Simultaneous or Sequential Orthogonal Gradient Formation in a 3D Cell Culture Microfluidic Platform

Small. 2016 Feb 3;12(5):612-22. doi: 10.1002/smll.201501905. Epub 2015 Nov 30.

Abstract

Biochemical gradients are ubiquitous in biology. At the tissue level, they dictate differentiation patterning or cell migration. Recapitulating in vitro the complexity of such concentration profiles with great spatial and dynamic control is crucial in order to understand the underlying mechanisms of biological phenomena. Here, a microfluidic design capable of generating diffusion-driven, simultaneous or sequential, orthogonal linear concentration gradients in a 3D cell-embedded scaffold is described. Formation and stability of the orthogonal gradients are demonstrated by computational and fluorescent dextran-based characterizations. Then, system utility is explored in two biological systems. First, stem cells are subjected to orthogonal gradients of morphogens in order to mimic the localized differentiation of motor neurons in the neural tube. Similarly to in vivo, motor neurons preferentially differentiate in regions of high concentration of retinoic acid and smoothened agonist (acting as sonic hedgehog), in a concentration-dependent fashion. Then, a rotating gradient is applied to HT1080 cancer cells and the change in migration direction is investigated as the cells adapt to a new chemical environment. The response time of ≈4 h is reported. These two examples demonstrate the versatility of this new design that can also prove useful in many applications including tissue engineering and drug screening.

Keywords: cancer cell migration; dynamic chemotaxis; microfluidics; orthogonal gradients; stem cell differentiation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Culture Techniques / methods*
  • Cell Differentiation
  • Cell Line
  • Chemotaxis / drug effects
  • Cyclohexylamines / pharmacology
  • Equipment Design
  • Humans
  • Hydrogel, Polyethylene Glycol Dimethacrylate / pharmacology
  • Mice
  • Microfluidic Analytical Techniques / instrumentation
  • Microfluidic Analytical Techniques / methods*
  • Motor Neurons / cytology
  • Motor Neurons / drug effects
  • Neural Tube / cytology
  • Neural Tube / embryology
  • Thiophenes / pharmacology
  • Time Factors
  • Tretinoin / pharmacology

Substances

  • Cyclohexylamines
  • SAG compound
  • Thiophenes
  • Hydrogel, Polyethylene Glycol Dimethacrylate
  • Tretinoin