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 in | PloS one Vol. 9; no. 10; p. e110475 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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. |
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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 |
Author_xml | – sequence: 1 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 – sequence: 2 givenname: Cam Ha T surname: Tran fullname: Tran, Cam Ha T organization: Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Hotchkiss Brain Institute, Calgary, Alberta, Canada – sequence: 3 givenname: Jeffery surname: LeDue fullname: LeDue, Jeffery organization: Department of Psychiatry, University of British Columbia, Brain Research Centre, Vancouver, British Columbia, Canada – sequence: 4 givenname: Ning surname: Zhou fullname: Zhou, Ning organization: Graduate Institute of Clinical Medical Science, China Medical University, Translational Medicine Research Center, Taichung, Taiwan – sequence: 5 givenname: Grant R 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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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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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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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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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 |
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