Desmoplakin is required for microvascular tube formation in culture

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...

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Veröffentlicht in:Journal of cell science 2004-07, Vol.117 (Pt 15), p.3129-3140
Hauptverfasser: Zhou, Xuan, Stuart, August, Dettin, Luis E, Rodriguez, Gisela, Hoel, Bonnie, Gallicano, G Ian
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container_end_page 3140
container_issue Pt 15
container_start_page 3129
container_title Journal of cell science
container_volume 117
creator Zhou, Xuan
Stuart, August
Dettin, Luis E
Rodriguez, Gisela
Hoel, Bonnie
Gallicano, G Ian
description 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.
doi_str_mv 10.1242/jcs.01132
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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). 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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Company of Biologists
subjects Alleles
Animals
Antigens, CD
Blotting, Western
Cadherins - metabolism
Capillaries - metabolism
Cell Adhesion
Cell Line
Collagen - pharmacology
Cytoskeletal Proteins - metabolism
Cytoskeletal Proteins - physiology
Desmoplakins
Desmosomes - metabolism
Drug Combinations
Endothelium, Vascular - metabolism
Green Fluorescent Proteins - metabolism
Humans
Immunohistochemistry
Laminin - pharmacology
Mice
Mice, Transgenic
Microcirculation
Microscopy, Electron
Microscopy, Fluorescence
Neovascularization, Physiologic
Proteoglycans - pharmacology
Reverse Transcriptase Polymerase Chain Reaction
RNA, Small Interfering - metabolism
Time Factors
title Desmoplakin is required for microvascular tube formation in culture
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