Expression patterns of endothelial permeability pathways in the development of the blood-retinal barrier in mice

被引:16
作者
van der Wijk, Anne-Eva [1 ,2 ]
Wisniewska-Kruk, Joanna [1 ,2 ]
Vogels, Ilse M. C. [1 ,2 ]
van Veen, Henk A. [3 ]
Ip, Wing Fung [1 ,2 ]
van der Wel, Nicole N. [3 ]
van Noorden, Cornelis J. F. [1 ,2 ,4 ,5 ]
Schlingemann, Reinier O. [1 ,2 ,6 ]
Klaassen, Ingeborg [1 ,2 ]
机构
[1] Univ Amsterdam, Dept Ophthalmol, Amsterdam UMC,Canc Ctr Amsterdam, Ocular Angiogenesis Grp,Amsterdam Cardiovasc Sci, Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Med Biol, Amsterdam UMC,Canc Ctr Amsterdam, Ocular Angiogenesis Grp,Amsterdam Cardiovasc Sci, Amsterdam, Netherlands
[3] Univ Amsterdam, Dept Med Biol, Amsterdam UMC, Electron Microscopy Ctr Amsterdam, Amsterdam, Netherlands
[4] Univ Amsterdam, Dept Med Biol, Amsterdam UMC, Cellular Imaging Core Facil, Amsterdam, Netherlands
[5] Natl Inst Biol, Dept Genet Toxicol & Tumor Biol, Ljubljana, Slovenia
[6] Univ Lausanne, Jules Gonin Eye Hosp, Dept Ophthalmol, Lausanne, Switzerland
基金
美国国家卫生研究院;
关键词
tight junctions; transcellular permeability; VEGF signaling; VESICLE-ASSOCIATED PROTEIN; HUMAN DIABETIC-RETINOPATHY; ANTIGEN PAL-E; VASCULAR DEVELOPMENT; GENE-EXPRESSION; UP-REGULATION; BRAIN-TUMOR; VEGF-A; ANGIOGENESIS; MARKER;
D O I
10.1096/fj.201801499RRR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Insight into the molecular and cellular processes in blood-retinal barrier (BRB) development, including the contribution of paracellular and transcellular pathways, is still incomplete but may help to understand the inverse process of BRB loss in pathologic eye conditions. In this comprehensive observational study, we describe in detail the formation of the BRB at the molecular level in physiologic conditions, using mice from postnatal day (P)3 to P25. Our data indicate that immature blood vessels already have tight junctions at P5, before the formation of a functional BRB. Expression of the endothelial cell-specific protein plasmalemma vesicle-associated protein (PLVAP), which is known to be involved in transcellular transport and associated with BRB permeability, decreased during development and was absent when a functional barrier was formed. Moreover, we show that PLVAP deficiency causes a transient delay in retinal vascular development and changes in mRNA expression levels of endothelial permeability pathway proteins.
引用
收藏
页码:5320 / 5333
页数:14
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