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Intravital imaging of fluorescent markers and FRET probes by DNA tattooing

Intravital imaging of fluorescent markers and FRET probes by DNA tattooing
Intravital imaging of fluorescent markers and FRET probes by DNA tattooing
BACKGROUND: Advances in fluorescence microscopy and mouse transgenesis have made it possible to image molecular events in living animals. However, the generation of transgenic mice is a lengthy process and intravital imaging requires specialized knowledge and equipment. Here, we report a rapid and undemanding intravital imaging method using generally available equipment. RESULTS: By DNA tattooing we transfect keratinocytes of living mice with DNA encoding fluorescent biosensors. Subsequently, the behavior of individual cells expressing these biosensors can be visualized within hours and using conventional microscopy equipment. Using this "instant transgenic" model in combination with a corrected coordinate system, we followed the in vivo behavior of individual cells expressing either FRET- or location-based biosensors for several days. The utility of this approach was demonstrated by assessment of in vivo caspase-3 activation upon induction of apoptosis. CONCLUSION: This "instant skin transgenic" model can be used to follow the in vivo behavior of individual cells expressing either FRET- or location-based probes for several days after tattooing and provides a rapid and inexpensive method for intravital imaging in murine skin.
Animals Apoptosis/physiology Caspase 3/*metabolism Cells, Cultured *DNA Probes Fluorescence Resonance Energy Transfer/*methods *Fluorescent Dyes Keratinocytes/cytology/*enzymology Mice Microscopy, Fluorescence/methods *Molecular Probe Techniques Transfection/*methods
1472-6750
Bins, A. D.
b12f0593-0096-479b-aced-0691242c3053
van Rheenen, J.
64841b09-2f62-415e-944e-34170c6b0715
Jalink, K.
81124fdb-185d-43c1-a659-cd22dd2d381c
Halstead, J. R.
019c9dab-c338-4f97-9318-353858ea82ac
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Spencer, D. M.
4affe9f6-353a-4507-8066-0180b8dc9eaf
Haanen, J. B.
2a61df35-770a-42e5-b49b-8c12281c6f41
Schumacher, T. N.
44698506-8bbf-45a5-bf6d-e4a1f12eeeab
Bins, A. D.
b12f0593-0096-479b-aced-0691242c3053
van Rheenen, J.
64841b09-2f62-415e-944e-34170c6b0715
Jalink, K.
81124fdb-185d-43c1-a659-cd22dd2d381c
Halstead, J. R.
019c9dab-c338-4f97-9318-353858ea82ac
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Spencer, D. M.
4affe9f6-353a-4507-8066-0180b8dc9eaf
Haanen, J. B.
2a61df35-770a-42e5-b49b-8c12281c6f41
Schumacher, T. N.
44698506-8bbf-45a5-bf6d-e4a1f12eeeab

Bins, A. D., van Rheenen, J., Jalink, K., Halstead, J. R., Divecha, N., Spencer, D. M., Haanen, J. B. and Schumacher, T. N. (2007) Intravital imaging of fluorescent markers and FRET probes by DNA tattooing. BMC Biotechnology, 7 (2), [2]. (doi:10.1186/1472-6750-7-2).

Record type: Article

Abstract

BACKGROUND: Advances in fluorescence microscopy and mouse transgenesis have made it possible to image molecular events in living animals. However, the generation of transgenic mice is a lengthy process and intravital imaging requires specialized knowledge and equipment. Here, we report a rapid and undemanding intravital imaging method using generally available equipment. RESULTS: By DNA tattooing we transfect keratinocytes of living mice with DNA encoding fluorescent biosensors. Subsequently, the behavior of individual cells expressing these biosensors can be visualized within hours and using conventional microscopy equipment. Using this "instant transgenic" model in combination with a corrected coordinate system, we followed the in vivo behavior of individual cells expressing either FRET- or location-based biosensors for several days. The utility of this approach was demonstrated by assessment of in vivo caspase-3 activation upon induction of apoptosis. CONCLUSION: This "instant skin transgenic" model can be used to follow the in vivo behavior of individual cells expressing either FRET- or location-based probes for several days after tattooing and provides a rapid and inexpensive method for intravital imaging in murine skin.

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More information

Accepted/In Press date: 3 January 2007
Published date: 3 January 2007
Additional Information: Bins, Adriaan D van Rheenen, Jacco Jalink, Kees Halstead, Jonathan R Divecha, Nullin Spencer, David M Haanen, John B A G Schumacher, Ton N M eng Research Support, Non-U.S. Gov't England 2007/01/05 BMC Biotechnol. 2007 Jan 3;7:2. doi: 10.1186/1472-6750-7-2.
Keywords: Animals Apoptosis/physiology Caspase 3/*metabolism Cells, Cultured *DNA Probes Fluorescence Resonance Energy Transfer/*methods *Fluorescent Dyes Keratinocytes/cytology/*enzymology Mice Microscopy, Fluorescence/methods *Molecular Probe Techniques Transfection/*methods

Identifiers

Local EPrints ID: 480159
URI: http://eprints.soton.ac.uk/id/eprint/480159
ISSN: 1472-6750
PURE UUID: a9685c8b-d7a9-439f-ae9f-e2bb1dfbe677

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Date deposited: 01 Aug 2023 16:55
Last modified: 17 Mar 2024 02:59

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Contributors

Author: A. D. Bins
Author: J. van Rheenen
Author: K. Jalink
Author: J. R. Halstead
Author: N. Divecha
Author: D. M. Spencer
Author: J. B. Haanen
Author: T. N. Schumacher

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