KIT expression reveals a population of precursor melanocytes in human skin
- PMID: 8618059
- DOI: 10.1111/1523-1747.ep12338471
KIT expression reveals a population of precursor melanocytes in human skin
Abstract
Human skin is believed to harbor a reservoir population of precursor melanocytes. It has been difficult to identify these putative cells experimentally, because they lack phenotypic features that define mature melanocytes. We have evaluated expression of the KIT tyrosine kinase receptor, which is critical for melanocyte development, as a possible marker of these cells. Sections of human skin were evaluated with single- and double-immunolabeling techniques. KIT-reactive dendritic cells were identified in the basal layer of the epithelia and were most numerous in the follicular infundibula and the rete ridges. These cells were located on the epithelial side of the basement membrane and lacked expression of cytokeratin and mast cell tryptase. The location of the KIT-reactive cells was distinctly different from that of Langerhans cells (identified with anti-CD1a) or Merkel cells (identified with CAM 5.2). Within the epidermis and upper follicular infundibulum the majority of the KIT-reactive dendritic cells also coexpressed TRP-1, a marker present in differentiated melanocytes. In the deeper follicular regions, the coexpression of TRP-1 in the KIT-reactive cells was absent. Throughout the epidermis and follicle, however, the KIT-reactive cells coexpressed BCL-2, a marker known to be increased in melanocytes. Thus, KIT expression reveals a population of intraepithelial cells that have immunophenotypic characteristics of mature melanocytes within the upper epithelial regions, but lack the differentiated melanocytic phenotype within the deeper follicular regions. We propose that these KIT(+), BCL-2(+), and TRP-1(-) cells constitute a precursor melanocyte reservoir of human skin.
Similar articles
-
The expression of the c-kit receptor by epidermal melanocytes may be reduced in vitiligo.Br J Dermatol. 1996 Feb;134(2):299-306. Br J Dermatol. 1996. PMID: 8746346
-
Kit(+) melanocytes seem to contribute to melanocyte proliferation after UV exposure as precursor cells.J Invest Dermatol. 2001 Jun;116(6):920-5. doi: 10.1046/j.0022-202x.2001.01370.x. J Invest Dermatol. 2001. PMID: 11407982
-
Stem cell factor/c-Kit signalling in normal and androgenetic alopecia hair follicles.J Endocrinol. 2008 Apr;197(1):11-23. doi: 10.1677/JOE-07-0522. J Endocrinol. 2008. PMID: 18372228
-
Review: melanocyte migration and survival controlled by SCF/c-kit expression.J Investig Dermatol Symp Proc. 2001 Nov;6(1):1-5. doi: 10.1046/j.0022-202x.2001.00006.x. J Investig Dermatol Symp Proc. 2001. PMID: 11764276 Review.
-
[Histology of skin and hair follicle].Med Sci (Paris). 2006 Feb;22(2):131-7. doi: 10.1051/medsci/2006222131. Med Sci (Paris). 2006. PMID: 16457751 Review. French.
Cited by
-
Molecular and cellular pathogenesis of melanoma initiation and progression.Cell Mol Life Sci. 2013 Nov;70(21):4055-65. doi: 10.1007/s00018-013-1324-2. Epub 2013 Mar 27. Cell Mol Life Sci. 2013. PMID: 23532409 Free PMC article. Review.
-
Differential expression of stem cell markers in human follicular bulge and interfollicular epidermal compartments.Histochem Cell Biol. 2010 Apr;133(4):455-65. doi: 10.1007/s00418-010-0684-z. Epub 2010 Mar 13. Histochem Cell Biol. 2010. PMID: 20229054
-
CD133-Dependent Activation of Phosphoinositide 3-Kinase /AKT/Mammalian Target of Rapamycin Signaling in Melanoma Progression and Drug Resistance.Cells. 2024 Jan 26;13(3):240. doi: 10.3390/cells13030240. Cells. 2024. PMID: 38334632 Free PMC article. Review.
-
Does melanoma begin in a melanocyte stem cell?J Skin Cancer. 2012;2012:571087. doi: 10.1155/2012/571087. Epub 2012 Dec 18. J Skin Cancer. 2012. PMID: 23316368 Free PMC article.
-
Extrafollicular dermal melanocyte stem cells and melanoma.Stem Cells Int. 2012;2012:407079. doi: 10.1155/2012/407079. Epub 2012 May 10. Stem Cells Int. 2012. PMID: 22666269 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical