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VEGF Signaling

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Cover of 'VEGF Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 VEGF Splicing and the Role of VEGF Splice Variants: From Physiological-Pathological Conditions to Specific Pre-mRNA Splicing.
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    Chapter 2 Detection and Quantification of VEGF Isoforms by ELISA
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    Chapter 3 Quantitation of Circulating Neuropilin-1 in Human, Monkey, Mouse, and Rat Sera by ELISA.
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    Chapter 4 Detection and Quantification of Vascular Endothelial Growth Factor Receptor Tyrosine Kinases in Primary Human Endothelial Cells
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    Chapter 5 Induction of VEGF Secretion in Cardiomyocytes by Mechanical Stretch
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    Chapter 6 Chromatin Immunoprecipitation Assay: Examining the Interaction of NFkB with the VEGF Promoter.
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    Chapter 7 An Overview of VEGF-Mediated Signal Transduction
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    Chapter 8 Identification of Receptor Tyrosine Kinase Inhibitors Using Cell Surface Biotinylation and Affinity Isolation
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    Chapter 9 VEGF Signaling
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    Chapter 10 In Vitro Angiogenesis Assays
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    Chapter 11 Chemotactic Migration of Endothelial Cells Towards VEGF-A 165
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    Chapter 12 Vasculogenesis and Angiogenesis in VEGF Receptor-1 Deficient Mice
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    Chapter 13 The Embryonic Mouse Hindbrain and Postnatal Retina as In Vivo Models to Study Angiogenesis
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    Chapter 14 VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Guinea Pigs to Enhance Fetal Growth
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    Chapter 15 VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Sheep to Enhance Fetal Growth
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    Chapter 16 Generation of Targeted Mutations in Zebrafish Using the CRISPR/Cas System.
Attention for Chapter 5: Induction of VEGF Secretion in Cardiomyocytes by Mechanical Stretch
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Citations

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Chapter title
Induction of VEGF Secretion in Cardiomyocytes by Mechanical Stretch
Chapter number 5
Book title
VEGF Signaling
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2917-7_5
Pubmed ID
Book ISBNs
978-1-4939-2916-0, 978-1-4939-2917-7
Authors

Michelle L. Matter, Matter, Michelle L.

Abstract

Cells respond to their environment by relaying mechanical force into biochemical stimuli that activate intracellular signal transduction pathways. Subjecting cells to in vitro mechanical stretch can mimic cellular responses to changes in the rigidity of the extracellular matrix. Here we describe an in vitro model system that mimics stretch overload in vivo. In this stretch-mediated hypertrophy model, adult rat cardiomyocytes attached to laminin-coated flexible membranes are subjected to cyclic mechanical stretch at an extension level of 10 % at 30 cycles/min. At various time points VEGF secretion into the media is collected and quantitated.