A high performance, cost-effective, open-source microscope for scanning two-photon microscopy that is modular and readily adaptable

Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo. However, there exist barriers for many laboratories to acquire two-photon microscopes. Additionally, if owned, typical systems are difficult to...

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Published inPloS one Vol. 9; no. 10; p. e110475
Main Authors Rosenegger, David G, Tran, Cam Ha T, LeDue, Jeffery, Zhou, Ning, Gordon, Grant R
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 21.10.2014
Public Library of Science (PLoS)
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Abstract Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo. However, there exist barriers for many laboratories to acquire two-photon microscopes. Additionally, if owned, typical systems are difficult to modify to rapidly evolving methodologies. A potential solution to these problems is to enable scientists to build their own high-performance and adaptable system by overcoming a resource insufficiency. Here we present a detailed hardware resource and protocol for building an upright, highly modular and adaptable two-photon laser scanning fluorescence microscope that can be used for in vitro or in vivo applications. The microscope is comprised of high-end componentry on a skeleton of off-the-shelf compatible opto-mechanical parts. The dedicated design enabled imaging depths close to 1 mm into mouse brain tissue and a signal-to-noise ratio that exceeded all commercial two-photon systems tested. In addition to a detailed parts list, instructions for assembly, testing and troubleshooting, our plan includes complete three dimensional computer models that greatly reduce the knowledge base required for the non-expert user. This open-source resource lowers barriers in order to equip more laboratories with high-performance two-photon imaging and to help progress our understanding of the cellular and physiological function of living systems.
AbstractList Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo. However, there exist barriers for many laboratories to acquire two-photon microscopes. Additionally, if owned, typical systems are difficult to modify to rapidly evolving methodologies. A potential solution to these problems is to enable scientists to build their own high-performance and adaptable system by overcoming a resource insufficiency. Here we present a detailed hardware resource and protocol for building an upright, highly modular and adaptable two-photon laser scanning fluorescence microscope that can be used for in vitro or in vivo applications. The microscope is comprised of high-end componentry on a skeleton of off-the-shelf compatible opto-mechanical parts. The dedicated design enabled imaging depths close to 1 mm into mouse brain tissue and a signal-to-noise ratio that exceeded all commercial two-photon systems tested. In addition to a detailed parts list, instructions for assembly, testing and troubleshooting, our plan includes complete three dimensional computer models that greatly reduce the knowledge base required for the non-expert user. This open-source resource lowers barriers in order to equip more laboratories with high-performance two-photon imaging and to help progress our understanding of the cellular and physiological function of living systems.
Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo . However, there exist barriers for many laboratories to acquire two-photon microscopes. Additionally, if owned, typical systems are difficult to modify to rapidly evolving methodologies. A potential solution to these problems is to enable scientists to build their own high-performance and adaptable system by overcoming a resource insufficiency. Here we present a detailed hardware resource and protocol for building an upright, highly modular and adaptable two-photon laser scanning fluorescence microscope that can be used for in vitro or in vivo applications. The microscope is comprised of high-end componentry on a skeleton of off-the-shelf compatible opto-mechanical parts. The dedicated design enabled imaging depths close to 1 mm into mouse brain tissue and a signal-to-noise ratio that exceeded all commercial two-photon systems tested. In addition to a detailed parts list, instructions for assembly, testing and troubleshooting, our plan includes complete three dimensional computer models that greatly reduce the knowledge base required for the non-expert user. This open-source resource lowers barriers in order to equip more laboratories with high-performance two-photon imaging and to help progress our understanding of the cellular and physiological function of living systems.
Audience Academic
Author Gordon, Grant R
Rosenegger, David G
Zhou, Ning
Tran, Cam Ha T
LeDue, Jeffery
AuthorAffiliation 2 Department of Psychiatry, University of British Columbia, Brain Research Centre, Vancouver, British Columbia, Canada
3 Graduate Institute of Clinical Medical Science, China Medical University, Translational Medicine Research Center, Taichung, Taiwan
University of Zurich, Switzerland
1 Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Hotchkiss Brain Institute, Calgary, Alberta, Canada
AuthorAffiliation_xml – name: 2 Department of Psychiatry, University of British Columbia, Brain Research Centre, Vancouver, British Columbia, Canada
– name: 3 Graduate Institute of Clinical Medical Science, China Medical University, Translational Medicine Research Center, Taichung, Taiwan
– name: University of Zurich, Switzerland
– name: 1 Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Hotchkiss Brain Institute, Calgary, Alberta, Canada
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  givenname: David G
  surname: Rosenegger
  fullname: Rosenegger, David G
  organization: Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Hotchkiss Brain Institute, Calgary, Alberta, Canada
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  surname: Tran
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  surname: LeDue
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  organization: Department of Psychiatry, University of British Columbia, Brain Research Centre, Vancouver, British Columbia, Canada
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  surname: Zhou
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  organization: Graduate Institute of Clinical Medical Science, China Medical University, Translational Medicine Research Center, Taichung, Taiwan
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  surname: Gordon
  fullname: Gordon, Grant R
  organization: Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Hotchkiss Brain Institute, Calgary, Alberta, Canada
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25333934$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright COPYRIGHT 2014 Public Library of Science
2014 Rosenegger et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2014 Rosenegger et al 2014 Rosenegger et al
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– notice: 2014 Rosenegger et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: DR CT JL NZ GG. Performed the experiments: DR CT GG. Analyzed the data: DR CT GG. Contributed to the writing of the manuscript: DR CT JL NZ GG.
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SSID ssj0053866
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Snippet Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo....
Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo ....
Two-photon laser scanning microscopy has revolutionized the ability to delineate cellular and physiological function in acutely isolated tissue and in vivo ....
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StartPage e110475
SubjectTerms Advantages
Animal models
Animals
Biology and Life Sciences
Brain
Brain - pathology
Brain research
Computer models
Confocal microscopy
Design
Engineering and Technology
Fluorescence
High performance systems
Image Processing, Computer-Assisted
In vivo methods and tests
Knowledge bases (artificial intelligence)
Laboratories
Lasers
Light
Maintenance
Mathematical models
Medicine
Mice
Microscopes
Microscopy
Microscopy, Electron, Scanning - economics
Microscopy, Electron, Scanning - instrumentation
Microscopy, Electron, Scanning - methods
Neuroimaging
Neurons
Optics
Pharmacology
Photons
Physiology
Research and Analysis Methods
Scanning microscopy
Signal-To-Noise Ratio
Software
Software industry
Three dimensional models
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Title A high performance, cost-effective, open-source microscope for scanning two-photon microscopy that is modular and readily adaptable
URI https://www.ncbi.nlm.nih.gov/pubmed/25333934
https://www.proquest.com/docview/1615771262
https://search.proquest.com/docview/1616477772
https://pubmed.ncbi.nlm.nih.gov/PMC4204885
https://doaj.org/article/268f5e69b13546b68c59222cda984f1c
http://dx.doi.org/10.1371/journal.pone.0110475
Volume 9
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