Title : Disulfide High-Mobility Group Box 1 Drives Ischemia-Reperfusion Injury in Human Liver Transplantation.

Pub. Date : 2021 Mar

PMID : 32426849






9 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Disulfide-HMGB1 Drives Ischemia-Reperfusion Injury in Human Liver Transplantation. Disulfides high mobility group box 1 Homo sapiens
2 Portal blood immediately following allograft reperfusion (liver flush, LF) had increased total HMGB1, but only LF from patients with histopathological IRI had increased disulfide-HMGB1 and induced TLR4-dependent TNFalpha production by macrophages. Disulfides high mobility group box 1 Homo sapiens
3 Disulfide HMGB1 levels increased concomitantly with IRI severity. Disulfides high mobility group box 1 Homo sapiens
4 IRI+ pre-reperfusion biopsies contained macrophages with hyperacetylated, lysosomal disulfide-HMGB1 that increased post-reperfusion at sites of injury, paralleling increased histone acetyltransferase GTF3C4 and decreased histone deacetylase HDAC5 expression. Disulfides high mobility group box 1 Homo sapiens
5 Purified disulfide-HMGB1 or IRI+ blood stimulated further production of disulfide-HMGB1 and increased pro-inflammatory molecule and cytokine expression in macrophages via a positive feedback loop. Disulfides high mobility group box 1 Homo sapiens
6 Purified disulfide-HMGB1 or IRI+ blood stimulated further production of disulfide-HMGB1 and increased pro-inflammatory molecule and cytokine expression in macrophages via a positive feedback loop. Disulfides high mobility group box 1 Homo sapiens
7 Purified disulfide-HMGB1 or IRI+ blood stimulated further production of disulfide-HMGB1 and increased pro-inflammatory molecule and cytokine expression in macrophages via a positive feedback loop. Disulfides high mobility group box 1 Homo sapiens
8 Purified disulfide-HMGB1 or IRI+ blood stimulated further production of disulfide-HMGB1 and increased pro-inflammatory molecule and cytokine expression in macrophages via a positive feedback loop. Disulfides high mobility group box 1 Homo sapiens
9 CONCLUSIONS: These data identify disulfide-HMGB1 as a mechanistic biomarker of, and therapeutic target for, minimizing sterile inflammation during human liver IRI. Disulfides high mobility group box 1 Homo sapiens