Fibroblast-Mediated Macrophage Recruitment Supports Acute Wound Healing

Epithelial and immune cells have long been appreciated for their contribution to the early immune response after injury; however, much less is known about the role of mesenchymal cells. Using single-nuclei RNA sequencing, we defined changes in gene expression associated with inflammation 1 day after wounding in mouse skin. Compared with those in keratinocytes and myeloid cells, we detected enriched expression of proinflammatory genes in fibroblasts associated with deeper layers of the skin. In particular, SCA1+ fibroblasts were enriched for numerous chemokines, including CCL2, CCL7, and IL-33, compared with SCA1- fibroblasts. Genetic deletion of Ccl2 in fibroblasts resulted in fewer wound-bed macrophages and monocytes during injury-induced inflammation, with reduced revascularization and re-epithelialization during the proliferation phase of healing. These findings highlight the important contribution of fibroblast-derived factors to injury-induced inflammation and the impact of immune cell dysregulation on subsequent tissue repair.

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Publication Details

Journal
Journal of Investigative Dermatology
Published
2024-11-22
DOI
https://doi.org/10.1016/j.jid.2024.10.609
Citations
14
Primary Topic
Wound Healing and Treatments
Type
article
Field-Weighted Citation Impact
3.50

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article

Fibroblast-Mediated Macrophage Recruitment Supports Acute Wound Healing

MaryEllen R. Haas, Chiraag Gohel, Brett A. Shook, Khatereh Khorsandi et al.
14 citations
Journal of Investigative Dermatology
Wound Healing and Treatments
3.50
article

Fibroblast-Mediated Macrophage Recruitment Supports Acute Wound Healing

MaryEllen R. Haas, Chiraag Gohel, Brett A. Shook, Khatereh Khorsandi, Anélia Horvath, Shatha Salameh, Ranojoy Chatterjee, Ali Rahnavard, Veronica M. Amuso, Paula O. Cooper, Sarah S Kleb, Sana Hafiz, Miguel F. Mazumder, Violet Josephson
article en
14 citations

Abstract

Epithelial and immune cells have long been appreciated for their contribution to the early immune response after injury; however, much less is known about the role of mesenchymal cells. Using single-nuclei RNA sequencing, we defined changes in gene expression associated with inflammation 1 day after wounding in mouse skin. Compared with those in keratinocytes and myeloid cells, we detected enriched expression of proinflammatory genes in fibroblasts associated with deeper layers of the skin. In particular, SCA1+ fibroblasts were enriched for numerous chemokines, including CCL2, CCL7, and IL-33, compared with SCA1- fibroblasts. Genetic deletion of Ccl2 in fibroblasts resulted in fewer wound-bed macrophages and monocytes during injury-induced inflammation, with reduced revascularization and re-epithelialization during the proliferation phase of healing. These findings highlight the important contribution of fibroblast-derived factors to injury-induced inflammation and the impact of immune cell dysregulation on subsequent tissue repair.

Journal of Investigative DermatologyVol. 145(7)
Milken Institute (US), George Washington University (US)
National Science Foundation, National Sleep Foundation, George Washington University, National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Zero hunger
Openalex Percentile: Top 7%
Wound Healing and Treatments
3.50
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