The FASEB JournalMolecular BiologyPeer-reviewed journal article
Distinct cAMP regulation in scleroderma lung and skin myofibroblasts governs their dedifferentiation via p38α inhibition
Jared D. BaasiD, John VargaiD, Carol A. Feghali‐BostwickiD, Marc L. Peters-GoldeniD, Sean M. FortieriD
Abstract
Fibrosis in systemic sclerosis/scleroderma (SSc) is characterized by the progressive accumulation and persistence in multiple organs of pathologic fibroblasts whose contractile properties and exuberant secretion of collagens promote tissue stiffness and scarring. Identifying a tractable mechanism for inactivating and possibly clearing these ultimate effector cells of fibrosis, conventionally termed myofibroblasts (MFs), represents an appealing therapeutic strategy for patients with SSc. This can be accomplished by their phenotypic dedifferentiation, a process known to be promoted by generation of the intracellular second messenger cyclic AMP (cAMP). Notably, however, the abilities of SSc fibroblasts derived from different tissues to generate cAMP - and dedifferentiate in response to it - have never been directly characterized or compared. Here we compared these two processes in lung and skin MFs derived from patients with SSc. While directly increasing intracellular cAMP induced comparable dedifferentiation of lung and skin SSc MFs, dedifferentiation in response to the well-recognized cAMP stimulus prostaglandin E2 (PGE2) was diminished or absent in MFs from skin as compared to lung, in part due to differences in the expression of its target G protein-coupled receptors (GPCRs). Importantly, treatment with a phosphodiesterase 4 inhibitor rescued the dedifferentiating effects of PGE2 in skin SSc MFs. Finally, both cAMP-mediated and direct pharmacologic inhibition of the MAPK p38 promoted dedifferentiation of lung and skin SSc MFs. We conclude that activation of the cAMP pathway and its subsequent inhibition of p38 dedifferentiates SSc MFs from both lung and skin, and may thus represent a therapeutic strategy to alleviate multi-organ fibrosis in SSc.
- organism: human
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: drug response / drug discovery
- approach: statistical model
- approach: experimental assay
- Citations
- 4
- FWCI
- 2.66
- Field percentile
- top 11%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- MONOCYTES STRONGLY INDUCE (MYO)FIBROBLAST CONTRACTION IN A NEW 3D SKIN MODEL TO UNDERSTAND THE INFLAMMATION-FIBROSIS AXIS IN SYSTEMIC SCLEROSIS
Djúlio César Zanin-Silva, Nienke J T van Kooten, … A. van Caam·bioRxiv·Feb 14, 2026
- Compartmental Profiling of PDE4B in Systemic Sclerosis
Astrid Hofman, Pietro Bearzi, … Oliver Distler·bioRxiv·Jul 28, 2026
- Imbalance of Ciliary Programs Drives Fibroblast Differentiation and Fibrotic Signaling in Systemic Sclerosis
Le My Tu Nguyen, Carlos E. Córdova, … Maria Eugenia Teves·bioRxiv·Feb 25, 2026
- Comparative molecular analysis of histopathologic subtypes reveals shared epithelial remodeling yet distinct fibroblast programs in scleroderma lung disease
Monica M. Yang, Vincent C Auyeung, … Paul J. Wolters·bioRxiv·Nov 4, 2026
- CD47 prevents the elimination of diseased fibroblasts in scleroderma
- A mast cell receptor is associated with fibrosis and itch in systemic sclerosis
Ruchita Kothari, Daniel Capuzzi, … Xinzhong P Dong·bioRxiv·Oct 10, 2026