TY - JOUR
T1 - Reversibly sealed multilayer microfluidic device for integrated cell perfusion and on-line chemical analysis of cultured adipocyte secretions
AU - Clark, Anna M.
AU - Sousa, Kyle M.
AU - Chisolm, Claire N.
AU - MacDougald, Ormond A.
AU - Kennedy, Robert T.
N1 - Funding Information:
Acknowledgments This work was supported by grants from the National Institutes of Health: R37 DK046960 (R.T.K.), NIBIB T32EB005582 (A.M.C.), DK070071, DE007057 (K.M.S.), and DK51563 (O.A.M.). K.M.S. also was supported by an Eli Lilly Postdoctoral Fellowship.
PY - 2010/8
Y1 - 2010/8
N2 - A three-layer microfluidic device was developed that combined perfusion of cultured cells with on-line chemical analysis for near real-time monitoring of cellular secretions. Two layers were reversibly sealed to form a cell chamber that allowed cells grown on coverslips to be loaded directly into the chip. The outlet of the chamber was in fluidic contact with a third layer that was permanently bonded. Perfusate from the cell chamber flowed into this third layer where a fluorescence enzyme assay for non-esterified fatty acid (NEFA) was performed on-line. The device was used to monitor efflux of NEFAs from ∼6,200 cultured adipocytes with 83 s temporal resolution. Perfusion of murine 3T3-L1 cultured adipocytes resulted in an average basal concentration of 24.2 ± 2.4 μM NEFA (SEM, n = 6) detected in the effluent corresponding to 3.31 × 10-5 nmol cell-1 min-1. Upon pharmacological treatment with a β-adrenergic agonist to stimulate lipolysis, a 6.9 ± 0.7-fold (SEM, n = 6) sustained increase in NEFA secretion was observed. This multilayer device provides a versatile platform that could be adapted for use with other cell types to study corresponding cellular secretions in near real-time. © 2010 Springer-Verlag.
AB - A three-layer microfluidic device was developed that combined perfusion of cultured cells with on-line chemical analysis for near real-time monitoring of cellular secretions. Two layers were reversibly sealed to form a cell chamber that allowed cells grown on coverslips to be loaded directly into the chip. The outlet of the chamber was in fluidic contact with a third layer that was permanently bonded. Perfusate from the cell chamber flowed into this third layer where a fluorescence enzyme assay for non-esterified fatty acid (NEFA) was performed on-line. The device was used to monitor efflux of NEFAs from ∼6,200 cultured adipocytes with 83 s temporal resolution. Perfusion of murine 3T3-L1 cultured adipocytes resulted in an average basal concentration of 24.2 ± 2.4 μM NEFA (SEM, n = 6) detected in the effluent corresponding to 3.31 × 10-5 nmol cell-1 min-1. Upon pharmacological treatment with a β-adrenergic agonist to stimulate lipolysis, a 6.9 ± 0.7-fold (SEM, n = 6) sustained increase in NEFA secretion was observed. This multilayer device provides a versatile platform that could be adapted for use with other cell types to study corresponding cellular secretions in near real-time. © 2010 Springer-Verlag.
KW - Adipocytes
KW - Enzyme assay
KW - Fatty acids
KW - Integration
KW - Microfluidics
KW - Microfluidic Analytical Techniques/instrumentation
KW - 3T3-L1 Cells
KW - Fatty Acids, Nonesterified/analysis
KW - Lipolysis
KW - Online Systems/instrumentation
KW - Animals
KW - Adipocytes/chemistry
KW - Mice
KW - Cell Culture Techniques
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UR - https://www.mendeley.com/catalogue/8cd2a2e4-2f56-3d00-972f-35137177f4af/
U2 - 10.1007/s00216-010-3897-z
DO - 10.1007/s00216-010-3897-z
M3 - Article
C2 - 20549489
SN - 1618-2642
VL - 397
SP - 2939
EP - 2947
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 7
ER -