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Cell Tissue Res. 2015 Apr;360(1):129-41. doi: 10.1007/s00441-015-2144-5. Epub 2015 Mar 6.

Light sheet-based fluorescence microscopy (LSFM) for the quantitative imaging of cells and tissues.

Author information

1
Physical Biology Group (FB 15, IZN), Buchmann Institute for Molecular Life Sciences (BMLS, CEF-MC), Goethe Universität Frankfurt am Main (Campus Riedberg), Max-von-Laue-Strasse 15, 60438, Frankfurt am Main, Germany, francesco.pampaloni@physikalischebiologie.de.

Abstract

In light sheet-based fluorescence microscopy (LSFM), only the focal plane is illuminated by a laser light sheet. Hence, only the fluorophores within a thin volume of the specimen are excited. This reduces photo-bleaching and photo-toxic effects by several orders of magnitude compared with any other form of microscopy. Therefore, LSFM (aka single/selective-plane illumination microscopy [SPIM] or digitally scanned light sheet microscopy [DSLM]) is the technique of choice for the three-dimensional imaging of live or fixed and of small or large three-dimensional specimens. The parallel recording of millions of pixels with modern cameras provides an extremely fast acquisition speed. Recent developments address the penetration depth, the resolution and the recording speed of LSFM. The impact of LSFM on research areas such as three-dimensional cell cultures, neurosciences, plant biology and developmental biology is increasing at a rapid pace. The development of high-throughput LSFM is the next leap forward, allowing the application of LSFM in toxicology and drug discovery screening.

PMID:
25743693
DOI:
10.1007/s00441-015-2144-5
[Indexed for MEDLINE]
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