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The unfolded protein sensor IRE1a is essential for homeostatic dendritic cell maturation

Sophie Janssens (UGent) , Victor Bosteels (UGent) , Sandra Maréchal (UGent) , Eva Cloots (UGent) , Laurien Van Heddegem, Simon Tavernier (UGent) , Sofie Rennen (UGent) , Clint De Nolf (UGent) , Seraja Amstelveen (UGent) , Jonathan Maelfait (UGent) , et al.
(2024)
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Abstract
The continuous engulfment of apoptotic cells initiates a homeostatic maturation program in conventional type I dendritic cells (cDC1s), hallmarked by the activation of the transcription factor LXRb, which mediates cholesterol efflux and dampens interferon stimulated gene expression. cDC1s are characterized by a high basal activation of the unfolded protein response (UPR) sensor IRE1, without concomitant induction of a proper UPR gene signature, a finding that has puzzled the field. Here we show that in absence of IRE1, the homeostatic maturation of cDC1s is blocked, while homeostatic maturation of cDC2s remains unaffected. IRE1 activation is strictly dependent on apoptotic cell engulfment and cholesterol influx, explaining its cDC1 subset specific activity. Stimulation of IRE1 endonuclease activity in cDC1s leads to a Regulated IRE1 Dependent Decay (RIDD) response, targeting miRNAs rather than mRNAs. This causes the degradation of miRNA-92a, which targets the cholesterol efflux transporter Abcg1. Loss of IRE1 leads to defects in cholesterol efflux in mature cDC1s and concomitant cell death, while cDC2s do not show any defects. Blocking miRNA synthesis or enforcing cholesterol efflux by treatment with reconstituted high-density lipoproteins rescues cDC1s from cell death. These data highlight the central role of IRE1 as a sensor of cholesterol influx in the ER, extending IRE1’s function beyond its canonical role in protein folding. Furthermore, they underscore the tight control of cholesterol metabolism during cDC1 maturation, uncovering a second pathway to coordinate cholesterol efflux that acts in parallel to LXRb.

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MLA
Janssens, Sophie, et al. The Unfolded Protein Sensor IRE1a Is Essential for Homeostatic Dendritic Cell Maturation. 2024, doi:10.21203/rs.3.rs-4763670/v1.
APA
Janssens, S., Bosteels, V., Maréchal, S., Cloots, E., Van Heddegem, L., Tavernier, S., … Goff, W. L. (2024). The unfolded protein sensor IRE1a is essential for homeostatic dendritic cell maturation. https://doi.org/10.21203/rs.3.rs-4763670/v1
Chicago author-date
Janssens, Sophie, Victor Bosteels, Sandra Maréchal, Eva Cloots, Laurien Van Heddegem, Simon Tavernier, Sofie Rennen, et al. 2024. “The Unfolded Protein Sensor IRE1a Is Essential for Homeostatic Dendritic Cell Maturation.” https://doi.org/10.21203/rs.3.rs-4763670/v1.
Chicago author-date (all authors)
Janssens, Sophie, Victor Bosteels, Sandra Maréchal, Eva Cloots, Laurien Van Heddegem, Simon Tavernier, Sofie Rennen, Clint De Nolf, Seraja Amstelveen, Jonathan Maelfait, Liesbet Martens, Evelien Van De Velde, Farzaneh Fayazpour, Kim Deswarte, Wouter Saelens, Louis Boon, Julie Van Duyse, Gert Van Isterdael, Isabelle Guillas, Yvan Saeys, Bart Lambrecht, Pieter Mestdagh, and Wilfried Le Goff. 2024. “The Unfolded Protein Sensor IRE1a Is Essential for Homeostatic Dendritic Cell Maturation.” doi:10.21203/rs.3.rs-4763670/v1.
Vancouver
1.
Janssens S, Bosteels V, Maréchal S, Cloots E, Van Heddegem L, Tavernier S, et al. The unfolded protein sensor IRE1a is essential for homeostatic dendritic cell maturation. 2024.
IEEE
[1]
S. Janssens et al., “The unfolded protein sensor IRE1a is essential for homeostatic dendritic cell maturation.” 2024.
@misc{01JW8QJAV9QCPXJ1Z08Z7DYZYV,
  abstract     = {{The continuous engulfment of apoptotic cells initiates a homeostatic maturation program in conventional type I dendritic cells (cDC1s), hallmarked by the activation of the transcription factor LXRb, which mediates cholesterol efflux and dampens interferon stimulated gene expression. cDC1s are characterized by a high basal activation of the unfolded protein response (UPR) sensor IRE1, without concomitant induction of a proper UPR gene signature, a finding that has puzzled the field. Here we show that in absence of IRE1, the homeostatic maturation of cDC1s is blocked, while homeostatic maturation of cDC2s remains unaffected. IRE1 activation is strictly dependent on apoptotic cell engulfment and cholesterol influx, explaining its cDC1 subset specific activity. Stimulation of IRE1 endonuclease activity in cDC1s leads to a Regulated IRE1 Dependent Decay (RIDD) response, targeting miRNAs rather than mRNAs. This causes the degradation of miRNA-92a, which targets the cholesterol efflux transporter Abcg1. Loss of IRE1 leads to defects in cholesterol efflux in mature cDC1s and concomitant cell death, while cDC2s do not show any defects. Blocking miRNA synthesis or enforcing cholesterol efflux by treatment with reconstituted high-density lipoproteins rescues cDC1s from cell death. These data highlight the central role of IRE1 as a sensor of cholesterol influx in the ER, extending IRE1’s function beyond its canonical role in protein folding. Furthermore, they underscore the tight control of cholesterol metabolism during cDC1 maturation, uncovering a second pathway to coordinate cholesterol efflux that acts in parallel to LXRb.}},
  author       = {{Janssens, Sophie and Bosteels, Victor and Maréchal, Sandra and Cloots, Eva and Van Heddegem, Laurien and Tavernier, Simon and Rennen, Sofie and De Nolf, Clint and Amstelveen, Seraja and Maelfait, Jonathan and Martens, Liesbet and Van De Velde, Evelien and Fayazpour, Farzaneh and Deswarte, Kim and Saelens, Wouter and Boon, Louis and Van Duyse, Julie and Van Isterdael, Gert and Guillas, Isabelle and Saeys, Yvan and Lambrecht, Bart and Mestdagh, Pieter and Goff, Wilfried Le}},
  language     = {{eng}},
  title        = {{The unfolded protein sensor IRE1a is essential for homeostatic dendritic cell maturation}},
  url          = {{http://doi.org/10.21203/rs.3.rs-4763670/v1}},
  year         = {{2024}},
}

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