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Hypercholesterolemic Mice Exhibit Lymphatic Vessel Dysfunction and Degeneration

机译:高胆固醇血症小鼠表现出淋巴管功能障碍和变性

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摘要

Lymphatic vessels are essential for lipid absorption and transport. Despite increasing numbers of observations linking lymphatic vessels and lipids, little research has been devoted to address how dysregulation of lipid balance in the blood, ie, dyslipidemia, may affect the functional biology of lymphatic vessels. Here, we show that hypercholesterolemia occurring in apolipoprotein E-deficient (apoE–/–) mice is associated with tissue swelling, lymphatic leakiness, and decreased lymphatic transport of fluid and dendritic cells from tissue. Lymphatic dysfunction results in part from profound structural abnormalities in the lymphatic vasculature: namely, initial lymphatic vessels were greatly enlarged, and collecting vessels developed notably decreased smooth muscle cell coverage and changes in the distribution of lymphatic vessel endothelial hyaluronic acid receptor-1 (LYVE-1). Our results provide evidence that hypercholesterolemia in adult apoE–/– mice is associated with a degeneration of lymphatic vessels that leads to decreased lymphatic drainage and provides an explanation for why dendritic cell migration and, thus, immune priming, are compromised in hypercholesterolemic mice.
机译:淋巴管对于脂质的吸收和运输至关重要。 尽管与淋巴管和脂质相关的观察数目不断增加,但很少有研究致力于解决 如何血液中脂质平衡的失调,即血脂异常,可能影响淋巴管的功能生物学。在这里, 我们证明了载脂蛋白 E缺乏(apoE – / – )小鼠中发生的高胆固醇血症与组织 肿胀,淋巴漏出和淋巴转运减少 。淋巴功能障碍 的部分原因是 淋巴管系统的深层结构异常:即,最初的淋巴管明显增大,而收集血管明显减少 平滑肌细胞覆盖以及淋巴管内皮透明质酸受体1(LYVE-1)分布的变化 我们的结果提供了证据成年 apoE – / – 小鼠的高胆固醇血症与 淋巴管的变性相关,导致淋巴引流减少 并解释了为什么高胆固醇血症小鼠会损害树突状细胞迁移 并因此导致免疫引发。

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  • 来源
    《American Journal of Pathology》 |2009年第3期|1328-1337|共10页
  • 作者单位

    From the Department of Microbiology,Immunology Programme, Yoon Loo Lin School of Medicine, National University of Singapore, Singapore;

    the Institute of Bioengineering,école Polytechnique Fédérale de Lausanne, Lausanne, Switzerland;

    and the Department of Gene and Cell Medicine,Mount Sinai School of Medicine, New York, New York;

    the Institute of Bioengineering,école Polytechnique Fédérale de Lausanne, Lausanne, Switzerland;

    the Institute of Bioengineering,école Polytechnique Fédérale de Lausanne, Lausanne, Switzerland;

    and the Department of Gene and Cell Medicine,Mount Sinai School of Medicine, New York, New York;

    From the Department of Microbiology,Immunology Programme, Yoon Loo Lin School of Medicine, National University of Singapore, Singapore|and the Department of Gene and Cell Medicine,Mount Sinai School of Medicine, New York, New York;

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