Spatial Transcriptomics Reveals Signatures of Histopathological Changes in Muscular Sarcoidosis.
Hippolyte LequainCyril DégletagneNathalie StreichenbergerJulie ValantinThomas SimonetLaurent SchaefferPascal SèvePascal LeblancPublished in: Cells (2023)
Sarcoidosis is a multisystemic disease characterized by non-caseating granuloma infiltrating various organs. The form with symptomatic muscular involvement is called muscular sarcoidosis. The impact of immune cells composing the granuloma on the skeletal muscle is misunderstood. Here, we investigated the granuloma-skeletal muscle interactions through spatial transcriptomics on two patients affected by muscular sarcoidosis. Five major transcriptomic clusters corresponding to perigranuloma, granuloma, and three successive muscle tissue areas (proximal, intermediate, and distal) around the granuloma were identified. Analyses revealed upregulated pathways in the granuloma corresponding to the activation of T-lymphocytes and monocytes/macrophages cytokines, the upregulation of extracellular matrix signatures, and the induction of the TGF-β signaling in the perigranuloma. A comparison between the proximal and distal muscles to the granuloma revealed an inverse correlation between the distance to the granuloma and the upregulation of cellular response to interferon-γ/α, TNF-α, IL-1,4,6, fibroblast proliferation, epithelial to mesenchymal cell transition, and the downregulation of muscle gene expression. These data shed light on the intercommunications between granulomas and the muscle tissue and provide pathophysiological mechanisms by showing that granuloma immune cells have a direct impact on proximal muscle tissue by promoting its progressive replacement by fibrosis via the expression of pro-inflammatory and profibrosing signatures. These data could possibly explain the evolution towards a state of disability for some patients.
Keyphrases
- skeletal muscle
- single cell
- gene expression
- extracellular matrix
- end stage renal disease
- poor prognosis
- ejection fraction
- newly diagnosed
- signaling pathway
- multiple sclerosis
- insulin resistance
- resistance training
- genome wide
- peritoneal dialysis
- stem cells
- rheumatoid arthritis
- rna seq
- dna methylation
- dendritic cells
- immune response
- electronic health record
- mass spectrometry
- machine learning
- big data
- adipose tissue
- body composition
- artificial intelligence
- epithelial mesenchymal transition
- patient reported
- long non coding rna