Extracellular epimorphin modulates epidermal differentiation signals mediated by epidermal growth factor receptor

Yoji Okugawa, Yohei Hirai
{"title":"Extracellular epimorphin modulates epidermal differentiation signals mediated by epidermal growth factor receptor","authors":"Yoji Okugawa,&nbsp;Yohei Hirai","doi":"10.1016/j.jdermsci.2012.11.006","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>The epidermal stratification/differentiation program is initiated in keratinocytes by a basement membrane-detachment cue and subsequently controlled by spatially and temporally regulated signaling molecules. The vital signals for the developmental behavior of the epidermis include those mediated by epidermal growth factor receptor (EGFR); however, regulatory elements responsible for activation have not yet been fully elucidated.</p></div><div><h3>Objective</h3><p>The objectives of this study were (1) to assess the effects of EGFR activation on epidermal differentiation, (2) to study the effects of epimorphin on the level of EGFR signaling degree dependent on matrix engagement, and (3) to address the impact of epimorphin modulation on EGFR-driven epidermal differentiation in a three-dimensional (3D) organotypic skin model.</p></div><div><h3>Methods</h3><p>We constructed skin-equivalent models with a well-stratified differentiated epidermis and utilized them to evaluate the epidermal behaviors.</p></div><div><h3>Results</h3><p>Extracellularly secreted epimorphin was identified as a strong candidate for signaling pathway<span> involvement. In a 3D epidermis model, EGF stimulation was sufficient for epidermal stratification. However, overactivation of EGFR led to irregular multicellular arrangements with an abnormal differentiation profile, which appeared to be reorganized back to the normal epidermal phenotype by extracellular epimorphin. Extracellular epimorphin interestingly attenuated EGF-stimulated EGFR phosphorylation, cell growth, and migration in adherent cells. In contrast to the results of adhesion culture, extracellular epimorphin reinforced EGFR activation in suspended cells.</span></p></div><div><h3>Conclusions</h3><p>These results demonstrate that epimorphin modulates the signaling pathways mediated by EGFR for epidermal tissue organization.</p></div>","PeriodicalId":94076,"journal":{"name":"Journal of dermatological science","volume":"69 3","pages":"Pages 236-242"},"PeriodicalIF":4.6000,"publicationDate":"2013-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jdermsci.2012.11.006","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of dermatological science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0923181112003350","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

Abstract

Background

The epidermal stratification/differentiation program is initiated in keratinocytes by a basement membrane-detachment cue and subsequently controlled by spatially and temporally regulated signaling molecules. The vital signals for the developmental behavior of the epidermis include those mediated by epidermal growth factor receptor (EGFR); however, regulatory elements responsible for activation have not yet been fully elucidated.

Objective

The objectives of this study were (1) to assess the effects of EGFR activation on epidermal differentiation, (2) to study the effects of epimorphin on the level of EGFR signaling degree dependent on matrix engagement, and (3) to address the impact of epimorphin modulation on EGFR-driven epidermal differentiation in a three-dimensional (3D) organotypic skin model.

Methods

We constructed skin-equivalent models with a well-stratified differentiated epidermis and utilized them to evaluate the epidermal behaviors.

Results

Extracellularly secreted epimorphin was identified as a strong candidate for signaling pathway involvement. In a 3D epidermis model, EGF stimulation was sufficient for epidermal stratification. However, overactivation of EGFR led to irregular multicellular arrangements with an abnormal differentiation profile, which appeared to be reorganized back to the normal epidermal phenotype by extracellular epimorphin. Extracellular epimorphin interestingly attenuated EGF-stimulated EGFR phosphorylation, cell growth, and migration in adherent cells. In contrast to the results of adhesion culture, extracellular epimorphin reinforced EGFR activation in suspended cells.

Conclusions

These results demonstrate that epimorphin modulates the signaling pathways mediated by EGFR for epidermal tissue organization.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
细胞外表吗啡调节由表皮生长因子受体介导的表皮分化信号
表皮分层/分化程序在角质形成细胞中由基底膜剥离提示启动,随后由空间和时间调节的信号分子控制。表皮发育行为的重要信号包括表皮生长因子受体(EGFR)介导的信号;然而,负责激活的调控元件尚未完全阐明。本研究的目的是(1)评估EGFR激活对表皮分化的影响,(2)研究表啡肽对EGFR信号传导程度依赖于基质接触水平的影响,以及(3)在三维(3D)器官型皮肤模型中解决表啡肽调节对EGFR驱动的表皮分化的影响。方法构建具有良好分层分化表皮的皮肤等效模型,并利用该模型评价表皮行为。结果胞外分泌的表吗啡被认为是参与信号通路的一个强有力的候选者。在3D表皮模型中,EGF刺激足以使表皮分层。然而,EGFR的过度激活导致不规则的多细胞排列和异常的分化特征,这似乎是通过细胞外表吗啡重组回到正常的表皮表型。有趣的是,细胞外表吗啡能减弱egf刺激的EGFR磷酸化、细胞生长和贴壁细胞的迁移。与黏附培养的结果相反,细胞外表吗啡增强悬浮细胞中的EGFR激活。结论epimorphin可调节EGFR介导的表皮组织信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
7.60
自引率
0.00%
发文量
0
期刊最新文献
Comparative analysis of cytotoxic mediators in Stevens-Johnson syndrome and toxic epidermal necrolysis using ex vivo human epidermis. Integrative analysis of bulk multiomics and single-cell transcriptomics reveals the value of neddylation in Skin Cutaneous Melanoma. Salvianolic acid B ameliorate alopecia by simultaneously targeting Wnt/β-catenin and mTORC2/Akt signaling. DcR3 reprograms macrophage plasticity to promote wound healing and hair regeneration. Low-temperature plasma-activated Ringer's lactate solution induces apoptosis in melanoma cells by downregulating heat shock proteins and by inducing mitochondrial dysfunction.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1