This paper presents a tubing-free microfluidic wound healing assay to quantify the migration of vascular smooth muscle cells (VSMCs), where gravity was used to generate a laminar flow within microfluidic channels, enabling cell seeding, culture, and wound generation. As the first systemic study to quantify the migration of VSMCs within microfluidic environments, the effects of channel geometries, surface modifications and chemokines on cellular migration were investigated, revealing that 1) height of the micro channels had a significant impact on cell migration; 2) the surface coating of collagen induced more migration of VSMCs than fibronectin coated surfaces and 3) platelet derived growth factor resulted in maximal cell migration compared...
Studying the rate of cell migration provides insight into fundamental cell biology as well as a tool...
We use a novel, microfluidics-based technique to deconstruct the classical wound healing scratch ass...
An in vitro tissue construct amenable to perfusion was formed by randomly packing mesenchymal stroma...
This paper presents a tubing-free microfluidic wound healing assay to quantify the migration of vasc...
This paper presents a tubing-free microfluidic wound healing assay to quantify the migration of vasc...
This paper presents a 384-well microfluidic wound-healing assay enabling the migration studies of va...
A microfluidic wound-healing assay for quantifying endothelial cell migration. Am J Physiol Heart Ci...
This paper presents a microfluidic device enabling culture of vascular smooth muscle cells (VSMCs) w...
In vitro scratch wound assays are commonly used strategies to measure cell repair rate, facilitating...
All cell migration and wound healing assays are based on the inherent ability of adherent cells to m...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
We use a novel, microfluidics-based technique to deconstruct the classical wound healing scratch ass...
Cell migration refers to the directional movement of cells to the surrounding cell-free zone in resp...
Vascular cell biology is an area of research with great biomedical relevance. Vascular dysfunction i...
<div><p>When living tissues are injured, they undergo a sequential process of homeostasis, inflammat...
Studying the rate of cell migration provides insight into fundamental cell biology as well as a tool...
We use a novel, microfluidics-based technique to deconstruct the classical wound healing scratch ass...
An in vitro tissue construct amenable to perfusion was formed by randomly packing mesenchymal stroma...
This paper presents a tubing-free microfluidic wound healing assay to quantify the migration of vasc...
This paper presents a tubing-free microfluidic wound healing assay to quantify the migration of vasc...
This paper presents a 384-well microfluidic wound-healing assay enabling the migration studies of va...
A microfluidic wound-healing assay for quantifying endothelial cell migration. Am J Physiol Heart Ci...
This paper presents a microfluidic device enabling culture of vascular smooth muscle cells (VSMCs) w...
In vitro scratch wound assays are commonly used strategies to measure cell repair rate, facilitating...
All cell migration and wound healing assays are based on the inherent ability of adherent cells to m...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
We use a novel, microfluidics-based technique to deconstruct the classical wound healing scratch ass...
Cell migration refers to the directional movement of cells to the surrounding cell-free zone in resp...
Vascular cell biology is an area of research with great biomedical relevance. Vascular dysfunction i...
<div><p>When living tissues are injured, they undergo a sequential process of homeostasis, inflammat...
Studying the rate of cell migration provides insight into fundamental cell biology as well as a tool...
We use a novel, microfluidics-based technique to deconstruct the classical wound healing scratch ass...
An in vitro tissue construct amenable to perfusion was formed by randomly packing mesenchymal stroma...