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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

In this protocol, a biomimetic microfluid assay, which can reproduce a physiologically relevant microvascular environment and reproduce the entire leukocyte adhesion/migration cascade, is employed to study leukocyte-endothelial cell interactions in inflammatory disease.

Abstract

Leukocyte-endothelial cell interactions play an important role in inflammatory diseases such as sepsis. During inflammation, excessive migration of activated leukocytes across the vascular endothelium into key organs can lead to organ failure. A physiologically relevant biomimetic microfluidic assay (bMFA) has been developed and validated using several experimental and computational techniques, which can reproduce the entire leukocyte rolling/adhesion/migration cascade to study leukocyte-endothelial cell interactions. Microvascular networks obtained from in vivo images in rodents were digitized using a Geographic Information System (GIS) approach and microfabricated with polydimethylsiloxane (PDMS) on a microscope slide. To study the effect of shear rate and vascular topology on leukocyte-endothelial cell interactions, a Computational Fluid Dynamics (CFD) model was developed to generate a corresponding map of shear rates and velocities throughout the network. The bMFA enables the quantification of leukocyte-endothelial cells interactions, including rolling velocity, number of adhered leukocytes in response to different shear rates, number of migrated leukocytes, endothelial cell permeability, adhesion molecule expression and other important variables. Furthermore, by using human-related samples, such as human endothelial cells and leukocytes, bMFA provides a tool for rapid screening of potential therapeutics to increase their clinical translatability.

Introduction

Inflammation is the host response to infection and injury, and the endothelium plays an important role in the inflammatory response1,2,3. Inflammatory dysregulation is the underlying cause of a number of disease pathologies such as sepsis, cardiovascular diseases, asthma, inflammatory bowel disease, cancer and COVID-19. Leukocyte-endothelial cell interactions play a central role in these inflammatory diseases. During inflammation, the release of PAMPS (pathogen-associated molecular patterns) from pathogens or DAMPS (damage-associated molecular patterns) from injured tiss....

Protocol

Heparinized human blood is obtained for neutrophil isolation from healthy adult donors (males and females, aged between 21 and 60 years old), following informed consent as approved by the Institutional Review Board of Temple University (Philadelphia, PA, USA).

1. Priming and coating the device with human fibronectin

NOTE: The bMFA has two inlet ports and two outlet ports connected to the vascular compartment. It also has one port connected to the tiss.......

Representative Results

After 48 h of culture under shear flow in bMFA, endothelial cells covered the surface of the vascular channels in bMFA and aligned in the direction of flow (Figure 6). Confocal microscopy indicated that all surfaces of the vascular channels were covered by endothelial cells, forming a complete 3D lumen in bMFA18.

Using this protocol, a neutrophil adhesion map can be acquired, showing that there is significant adhesion of neutrophils to.......

Discussion

The bMFA reproduces the topography and flow conditions of the in vivo microvascular networks and can be used to study leukocyte-endothelial cell interaction and endothelial function in vitro under physiologically realistic conditions. In the microvasculature of either mouse or human, the geometry of the microvascular networks are self-similar and fractal, and the Reynolds number << 1, indicating that vascular geometry does not significantly impact flow patterns. Therefore, the bFMA can be used t.......

Acknowledgements

This work was supported by the National Institutes of Health, Grant Number: GM114359 and GM134701 (M.F.K. and L.E.K.), 1F31AI164870-01 (J.C.L.), and Defense Threat Reduction Agency, Grant Number: HDTRA11910012 (M.F.K. and L.E.K.).

....

Materials

NameCompanyCatalog NumberComments
1 mL syringeFisher Scientific14-823-30
Biomimetic microfluidic assay (bMFA)SynVivoSMN1-C001Exclusive at SynVivo
Blunt needleJensen GlobalJG24-0.5
Calcium ChlorideFisher ScientificC70-500
CFDA, SEThermoFisherC1157
Dextran, 250,000, PowderSpectrum Chemical Mfg. CorpDE-130
Ficoll-Paque PremiumGE Health Care17-5442-02Leukocyte isolation media
fMLPSigma-AldrichF3506
HepesFisher ScientificAAJ1692630
Human fibronectinFisher Scientific33-016-015use vendor recommended ECM for different cell lines
Microvascular Endothelial Cell Growth Medium-2 BulletKitLonzacc-3202Human lung microvascular endothelial cell culture medium (HLMVEC).
Human lung microvascular endothelial cellsLonzacc-2527use vedor remommended trypsin-EDTA and TNS
Magnesium ChlorideFisher ScientificBP214-500
Nikon Eclipse Ti2Nikon Instruments Inc.Microscope
NIS-elements, 5.20.01Nikon Instruments Inc.Imaging software
PBSFisher ScientificMT21040CV
PhD Ultra Syringe PumpHarvard Apparatus70-3007Syringe Pump
Potassium HydroxideFisher Scientific02-003-763
Recombinant Human TNF-alphaR&D Systems210-TA
Slide clampSynVivo
Sodium ChlorideFisher ScientificS640-500
Synvivo Pneumatic PrimerSynVivo
Trypsin-EDTA, Trypsin Neutralization Solution(TNS)Lonzacc-5034
Tygon tubingFisher Scientific50-206-8921Tubing

References

  1. Kolaczkowska, E., Kubes, P. Neutrophil recruitment and function in health and inflammation. Nature Reviews Immunology. 13 (3), 159-175 (2013).
  2. Yang, Q., Wijerathne, H., Langston, J. C., Kiani, M. F., Kilpatrick, L. E.

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