Transplant Immunology, Год журнала: 2024, Номер 87, С. 102148 - 102148
Опубликована: Ноя. 14, 2024
Язык: Английский
Transplant Immunology, Год журнала: 2024, Номер 87, С. 102148 - 102148
Опубликована: Ноя. 14, 2024
Язык: Английский
Journal of Cellular and Molecular Medicine, Год журнала: 2025, Номер 29(4)
Опубликована: Фев. 1, 2025
ABSTRACT Hepatic ischemia/reperfusion injury (IRI) commonly complicates liver transplantation (LT). However, the precise mechanisms underlying hepatic IRI remain incompletely understood. We acquired single‐cell RNA sequencing (scRNA‐seq) and transcriptome data of LT patients from GEO database. Employing scRNA‐seq, we delved into interplay between non‐immune immune cells in IRI, pinpointing genes exhibiting altered expression patterns. Integrating insights gleaned scRNA‐seq datasets, deepened our comprehension cellular interactions IRI. Additionally, conducted preliminary validation identified gene alterations using immunofluorescence techniques. Using detected significant changes populations sinusoidal endothelial (LSECs) monocytes after ischemia–reperfusion (IRI). By integrating with bulk data, key dysregulated LSECs (ICAM1, SOCS3, NFKBIZ, JUND, TNFRSF12A HSPA6) (SOCS3, FPR2 NR4A2). Our analysis cell communication indicated that ANXA1‐FPR2 axis might be a pivotal signature mediating monocytes. then established mouse model for further analyses flow cytometry showed increase monocyte proportion post‐IR ( p < 0.01). Consistently, Western Blot also revealed upregulation ANXA1 study elucidated signalling pathways following The likely triggers cascade events, promoting infiltration amplifying inflammatory responses, thus worsening deleterious effects
Язык: Английский
Процитировано
0Surgery, Год журнала: 2024, Номер unknown
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
1Transplant Immunology, Год журнала: 2024, Номер 87, С. 102148 - 102148
Опубликована: Ноя. 14, 2024
Язык: Английский
Процитировано
0