Desmoplakin is required for microvascular tube formation in culture

桥粒蛋白 粘合连接 基质凝胶 细胞生物学 血管生成 生物 普氏球蛋白 桥粒 血管生成 转分化 内皮干细胞 癌症研究 钙粘蛋白 细胞 干细胞 信号转导 遗传学 体外 Wnt信号通路 连环素 祖细胞
作者
Xuan Zhou,August Stuart,Luis E. Dettin,Gisela Pita Rodríguez,Bonnie Hoel,G. Ian Gallicano
出处
期刊:Journal of Cell Science [The Company of Biologists]
卷期号:117 (15): 3129-3140 被引量:43
标识
DOI:10.1242/jcs.01132
摘要

Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells that line capillaries. Few studies have focused on the function of DP in de novo capillary formation (vasculogenesis) and branching (angiogenesis) during tumorigenesis, embryonic development, cardiovascular development or wound healing. Only recently have investigations begun to determine the effect the loss of DP has on capillaries during embryogenesis (i.e. in DP–/– mice). Evidence shows that the loss of desmoplakin in vivo results in leaky capillaries and/or capillary malformation. Consequently, the goal of this study was to determine the function of DP in complexus adherens junctions during capillary formation. To accomplish this goal, we used siRNA technology to knock down desmoplakin expression in endothelial cells before they were induced to form microvascular tubes on matrigel. DP siRNA treated cells sent out filopodia and came in close contact with each other when plated onto matrigel; however, in most cases they failed to form tubes as compared with control endothelial cells. Interestingly, after siRNA degradation, endothelial cells were then capable of forming microvascular tubes. In depth analyses into the function of DP in capillary formation were not previously possible because the tools and experimental approaches only recently have become available (i.e. siRNA). Consequently, fully understanding the role of desmoplakin in capillary formation may lead to a novel approach for inhibiting vasculo- and angiogenesis in tumor formation.

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