Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device

The establishment and maintenance of axonal patterning is crucial for neuronal function. To identify the molecular systems that operate locally to control axonal structure, it is important to manipulate molecular functions in restricted subcellular areas for a long period of time. Microfluidic devic...

Full description

Bibliographic Details
Main Authors: Daiki Uryu, Tomohiro Tamaru, Azusa Suzuki, Rie Sakai, Yoshiyuki Konishi
Format: Article
Language:English
Published: Taylor & Francis Group 2016-01-01
Series:Science and Technology of Advanced Materials
Subjects:
Online Access:http://dx.doi.org/10.1080/14686996.2016.1241131
id doaj-2d9362928ca54bfa83143769a890a7c5
record_format Article
spelling doaj-2d9362928ca54bfa83143769a890a7c52021-07-06T11:30:14ZengTaylor & Francis GroupScience and Technology of Advanced Materials1468-69961878-55142016-01-0117169169710.1080/14686996.2016.12411311241131Study of local intracellular signals regulating axonal morphogenesis using a microfluidic deviceDaiki Uryu0Tomohiro Tamaru1Azusa Suzuki2Rie Sakai3Yoshiyuki Konishi4Department of Human and Artificial Intelligent Systems, Faculty of Engineering, University of FukuiDepartment of Human and Artificial Intelligent Systems, Faculty of Engineering, University of FukuiDepartment of Human and Artificial Intelligent Systems, Faculty of Engineering, University of FukuiDepartment of Human and Artificial Intelligent Systems, Faculty of Engineering, University of FukuiDepartment of Human and Artificial Intelligent Systems, Faculty of Engineering, University of FukuiThe establishment and maintenance of axonal patterning is crucial for neuronal function. To identify the molecular systems that operate locally to control axonal structure, it is important to manipulate molecular functions in restricted subcellular areas for a long period of time. Microfluidic devices can be powerful tools for such purposes. In this study, we demonstrate the application of a microfluidic device to clarify the function of local Ca2+ signals in axons. Membrane depolarization significantly induced axonal branch-extension in cultured cerebellar granule neurons (CGNs). Local application of nifedipine using a polydimethylsiloxane (PDMS)-based microfluidic device demonstrated that Ca2+ entry from the axonal region via L-type voltage-dependent calcium channels (L-VDCC) is required for branch extension. Furthermore, we developed a method for locally controlling protein levels by combining genetic techniques and use of a microfluidic culture system. A vector for enhanced green fluorescent protein (EGFP) fused to a destabilizing domain derived from E. coli dihydrofolate reductase (ecDHFR) is introduced in neurons by electroporation. By local application of the DHFR ligand, trimethoprim (TMP) using a microfluidic device, we were able to manipulate differentially the level of fusion protein between axons and somatodendrites. The present study revealed the effectiveness of microfluidic devices to address fundamental biological issues at subcellular levels, and the possibility of their development in combination with molecular techniques.http://dx.doi.org/10.1080/14686996.2016.1241131microfluidic devicecerebellar granule neuronsaxondepolarizationdihydrofolate reductase
collection DOAJ
language English
format Article
sources DOAJ
author Daiki Uryu
Tomohiro Tamaru
Azusa Suzuki
Rie Sakai
Yoshiyuki Konishi
spellingShingle Daiki Uryu
Tomohiro Tamaru
Azusa Suzuki
Rie Sakai
Yoshiyuki Konishi
Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
Science and Technology of Advanced Materials
microfluidic device
cerebellar granule neurons
axon
depolarization
dihydrofolate reductase
author_facet Daiki Uryu
Tomohiro Tamaru
Azusa Suzuki
Rie Sakai
Yoshiyuki Konishi
author_sort Daiki Uryu
title Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
title_short Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
title_full Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
title_fullStr Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
title_full_unstemmed Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
title_sort study of local intracellular signals regulating axonal morphogenesis using a microfluidic device
publisher Taylor & Francis Group
series Science and Technology of Advanced Materials
issn 1468-6996
1878-5514
publishDate 2016-01-01
description The establishment and maintenance of axonal patterning is crucial for neuronal function. To identify the molecular systems that operate locally to control axonal structure, it is important to manipulate molecular functions in restricted subcellular areas for a long period of time. Microfluidic devices can be powerful tools for such purposes. In this study, we demonstrate the application of a microfluidic device to clarify the function of local Ca2+ signals in axons. Membrane depolarization significantly induced axonal branch-extension in cultured cerebellar granule neurons (CGNs). Local application of nifedipine using a polydimethylsiloxane (PDMS)-based microfluidic device demonstrated that Ca2+ entry from the axonal region via L-type voltage-dependent calcium channels (L-VDCC) is required for branch extension. Furthermore, we developed a method for locally controlling protein levels by combining genetic techniques and use of a microfluidic culture system. A vector for enhanced green fluorescent protein (EGFP) fused to a destabilizing domain derived from E. coli dihydrofolate reductase (ecDHFR) is introduced in neurons by electroporation. By local application of the DHFR ligand, trimethoprim (TMP) using a microfluidic device, we were able to manipulate differentially the level of fusion protein between axons and somatodendrites. The present study revealed the effectiveness of microfluidic devices to address fundamental biological issues at subcellular levels, and the possibility of their development in combination with molecular techniques.
topic microfluidic device
cerebellar granule neurons
axon
depolarization
dihydrofolate reductase
url http://dx.doi.org/10.1080/14686996.2016.1241131
work_keys_str_mv AT daikiuryu studyoflocalintracellularsignalsregulatingaxonalmorphogenesisusingamicrofluidicdevice
AT tomohirotamaru studyoflocalintracellularsignalsregulatingaxonalmorphogenesisusingamicrofluidicdevice
AT azusasuzuki studyoflocalintracellularsignalsregulatingaxonalmorphogenesisusingamicrofluidicdevice
AT riesakai studyoflocalintracellularsignalsregulatingaxonalmorphogenesisusingamicrofluidicdevice
AT yoshiyukikonishi studyoflocalintracellularsignalsregulatingaxonalmorphogenesisusingamicrofluidicdevice
_version_ 1721317512350531584