A continuous flow cell culture system for precision cell stimulation and time-resolved profiling of cell secretion.


Journal

Analytical biochemistry
ISSN: 1096-0309
Titre abrégé: Anal Biochem
Pays: United States
ID NLM: 0370535

Informations de publication

Date de publication:
15 07 2021
Historique:
received: 19 01 2021
revised: 04 04 2021
accepted: 14 04 2021
pubmed: 23 4 2021
medline: 28 9 2021
entrez: 22 4 2021
Statut: ppublish

Résumé

Cells exchange substances with their surroundings during metabolism, signaling, and other functions. These fluxes are dynamic, changing in response to external cues and internal programs. Static cultures are inadequate for measuring these dynamics because the environments of the cells change as substances accumulate or deplete from medium, unintentionally affecting cell behavior. Static cultures offer limited time resolution due to the impracticality of frequent or prolonged manual sampling, and cannot expose cells to smooth, transient changes in stimulus concentrations. In contrast, perfusion cultures constantly maintain cellular environments and continuously sample the effluent stream. Existing perfusion culture systems are either microfluidic, which are difficult to make and use, or macrofluidic devices built from custom parts that neglect solute dispersion. In this study, a multiplexed macrofluidic perfusion culture platform was developed to measure secretion and absorption rates of substances by cells in a temporally controlled environment. The modular platform handles up to 31 streams with automated fraction collection. This paper presents the assembly of this dynamic bioreactor from commercially available parts, and a method for quantitatively handling the effects of dispersion using residence time distributions. The system is then applied to monitor the secretion of a circadian clock gene-driven reporter from engineered cells.

Identifiants

pubmed: 33887234
pii: S0003-2697(21)00114-7
doi: 10.1016/j.ab.2021.114213
pmc: PMC8154734
mid: NIHMS1698271
pii:
doi:

Substances chimiques

Culture Media 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

114213

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM135141
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI134116
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB012521
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008339
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM127353
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Patrick Erickson (P)

Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, NJ, 08854, USA.

Tony Houwayek (T)

Department of Biomedical Engineering, Rutgers University, Piscataway, NJ, 08854, USA.

Alexandra Burr (A)

Department of Biomedical Engineering, Rutgers University, Piscataway, NJ, 08854, USA.

Matthew Teryek (M)

Department of Biomedical Engineering, Rutgers University, Piscataway, NJ, 08854, USA.

Biju Parekkadan (B)

Department of Biomedical Engineering, Rutgers University, Piscataway, NJ, 08854, USA; Department of Medicine, Rutgers Biomedical Health Sciences, New Brunswick, NJ, 08852, USA. Electronic address: biju.parekkadan@rutgers.edu.

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Classifications MeSH