Combinations of peptides synergistically activate the regenerative capacity of skin cells in vitro

• Published in: International journal of cosmetic science 2021-10, Vol.43 (5), p.518-529
• Main Authors: Flagler, Michael J., Tamura, Makio, Laughlin, Tim, Hartman, Scott, Ashe, Julie, Adams, Rachel, Kozak, Kim, Cresswell, Kellen, Mullins, Lisa, Jarrold, Bradley B., Isfort, Robert J., Sherrill, Joseph D.
• Format: Article
• Language: English
• Subjects: Associations; ATP; Bioinformatics; Cell Line; Cell lines; Cellular stress response; Combinatorial analysis; DNA microarrays; Drug Synergism; Gene Expression; Humans; Keratinocytes; Keratinocytes - drug effects; Lasers; Niacinamide - pharmacology; Nicotinamide; Original; Oxidative stress; Peptides; Peptides - pharmacology; Regeneration; Rejuvenation; Repair; Resurfacing; Skin; Skin Aging - drug effects; Surfacing; Synergistic effect; Transcription
• ISSN: 0142-5463; 1468-2494
• DOI: 10.1111/ics.12725

Objective To explore synergistic effects related to skin regeneration, peptides with distinct biological mechanisms of action were evaluated in combination with different skin cell lines in the presence or absence of niacinamide (Nam). Furthermore, the synergistic responses of peptide combinations on global gene expression were compared with the changes that occur with fractional laser resurfacing treatment, a gold standard approach for skin rejuvenation, to further define optimal peptide combinations. Methods Microarray profiling was used to characterize the biological responses of peptide combinations (+/− Nam) relative to the individual components in epidermal keratinocyte and dermal fibroblast cell lines. Cellular functional assays were utilized to confirm the synergistic effects of peptide combinations. Bioinformatics approaches were used to link the synergistic effects of peptide combinations on gene expression to the transcriptomics of the skin rejuvenation response from fractional laser treatment. Results Microarray analysis of skin cells treated with peptide combinations revealed synergistic changes in gene expression compared with individual peptide controls. Bioinformatic analysis of synergy genes in keratinocytes revealed the activation of NRF2‐mediated oxidative stress responses by a combination of Ac‐PPYL, Pal‐KTTKS and Nam. Additional analysis revealed direct downstream transcriptional targets of NRF2/ARE exhibiting synergistic regulation by this combination of materials, which was corroborated by a cellular reporter assay. NRF2‐mediated oxidative stress response pathways were also found to be activated in the transcriptomics of the early skin rejuvenation response to fractional laser treatment, suggesting the importance of this biology in the early stages of tissue repair. Additionally, the second combination of peptides (pal‐KT and Ac‐PPYL) was found to synergistically restore cellular ATP levels that had been depleted due to the presence of ROS, indicating an additional mechanism, whereby peptide synergies may accelerate skin repair. Conclusion Through combinatorial synergy studies, we have identified additional in vitro skin repair mechanisms beyond the previously described functions of individual peptides and correlated these to the transcriptomics of the skin rejuvenation response of fractional laser treatment. These findings suggest that specific peptides can act together, via complementary and synergistic mechanisms, to holistically