Journal
CELL PROLIFERATION
Volume 54, Issue 9, Pages -Publisher
WILEY
DOI: 10.1111/cpr.13106
Keywords
3D co-culture system; amphiregulin; hair follicle; MAPK; PI3K; skin-derived precursors
Categories
Funding
- National Natural Science Foundation of China [31801196, 31900540]
- Shenzhen Science and Technology Innovation Committee [JCYJ201803073000199, JCYJ20200109142444449]
- Central University Basic Research Fund of China [19ykpy16]
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The study revealed that AREG enhances SKP stemness through the PI3K and MAPK pathways, promoting their proliferation and hair-inducing capacity, suggesting AREG therapy as a potentially promising approach for treating alopecia.
Objectives There are significant clinical challenges associated with alopecia treatment, including poor efficiency of related drugs and insufficient hair follicles (HFs) for transplantation. Skin-derived precursors (SKPs) exhibit great potential as stem cell-based therapies for hair regeneration; however, the proliferation and hair-inducing capacity of SKPs gradually decrease during culturing. Materials and Methods We describe a 3D co-culture system accompanied by kyoto encyclopaedia of genes and genomes and gene ontology enrichment analyses to determine the key factors and pathways that enhance SKP stemness and verified using alkaline phosphatase assays, Ki-67 staining, HF reconstitution, Western blot and immunofluorescence staining. The upregulated genes were confirmed utilizing corresponding recombinant protein or small-interfering RNA silencing in vitro, as well as the evaluation of telogen-to-anagen transition and HF reconstitution in vivo. Results The 3D co-culture system revealed that epidermal stem cells and adipose-derived stem cells enhanced SKP proliferation and HF regeneration capacity by amphiregulin (AREG), with the promoted stemness allowing SKPs to gain an earlier telogen-to-anagen transition and high-efficiency HF reconstitution. By contrast, inhibitors of the phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase (MAPK) pathways downstream of AREG signalling resulted in diametrically opposite activities. Conclusions By exploiting a 3D co-culture model, we determined that AREG promoted SKP stemness by enhancing both proliferation and hair-inducing capacity through the PI3K and MAPK pathways. These findings suggest AREG therapy as a potentially promising approach for treating alopecia.
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