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Cited 79 time in webofscience Cited 91 time in scopus
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Isolation of a mesenchymal cell population from murine dermis that contains progenitors of multiple cell lineagesopen access

Authors
Crigler, LaurenKazhanie, AmitaYoon, Tae-JinZakhari, JuliaAnders, JoannaTaylor, BarbaraVirador, Victoria M.
Issue Date
Jul-2007
Publisher
WILEY
Keywords
epidermal precursors; murine organotypic culture; keratinocytes
Citation
FASEB JOURNAL, v.21, no.9, pp 2050 - 2063
Pages
14
Indexed
SCIE
SCOPUS
Journal Title
FASEB JOURNAL
Volume
21
Number
9
Start Page
2050
End Page
2063
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/28342
DOI
10.1096/fj.06-5880com
ISSN
0892-6638
1530-6860
Abstract
The skin contains two known subpopulations of stem cells/epidermal progenitors: a basal keratinocyte population found in the interfollicular epithelium and cells residing in the bulge region of the hair follicle. The major role of the interfollicular basal keratinocyte population may be epidermal renewal, whereas the bulge population may only be activated and recruited to form a cutaneous epithelium in case of trauma. Using 3-dimensional cultures of murine skin under stress conditions in which only reserve epithelial cells would be expected to survive and expand, we demonstrate that a mesenchymal population resident in neonatal murine dermis has the unique potential to develop an epidermis in vitro. In monolayer culture, this dermal subpopulation has long-term survival capabilities in restricted serum and an inducible capacity to evolve into multiple cell lineages, both epithelial and mesenchymal, depending on culture conditions. When grafted subcutaneously, this dermal subpopulation gave rise to fusiform structures, reminiscent of disorganized muscle, that stained positive for smooth muscle actin and desmin; on typical epidermal grafts, abundant melanocytes appeared throughout the dermis that were not associated with hair follicles. The multipotential cells can be repeatedly isolated from neonatal murine dermis by a sequence of differential centrifugation and selective culture conditions. These results suggest that progenitors capable of epidermal differentiation exist in the mesenchymal compartment of an abundant tissue source and may have a function in mesenchymal-epithelial transition upon insult. Moreover, these cells could be available in sufficient quantities for lineage determination or tissue engineering applications.
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