358 Can Immune Cells Become Skin Cells in Large Burn Injury?

Abstract Introduction Upon any kind of dermal injury, keratinocytes and fibroblasts migrate from the edge of injury site to the wound site where they proliferate and promote wound healing. However, it is unlikely that these cells from the edges of large burn injury be able to migrate to a very long...

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Veröffentlicht in:Journal of burn care & research 2018-04, Vol.39 (suppl_1), p.S149-S149
Hauptverfasser: Li, Y, Kilani, R, Ghahary, A
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract Introduction Upon any kind of dermal injury, keratinocytes and fibroblasts migrate from the edge of injury site to the wound site where they proliferate and promote wound healing. However, it is unlikely that these cells from the edges of large burn injury be able to migrate to a very long distance to cover the injury site. Here, we hypothesize that skin injury initiates a signal through which a subset of circulating immune cells become de-differentiated into stem like cells and these cells then become the major source of skin cells during the healing process. Methods The potential role of releasable factors from the proliferating fibroblasts on trans-differentiation of immune cells to multi-potent stem like cells was evaluated by culturing immune cells in fibroblast conditioned medium for 6 days. Cells were then examined for their morphology and the expression of a set of stem cell markers and their capacity to further differentiation into other cell types. Results The finding showed that culturing a subset of blood derived immune cells have the capacity to be de-differentiated into fibroblast like cells when co-cultured with proliferating fibroblasts. These cells were then identified to be fibroblast like cells with capacity to express a panel of stem cell markers such as alkaline phosphatase, formation of embryonic bodies, and expression of other pluripotent stem cells markers. Further, these cells showed a capacity to further differentiate into fibroblasts, osteocytes, adipocytes, smooth muscle cells, endothelial cells, neural cells. This finding was further confirmed in a mouse model by showing an easy detection of SSEA-1, a main marker for PSCs in wounded but not in normal tissues. Conclusions These data confirm that a subset of circulating immune cells have the capacity to become de-differentiated into PSCs within the wound environment and that these cells become the main source of skin cells in large wounds including burn. Applicability of Research to Practice Identifying the factors responsible for conversion of immune cells to skin cells would make it possible to topically apply these factors to promote the healing and reduce inflammation in large burn injury.
ISSN:1559-047X
1559-0488
DOI:10.1093/jbcr/iry006.280