Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Sublethal necroptosis signaling promotes inflammation and liver cancer.
Immunity 56, 1578-1595.e8 (2023)
It is currently not well known how necroptosis and necroptosis responses manifest in vivo. Here, we uncovered a molecular switch facilitating reprogramming between two alternative modes of necroptosis signaling in hepatocytes, fundamentally affecting immune responses and hepatocarcinogenesis. Concomitant necrosome and NF-κB activation in hepatocytes, which physiologically express low concentrations of receptor-interacting kinase 3 (RIPK3), did not lead to immediate cell death but forced them into a prolonged “sublethal” state with leaky membranes, functioning as secretory cells that released specific chemokines including CCL20 and MCP-1. This triggered hepatic cell proliferation as well as activation of procarcinogenic monocyte-derived macrophage cell clusters, contributing to hepatocarcinogenesis. In contrast, necrosome activation in hepatocytes with inactive NF-κB-signaling caused an accelerated execution of necroptosis, limiting alarmin release, and thereby preventing inflammation and hepatocarcinogenesis. Consistently, intratumoral NF-κB-necroptosis signatures were associated with poor prognosis in human hepatocarcinogenesis. Therefore, pharmacological reprogramming between these distinct forms of necroptosis may represent a promising strategy against hepatocellular carcinoma.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Hcc ; Intravital Imaging ; Mlkl ; Nf-κb ; Rip1 ; Rip3 ; Ripk1 ; Ripk3 ; Traf2 ; Undead Cells; Nf-kappa-b; Gene-expression Signature; Cell-death; Hepatocellular-carcinoma; Mouse Hepatocytes; Activation; Traf2; Rip3; Tak1; Hepatocarcinogenesis
ISSN (print) / ISBN
1074-7613
e-ISSN
1097-4180
Zeitschrift
Immunity
Quellenangaben
Band: 56,
Heft: 7,
Seiten: 1578-1595.e8
Verlag
Cell Press
Verlagsort
Cambridge, Mass.
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Research Unit Radiation Cytogenetics (ZYTO)
Förderungen
Cancer Research UK