PDRN, a Bioactive Natural Compound, Ameliorates Imiquimod-Induced Psoriasis through NF-κB Pathway Inhibition and Wnt/β-Catenin Signaling Modulation

被引:22
作者
Irrera, Natasha [1 ]
Bitto, Alessandra [1 ]
Vaccaro, Mario [1 ]
Mannino, Federica [1 ]
Squadrito, Violetta [1 ]
Pallio, Giovanni [1 ]
Arcoraci, Vincenzo [1 ]
Minutoli, Letteria [1 ]
Ieni, Antonio [2 ]
Lentini, Maria [2 ]
Altavilla, Domenica [3 ]
Squadrito, Francesco [1 ]
机构
[1] Univ Messina, Dept Clin & Expt Med, AOU Policlin G Martino, Via C Valeria Gazzi, I-98125 Messina, Italy
[2] Univ Messina, Dept Human Pathol Adult & Dev Age Gaetano Barresi, AOU Policlin G Martino, Via C Valeria Gazzi, I-98125 Messina, Italy
[3] Univ Messina, Dept Biomed & Dent Sci & Morphol & Funct Sci, AOU Policlin G Martino, Via C Valeria Gazzi, I-98125 Messina, Italy
关键词
adenosine A2A receptor; psoriasis; NF-kappa B; Wnt/beta-catenin pathway; ADENOSINE RECEPTOR STIMULATION; PATHOGENESIS; MECHANISMS;
D O I
10.3390/ijms21041215
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear factor-kappa B (NF-kappa B) plays a central role in psoriasis and canonical Wnt/beta-catenin pathway blunts the immune-mediated inflammatory cascade in psoriasis. Adenosine A2A receptor activation blocks NF-kappa B and boosts the Wnt/beta-catenin signaling. PDRN (Polydeoxyribonucleotide) is a biologic agonist of the A2A receptor and its effects were studied in an experimental model of psoriasis. Psoriasis-like lesions were induced by a daily application of imiquimod (IMQ) on the shaved back skin of mice for 7 days. Animals were randomly assigned to the following groups: Sham psoriasis challenged with Vaseline; IMQ animals challenged with imiquimod; and IMQ animals treated with PDRN (8 mg/kg/ip). An additional arm of IMQ animals was treated with PDRN plus istradefylline (KW6002; 25 mg/kg/ip) as an A2A antagonist. PDRN restored a normal skin architecture, whereas istradefylline abrogated PDRN positive effects, thus pointing out the mechanistic role of the A2A receptor. PDRN decreased pro-inflammatory cytokines, prompted Wnt signaling, reduced IL-2 and increased IL-10. PDRN also reverted the LPS repressed Wnt-1/beta-catenin in human keratinocytes and these effects were abolished by ZM241385, an A2A receptor antagonist. Finally, PDRN reduced CD3+ cells in superficial psoriatic dermis. PDRN anti-psoriasis potential may be linked to a "dual mode" of action: NF-kappa B inhibition and Wnt/beta-catenin stimulation.
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页数:14
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