A non-bactericidal cathelicidin with antioxidant properties ameliorates UVB-induced mouse skin photoaging via intracellular ROS scavenging and Keap1/Nrf2 pathway activation

IF 7.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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Abstract

Cathelicidins, a category of critical host defense molecules in vertebrates, have been extensively studied for their bactericidal functions, but little is known about their non-bactericidal properties. Herein, a novel cathelicidin peptide (Atonp2) was identified from the plateau frog Nanorana ventripunctata. It did not exhibit bactericidal activity but showed significant therapeutic effects in chronic UVB radiation-induced mouse skin photoaging through inhibiting thickening, pyroptosis and inflammation in the epidermis, while inhibiting cellular senescence, collagen fibre breakage and type Ⅰ collagen reduction in the dermis. Further studies indicated that Atonp2 effectively scavenged UVB-induced intracellular ROS via tyrosines at positions 9 and 10, while activating the Keap1/Nrf2 pathway to protect epidermal keratinocytes against UVB radiation, which in turn indirectly reversed the senescence and collagen degradation of dermal fibroblasts, thereby ameliorating UVB-induced skin photoaging. As such, this study identified a non-bactericidal cathelicidin peptide with potent antioxidant functions, highlighting its potential to treat and prevent skin photoaging.

Abstract Image

一种具有抗氧化特性的非杀菌性白头翁素能通过清除细胞内 ROS 和激活 Keap1/Nrf2 通路改善紫外线诱导的小鼠皮肤光老化。
柔毛素是脊椎动物中一类关键的宿主防御分子,其杀菌功能已被广泛研究,但对其非杀菌特性却知之甚少。在此,研究人员从高原蛙Nanorana ventripunctata身上鉴定出了一种新型的柔毛肽(Atonp2)。它不具有杀菌活性,但对慢性紫外线辐射诱导的小鼠皮肤光老化有显著的治疗效果,能抑制表皮的增厚、脓毒血症和炎症,同时抑制真皮层的细胞衰老、胶原纤维断裂和Ⅰ型胶原减少。进一步的研究表明,Atonp2 可通过第 9 位和第 10 位的酪氨酸有效清除紫外线诱导的细胞内 ROS,同时激活 Keap1/Nrf2 通路,保护表皮角质细胞免受紫外线辐射,进而间接逆转真皮成纤维细胞的衰老和胶原降解,从而改善紫外线诱导的皮肤光老化。因此,这项研究发现了一种具有强大抗氧化功能的非杀菌柔毛肽,凸显了其治疗和预防皮肤光老化的潜力。
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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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