A novel three-dimensional flow chamber device to study chemokine-directed extravasation of cells circulating under physiological flow conditions.

Valentina Goncharova, Sophia K Khaldoyanidi
Author Information
  1. Valentina Goncharova: Torrey Pines Institute for Molecular Studies.

Abstract

Extravasation of circulating cells from the bloodstream plays a central role in many physiological and pathophysiological processes, including stem cell homing and tumor metastasis. The three-dimensional flow chamber device (hereafter the 3D device) is a novel in vitro technology that recreates physiological shear stress and allows each step of the cell extravasation cascade to be quantified. The 3D device consists of an upper compartment in which the cells of interest circulate under shear stress, and a lower compartment of static wells that contain the chemoattractants of interest. The two compartments are separated by porous inserts coated with a monolayer of endothelial cells (EC). An optional second insert with microenvironmental cells of interest can be placed immediately beneath the EC layer. A gas exchange unit allows the optimal CO2 tension to be maintained and provides an access point to add or withdraw cells or compounds during the experiment. The test cells circulate in the upper compartment at the desired shear stress (flow rate) controlled by a peristaltic pump. At the end of the experiment, the circulating and migrated cells are collected for further analyses. The 3D device can be used to examine cell rolling on and adhesion to EC under shear stress, transmigration in response to chemokine gradients, resistance to shear stress, cluster formation, and cell survival. In addition, the optional second insert allows the effects of crosstalk between EC and microenvironmental cells to be examined. The translational applications of the 3D device include testing of drug candidates that target cell migration and predicting the in vivo behavior of cells after intravenous injection. Thus, the novel 3D device is a versatile and inexpensive tool to study the molecular mechanisms that mediate cellular extravasation.

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Grants

  1. R21 DK067084/NIDDK NIH HHS
  2. R43 CA141782/NCI NIH HHS
  3. R43CA141782/NCI NIH HHS
  4. R21DK067084/NIDDK NIH HHS

MeSH Term

Animals
Bone Marrow Cells
Cell Movement
Chemokines
Cytological Techniques
Endothelial Cells
Human Umbilical Vein Endothelial Cells
Humans
Mice

Chemicals

Chemokines