Hypercholesterolemic Mice Exhibit Lymphatic Vessel Dysfunction and Degeneration

被引:139
作者
Lim, Hwee Ying
Rutkowski, Joseph M. [2 ]
Helft, Julie [3 ]
Reddy, Sai T. [2 ]
Swartz, Melody A. [2 ]
Randolph, Gwendalyn J. [3 ]
Angeli, Veronique [1 ,3 ]
机构
[1] Natl Univ Singapore, Dept Microbiol, Yoon Loo Lin Sch Med, Immunol Programme,Ctr Life Sci, Singapore 117456, Singapore
[2] Ecole Polytech Fed Lausanne, Inst Bioengn, Lausanne, Switzerland
[3] Mt Sinai Sch Med, Dept Gene & Cell Med, New York, NY USA
基金
瑞士国家科学基金会; 美国国家卫生研究院; 英国医学研究理事会;
关键词
E-DEFICIENT MICE; DENDRITIC CELL MOBILIZATION; ENDOTHELIAL-CELLS; ATHEROSCLEROSIS; NODES; LYMPHANGIOGENESIS; INFLAMMATION; CHOLESTEROL; LYMPHEDEMA; FAILURE;
D O I
10.2353/ajpath.2009.080963
中图分类号
R36 [病理学];
学科分类号
100104 ;
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. (Am J Pathol 2009, 175:1328-1337; DOI. 10.2353/ajpath.2009.080963)
引用
收藏
页码:1328 / 1337
页数:10
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