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...
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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 |
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1721317512350531584 |