Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq

Figure 1

In vitro assessment of the effect of different concentrations of porphyra extract and porphyra-334 on cell viability and collagen synthesis. The effect of three different concentrations (1, 5, and 10 ppm) of porphyra extract and porphyra-334 on the cell viability of Detroit 551 cells was examined by MTT assay (a). C indicates control cells treated with distilled water. (b) PIP content was measured in Detroit 551 cells after treatment with different concentrations of porphyra extract and porphyra-334. TGF-β1, which is known to promote collagen formation, cell proliferation, and the differentiation of dermal fibroblasts, was used as a positive control. (c) PIP content was measured in HFDP cells after treatment with different concentrations of porphyra-334. For the comparisons between the positive sample (TGF-β1) and the treatment group, we conducted independent t-tests. ^∗∗.

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