Landscape of Immune Cells Heterogeneity in Liver Transplantation by Single-Cell RNA Sequencing Analysis.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 05 03 2022
accepted: 11 04 2022
entrez: 27 5 2022
pubmed: 28 5 2022
medline: 31 5 2022
Statut: epublish

Résumé

Rejection is still a critical barrier to the long-term survival of graft after liver transplantation, requiring clinicians to unveil the underlying mechanism of liver transplant rejection. The cellular diversity and the interplay between immune cells in the liver graft microenvironment remain unclear. Herein, we performed single-cell RNA sequencing analysis to delineate the landscape of immune cells heterogeneity in liver transplantation. T cells, NK cells, B cells, and myeloid cell subsets in human liver and blood were enriched to characterize their tissue distribution, gene expression, and functional modules. The proportion of CCR6+CD4+ T cells increased within an allograft, suggesting that there are more memory CD4+ T cells after transplantation, in parallel with exhausted CTLA4+CD8+ T and actively proliferating MKI67+CD8+ T cells increased significantly, where they manifested heterogeneity, distinct function, and homeostatic proliferation. Remarkably, the changes of CD1c+ DC, CADM+ DC, MDSC, and FOLR3+ Kupffer cells increase significantly, but the proportion of CD163+ Kupffer, APOE+ Kupffer, and GZMA+ Kupffer decreased. Furthermore, we identified LDLR as a novel marker of activated MDSC to prevent liver transplant rejection. Intriguingly, a subset of CD4+CD8+FOXP3+ T cells included in CTLA4+CD8+ T cells was first detected in human liver transplantation. Furthermore, intercellular communication and gene regulatory analysis implicated the LDLR+ MDSC and CTLA4+CD8+ T cells interact through TIGIT-NECTIN2 signaling pathway. Taken together, these findings have gained novel mechanistic insights for understanding the immune landscape in liver transplantation, and it outlines the characteristics of immune cells and provides potential therapeutic targets in liver transplant rejection.

Identifiants

pubmed: 35619708
doi: 10.3389/fimmu.2022.890019
pmc: PMC9127089
doi:

Substances chimiques

CTLA-4 Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

890019

Informations de copyright

Copyright © 2022 Li, Li, Wu, Xu, Teng, Yang, Sun, Zhao, Li, Liu, Yang, Gong and Cai.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Xinqiang Li (X)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.

Shipeng Li (S)

Department of General Surgery, Jiaozuo Women's and Children's Hospital, Jiaozuo, China.
The Second Clinical Medical College, Capital Medical University, Beijing, China.

Bin Wu (B)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Qingguo Xu (Q)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Dahong Teng (D)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Tongwang Yang (T)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Yandong Sun (Y)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Yang Zhao (Y)

Department of Urology Surgery, Peking Union Medical College Hospital, Beijing, China.

Tianxiang Li (T)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Dan Liu (D)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

Shuang Yang (S)

Department of Molecular Biology, Medical College, Nankai University, Tianjin, China.

Weihua Gong (W)

Department of Surgery, Second Affiliated Hospital of School of Medicine, Zhejiang University, Hangzhou, China.

Jinzhen Cai (J)

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

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