Tie2激活通过改善淋巴内皮的完整性来增强淋巴水肿的血管化淋巴结转移。

IF 3.4 2区 医学 Q1 SURGERY
Do Young Park, Bo-Yoon Park, Dong Hyun Seo, Tae Hyun Kong, Sang-Oh Lee, Kyoo-Ri Kwon, Du-Hyong Cho, Yong-Ha Kim, Choong-Kun Lee, Il-Kug Kim
{"title":"Tie2激活通过改善淋巴内皮的完整性来增强淋巴水肿的血管化淋巴结转移。","authors":"Do Young Park, Bo-Yoon Park, Dong Hyun Seo, Tae Hyun Kong, Sang-Oh Lee, Kyoo-Ri Kwon, Du-Hyong Cho, Yong-Ha Kim, Choong-Kun Lee, Il-Kug Kim","doi":"10.1097/PRS.0000000000012473","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Lymphedema is characterized by inadequate interstitial fluid drainage due to disrupted lymphatic vasculature. Despite the pivotal role of angiopoietin (Ang)-Tie2 signaling in lymphatics, the therapeutic potential of Tie2 modulation in lymphedema remains unknown.</p><p><strong>Methods: </strong>To investigate the molecular and pathological changes associated with lymphedema, fat tissues were collected from lymphedema patients and subjected to immunohistochemistry and transcriptomic analyses. Additionally, a mouse hindlimb lymphedema model was established by obstructing superficial and deep lymphatic drainage, allowing the evaluation of structural, functional, and molecular alterations accompanying lymphedema. The effects of systemically administered Ang2-binding and Tie2-activating antibody (ABTAA) on lymphedema were assessed, both independently and in combination with vascularized lymph node transfer (VLNT).</p><p><strong>Results: </strong>Immunohistochemistry and transcriptomic analyses of tissues from lymphedema patients revealed significant impairment of lymphatic endothelial cell (LEC) junctions and alterations in Ang-Tie2 signaling. A mouse hindlimb lymphedema model demonstrated the hallmarks of lymphedema, including fluid drainage impairment along with tissue edema, disintegrated LECs, and remodeling of lymphatic vessels. ABTAA significantly improved all the features of lymphedema by activating lymphatic endothelial Tie2, leading to increased LEC junctional stability. Notably, ABTAA exerted an additive effect in relieving lymphedema when combined with VLNT, which was supported by transcriptomic analysis results that indicated enhanced lymphatic vascular integrity, reduced inflammation, and increased vasculogenesis upon treatment.</p><p><strong>Conclusions: </strong>Tie2 activation with ABTAA ameliorates lymphedema in a mouse model, both independently and in combination with VLNT treatment. These findings suggest that Tie2 activation may present a novel and effective option, potentially improving the current treatment of lymphedema.</p><p><strong>Clinical relevance statement: </strong>The results of the study highlight the potential of ABTAA treatment in enhancing lymphatic stability, offering plastic surgeons a novel therapeutic approach to improving outcomes in patients undergoing vascularized lymph node transfer for lymphedema.</p><p><strong>Graphical abstract: </strong>A graphical abstract is available for this article.</p>","PeriodicalId":20128,"journal":{"name":"Plastic and reconstructive surgery","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tie2 activation enhances vascularized lymph node transfer in lymphedema by improving lymphatic endothelial integrity.\",\"authors\":\"Do Young Park, Bo-Yoon Park, Dong Hyun Seo, Tae Hyun Kong, Sang-Oh Lee, Kyoo-Ri Kwon, Du-Hyong Cho, Yong-Ha Kim, Choong-Kun Lee, Il-Kug Kim\",\"doi\":\"10.1097/PRS.0000000000012473\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Lymphedema is characterized by inadequate interstitial fluid drainage due to disrupted lymphatic vasculature. Despite the pivotal role of angiopoietin (Ang)-Tie2 signaling in lymphatics, the therapeutic potential of Tie2 modulation in lymphedema remains unknown.</p><p><strong>Methods: </strong>To investigate the molecular and pathological changes associated with lymphedema, fat tissues were collected from lymphedema patients and subjected to immunohistochemistry and transcriptomic analyses. Additionally, a mouse hindlimb lymphedema model was established by obstructing superficial and deep lymphatic drainage, allowing the evaluation of structural, functional, and molecular alterations accompanying lymphedema. The effects of systemically administered Ang2-binding and Tie2-activating antibody (ABTAA) on lymphedema were assessed, both independently and in combination with vascularized lymph node transfer (VLNT).</p><p><strong>Results: </strong>Immunohistochemistry and transcriptomic analyses of tissues from lymphedema patients revealed significant impairment of lymphatic endothelial cell (LEC) junctions and alterations in Ang-Tie2 signaling. A mouse hindlimb lymphedema model demonstrated the hallmarks of lymphedema, including fluid drainage impairment along with tissue edema, disintegrated LECs, and remodeling of lymphatic vessels. ABTAA significantly improved all the features of lymphedema by activating lymphatic endothelial Tie2, leading to increased LEC junctional stability. Notably, ABTAA exerted an additive effect in relieving lymphedema when combined with VLNT, which was supported by transcriptomic analysis results that indicated enhanced lymphatic vascular integrity, reduced inflammation, and increased vasculogenesis upon treatment.</p><p><strong>Conclusions: </strong>Tie2 activation with ABTAA ameliorates lymphedema in a mouse model, both independently and in combination with VLNT treatment. These findings suggest that Tie2 activation may present a novel and effective option, potentially improving the current treatment of lymphedema.</p><p><strong>Clinical relevance statement: </strong>The results of the study highlight the potential of ABTAA treatment in enhancing lymphatic stability, offering plastic surgeons a novel therapeutic approach to improving outcomes in patients undergoing vascularized lymph node transfer for lymphedema.</p><p><strong>Graphical abstract: </strong>A graphical abstract is available for this article.</p>\",\"PeriodicalId\":20128,\"journal\":{\"name\":\"Plastic and reconstructive surgery\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plastic and reconstructive surgery\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1097/PRS.0000000000012473\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"SURGERY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plastic and reconstructive surgery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/PRS.0000000000012473","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

