords: Alpha-1,3-galactosyltransferase knockout pig; Codon optimization; Membrane cofactor protein; Thrombomodulin
Year: 2020 PMID: 32095422 PMCID: PMC7008109 DOI: 10.1007/s13205-020-2091-z
Source DB: PubMed Journal: 3 Biotech ISSN: 2190-5738 Impact factor: 2.406