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An Automated Perifusion System for Modifying Cell Culture Conditions over Time

BACKGROUND: Cells are continuously exposed to changes in their environment. Endocrine systems, in particular, communicate by rhythms and feedback loops. In this study, we developed an automated system to produce such conditions for cultured cells in a precisely timed manner. We utilized a programmab...

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Autores principales: Whitticar, Nicholas B., Strahler, Elisha W., Rajan, Parthiban, Kaya, Savas, Nunemaker, Craig S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117600/
https://www.ncbi.nlm.nih.gov/pubmed/27895534
http://dx.doi.org/10.1186/s12575-016-0049-7
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author Whitticar, Nicholas B.
Strahler, Elisha W.
Rajan, Parthiban
Kaya, Savas
Nunemaker, Craig S.
author_facet Whitticar, Nicholas B.
Strahler, Elisha W.
Rajan, Parthiban
Kaya, Savas
Nunemaker, Craig S.
author_sort Whitticar, Nicholas B.
collection PubMed
description BACKGROUND: Cells are continuously exposed to changes in their environment. Endocrine systems, in particular, communicate by rhythms and feedback loops. In this study, we developed an automated system to produce such conditions for cultured cells in a precisely timed manner. We utilized a programmable pair of syringe pumps for inflow and a peristaltic pump for outflow to create rhythmic pulses at 5-min intervals in solutions that mimic the endogenous patterns of insulin produced by pancreatic islets as a test case. RESULTS: This perifusion system was first tested by measuring trypan blue absorbance, which was intermittently added and washed out at 3:3 and 2:3 min (in:out). Absorbance corresponded with patterns of trypan blue delivery. We then created patterns of forced oscillations in islets by intermittently switching between solutions containing 28 millimolar (mM) glucose (producing high levels of intracellular calcium ([Ca(2+)](i)) and insulin secretion) and 28 mM glucose + calcium-channel blocker nifedipine (producing low levels of [Ca(2+)](i) and insulin secretion). Forced perifusion effects were monitored by fura-2 AM fluorescence measurements of [Ca(2+)](i). Islets showed uniform oscillations in [Ca(2+)](i) at time intervals consistent with the perifusion pattern, mimicking endogenous pulsatility. CONCLUSIONS: This study highlights a valuable method to modify the environment of the cell culture over a period of hours to days.
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spelling pubmed-51176002016-11-28 An Automated Perifusion System for Modifying Cell Culture Conditions over Time Whitticar, Nicholas B. Strahler, Elisha W. Rajan, Parthiban Kaya, Savas Nunemaker, Craig S. Biol Proced Online Methodology BACKGROUND: Cells are continuously exposed to changes in their environment. Endocrine systems, in particular, communicate by rhythms and feedback loops. In this study, we developed an automated system to produce such conditions for cultured cells in a precisely timed manner. We utilized a programmable pair of syringe pumps for inflow and a peristaltic pump for outflow to create rhythmic pulses at 5-min intervals in solutions that mimic the endogenous patterns of insulin produced by pancreatic islets as a test case. RESULTS: This perifusion system was first tested by measuring trypan blue absorbance, which was intermittently added and washed out at 3:3 and 2:3 min (in:out). Absorbance corresponded with patterns of trypan blue delivery. We then created patterns of forced oscillations in islets by intermittently switching between solutions containing 28 millimolar (mM) glucose (producing high levels of intracellular calcium ([Ca(2+)](i)) and insulin secretion) and 28 mM glucose + calcium-channel blocker nifedipine (producing low levels of [Ca(2+)](i) and insulin secretion). Forced perifusion effects were monitored by fura-2 AM fluorescence measurements of [Ca(2+)](i). Islets showed uniform oscillations in [Ca(2+)](i) at time intervals consistent with the perifusion pattern, mimicking endogenous pulsatility. CONCLUSIONS: This study highlights a valuable method to modify the environment of the cell culture over a period of hours to days. BioMed Central 2016-11-21 /pmc/articles/PMC5117600/ /pubmed/27895534 http://dx.doi.org/10.1186/s12575-016-0049-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Whitticar, Nicholas B.
Strahler, Elisha W.
Rajan, Parthiban
Kaya, Savas
Nunemaker, Craig S.
An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title_full An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title_fullStr An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title_full_unstemmed An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title_short An Automated Perifusion System for Modifying Cell Culture Conditions over Time
title_sort automated perifusion system for modifying cell culture conditions over time
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117600/
https://www.ncbi.nlm.nih.gov/pubmed/27895534
http://dx.doi.org/10.1186/s12575-016-0049-7
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