Morphology: size, shape, optical density, motility, division, organelle configuration, non-translational motion, nuclear shape |
Force: shear, tension, deformation |
Intracellular signaling (optical, MALDI-IM-MS): GFP/luciferase reporters, [Ca]I, pHi, Vm, MMP, GFP, GFP-FRET |
Extracellular electrolytes (electrochemical): [Na]e, [Ca]e, [K]e, [Mg]e, [PO4]e, [Cl]e, [HCO3]e
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Neurotransmitters (electrochemical): serotonin, acetylcholine, GAB A, … |
Extracellular metabolites (electrochemical): [glucose](t), [lactate](t), [pH](t), [O2](t), [NO](t), [H2O2](t),… |
Extracellular metabolites (GC/UPLC-IM-MS): amino acids, carbohydrates, small metabolites, stable isotopic markers |
Surface expression: specific affinity probes (dyes, Q-dots) |
Soluble gene expression (Luminex, nESI-IM-MS): cytokines, growth factors, hormones, enzymes |
Cytosolic proteins and membrane lipids (GFPs, MALDI-IM-MS) |
Gene expression (mRNA arrays, RT-PCR) |
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Parameters that can be controlled (actuators) |
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Base formulation of universal perfusion medium (blood surrogate) |
[glucose](t), [lactate](t), amino acids (~15), cytokines (N»1), growth factors (N»1), hormones (N»1), toxins and drugs (N»1) |
[Na]e(t), [Ca]e(t), [K]e(t), [Mg]e(t), pH(t), [O2](t), [PO4]e(t) |
Mechanical, electrical, optical, thermal, genetic (siRNA, optogenetic). |