摘要

背景:淋巴水肿的特点是由于淋巴血管系统紊乱导致间质液排出不足。尽管血管生成素(Ang)-Tie2信号在淋巴系统中起着关键作用,但Tie2调节在淋巴水肿中的治疗潜力尚不清楚。方法:收集淋巴水肿患者的脂肪组织,进行免疫组织化学和转录组学分析,探讨与淋巴水肿相关的分子和病理变化。此外,通过阻塞浅层和深层淋巴引流建立小鼠后肢淋巴水肿模型,以评估淋巴水肿伴随的结构、功能和分子改变。系统给药ang2结合抗体和tie2活化抗体(ABTAA)对淋巴水肿的影响被评估,单独和联合血管化淋巴结转移(VLNT)。结果:淋巴水肿患者组织的免疫组织化学和转录组学分析显示淋巴内皮细胞(LEC)连接明显受损,Ang-Tie2信号通路改变。小鼠后肢淋巴水肿模型显示出淋巴水肿的特征,包括伴随组织水肿的液体排泄障碍、LECs解体和淋巴管重塑。ABTAA通过激活淋巴内皮Tie2显著改善淋巴水肿的所有特征,导致LEC连接稳定性增加。值得注意的是,当ABTAA与VLNT联合使用时,在缓解淋巴水肿方面发挥了附加效应,转录组分析结果表明,治疗后淋巴血管完整性增强,炎症减少,血管生成增加。结论:用ABTAA激活Tie2可单独或联合VLNT治疗小鼠淋巴水肿。这些发现表明,激活Tie2可能是一种新颖有效的选择,有可能改善目前淋巴水肿的治疗。临床相关性声明:该研究结果强调了ABTAA治疗在增强淋巴稳定性方面的潜力,为整形外科医生提供了一种新的治疗方法,以改善因淋巴水肿而接受血管化淋巴结转移的患者的预后。图形摘要:本文提供图形摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tie2 activation enhances vascularized lymph node transfer in lymphedema by improving lymphatic endothelial integrity.

Background: Lymphedema is characterized by inadequate interstitial fluid drainage due to disrupted lymphatic vasculature. Despite the pivotal role of angiopoietin (Ang)-Tie2 signaling in lymphatics, the therapeutic potential of Tie2 modulation in lymphedema remains unknown.

Methods: To investigate the molecular and pathological changes associated with lymphedema, fat tissues were collected from lymphedema patients and subjected to immunohistochemistry and transcriptomic analyses. Additionally, a mouse hindlimb lymphedema model was established by obstructing superficial and deep lymphatic drainage, allowing the evaluation of structural, functional, and molecular alterations accompanying lymphedema. The effects of systemically administered Ang2-binding and Tie2-activating antibody (ABTAA) on lymphedema were assessed, both independently and in combination with vascularized lymph node transfer (VLNT).

Results: Immunohistochemistry and transcriptomic analyses of tissues from lymphedema patients revealed significant impairment of lymphatic endothelial cell (LEC) junctions and alterations in Ang-Tie2 signaling. A mouse hindlimb lymphedema model demonstrated the hallmarks of lymphedema, including fluid drainage impairment along with tissue edema, disintegrated LECs, and remodeling of lymphatic vessels. ABTAA significantly improved all the features of lymphedema by activating lymphatic endothelial Tie2, leading to increased LEC junctional stability. Notably, ABTAA exerted an additive effect in relieving lymphedema when combined with VLNT, which was supported by transcriptomic analysis results that indicated enhanced lymphatic vascular integrity, reduced inflammation, and increased vasculogenesis upon treatment.

Conclusions: Tie2 activation with ABTAA ameliorates lymphedema in a mouse model, both independently and in combination with VLNT treatment. These findings suggest that Tie2 activation may present a novel and effective option, potentially improving the current treatment of lymphedema.

Clinical relevance statement: The results of the study highlight the potential of ABTAA treatment in enhancing lymphatic stability, offering plastic surgeons a novel therapeutic approach to improving outcomes in patients undergoing vascularized lymph node transfer for lymphedema.

Graphical abstract: A graphical abstract is available for this article.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.00
自引率
13.90%
发文量
1436
审稿时长
1.5 months
期刊介绍: For more than 70 years Plastic and Reconstructive Surgery® has been the one consistently excellent reference for every specialist who uses plastic surgery techniques or works in conjunction with a plastic surgeon. Plastic and Reconstructive Surgery® , the official journal of the American Society of Plastic Surgeons, is a benefit of Society membership, and is also available on a subscription basis. Plastic and Reconstructive Surgery® brings subscribers up-to-the-minute reports on the latest techniques and follow-up for all areas of plastic and reconstructive surgery, including breast reconstruction, experimental studies, maxillofacial reconstruction, hand and microsurgery, burn repair, cosmetic surgery, as well as news on medicolegal issues. The cosmetic section provides expanded coverage on new procedures and techniques and offers more cosmetic-specific content than any other journal. All subscribers enjoy full access to the Journal''s website, which features broadcast quality videos of reconstructive and cosmetic procedures, podcasts, comprehensive article archives dating to 1946, and additional benefits offered by the newly-redesigned website.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信