Bee Venom Stimulates Growth Factor Release from Adipose-Derived Stem Cells to Promote Hair Growth.
Jung-Hyun KimTae Yoon KimBon-Hyuk GooYeoncheol ParkPublished in: Toxins (2024)
Limited evidence suggests that stimulating adipose-derived stem cells (ASCs) indirectly promotes hair growth. We examined whether bee venom (BV) activated ASCs and whether BV-induced hair growth was facilitated by enhanced growth factor release by ASCs. The induction of the telogen-to-anagen phase was studied in mice. The underlying mechanism was investigated using organ cultures of mouse vibrissa hair follicles. When BV-treated ASCs were injected subcutaneously into mice, the telogen-to-anagen transition was accelerated and, by day 14, the hair weight increased. Quantitative polymerase chain reaction (qPCR) revealed that BV influenced the expression of several molecules, including growth factors, chemokines, channels, transcription factors, and enzymes. Western blot analysis was employed to verify the protein expression levels of extracellular-signal-regulated kinase (ERK) and phospho-ERK. Both the Boyden chamber experiment and scratch assay confirmed the upregulation of cell migration by BV. Additionally, ASCs secreted higher levels of growth factors after exposure to BV. Following BV therapy, the gene expression levels of alkaline phosphatase (ALP), fibroblast growth factor (FGF)-1 and 6, endothelial cell growth factor, and platelet-derived growth factor (PDGF)-C were upregulated. The findings of this study suggest that bee venom can potentially be utilized as an ASC-preconditioning agent for hair regeneration.
Keyphrases
- growth factor
- lps induced
- lipopolysaccharide induced
- inflammatory response
- gene expression
- cell migration
- transcription factor
- cell proliferation
- endothelial cells
- stem cells
- high fat diet induced
- high glucose
- dna methylation
- south africa
- weight loss
- bone marrow
- adipose tissue
- insulin resistance
- body mass index
- mass spectrometry
- diabetic rats
- brain injury
- tyrosine kinase
- single cell
- oxidative stress
- drug induced
- atomic force microscopy
- wild type
- long non coding rna
- dna binding
- smoking cessation
- vascular endothelial growth factor