Myo/Nog cells in normal, wounded and tumor-bearing skin

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Abstract

Murine and human skin were examined for the presence of Myo/Nog cells that were originally discovered in the chick embryo by their expression of MyoD mRNA, noggin and the G8 antigen. Myo/Nog cells are the primary source of noggin in telogen hair follicles. They are scarce within the interfollicular dermis and absent in the epidermis. Within 24 h following epidermal abrasion, Myo/Nog cells increase in number in the follicles and appear in the wound. Myo/Nog cells are also recruited to the stroma of tumors formed from v-Ras-transformed keratinocytes (Ker/Ras). Human squamous cell carcinomas and malignant melanomas contain significantly more Myo/Nog cells than basal cell carcinomas. Myo/Nog cells are distinct from macrophages, granulocytes and cells expressing alpha smooth muscle actin in the tumor stroma. Myo/Nog cells may be modulators of skin homoeostasis and wound healing, and potential diagnostic and therapeutic targets in skin cancer. © 2012 John Wiley & Sons A/S.

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Gerhart, J., Hayes, C., Scheinfeld, V., Chernick, M., George-Weinstein, M., & Gilmour, S. (2012, June). Myo/Nog cells in normal, wounded and tumor-bearing skin. Experimental Dermatology. https://doi.org/10.1111/j.1600-0625.2012.01503.x

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