hfdpcs (PromoCell)
Structured Review

Hfdpcs, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 122 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hfdpcs/product/PromoCell
Average 95 stars, based on 122 article reviews
Images
1) Product Images from "Anti-Hair Loss Activity of Healthy Human Scalp-Derived Staphylococcus capitis KMH304 Ferment Filtrate in Human Hair-Follicle Dermal Papilla and Keratinocyte Cells"
Article Title: Anti-Hair Loss Activity of Healthy Human Scalp-Derived Staphylococcus capitis KMH304 Ferment Filtrate in Human Hair-Follicle Dermal Papilla and Keratinocyte Cells
Journal: Microorganisms
doi: 10.3390/microorganisms14040929
Figure Legend Snippet: Effect of SCFF on HFDPC and HaCaT cell viability and proliferation. HFDPCs and HaCaT cells were treated with different concentrations of SCFF as indicated for 24 h. ( a ) HFDPC and ( b ) HaCaT viability and proliferation were assessed at various SCFF concentrations (50, 100, 250, 500, 1000, 2500, 5000 μg/mL) using a CCK-8 assay. Values are mean ± SD of three independent experiments. ( a – c ) *** p < 0.001, ** p < 0.01 and * p < 0.05 versus NC group (100%). ( c ) Representative images of cellular proliferation activity in HFDPCs and HaCaT cells after 48 h of incubation ( n = 3; Scale bar = 200 μm). SCFF, Staphylococcus capitis KMH304 ferment filtrate; HFDPCs, human follicle dermal papilla cells; NC, negative control.
Techniques Used: CCK-8 Assay, Activity Assay, Incubation, Negative Control
Figure Legend Snippet: Hair growth-related and AGA-inducing signature gene expression following SCFF treatment in HFDPCs. HFDPCs were treated with different SCFF concentrations for 24 h, and gene expression was evaluated using qPCR. ( a ) Hair growth-related factors (KGF, IGF-1, and HGF). ( b ) AGA-inducing factors (AR and TGF-β2). MXD at 5 μg/mL was used as PC for TGF-β2, and 2.5 μg/mL MXD was used as PC for other markers. Data are mean ± SD of three independent experiments. *** p < 0.001, ** p < 0.01 and * p < 0.05 versus NC group (100%). SCFF, Staphylococcus capitis KMH304 ferment filtrate; HFDPCs, human follicle dermal papilla cells; MXD, minoxidil; PC, positive control.
Techniques Used: Gene Expression, Positive Control
Figure Legend Snippet: The regulation of cellular senescence by SCFF in HFDPCs. HFDPCs were treated with different concentrations of SCFF for 24 h, followed by analysis using qPCR and SA-β-gal staining. ( a , b ) Anti-aging factors (SIRT1, SIRT7, COL13A1, and p21). ( c ) SA-β-gal staining in young (P6) and senescent (P16) passage cells. Quantitative and representative images of SA-β-gal-positive cells compared with senescent cells (Scale bar = 200 μm). For SIRT, 1 μg/mL fisetin (Fis) was used as a positive control (PC), and for COL13 and p21, 1 μg/mL Fis was used as PC. Data are the mean ± SD of three independent experiments. **** p < 0.0001, *** p < 0.001, ** p < 0.01, and * p < 0.05 versus the negative control (NC) and the senescent group (100%). SCFF, Staphylococcus capitis KMH304 ferment filtrate; HFDPCs, human follicle dermal papilla cells.
Techniques Used: Staining, Positive Control, Negative Control
Figure Legend Snippet: Overall effect of SCFF in HFDPCs and HaCaT cells. In keratinocytes, SCFF enhanced barrier function and antioxidant activity. SCFF not only regulated cellular aging through longevity-, collagen-, and p21-related genes, but also promoted hair growth by increasing the expression of hair-growth–associated factors and suppressing hair loss-inducing factors in HFDPCs. SCFF, Staphylococcus capitis KMH304 ferment filtrate; HFDPCs, human follicle dermal papilla cells.
Techniques Used: Antioxidant Activity Assay, Expressing