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Resolution: standard / high Figure 3.
Endogenous sensory axon regeneration across GDA-transplanted dorsal column injuries
at 8 days after lesion and transplantation. (a) A montaged, low-magnification confocal image scanned from a single 25-μm thick sagittal
section, showing BDA-labeled ascending dorsal column axons (green) that have entered,
grown within and exited a hPAP+ (red) GDA-transplanted dorsal column lesion. LC, lesion center. (b) A high-magnification image of a rostral graft/host interface showing BDA+ axons exiting the GDA graft and entering host white matter. A few axons were observed
to have turned away from the interface and grown back towards the lesion center (arrowhead).
(c) In control lesions, the vast majority of BDA+ axons have formed dystrophic endings and failed to leave the caudal margins of the
lesion, marked by hypertrophic GFAP+ astrocytes (red). (d) A high-magnification image showing numerous BDA+ axons that have successfully crossed the host/graft interface at the caudal lesion
margin. A few cut axons (arrowheads) have, however, failed to leave the caudal lesion
interface and can be seen to have turned and/or formed dystrophic endings, particularly
in regions containing few hPAP+ GDAs (red). (e) BDA+ axons located near the pial surface and ventral regions of cuneate white matter at
1.5 mm rostral to a GDA-bridged lesion site. (f) BDA+ axon growth cones in white matter 1.5 mm rostral to the lesion site often display
streamlined growth cones indicative of rapid growth. Scale bars: (a,c) 100 μm; (b-e)
50 μm; (f) 5 μm (top) and 10 μm (bottom).
Davies et al. Journal of Biology 2006 5:7 doi:10.1186/jbiol35 |