Myo/Nog cells in normal, wounded and tumor-bearing skin
Document Type
Article
Publication Date
2012
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.
Publication Title
Experimental dermatology
Volume
21
Issue
6
First Page
466
Last Page
468
Recommended Citation
Gerhart, Jacquelyn; Hayes, C.; Scheinfeld, V.; Chernick, M.; George-Weinstein, Mindy; and Gilmour, S., "Myo/Nog cells in normal, wounded and tumor-bearing skin" (2012). PCOM Scholarly Works. 1664.
https://digitalcommons.pcom.edu/scholarly_papers/1664
Comments
This article was published in Experimental dermatology, Volume 21, Issue 6, Pages 466-468.
The published version is available at http://dx.doi.org/10.1111/j.1600-0625.2012.01503.
Copyright © 2012 Wiley.