Publication: Melanocyte stem cells in skin diseases and their potential in cell-based therapy
Authors
Wang, Zi Han ; Liu, Li-Ping ; Zheng, Yun-Wen
item.page.secondaryauthor
item.page.director
Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
publication.page.editor
publication.page.department
DOI
https://doi.org/ 10.14670/HH-18-470
item.page.type
info:eu-repo/semantics/article
Description
Abstract
Melanocytes have a complex function and
play an important role in a variety of regulatory
mechanisms in the human system. Melanocyte stem cells
(MelSCs) serve as a reservoir to replenish the
melanocytes by regenerating new ones, and they are
capable of self-renewal and differentiation to maintain
their homeostasis, repair, and regeneration in tissues.
The numerical decrease and functional impairment of
MelSCs may be closely related to the development and
treatment response of many skin diseases. However, the
current knowledge about MelSCs mainly comes from
studies in mice, and little is known about human MelSC
markers; especially, their markers are still unclear or
lack consensus. This leads to uncertainty in clinical
findings, which further limits our comprehensive
understanding of pigmentary disorders and also hinders
the progress of new treatments. Thus, in this review
article, combined with our previous and current work,
we summarize and update the recent advances in MelSC
research, including the molecular markers of human
MelSCs and their niche, as well as the association of
MelSCs with skin diseases, including vitiligo, hair
greying, and melanoma. Due to the limited tools
available to explore the identified characteristics of
human MelSCs, pluripotent stem cells can provide a new
research model for further study, especially combined
with CRISPR/Cas9 technology. The visualization of
human MelSCs’ development and differentiation can
help to identify their molecular characteristics and
understand their cellular fate dynamically, which will
allow us not only to further explore their roles in
associated diseases, but also to achieve MelSC-based
cellular therapy.
publication.page.subject
Citation
Histology and Histopathology Vol. 37, nÂş10 (2022)
item.page.embargo
Ir a EstadĂsticas
Este Ătem está sujeto a una licencia Creative Commons. http://creativecommons.org/licenses/by-nc-nd/4.0/