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RETREG1‐Mediated Reticulophagy is Essential for Dendritic Cell Maturation and Function in Sepsis

Year: 2026
Type: article
Abstract: ABSTRACT Dendritic cells (DCs) are crucial antigen‐presenting cells that mediate the interplay between innate and adaptive immunity during lethal infections. Here, we report the key role of reticulophagy regulator 1 (RETREG1), a selective autophagy receptor, in maintaining DC maturation and function in the early stage of sepsis. Mechanistically, activating transcription factor 6 (ATF6) acts as a direct transcription factor regulating RETREG1 expression in response to bacterial lipopolysaccharide‐induced endoplasmic reticulum (ER) stress. RETREG1‐mediated reticulophagy reduces excessive ER stress via the eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3) signaling pathway and inhibits membrane‐associated RING‐CH‐type finger 8 (MARCH8)‐dependent major histocompatibility complex class II (MHC‐II) ubiquitination to maintain antigen presentation in DCs. Consequently, Cd11c cre Retreg1 fl/fl , Retreg1 −/− , and Atf6 −/− mice exhibit impaired DC function, leading to immunosuppression and multiple organ failure in experimental sepsis. Exploration of samples from septic patients, combined with single‐cell bioinformatics analysis, further suggests that a deficit in reticulophagy in DCs is associated with the development of human sepsis.
Language: English
Subfield: Epidemiology
Field: Medicine
Open Access status: gold
Estimated APC paid: $6,730
OpenAlex ID: W7140216466
FWCI: 4.471
Cites: 52
Cited by: 1
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