Defective remodeling and maturation of the lymphatic vasculature in Angiopoietin-2 deficient mice

被引:148
作者
Dellinger, Michael [1 ]
Hunter, Robert [2 ]
Bernas, Michael [2 ]
Gale, Nicholas [4 ]
Yancopoulos, George [4 ]
Erickson, Robert [1 ,3 ]
Witte, Marlys [2 ]
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Surg, Tucson, AZ USA
[3] Univ Arizona, Dept Pediat, Tucson, AZ 85721 USA
[4] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
关键词
Ang2; Angpt2; Angiopoietin-2; Ang2 knock-out mice; Angiopoietin-1; tie-2; lymphedema; lymphangiogenesis; lymphatic development; lymphatic remodeling;
D O I
10.1016/j.ydbio.2008.04.024
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular mechanisms regulating the remodeling of the lymphatic vasculature from an immature plexus of vessels to a hierarchal network of initial and collecting lymphatics are not well understood. One gene thought to be important for this process is Angiopoietin-2 (Ang-2). Ang2(-/-) mice have previously been reported to exhibit an abnormal lymphatic phenotype but the precise nature of the lymphatic defects and the underlying mechanisms have yet to be defined. Here we demonstrate by whole-mount immunofluorescence staining of ear skin and mesentery that lymphatic vessels in Ang2(-/-) mice fail to mature and do not exhibit a collecting vessel phenotype. Furthermore, dermal lymphatic vessels in Ang2(-/-) pups prematurely recruit smooth muscle cells and do not undergo proper postnatal remodeling. In contrast, Ang2 knock-out Ang1 knock-in mice do develop a hierarchal lymphatic vasculature, suggesting that activation of Tie-2 is required for normal lymphatic development. Taken together, this work pinpoints a specific lymphatic defect of Ang2(-/-) mice and further defines the sequential steps in lymphatic vessel remodeling. Published by Elsevier Inc.
引用
收藏
页码:309 / 320
页数:12
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