This work was supported by NIH/NHLBI grant R01 HL082689 to Scott I. Simon and Anthony G. Passerini.

1. Cell Culture and Substrate Preparation
 <ol>
 <li>Cut 3-inch circular substrates from a 100 x 20 mm tissue culture dish (BD Falcon) using a lathe. Sterilize substrates by submersion in 70% ethanol. Place in a Petri dish and coat with 4 ml type-I collagen (100 &mu;g/ml) for 1 hr at room temperature, then rinse with 4 ml 1 x PBS. </li>
 <li>Suspend Human Aortic Endothelial Cells (HAEC, passage 4-6) at 6.5x105 cells/ml and seed by applying 1 ml directly to substrate. Place in a 37 &deg;C, 5% CO<s...

<ol>
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No conflicts of interest declared.

We describe the use of microfluidic PDMS devices for the on-chip assessment of endothelial inflammatory phenotype through the real-time imaging of CAM expression and monocyte adhesion. A major advantage of our approach lies in the ability to quantify outcomes associated with endothelial dysfunction in cells exposed to inflammatory mediators such as dietary lipids and cytokines under defined hydrodynamic conditions that mirror shear stress in atherogenic vessels. The VMMC facilitate the use of small amounts of reagents or...

<table border="1">
<tbody>
 <tr>
 <td>Item</td>
 <td>Company</td>
 <td>Catalogue Number</td>
 </tr>
 <tr>
 <td>100 x 20mm Petri Dishes</td>
 <td>BD Falcon</td>
 <td>353003</td>
 </tr>
 <tr>
 <td>Ethanol 95%</td>
 <td>EMD Chemicals</td>
 <td>EX0290-1</td>
 </tr>
 <tr>
 <td>DPBS</td>
 <td>Cellgro</td>
 <td>21-031-CV</td>
 </tr>
 <tr>
 <td>Type I Rat Tail Derived Collagen</td>
 <td>Gibco</td>
 <td>A10483-01</td>
 </tr>
 <tr>
 <td>Human Aortic Endothelial Cells</td>
 <td>Genlantis</td>
 <td>PH30405A</td>
 </tr>
 <tr>
 <td>Antibiotic-Antimycotic Solution</td>
 <td>Invitrogen</td>
 <td>15240-062</td>
 </tr>
 <tr>
 <td>Endothelial BulletKit</td>
 <td>Lonza</td>
 <td>CC-4176</td>
 </tr>
 <tr>
 <td>Endothelial Basal Media-2</td>
 <td>Lonza</td>
 <td>CC-3156</td>
 </tr>
 <tr>
 <td>10 ml Syringes</td>
 <td>BD Falcon</td>
 <td>309604 </td>
 </tr>
 <tr>
 <td>Polyurethane tubing</td>
 <td>Tygon</td>
 <td>ABW0001</td>
 </tr>
 <tr>
 <td>Leibovitz-15 Media</td>
 <td>Gibco</td>
 <td>11415-069</td>
 </tr>
 <tr>
 <td>Sylgard 184 Silicone Elastomer Base</td>
 <td>Dow Corning</td>
 <td>184</td>
 </tr>
 <tr>
 <td>Sylgard 184 Silicone Elastomer Curing Agent</td>
 <td>Dow Corning</td>
 <td>184</td>
 </tr>
 <tr>
 <td>SU8 Photoresist Master Wafer</td>
 <td>UC Davis Pan Lab</td>
 <td>N/A</td>
 </tr>
 <tr>
 <td>Eclipse TE200 Inverted Microscope</td>
 <td>Nikon</td>
 <td>Eclipse TE200</td>
 </tr>
 <tr>
 <td>Syringe Pump</td>
 <td>Harvard Apparatus</td>
 <td>PHD2000</td>
 </tr>
 <tr>
 <td>19 gauge hypodermic needle</td>
 <td>Kendall</td>
 <td>8881</td>
 </tr>
 <tr>
 <td>THP-1 Monocytic Cell Line</td>
 <td>ATCC</td>
 <td>TIB-202</td>
 </tr>
 <tr>
 <td>HBSS (Hanks Buffered Saline Solution) with Ca2+/Mg2+ </td>
 <td>Gibco</td>
 <td>14025-092</td>
 </tr>
 <tr>
 <td>Tumor Necrosis Factor Alpha (TNF-&alpha;)</td>
 <td>R&amp;D Systems</td>
 <td>210-TA-010</td>
 </tr>
 <tr>
 <td>Stromal Derived Factor - 1 (SDF-1)</td>
 <td>R&amp;D Systems</td>
 <td>350-NS-010</td>
 </tr>
 <tr>
 <td>RPMI 1640</td>
 <td>Cellgro </td>
 <td>10-040-CV</td>
 </tr>
 <tr>
 <td>Human Serum Albumin (HSA)</td>
 <td>ZLB Behring</td>
 <td>NDC 0053-7680-32</td>
 </tr>
 </tbody>
</table>
Table 2. Specific reagents and equipment.

on-chip endothelial inflammatory phenotyping

Atherogenesis is potentiated by metabolic abnormalities that contribute to a heightened state of systemic inflammation resulting in endothelial dysfunction. However, early functional changes in endothelium that signify an individual's level of risk are not directly assessed clinically to help guide therapeutic strategy. Moreover, the regulation of inflammation by local hemodynamics contributes to the non-random spatial distribution of atherosclerosis, but the mechanisms are difficult to delineate in vivo. We describe a lab-on-a-chip based approach to quantitatively assay metabolic perturbation of inflammatory events in human endothelial cells (EC) and monocytes under precise flow conditions. Standard methods of soft lithography are used to microfabricate vascular mimetic microfluidic chambers (VMMC), which are bound directly to cultured EC monolayers.1 These devices have the advantage of using small volumes of reagents while providing a platform for directly imaging the inflammatory events at the membrane of EC exposed to a well-defined shear field. We have successfully applied these devices to investigate cytokine-,2 lipid-3, 4 and RAGE-induced5 inflammation in human aortic EC (HAEC). Here we document the use of the VMMC to assay monocytic cell (THP-1) rolling and arrest on HAEC monolayers that are conditioned under differential shear characteristics and activated by the inflammatory cytokine TNF-&alpha;. Studies such as these are providing mechanistic insight into atherosusceptibility under metabolic risk factors.

Watch this Scientific Journal Video about On-Chip Endothelial Inflammatory Phenotyping at JoVE.com

On-Chip Endothelial Inflammatory Phenotyping

Microfluidic flow chambers etched by photolithography and fabricated from PDMS are applied to probe functional outcomes associated with EC dysfunction and inflammation. In a representative experiment, the ability of differential shear stress to modulate monocytic cell adhesion to cytokine activated EC monolayers is demonstrated.

Atherogenesis is potentiated by metabolic abnormalities that contribute to a heightened state of systemic inflammation resulting in endothelial ...

on-chip-endothelial-inflammatory-phenotyping

Research

JoVE Journal

Bioengineering

10.8K vues.  University of California, Davis. Chambres d'écoulement microfluidiques gravés par photolithographie et fabriqué à partir de PDMS sont appliqués à sonder les résultats fonctionnels associés à une dysfonction CE et de l'inflammation. Dans une expérience représentative, la capacité de contrainte de cisaillement différentiel de moduler l'adhésion cellulaire monocytaire à cytokine activé monocouches CE est démontrée.