Neurite Outgrowth Inhibition by Chondroitin Sulfate Proteoglycan: Stalling/Stopping Exceeds Turning in Human Neuroblastoma Growth Cones

2002 ◽  
Vol 175 (1) ◽  
pp. 301-302 ◽  
Author(s):  
DiAnna L. Hynds ◽  
Diane M. Snow
1991 ◽  
Vol 56 (2) ◽  
pp. 706-708 ◽  
Author(s):  
Noboru Iijima ◽  
Atsuhiko Oohira ◽  
Toshio Mori ◽  
Katsuaki Kitabatake ◽  
Shinichi Kohsaka

Development ◽  
1991 ◽  
Vol 113 (4) ◽  
pp. 1473-1485 ◽  
Author(s):  
D.M. Snow ◽  
M. Watanabe ◽  
P.C. Letourneau ◽  
J. Silver

In the developing retina, retinal ganglion cell (RGC) axons elongate toward the optic fissure, even though no obvious directional restrictions exist. Previous studies indicate that axon-matrix interactions are important for retinal ganglion cell axon elongation, but the factors that direct elongation are unknown. Chondroitin sulfate proteoglycan (CS-PG), a component of the extracellular matrix, repels elongating dorsal root ganglion (DRG) axons in vitro and is present in vivo in the roof plate of the spinal cord, a structure that acts as a barrier to DRG axons during development. In this study, we examined whether CS-PG may regulate the pattern of retinal ganglion cell outgrowth in the developing retina. Immunocytochemical analysis showed that CS-PG was present in the innermost layers of the developing rat retina. The expression of CS-PG moved peripherally with retinal development, always remaining at the outer edge of the front of the developing axons. CS-PG was no longer detectable with immunocytochemical techniques when RGC axon elongation in the retina is complete. Results of studies in vitro showed that CS-PG, isolated from bovine nasal cartilage and chick limb, was inhibitory to elongating RGC axons and that RGC growth cones were more sensitive to CS-PG than were DRG neurites tested at the same concentrations of CS-PG. The behavior of retinal growth cones as they encounter CS-PG was characterized using time-lapse video microscopy. Filopodia of the RGC growth cones extended to and sampled the CS-PG repeatedly. With time, the growth cones turned to avoid outgrowth on the CS-PG and grew only on laminin. While numerous studies have shown the presence of positive factors within the retina that may guide developing RGC axons, this is the first demonstration of an inhibitory or repelling molecule in the retina that may regulate axon elongation. Taken together, these data suggest that the direction of RGC outgrowth in the retina may be regulated by the proper ratio of growth-promoting molecules, such as laminin, to growth-inhibiting molecules, like CS-PG, present in the correct pattern and concentrations along the retinal ganglion cell pathway.


1996 ◽  
Vol 109 (8) ◽  
pp. 2031-2040 ◽  
Author(s):  
J.F. Challacombe ◽  
D.M. Snow ◽  
P.C. Letourneau

The extracellular matrix through which growth cones navigate contains molecules, such as chondroitin sulfate proteoglycan, that can inhibit growth cone advance and induce branching and turning. Growth cone turning is accompanied by rearrangement of the cytoskeleton. To identify changes in the organization of actin filaments and microtubules that occur as growth cones turn, we used time-lapse phase contrast videomicroscopy to observe embryonic chick dorsal root ganglion neuronal growth cones at a substratum border between fibronectin and chondroitin sulfate proteoglycan, in the presence and absence of cytochalasin B. Growth cones were fixed and immunocytochemically labeled to identify actin filaments and dynamic and stable microtubules. Our results suggest that microtubules are rearranged within growth cones to accomplish turning to avoid chondroitin sulfate proteoglycan. Compared to growth cones migrating on fibronectin, turning growth cones were more narrow, and they contained dynamic microtubules that were closer to the leading edge and were more bundled. Cytochalasin B-treated growth cones sidestepped laterally along the border instead of turning, and in sidestepping growth cones, microtubules were not bundled and aligned. We conclude that actin filament bundles are required for microtubule reorientation and growth cone turning to avoid chondroitin sulfate proteoglycan.


2008 ◽  
Vol 86 (10) ◽  
pp. 2214-2226 ◽  
Author(s):  
Sujatha M. Gopalakrishnan ◽  
Nicole Teusch ◽  
Christiane Imhof ◽  
Margot H. M. Bakker ◽  
Mark Schurdak ◽  
...  

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