| Literature DB >> 33451076 |
Min Young Park1, Bala Murali Krishna Vasamsetti2, Wan Seop Kim3, Hee Jung Kang4, Do-Young Kim1, Byeonghwi Lim1, Kahee Cho5, Jun Seok Kim6, Hyun Keun Chee6, Jung Hwan Park7, Hyun Suk Yang8, Harikrishna Reddy Rallabandi2, Sun A Ock2, Mi-Ryung Park2, Heasun Lee2, In-Sul Hwang2, Jun-Mo Kim1, Keon Bong Oh2, Ik Jin Yun9.
Abstract
Porcine heart xenotransplantation is a potential treatment for patients with end-stage heart failure. To understand molecular mechanisms of graft rejection after heart transplantation, we transplanted a 31-day-old alpha-1,3-galactosyltransferase knockout (GTKO) porcine heart to a five-year-old cynomolgus monkey. Histological and transcriptome analyses were conducted on xenografted cardiac tissue at rejection (nine days after transplantation). The recipient monkey's blood parameters were analyzed on days -7, -3, 1, 4, and 7. Validation was conducted by quantitative real-time PCR (qPCR) with selected genes. A non-transplanted GTKO porcine heart from an age-matched litter was used as a control. The recipient monkey showed systemic inflammatory responses, and the rejected cardiac graft indicated myocardial infarction and cardiac fibrosis. The transplanted heart exhibited a total of 3748 differentially expressed genes compared to the non-transplanted heart transcriptome, with 2443 upregulated and 1305 downregulated genes. Key biological pathways involved at the terminal stage of graft rejection were cardiomyopathies, extracellular interactions, and ion channel activities. The results of qPCR evaluation were in agreement with the transcriptome data. Transcriptome analysis of porcine cardiac tissue at graft rejection reveals dysregulation of the key molecules and signaling pathways, which play relevant roles on structural and functional integrities of the heart.Entities:
Keywords: Xenotransplatation; heart failure; porcine cardiac tissue; transcriptome analysis (or RNA-seq analysis)
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Year: 2021 PMID: 33451076 PMCID: PMC7828557 DOI: 10.3390/ijms22020751
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923