In vitro and in vivo models of angiogenesis
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In Vitro and in Vivo Models for Studying Angiogenesis
Vijay Avin BR, Molecular Biomedicine Laboratory, Sahyadri Sceince College, Shimoga, Karnataka, India
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Growth of new blood vesselsAdvanced cancers can secrete
angiogenic factors (VEGF, bFGF etc).
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Basic research to elucidate molecular mechanisms of angiogenesis:Identify and characterize regulatory pathways that mediate various steps of angiogenesis such as endothelial cell migration, invasion, and tubulogenesis.
To develop treatments for cancer and other diseases associated with angiogenesis: Identification of compounds that inhibit or stimulate key steps in the angiogenesis process.
Angiogenesis Research
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Methods to Study Angiogenesis
In vitro ModelsIn Vivo Models
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Important Considerations forDeveloping
Angiogenesis Studies Choose appropriate endothelial cell source.
Establish acceptable dynamic range to measure stimulation and/or inhibition of angiogenesis.
Incorporate appropriate extracellular matrix (ECM) protein(s) to facilitate cell functionality and assay outcome.
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Endothelial Cells are the most important tool for
in vitro studies of
Angiogenesis……
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Tumor cell survival is dependent on the health and proliferation of endothelial cells in surrounding blood
vessels………
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Sources of Endothelial CellsLarge vessel– aortic (e.g., HAEC)– umbilical vein (e.g. HUVEC)– pulmonary artery
Microvascular (e.g., HMVEC)– brain– lung– dermis (e.g., HDMEC)– myocardium
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Human Umbilical Vein Endothelial Cells HUVEC
Most commonly used EC type for angiogenesis studies
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ECM provides a physiological substrate that supports key cellular functions:
• Structural organization of cells and tissue.
• Cell attachment, survival, and proliferation.
• Induction and maintenance of cell differentiation.
• Can influence signal transduction and regulation of gene expression.
Examples: gelatin, fibronectin, vitronectin, laminin, collagen & Matrigel
Extracellular Matrix
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In vitro models for AngiogenesisCord Formation Assay
Tube Formation Assay
Cell Migration Assay
Cell Proliferation Assay
Gelatin Zymography
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Cord Formation Assay
Endothelial cells are incubated in growth factor containing matrigel
Then they were trypsinized and resuspended in the same medium and dispersed onto the matrigel.
Cord formation in each well is monitored and photographed using an inverted microscope.
Control
+ Inhibitor
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The endothelial cells are isolated and cultured in medium in gelatin coated flasks.
After gelation at 37C for 30 min the gels are overlaid with basal medium supplemented with test substances at desired concentrations.
Gels are examined and the tube length is determined for each well followed by determination of each group by using software.
Tube Formation Assay
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Cell Migration Assay
Polycarbonate + 12uM
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Cell Proliferation AssayControl
+ Inhibitor
The proliferation studies are based on cell counting, thymidine incorporation (or) Immunohistochemical staining for proliferation (or) cell death.
Endothelial cells are isolated and cultured in medium at 37C in a humidified atmosphere containing 5 % CO2. Cell proliferation is determined using a 5-bromo-2'-deoxyuridine (BrdU) colorimetric assay kit.
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Gelatin Zymography
MMP MMP +Inhibitor
This assay can also be called as Matrix Metalloproteinase (MMP) assay.
Gelatin is used as a substrate and is incorporated into poly acryl amide gels.
Samples are mixed with buffer loaded onto the gel and electrophoreses.
After electrophoreses the gels are incubated in activity buffer analyzed by densitography
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Invasion assay
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Rabbit or rat corneal assaySponge implantation modelsMatrigel plugsWound healing assay
In Vivo Models
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Sponge Implantation Method
This model is used for the evaluation of angiogenesis and anti- angiogenic agents.
The mechanism involved in this is stimulation of inflammation by foreign substance leads to the
angiogenesis.
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Sponge implant modelsSterile absorbable gel foam is used as a sponge .Incision is made at midline of the anaesthetized animal and gel piece is inserted in to subcutaneously.At 14th day the animals are sacrificed and gel foams are harvested and quantification is done for angiogenesis activity.
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Matrigel plug AssayUsed for the evaluation of both angiogenic and anti-angiogenic agents.
The mostly used animal model is mice.
The mechanism involved in this model is injection of foreign substances in to the animal leads to the stimulation of the inflammatory cells including macrophages and neutrophils that leads to the stimulation of angiogenesis.
Matrigel is a gelatinous material derived from mouse tumor cells
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Matrigel plugs
Mice injected with VEGF supplemented Matrigel were left untreated or were treated with the angiogenesis inhibitor which fully
suppresses angiogenesis, as visible macroscopically and microscopically.
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Corneal Angiogenesis AssayA pocket is created in the cornea where the compound of interest is inserted.
To induce an angiogenic response, a variety of materials including sponges, ethylene vinyl copolymer, or Hydron, containing an angiogenic substance (i.e. FGF-2 of VEGF) are implanted in "pockets"
The vascular response can then be monitored by direct observation using either a microscope or can be quantified by computer image analysis after perfusion of the cornea.
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Wound Healing Assay
Two circular holes of approximately 5 mm in diameter are punched with a tissue puncher through the dorsal skin of an anesthetized mouse.
Wound size, scar formation and re-epithelization of the wounds should be recorded daily by photography and by measuring the wound area with calipers.
Treatment can consist of pro-or anti-angiogenic compounds, and their effects on angiogenesis is determined post mortem after the regenerated tissue has been excised, fixed and stained. Transgenic or knock-out mice can be used, when available, to study the specific effects of particular genes.
Inflammation, new tissue formation and remodeling
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Hind Limb Ischemia Model
This method is mostly used for the evaluation of angiogenesis substances.
The mechanism involved in this model is haemodynamic changes leads to the formation of new blood vessels i.e. while large vessels with low flow tend to augmentation of blood flow which leads to the stimulation of vascular sprouting and maintain the potency of the newly formed collateral vessels thereby providing blood flow to theischemic tissue
the animals are anaesthetized and incision is making in the skin overlying the middle portion of the hind limb. Then the proximal end of the femoral artery is ligating and distal portion of saphenous artery is ligating and artery and their side branches were dissected free. The femoral artery and attached side branched are excised and overlying skin is then closed.
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IN- OVA ASSAY
Pilot method for most of the angiogenesis evaluation studies.
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Fertilized chicken eggs on the second day of incubation is and incubated at 37C at constant humidity.
On day 3 small hole is drill at narrow end and the albumin is withdrawn.
At the 7th day of incubation a small square window is open in the shell and test substances are implanted on the top of the membrane.
The window was sealed and reincubated. Eggs are incubated up to appropriate incubation time and angiogenesis is quantified
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Xenograft model On day third window made
and removing 2-3 drops of albumin
Resealed and kept for incubation
On day 10 plastic rings along with cells were placed and kept for incubation
On day 17th the eggs were opened and observed for the formation of solid tumor
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Thank you