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本文引用的文献

1
Transforming Growth Factor-β and Endoglin Signaling Orchestrate Wound Healing.转化生长因子-β与内皮糖蛋白信号协同调控伤口愈合。
Front Physiol. 2011 Nov 29;2:89. doi: 10.3389/fphys.2011.00089. eCollection 2011.
2
Prx-1 expression in Xenopus laevis scarless skin-wound healing and its resemblance to epimorphic regeneration.爪蟾无痕皮肤创伤愈合过程中 Prx-1 的表达及其与胚胎后再生的相似性。
J Invest Dermatol. 2011 Dec;131(12):2477-85. doi: 10.1038/jid.2011.223. Epub 2011 Jul 21.
3
Ex vivo generation of a functional and regenerative wound epithelium from axolotl (Ambystoma mexicanum) skin.从美西螈(Ambystoma mexicanum)皮肤体外生成具有功能和再生能力的创面上皮。
Dev Growth Differ. 2010 Oct;52(8):715-24. doi: 10.1111/j.1440-169X.2010.01208.x.
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Skin wound healing modulation by macrophages.巨噬细胞对皮肤伤口愈合的调节作用。
Int J Clin Exp Pathol. 2010 Jul 25;3(7):643-53.
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Molecular pathology of wound healing.伤口愈合的分子病理学。
Forensic Sci Int. 2010 Dec 15;203(1-3):93-8. doi: 10.1016/j.forsciint.2010.07.004. Epub 2010 Aug 23.
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The UV response of the skin: a review of the MAPK, NFkappaB and TNFalpha signal transduction pathways.皮肤的紫外线反应:MAPK、NFkappaB 和 TNFalpha 信号转导通路综述。
Arch Dermatol Res. 2010 Jan;302(1):5-17. doi: 10.1007/s00403-009-0994-y. Epub 2009 Sep 16.
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Growth factors and cytokines in wound healing.伤口愈合中的生长因子和细胞因子。
Wound Repair Regen. 2008 Sep-Oct;16(5):585-601. doi: 10.1111/j.1524-475X.2008.00410.x.
8
The p38 mitogen-activated protein kinase (MAPK) pathway in rheumatoid arthritis.类风湿关节炎中的p38丝裂原活化蛋白激酶(MAPK)信号通路
Ann Rheum Dis. 2008 Jul;67(7):909-16. doi: 10.1136/ard.2007.074278. Epub 2007 Sep 7.
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Pathophysiology of acute wound healing.急性伤口愈合的病理生理学
Clin Dermatol. 2007 Jan-Feb;25(1):9-18. doi: 10.1016/j.clindermatol.2006.09.007.
10
Collagen loss and impaired wound healing is associated with c-Myb deficiency.胶原蛋白流失和伤口愈合受损与c-Myb缺乏有关。
J Pathol. 2007 Feb;211(3):351-61. doi: 10.1002/path.2113.

一种来自蝾螈皮肤的具有促进伤口愈合潜力的肽。

A potential wound-healing-promoting peptide from salamander skin.

作者信息

Mu Lixian, Tang Jing, Liu Han, Shen Chuanbin, Rong Mingqiang, Zhang Zhiye, Lai Ren

机构信息

Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China; and Kunming College of Life Science, University of Chinese Academy of Sciences, Beijing, China.

Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China; and.

出版信息

FASEB J. 2014 Sep;28(9):3919-29. doi: 10.1096/fj.13-248476. Epub 2014 May 27.

DOI:10.1096/fj.13-248476
PMID:24868009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5395725/
Abstract

Although it is well known that wound healing proceeds incredibly quickly in urodele amphibians, such as newts and salamanders, little is known about skin-wound healing, and no bioactive/effector substance that contributes to wound healing has been identified from these animals. As a step toward understanding salamander wound healing and skin regeneration, a potential wound-healing-promoting peptide (tylotoin; KCVRQNNKRVCK) was identified from salamander skin of Tylototriton verrucosus. It shows comparable wound-healing-promoting ability (EC50=11.14 μg/ml) with epidermal growth factor (EGF; NSDSECPLSHDGYCLHDGVCMYIEALDKYACNCVVGYIGERCQYRDLKWWELR) in a murine model of full-thickness dermal wound. Tylotoin directly enhances the motility and proliferation of keratinocytes, vascular endothelial cells, and fibroblasts, resulting in accelerated reepithelialization and granulation tissue formation in the wound site. Tylotoin also promotes the release of transforming growth factor β1 (TGF-β1) and interleukin 6 (IL-6), which are essential in the wound healing response. Gene-encoded tylotoin secreted in salamander skin is possibly an effector molecule for skin wound healing. This study may facilitate understanding of the cellular and molecular events that underlie quick wound healing in salamanders.

摘要

虽然众所周知,诸如蝾螈和火蜥蜴等有尾两栖动物的伤口愈合速度极快,但关于皮肤伤口愈合的了解却很少,而且尚未从这些动物中鉴定出任何有助于伤口愈合的生物活性/效应物质。作为迈向了解蝾螈伤口愈合和皮肤再生的一步,从疣螈的蝾螈皮肤中鉴定出了一种潜在的促进伤口愈合的肽(tylotoin;KCVRQNNKRVCK)。在全层皮肤伤口的小鼠模型中,它显示出与表皮生长因子(EGF;NSDSECPLSHDGYCLHDGVCMYIEALDKYACNCVVGYIGERCQYRDLKWWELR)相当的促进伤口愈合的能力(EC50 = 11.14 μg/ml)。Tylotoin直接增强角质形成细胞、血管内皮细胞和成纤维细胞的运动性和增殖,从而加速伤口部位的上皮再形成和肉芽组织形成。Tylotoin还促进转化生长因子β1(TGF-β1)和白细胞介素6(IL-6)的释放,这两种物质在伤口愈合反应中至关重要。蝾螈皮肤中分泌的基因编码tylotoin可能是皮肤伤口愈合的效应分子。这项研究可能有助于理解蝾螈快速伤口愈合背后的细胞和分子事件。