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5 protocols using ab178676

1

Thymocid Modulates Melanogenesis Genes

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B16F10 cells were seeded in 6-well plates at a density of 1.0 × 105 cells per well and allowed to grow for 24 h and were then treated with Thymocid® (2.5 and 10 µg/mL) and cultured for 72 h. After washing with PBS, B16F10 cells were harvested, whole-cell lysates were prepared and quantified, and the protein expressions of MITF, TYR, TYRP1, and TYRP2 were quantified by Western blot assay, as described previously [27 (link)]. Antibodies including anti-MITF (ab3201), anti-TYRP1 (ab178676), anti-TYRP2 (ab103463), and anti-β-Actin antibody (ab8227) were obtained from Abcam, Cambridge, MA, USA. The western blot (WB) bands were detected on X-ray films using an enhanced chemiluminescence (ECL) detection kit (GE Healthcare, Piscataway, NJ, USA) according to the manufacturer’s protocol.
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2

Quantifying Melanosome Transfer in MC-KC Co-culture

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Quantitative assessments for melanosome transfer in MC-KC co-culture. Cells in co-culture were treated with the indicated compounds for 48 h. To quantitatively assay melanosome transfer. The co-cultured cells were harvested and washed with cold PBS, fixed in 4% paraformaldehyde for 10 min, washed with PBS containing 0.1% Triton-X100 for 5 min. MCs were immunostained with anti-TRP1 antibody (ab178676, Abcam, Cambridge, UK) and goat anti-mouse IgG H&L/PE secondary antibody (bs-0296G-PE, Bioss, Beijing, China) and KCs were incubated with anti-pan cytokeratin antibody conjugated with alexa fluor 488 (ab277270, Abcam, Cambridge, UK). Stained cells were analysed by flow cytometry. A total of 10 000 events were collected on the CytoFLEX Flow Cytometer (Beckman coulter, Brea, CA, USA). The ratio of percentage of cells positive for both cytokeratin and tyrosinase to that of cells positive for cytokeratin only represents melanosome transfer efficacy [30 (link),34 (link),35 (link)].
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3

Immunostaining of Co-cultured Cells

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The co-cultured cells were washed with ice-cold PBS, fixed in 4% paraformaldehyde for 10 min, and washed with PBS containing 0.25% Triton-X100 for 10 min to permeabilize the membrane. Add blocking buffer (Beyotime, Shanghai, China) for 10 min at 37 ℃. Then MCs were immunostained with anti-TRP1 antibody (ab178676, Abcam, Cambridge, UK) and goat anti-mouse IgG H&L/PE secondary antibody (bs-0296G-PE, Bioss, Beijing, China) and KCs were incubated with anti-pan cytokeratin antibody conjugated with alexa fluor 488 (ab277270, Abcam, Cambridge, UK). Nucleus were stained with DAPI. Images were obtained with an Inverted fluorescence microscope (Mshot, Guangzhou, China) and dealt with Image pro plus [36 (link)].
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Argan Leaf Saponin and Arbutin Effects on Melanogenesis Proteins

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B16 cells (5 × 104 cells/Petri dishes) were seeded and incubated at 37 °C in an incubator with 5% CO2. After 24 h incubation, the growth medium was replaced with a fresh growth medium with or without 10 μg argan leaf saponin and 100 μM arbutin, and incubated further for 24 h and 48 h. After the specified incubation time, the protein samples were extracted using a RIPA (radio immunoprecipitation assay) lysis buffer (SIGMA; St. Louis, MO, USA) with 0.1% protease inhibitor cocktail (SIGMA; St. Louis, MO, USA) following the manufacturer’s instructions. The protein samples were then loaded into 10% SDS-polyacrylamide gel and subjected to electrophoresis (SDS-PAGE). The proteins in the gel were transferred onto a PVDF membrane and incubated in specific primary antibodies against MITF (ab140606, Abcam, Waltham, MA, USA), TYR (ab180753, Abcam, Waltham, MA, USA), TYRP1 (ab221144, Abcam, Waltham, MA, USA), DCT (ab178676, Abcam, Waltham, MA, USA), and GAPDH (ab181602, ab9485, Abcam, Waltham, MA, USA). Membranes were washed with PBS with Tween-20 (PBST) before incubation with goat anti-mouse IRDye 680LT or goat anti-rabbit IRDye 800CW (LI-COR) secondary antibodies at room temperature.
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5

Protein Expression Analysis in Exosomes

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Cells were lysed in RIPA buffer (P0013C, Beyotime, Shanghai, China) with a protease inhibitor cocktail (P8340, Sigma‐Aldrich). The total proteins of lysates or exosomes were separated by SDS polyacrylamide gels and transferred onto PVDF membranes (Millipore, USA). Then, these membranes were blocked with 5% BSA for one hour at room temperature and incubated with primary antibodies overnight at 4°C. Afterwards, the secondary antibodies were added. The blots were observed using the Azure Biosystems C300. The antibodies are listed, as follows: rabbit anti‐Tyrosinase (ab170905; Abcam, Cambridge, MA, USA), rabbit anti‐TRP1 (ab178676, Abcam), rabbit anti‐TRP2/DCT (ab221144, Abcam), rabbit anti‐MITF (ab140606, Abcam), rabbit anti‐β‐catenin (51067‐2‐AP; Proteintech, Wuhan, China), rabbit anti‐SOX1 (20744‐1‐AP, Proteintech), rabbit anti‐CD63 (25682‐1‐AP, Proteintech), rabbit anti‐TSG101 (14497‐1‐AP, Proteintech), Lamin B1 antibody (12987‐1‐AP, Proteintech) and β‐actin (no.3700, Cell Signaling Technology, Danvers, MA, USA).
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