利用肉眼显微镜量化淋巴管在小鼠淋巴水肿尾部模型中的生成情况

IF 1.6 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Lymphatic research and biology Pub Date : 2024-06-01 Epub Date: 2024-05-03 DOI:10.1089/lrb.2023.0048
Ganesh Mohan, Imran Khan, Stephanie M Diaz, Malgorzata M Kamocka, Luci A Hulsman, Shahnur Ahmed, Colby R Neumann, Miguel D Jorge, Gayle M Gordillo, Chandan K Sen, Mithun Sinha, Aladdin H Hassanein
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引用次数: 0

摘要

背景:淋巴水肿是淋巴功能障碍导致的慢性肢体肿胀。估计有 500 万美国人患有此病。这种疾病无法治愈。评估淋巴生长对开发新型疗法至关重要。内视显微镜(IVM)是一种强大的成像工具,可用于研究活体动物的各种生物过程。组织纳米转染技术(TNT)通过使用带有纳米通道孔隙的芯片,可快速直接经皮传递非病毒载体基因(方法与结果):利用小鼠尾部淋巴水肿模型。将 TNT 直接应用于小鼠尾部(第 0 天)的手术部位,并将基因货物装入 TNT 储库:TNTpCMV6 组接受 pCMV6(单独表达载体骨架)(n = 6);TNTProx1 组接受 pCMV6-Prox1(n = 6)。用共聚焦/多光子显微镜分析淋巴管(异硫氰酸荧光素[FITC]-葡聚糖染色)和淋巴分支点(表明淋巴管生成)。与 TNTpCMV6 组相比,实验组 TNTProx1 的术后尾部淋巴水肿减轻,淋巴分布增加。在 TNTProx1 组的 TNT 位点观察到更多的淋巴分支点(>3 倍)。结论:本研究展示了一种新颖、强大的成像工具,可用于研究活体鼠尾淋巴水肿模型中的淋巴管。IVM 可用于淋巴管的功能评估以及基因疗法后淋巴管生成的可视化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantification of Lymphangiogenesis in the Murine Lymphedema Tail Model Using Intravital Microscopy.

Background: Lymphedema is chronic limb swelling resulting from lymphatic dysfunction. It affects an estimated five million Americans. There is no cure for this disease. Assessing lymphatic growth is essential in developing novel therapeutics. Intravital microscopy (IVM) is a powerful imaging tool for investigating various biological processes in live animals. Tissue nanotransfection technology (TNT) facilitates a direct, transcutaneous nonviral vector gene delivery using a chip with nanochannel poration in a rapid (<100 ms) focused electric field. TNT was used in this study to deliver the genetic cargo in the murine tail lymphedema to assess the lymphangiogenesis. The purpose of this study is to experimentally evaluate the applicability of IVM to visualize and quantify lymphatics in the live mice model. Methods and Results: The murine tail model of lymphedema was utilized. TNT was applied to the murine tail (day 0) directly at the surgical site with genetic cargo loaded into the TNT reservoir: TNTpCMV6 group receives pCMV6 (expression vector backbone alone) (n = 6); TNTProx1 group receives pCMV6-Prox1 (n = 6). Lymphatic vessels (fluorescein isothiocyanate [FITC]-dextran stained) and lymphatic branch points (indicating lymphangiogenesis) were analyzed with the confocal/multiphoton microscope. The experimental group TNTProx1 exhibited reduced postsurgical tail lymphedema and increased lymphatic distribution compared to TNTpCMV6 group. More lymphatic branching points (>3-fold) were observed at the TNT site in TNTProx1 group. Conclusions: This study demonstrates a novel, powerful imaging tool for investigating lymphatic vessels in live murine tail model of lymphedema. IVM can be utilized for functional assessment of lymphatics and visualization of lymphangiogenesis following gene-based therapy.

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来源期刊
Lymphatic research and biology
Lymphatic research and biology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.10
自引率
7.10%
发文量
85
审稿时长
>12 weeks
期刊介绍: Lymphatic Research and Biology delivers the most current peer-reviewed advances and developments in lymphatic biology and pathology from the world’s leading biomedical investigators. The Journal provides original research from a broad range of investigative disciplines, including genetics, biochemistry and biophysics, cellular and molecular biology, physiology and pharmacology, anatomy, developmental biology, and pathology. Lymphatic Research and Biology coverage includes: -Vasculogenesis and angiogenesis -Genetics of lymphatic disorders -Human lymphatic disease, including lymphatic insufficiency and associated vascular anomalies -Physiology of intestinal fluid and protein balance -Immunosurveillance and immune cell trafficking -Tumor biology and metastasis -Pharmacology -Lymphatic imaging -Endothelial and smooth muscle cell biology -Inflammation, infection, and autoimmune disease
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