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PMID: 11733043 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Applying multiphoton imaging to the study of membrane dynamics in living cells.

Traffic (Copenhagen, Denmark) ·Vol. 2 ·No. 11 ·2001-11-00 ·Pages 775-80

White JG, Squirrell JM, Eliceiri KW

Abstract

The endomembrane system of a cell is a highly dynamic, ephemeral structure that is difficult to visualize. Reconstructions from sections of fixed material can provide high-resolution information on intercellular membrane architecture, but such techniques are fraught with artifacts and are of little help in understanding the dynamics of intracellular membrane traffic. Recently, the availability of fluorescent membrane probes and the development of techniques for optically sectioning intact specimens have allowed glimpses of membrane dynamics to be visualized in living tissue. In this review we discuss the potential of a new optical sectioning technique, multiphoton imaging, for visualizing membrane dynamics in living cells. Multiphoton microscopy offers an unparalleled ability to obtain images from deep within specimens while minimizing the effects of phototoxicity.

MeSH Terms
Animals Cell Membrane Microscopy, Confocal Optics and Photonics Photons
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
White J G
LOCI, Laboratory of Molecular Biology, University of Wisconsin, Madison, WI 53706, USA. jwhite1@facstaff.wisc.edu
Squirrell J M
Eliceiri K W
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Article Info
Journal
Traffic (Copenhagen, Denmark)
Abbr.
Traffic
ISSN
1398-9219
Published
2001-11-00
Pages
775-80
Language
English
Region
England
NLM ID
100939340
PMCID
PMC5428986
Subset
IM
Grants
NIGMS NIH HHS · R01 GM057583 · United States
NCRR NIH HHS · R01 RR000570 · United States
NIGMS NIH HHS · R01-GM57583 · United States
NCRR NIH HHS · R01-RR00570 · United States
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