Phenotypic plasticity of melanocytes derived from human adult skin.
Dániel László VidácsZoltán VerébRenáta BozóLili Borbála FlinkHilda PolyánkaIstván Balázs NémethSzilárd PóliskaBenjamin Tamás PappMáté ManczingerRóbert GáspárSeyedmohsen MirdamadiLajos KeményZsuzsanna Bata-CsörgőPublished in: Pigment cell & melanoma research (2021)
We previously described a novel in vitro culture technique for dedifferentiated human adult skin melanocytes. Melanocytes cultured in a defined, cholera toxin and PMA free medium became bipolar, unpigmented, and highly proliferative. Furthermore, TRP-1 and c-Kit expression disappeared and EGFR receptor and nestin expression were induced in the cells. Here, we further characterized the phenotype of these dedifferentiated cells and by comparing them to mature pigmented melanocytes we detected crucial steps in their phenotype change. Our data suggest that normal adult melanocytes easily dedifferentiate into pluripotent stem cells given the right environment. This dedifferentiation process described here for normal melanocyte is very similar to what has been described for melanoma cells, indicating that phenotype switching driven by environmental factors is a general characteristic of melanocytes that can occur independent of malignant transformation.
Keyphrases
- pluripotent stem cells
- endothelial cells
- induced apoptosis
- poor prognosis
- cell cycle arrest
- high glucose
- small cell lung cancer
- escherichia coli
- induced pluripotent stem cells
- soft tissue
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- epidermal growth factor receptor
- diabetic rats
- pi k akt
- machine learning
- young adults
- long non coding rna
- deep learning
- data analysis