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两栖动物衍生肽同源二聚体促进皮肤伤口再生。

Amphibian-derived peptide homodimer promotes regeneration of skin wounds.

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Basic Medical Science, Kunming Medical University, Kunming 650500, Yunnan, China.

Public Technical Service Center, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, Yunnan, China.

出版信息

Biomed Pharmacother. 2022 Feb;146:112539. doi: 10.1016/j.biopha.2021.112539. Epub 2021 Dec 20.

Abstract

Despite the increasing treatments in skin wound repair, existing therapeutic drugs cannot meet current needs. As such, skin wound repair remains a considerable clinical challenge, and thus the discovery of new pro-healing agents is crucial. Here, we identified the first naturally occurring peptide homodimer named as OA-GP11 dimer (OA-GP11d) from Odorrana andersonii (odorous frog) through the combinational methods of peptidomics and genomics. OA-GP11d was linked by the intramolecular disulfide formed by the 10 cysteine residues from the monomer of peptide with sequence of GPLSGINAECM, which effectively promoted the repair of full-thickness and burn wounds in mice. The underlying molecular mechanisms revealed that OA-GP11d not only accelerated the migration and cell-scratch healing of mouse keratinocytes, but also activated the mitogen-activated protein kinases (MAPKs) signaling pathway (phosphorylation of p38 and ERK subgroups) in immortalized human keratinocytes (HaCaT). Besides, OA-GP11d reduced the phosphorylation of nuclear factor-κB (NF-κB) and inhibitor of NF-κB (I-κB) induced by lipopolysaccharide stimulation in mouse macrophages, and inhibited the release of associated inflammatory factors tumor necrosis factor (TNF)-α and interleukin (IL)-6. OA-GP11d is the first identified naturally occurring peptide dimer with significant pro-healing potency. Our results highlight the importance of amphibians as a source of novel pro-healing agents and suggest OA-GP11d as a potential new pro-regenerative drug candidate.

摘要

尽管皮肤伤口修复的治疗方法不断增加,但现有的治疗药物仍无法满足当前的需求。因此,皮肤伤口修复仍然是一个相当大的临床挑战,因此发现新的促愈剂至关重要。在这里,我们通过肽组学和基因组学的组合方法,从 Odorrana andersonii(臭蛙)中鉴定出第一个天然存在的肽同源二聚体,命名为 OA-GP11 二聚体(OA-GP11d)。OA-GP11d 由单体肽中的 10 个半胱氨酸残基形成的分子内二硫键连接,序列为 GPLSGINAECM,有效促进了小鼠全层和烧伤伤口的修复。潜在的分子机制表明,OA-GP11d 不仅加速了小鼠角质形成细胞的迁移和细胞划痕愈合,而且激活了永生化人角质形成细胞(HaCaT)中的丝裂原活化蛋白激酶(MAPKs)信号通路(p38 和 ERK 亚组的磷酸化)。此外,OA-GP11d 降低了脂多糖刺激小鼠巨噬细胞中核因子-κB(NF-κB)和 NF-κB 抑制剂(I-κB)的磷酸化,并抑制相关炎症因子肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6 的释放。OA-GP11d 是第一个被鉴定为具有显著促愈活性的天然存在的肽二聚体。我们的研究结果强调了两栖动物作为新型促愈剂来源的重要性,并表明 OA-GP11d 可能成为一种新的促再生药物候选物。

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