淋巴水肿
病理生理学
水肿
淋巴管新生
脂肪生成
医学
组织学
炎症
脂肪组织
淋巴
病理
渗透(HVAC)
免疫组织化学
淋巴系统
内科学
材料科学
癌症
乳腺癌
复合材料
转移
作者
Germano José Ferraz de Arruda,Suely Kunimi Kubo Ariga,TM de Lima,Heraldo Possolo de Souza,Mauro Andrade
出处
期刊:Lymphology
[University of Arizona]
日期:2020-06-02
卷期号:53 (1)
被引量:4
摘要
One of the main obstacles to studying the pathophysiology of lymphedema development is the lack of appropriate experimental models. Following up on a mouse-tail method that has been described, we performed changes to the method which made it easier to perform in our hands and demonstrated similar results. Twenty C57Black mice were operated on using the previous technique and euthanized after 3 or 6 weeks. Another twenty mice were submitted to the new technique developed in our laboratory and euthanized at the same time points. Tissue samples were collected from the proximal part of the tail (control) and from the distal part (lymphedema) for both models. Animals in both operative groups developed marked edema in the distal part of the tail. This was characterized by lymph vessels dilation, edema, inflammatory cell infiltration, and adipose tissue deposition. Lymphedema was detected after 3 weeks in both models, reaching its maximum after 6 weeks. Adipocytes detected by histology (Oil red O staining) and molecular markers for adipogenesis, lymphangiogenesis and inflammation (lipin 1 and 2, SLP76, and F4-80) were demonstrated to be increased equally in both models. In conclusion, both models provide a reliable method to study lymphedema pathophysiology. However, our modified technique is easier and faster to perform while still providing reliable and consistent results.
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