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Tue, 5 Apr 2011 18:48:41 -0700 |
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*****
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Based on their spectra, I wouldn't expect the fluorescence of esters of
retinoids to be fluorescent in the Cy3 channel but more in the DAPI
channel. Also I mainly see those structures around the round nucleus of
hepatocytes.
> Lipid droplets in stellate (Ito) cells are highly autofluorescent
> due to their content of esters of retinoic acid. These are probably
> your structures.
> --
> John J. Lemasters, MD, PhD
> Professor and GlaxoSmithKline Distinguished Endowed Chair
> Director, Center for Cell Death, Injury and Regeneration
> Departments of Pharmaceutical & Biomedical Sciences and Biochemistry
> & Molecular Biology
> Medical University of South Carolina
> QF213 Quadrangle Building
> 280 Calhoun Street, MSC 140
> Charleston, SC 29425
> Office: 843-792-2153
> Lab: 843-792-3530
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> http://academicdepartments.musc.edu/ccdir
>
> -----Original Message-----
> From: Confocal Microscopy List [mailto:[log in to unmask]
> EDU] On Behalf Of Jean-Pierre CLAMME
> Sent: Tuesday, April 05, 2011 9:06 PM
> To: [log in to unmask]
> Subject: Experience with liver tissue autofluorescence ?
> *****
> To join, leave or search the confocal microscopy listserv, go to:
> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
> *****
> Hi,
> I'm looking for someone having experience with confocal imaging of
> liver tissue. I'm imaging mouse liver tissue and I have some issues
> with autofluorescence in the cy3 channel coming from structure
> appearing like vesicle in hepatocytes. Those vesicles mainly show up
> in the Cy3 channel but are also visible in the FITC channel
> (depending on the power I use).
> A spectral image with excitation at 488, shows a broad signal with a
> maximum around 580 nm.
> Could someone comment on the origin of this fluorescence ? Is it
> possible that it is lipofuscine ?
> Thank you,
> JP
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