| Literature DB >> 27168117 |
Despina Soteriou1, Lana Kostic1, Egor Sedov1, Yahav Yosefzon1, Hermann Steller2, Yaron Fuchs3.
Abstract
The hair follicle (HF) is an ideal system for studying the biology and regulation of adult stem cells (SCs). This dynamic mini organ is replenished by distinct pools of SCs, which are located in the permanent portion of the HF, a region known as the bulge. These multipotent bulge SCs were initially identified as slow cycling label retaining cells; however, their isolation has been made feasible after identification of specific cell markers, such as CD34 and keratin 15 (K15). Here, we describe a robust method for isolating bulge SCs and epidermal keratinocytes from mouse HFs utilizing fluorescence activated cell-sorting (FACS) technology. Isolated hair follicle SCs (HFSCs) can be utilized in various in vivo grafting models and are a valuable in vitro model for studying the mechanisms that govern multipotency, quiescence and activation.Entities:
Mesh:
Year: 2016 PMID: 27168117 PMCID: PMC4942017 DOI: 10.3791/53931
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355