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Resolution: standard / high Figure 4.
Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H).
A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue)
and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals
were found in the cytoplasm and highly enriched inside the nucleus sparing out the
nucleoli as indicated by the DNA staining. The reticular and vesicular staining of
the lysosomal marker adjacent to the nuclear indentation did not overlap with EGFP
signals. Obj. 40×/1.30 Oil. Processing of recombinant CB(SC) and influence of the
fluorescent protein marker or the total molecule size on its localization were proven
by differential tagging (N- or C-terminus, respectively) as well as by means of immunocytochemistry
using a N-terminal myc-epitope. C, D. Double-tagged ECFP-CB(SC)-EYFP was distributed
mainly in the nucleus analogously to CB(SC), which was marked at its C-terminus only.
Accumulates were found within the nucleus and adjacent to it. Fluorescence also appeared
in the ring shaped midbody matrix (enlarged region in the upper right corner). Obj.
40×/0.60; processed by deconvolution. E, F. Cells coexpressing myc-CB(SC) and CB(SC)-EGFP
were fixed by acetone/methanol and immunostained against myc and GFP. A tight colocalization
of both was found (E and F); the constructs were found mainly in the nucleus and stained
the midbody (marked by the arrowhead; see inset). Obj. 40×/0.60. G, H. Optical sections
of CB(SC)-EYFP expressing cells were subjected to spatial reconstruction (G: 3D-visualisation;
H: orthogonal projection). Isosurfaces obtained by arbitrary fluorescence intensity
thresholds represent distinct compartments (granules: opaque; nucleus and midbody:
transparent). In the given cellular state, only a weak expression in the cytoplasm
is found. The main signals arise from granular inclusions within the nucleus including
distinct regions inside the nucleoli (marked by dashed lines in H) as well as from
enrichment in the midbody (arrow). Obj. 63×/1.32 Oil. ROI: 72 × 59 × 11 μm3 (= 464 × 380 × 25 voxels).
Bestvater et al. BMC Cell Biology 2005 6:16 doi:10.1186/1471-2121-6-16 |