题名 | NGF Accelerates Cutaneous Wound Healing by Promoting the Migration of Dermal Fibroblasts via the PI3K/Akt-Rac1-JNK and ERK Pathways |
作者 | |
发表日期 | 2014-12-31 |
发表期刊 | BIOMED RESEARCH INTERNATIONAL 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
其他关键词 | NERVE-GROWTH-FACTOR ; ACTIVATED PROTEIN-KINASE ; MAST-CELLS ; EXPRESSION ; RECEPTOR ; JNK ; PROLIFERATION ; KERATINOCYTES ; FAMILY ; BETA |
摘要 | As a well-known neurotrophic factor, nerve growth factor (NGF) has also been extensively recognized for its acceleration of healing in cutaneous wounds in both animal models and randomized clinical trials. However, the underlying mechanisms accounting for the therapeutic effect of NGF on skin wounds are not fully understood. NGF treatment significantly accelerated the rate of wound healing by promoting wound reepithelialization, the formation of granulation tissue, and collagen production. To explore the possible mechanisms of this process, the expression levels of CD68, VEGF, PCNA, and TGF-beta 1 in wounds were detected by immunohistochemical staining. The levels of these proteins were all significantly raised in NGF-treated wounds compared to untreated controls. NGF also significantly promoted the migration, but not the proliferation, of dermal fibroblasts. NGF induced a remarkable increase in the activity of PI3K/Akt, JNK, ERK, and Rac1, and blockade with their specific inhibitors significantly impaired the NGF-induced migration. In conclusion, NGF significantly accelerated the healing of skin excisional wounds in rats and the fibroblast migration induced by NGF may contribute to this healing process. The activation of PI3K/Akt, Rac1, JNK, and ERK were all involved in the regulation of NGF-induced fibroblast migration. |
资助项目 | National Natural Science Funding of ChinaNational Natural Science Foundation of China (NSFC) [81372112]; Ningbo City Natural Science Foundation [2012A610254]; Zhejiang Provincial Project of Key Group [2010R50042] |
出版者 | HINDAWI LTD |
出版地 | LONDON |
ISSN | 2314-6133 |
EISSN | 2314-6141 |
卷号 | 2014页码:547187 |
DOI | 10.1155/2014/547187 |
页数 | 13 |
WOS类目 | Biotechnology & Applied Microbiology ; Medicine, Research & Experimental |
WOS研究方向 | Biotechnology & Applied Microbiology ; Research & Experimental Medicine |
WOS记录号 | WOS:000336606800001 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 25006578 |
PMC记录号 | PMC4055427 |
SCOPUSEID | 2-s2.0-84902164765 |
通讯作者地址 | [Wei, Xiao-Jie]Translation Medicine Research Center, Cixi People's Hospital, Wenzhou Medical University,China |
Scopus学科分类 | Biochemistry, Genetics and Molecular Biology (all);Immunology and Microbiology (all) |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/15560 |
专题 | 附属第一医院 药学院(分析测试中心) 其他_附属台州医院(浙江省台州医院) 其他_附属慈溪医院(慈溪市人民医院) |
通讯作者 | Wei, Xiao-Jie |
作者单位 | 1.Department of Gastrointestinal Surgery, First Affiliate Hospital, Wenzhou Medical University,China; 2.School of Pharmacy, Wenzhou Medical University,China; 3.Wound Treatment Center, First Affiliate Hospital, Wenzhou Medical University,China; 4.Emergency Department, Taizhou Hospital, Wenzhou Medical University,China; 5.Translation Medicine Research Center, Cixi People's Hospital, Wenzhou Medical University,China; 6.Departmant of Pharmacy, Second Affiliate Hospital, Wenzhou Medical University,China |
第一作者单位 | 温州医科大学 |
通讯作者单位 | 温州医科大学 |
第一作者的第一单位 | 温州医科大学 |
推荐引用方式 GB/T 7714 | Chen, Ji-Cai,Lin, Bei-Bei,Hu, Hou-Wen,et al. NGF Accelerates Cutaneous Wound Healing by Promoting the Migration of Dermal Fibroblasts via the PI3K/Akt-Rac1-JNK and ERK Pathways[J]. BIOMED RESEARCH INTERNATIONAL,2014,2014:547187. |
APA | Chen, Ji-Cai., Lin, Bei-Bei., Hu, Hou-Wen., Lin, Cai., Jin, Wen-Yang., ... & Chen, Rui-Jie. (2014). NGF Accelerates Cutaneous Wound Healing by Promoting the Migration of Dermal Fibroblasts via the PI3K/Akt-Rac1-JNK and ERK Pathways. BIOMED RESEARCH INTERNATIONAL, 2014, 547187. |
MLA | Chen, Ji-Cai,et al."NGF Accelerates Cutaneous Wound Healing by Promoting the Migration of Dermal Fibroblasts via the PI3K/Akt-Rac1-JNK and ERK Pathways".BIOMED RESEARCH INTERNATIONAL 2014(2014):547187. |
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