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Woo, M.S.* ; Mayer, C.* ; Binkle-Ladisch, L.* ; Sonner, J.K.* ; Rosenkranz, S.C.* ; Shaposhnykov, A.* ; Rothammer, N.* ; Tsvilovskyy, V.* ; Lorenz, S. ; Raich, L.* ; Bal, L.C.* ; Vieira, V.* ; Wagner, I.* ; Bauer, S.* ; Glatzel, M.* ; Conrad, M. ; Merkler, D.* ; Freichel, M.* ; Friese, M.A.*

STING orchestrates the neuronal inflammatory stress response in multiple sclerosis.

Cell 187, 4043-4060.e30 (2024)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Inflammation-induced neurodegeneration is a defining feature of multiple sclerosis (MS), yet the underlying mechanisms remain unclear. By dissecting the neuronal inflammatory stress response, we discovered that neurons in MS and its mouse model induce the stimulator of interferon genes (STING). However, activation of neuronal STING requires its detachment from the stromal interaction molecule 1 (STIM1), a process triggered by glutamate excitotoxicity. This detachment initiates non-canonical STING signaling, which leads to autophagic degradation of glutathione peroxidase 4 (GPX4), essential for neuronal redox homeostasis and thereby inducing ferroptosis. Both genetic and pharmacological interventions that target STING in neurons protect against inflammation-induced neurodegeneration. Our findings position STING as a central regulator of the detrimental neuronal inflammatory stress response, integrating inflammation with glutamate signaling to cause neuronal cell death, and present it as a tractable target for treating neurodegeneration in MS.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Sting ; Calcium Signaling ; Cell Death ; Excitotoxicity ; Ferroptosis ; Multiple Sclerosis ; Neurodegeneration ; Neuroinflammation; Cyclic Gmp-amp; T-cells; Dna; Activation; Degeneration; Ferroptosis; Synthase; Release; Sensor; Stim1
ISSN (print) / ISBN 0092-8674
e-ISSN 1097-4172
Zeitschrift Cell
Quellenangaben Band: 187, Heft: 15, Seiten: 4043-4060.e30 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Cambridge, Mass.
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Metabolism and Cell Death (MCD)
Förderungen Hertie-Stiftung
Memorial Stipend