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Mast cells are dispensable for normal and activin‐promoted wound healing and skin carcinogenesis
Abstract
The growth and differentiation factor activin A is a key regulator of tissue repair, inflammation, fibrosis, and tumorigenesis. However, the cellular targets, which mediate the different activin functions, are still largely unknown. In this study, we show that activin increases the number of mature mast cells in mouse skin in vivo. To determine the relevance of this finding for wound healing and skin carcinogenesis, we mated activin transgenic mice with CreMaster mice, which are characterized by Cre recombinase-mediated mast cell eradication. Using single- and double-mutant mice, we show that loss of mast cells neither affected the stimulatory effect of overexpressed activin on granulation tissue formation and reepithelialization of skin wounds nor its protumorigenic activity in a model of chemically induced skin carcinogenesis. Furthermore, mast cell deficiency did not alter wounding-induced inflammation and new tissue formation or chemically induced angiogenesis and tumorigenesis in mice with normal activin levels. These findings reveal that mast cells are not major targets of activin during wound healing and skin cancer development and also argue against nonredundant functions of mast cells in wound healing and skin carcinogenesis in general.
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“Finally, several mouse studies have found that the absence of mast cells has no effect on skin carcinogenesis or the growth of subcutaneously inoculated melanoma. 231 , 232 , 233”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [233]
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“cancer (27) and because mast cells had been proposed, based on work in Kit mutants, to contribute to human papilloma virus (HPV) 16-induced skin carcinogenesis (28), we asked whether these cells also play a role in chemically induced skin carcinogenesis.”
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Cited by
Sorted by citations
Wound repair and regeneration: Mechanisms, signaling, and translation
Eming, S. A., Martin, P., & Tomic-Canic, M. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3009337 · Cited by 3,562
Are mast cells instrumental for fibrotic diseases?
Overed-Sayer, C., Rapley, L., Mustelin, T., & Clarke, D. L. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2013.00174 · Cited by 105
Mast cell ontogeny: From fetal development to life‐long health and disease
Chia, S. L., Kapoor, S., Carvalho, C., Bajénoff, M., & Gentek, R. (2023) · Immunological Reviews · doi:10.1111/imr.13191 · Cited by 60
Metadata
- Authors
- Antsiferova, M., Martin, C., Huber, M., Feyerabend, T. B., Förster, A., Hartmann, K., Rodewald, H.-R., Hohl, D., & Werner, S.
- Affiliations
- Department of Biology, Institute of Molecular Health Sciences, Swiss Federal Institute of Technology Zurich , 8093 Zürich,
- Department of Dermatology, University of Lausanne , 1011 Lausanne,
- German Cancer Research Center , 69120 Heidelberg,
- Department of Dermatology, University of Cologne , 50937 Cologne,
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2013-12
- Volume
- 191
- Issue
- 12
- Pages
- 6147-6155
- ISSN
- 0022-1767
- 1550-6606
- Cited by
- 75
- References
- 1
- Language
- en
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- Antsiferova, M., Martin, C., Huber, M., Feyerabend, T. B., Förster, A., Hartmann, K., Rodewald, H.-R., Hohl, D., & Werner, S. (2013). Mast cells are dispensable for normal and activin‐promoted wound healing and skin carcinogenesis. The Journal of Immunology. https://doi.org/10.4049/jimmunol.1301350