First Direct In Vitro Comparison Between Cordycepin (MDRN) and PDRN: Skin-Repair-Related Cellular Responses at Lower Tested Mass Concentrations
Gyeonghyeon Kim, Byeongho Park, Sae Woong Oh, Yeonsoo Kim, Seon Bin Lee, Eui Su Choung, Hye Jin Kim, Seung Hui Yu, Kwanje Cho, Jongsung Lee, Won-Sang SeoThis study introduces the concept of MDRN, referring to monomeric deoxyribonucleoside, and evaluates cordycepin (251.24 Da) as a low-molecular-weight alternative to polydeoxyribonucleotide (PDRN). Cordycepin (1–20 μM) was compared with PDRN (100 μg/mL) in human keratinocytes and dermal fibroblasts. Molecular simulations and cellular thermal-shift assays supported a potential interaction with the adenosine A2A receptor, while 3,7-dimethyl-1-propargylxanthine (DMPX), an adenosine receptor antagonist, attenuated selected signaling responses. Cordycepin reduced UVA-induced oxidative and inflammatory responses in keratinocytes, altered autophagy-related reporter signals in HEK293T cells, and selectively modulated barrier- and tight-junction-related gene expression. In fibroblasts, it decreased MMP-1 expression and increased COL1A1 expression. Cordycepin also increased scratch-wound closure in both cell types at selected concentrations. Selected cordycepin treatments significantly increased fibroblast scratch-wound closure and the expression of specific keratinocyte barrier-associated genes compared with PDRN. These comparative responses depended on the endpoint and concentration. Notably, 20 μM cordycepin corresponds to approximately 5.02 μg/mL, one-twentieth of the tested PDRN mass concentration. These findings support cordycepin as an MDRN candidate that elicits skin-repair-related cellular responses at substantially lower mass concentrations than PDRN. Further studies are required to establish relative potency and topical applicability.