Impact of intercellular crosstalk between epidermal keratinocytes and dermal fibroblasts on skin homeostasis
Open accessAbstract
Dermal fibroblasts seem critical for epidermal maturation and differentiation and recent work demonstrated that diseased fibroblasts may drive pathophysiological processes. Nevertheless, still very little is known about the actual crosstalk between epidermal keratinocytes and dermal fibroblasts and the impact of dermal fibroblasts on epidermal maturation and differentiation. Aiming for a more fundamental understanding of the impact of the cellular crosstalk between keratinocytes and fibroblasts on the skin homeostasis, we generated full-thickness skin equivalents with and without fibroblasts and subsequently analysed them for the expression of skin differentiation markers, their barrier function, skin lipid content and epidermal cell signalling. Skin equivalents without fibroblasts consistently showed an impaired differentiation and dysregulated expression of skin barrier and tight junction proteins, increased skin permeability, and a decreased skin lipid/protein ratio. Most interestingly, impaired Ras/Raf/ERK/MEK signalling was evident in skin equivalents without fibroblasts. Our data clearly indicate that the epidermal-dermal crosstalk between keratinocytes and fibroblasts is critical for adequate skin differentiation and that fibroblasts orchestrate epidermal differentiation processes.
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The two-layer design of HSEs allows optimal differentiation of the epidermis and replication of complex interactions between keratinocytes and fibroblasts, which are crucial for maintaining skin homeostasis.
“This design allows for the optimal differentiation of the epidermis and the replication of the complex interactions between KCs and Fibs, which are crucial for maintaining skin homeostasis [32].”
From Diversity of human skin three-dimensional organotypic cultures (2024) · cites this paper as [32]
HSEs show marked molecular differences in basal and terminal gene expression, suggesting epidermal differentiation is not quite analogous to in vivo counterparts.
“Many studies defining HSEs have shown marked molecular differences in basal and terminal gene expression that suggest that epidermal differentiation is not quite analogous to the in vivo counterparts.”
From Single-cell transcriptomics of human-skin-equivalent organoids (2023) · cites this paper as [21]
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References 37 · Cited by 75
- Authors
- Jevtić, M., Löwa, A., Nováčková, A., Kováčik, A., Kaessmeyer, S., Erdmann, G., Vávrová, K., & Hedtrich, S.
- Affiliations
- Freie Universität Berlin (DE)
- Charles University (CZ)
- University of British Columbia (CA)
- Corresponding author
- Hedtrich, Sarah
- ORCID
- Venue
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Publisher
- Elsevier BV
- Published
- 2020-08
- Volume
- 1867
- Issue
- 8
- Pages
- 118722
- ISSN
- 0167-4889 (ISSN-L)
- OpenAlex
- W3016714209
- Cited by
- 75
- References
- 37
- Citations by year
- 2026: 12 · 2025: 15 · 2024: 14 · 2023: 11 · 2022: 11 · 2021: 9 · 2020: 3
- FWCI
- 4.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (publishedVersion)
- PubMed (publishedVersion)
- MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
- Health Sciences › Medicine › Urology › Hair Growth and Disorders
- Keywords
- keratinocytes, dermal fibroblasts, cell-cell crosstalk, epidermal differentiation, skin homeostasis, skin equivalents, skin barrier function, tight junction proteins, skin permeability, epidermal-dermal interaction
- MeSH terms
- Epidermal Cells, Cell Differentiation, Epidermis, Fibroblasts, Homeostasis, Humans, Permeability, Skin, Skin Absorption, Keratinocytes
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