Altered X-chromosome inactivation of the TLR7/8 locus and heterogeneity of pDCs in systemic sclerosis

Systemic sclerosis (SSc) is an autoimmune disease that has a strong female predominance. Both the X-linked TLR7 and TLR8 can induce type I IFN (IFN-I) by plasmacytoid DCs (pDCs), which can promote fibrosis. We identified five subclusters of pDCs, including ISGhigh clusters that were over-represented in SSc patients. We observed that both TLR7 and TLR8 genes escape from X chromosome inactivation (XCI) at higher frequency in pDCs of SSc patients, which was associated with changes in TLR7 protein profile. Combined DNA/RNA FISH analysis revealed that the TLR7/8 locus is preferentially located outside of the inactive X (Xi) territory when TLR7 is expressed, suggesting that higher-order loop formation is linked to TLR7/8 expression from the Xi. Furthermore, the expression levels of XIST and the transcriptional repressor SPEN were reduced in SSc pDCs. Hence, our data revealed the heterogeneity of pDCs in SSc and suggested that altered XCI at the TLR7/8 locus may contribute to the chronic IFN-I activity of pDCs in female SSc patients.

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Publication Details

Journal
The Journal of Experimental Medicine
Published
2024-12-13
DOI
https://doi.org/10.1084/jem.20231809
Citations
17
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
7.22

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article

Altered X-chromosome inactivation of the TLR7/8 locus and heterogeneity of pDCs in systemic sclerosis

Robert Spiera, Kimberly S. Lakin, Franck J. Barrat, Michael Pierides et al.
17 citations
The Journal of Experimental Medicine
Systemic Sclerosis and Related Diseases
7.22
article

Altered X-chromosome inactivation of the TLR7/8 locus and heterogeneity of pDCs in systemic sclerosis

Robert Spiera, Kimberly S. Lakin, Franck J. Barrat, Michael Pierides, Marie‐Elise Truchetet, Berenice Faz-López, Marie Dominique Ah Kioon, Jessica Gordon, Julie Chaumeil, Claire Cénac, Jean‐Charles Guéry, Yong Du
article en
17 citations

Abstract

Systemic sclerosis (SSc) is an autoimmune disease that has a strong female predominance. Both the X-linked TLR7 and TLR8 can induce type I IFN (IFN-I) by plasmacytoid DCs (pDCs), which can promote fibrosis. We identified five subclusters of pDCs, including ISGhigh clusters that were over-represented in SSc patients. We observed that both TLR7 and TLR8 genes escape from X chromosome inactivation (XCI) at higher frequency in pDCs of SSc patients, which was associated with changes in TLR7 protein profile. Combined DNA/RNA FISH analysis revealed that the TLR7/8 locus is preferentially located outside of the inactive X (Xi) territory when TLR7 is expressed, suggesting that higher-order loop formation is linked to TLR7/8 expression from the Xi. Furthermore, the expression levels of XIST and the transcriptional repressor SPEN were reduced in SSc pDCs. Hence, our data revealed the heterogeneity of pDCs in SSc and suggested that altered XCI at the TLR7/8 locus may contribute to the chronic IFN-I activity of pDCs in female SSc patients.

The Journal of Experimental MedicineVol. 222(3)
Hospital for Special Surgery (US), Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Université de Bordeaux (FR), Inserm (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Université Paris Cité (FR), Cornell University (US), Centre Hospitalier Universitaire de Bordeaux (FR), Immunology from Concept and Experiments to Translation (FR), Société Française de Rhumatologie (FR), Institut Cochin (FR)
Scleroderma Foundation, Scleroderma Research Foundation, Tow Foundation, Agence Nationale de la Recherche, Foundation for Research in Rheumatology, Région Occitanie Pyrénées-Méditerranée, National Institutes of Health, Weill Cornell Medical College, University of Texas MD Anderson Cancer Center
Life below water
Openalex Percentile: Top 2%
Systemic Sclerosis and Related Diseases
7.22
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