2. Behavioral Biology TALKS - Deutsche Zoologische Gesellschaft
2. Behavioral Biology TALKS - Deutsche Zoologische Gesellschaft
2. Behavioral Biology TALKS - Deutsche Zoologische Gesellschaft
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13. Neurobiology POSTERS<br />
����134 Gerd Bicker<br />
A dog is man's best friend, but can its olfactory ensheathing cells help human<br />
neurons?<br />
Authors: Gerd Bicker 1/6 , F. Roloff 1 , S. Ziege 2 , S. Strauss 3 , K. Reimers 3 , J.D. Kocsis 4/5 ,<br />
C. Radtke 3 , W. Baumgärtner 2/6 ,K. Wewetzer 2/6<br />
Affiliations: 1 Division of Cell <strong>Biology</strong>, University of Veterinary Medicine Hannover;<br />
2 Department of Pathology, University of Veterinary Medicine Hannover;<br />
3 Department of Plastic, Hand- and Reconstructive Surgery, Hannover Medical<br />
School; 4 Department of Neurology and Center for Neuroscience and<br />
Regeneration Research, Yale University School of Medicine, New Haven,<br />
Connecticut; 5 Neuroscience Research Center, Veterans Affairs Connecticut<br />
Healthcare System, West Haven, Connecticut; 6 Center for Systems<br />
Neuroscience Hannover<br />
Transplantation of olfactory ensheathing cells (OEC) and Schwann cells (SC) is a<br />
promising therapeutic strategy to facilitate axon regeneration and remyelination<br />
after spinal cord injury. However, the close phenotypic resemblance of OECs and SCs<br />
including the expression of marker molecules, e.g. the neurotrophin receptor p75<br />
(p75NTR) and S100 so far did not allow selective identification and purification of<br />
OECs. Using magnetic activated cell sorting, we depleted contaminating SCs from<br />
OEC preparations and purified canine OECs from olfactory bulb (OB-OECs), olfactory<br />
mucosa (OM-OECs), and SCs from fibular nerve for in vitro analysis. To compare the<br />
motility of the purified glial cells, we used a scratch migration assay which measures<br />
cell migration during the closure of a ?wound? that is scratched into a confluent cell<br />
monolayer. Closure of the gap was followed by monitoring the advancement of the<br />
cell front over 8 hrs. Because this time interval is too short for significant cell<br />
proliferation, the presence of cells in the gap reflects migration. A quantitative<br />
evaluation shows that OB-OECs and SCs migrated faster than the OM-OECs. The OB-<br />
OECs and SCs covered a distance of about 120 µm in 8 hrs, as compared to about 80<br />
µm for the OM-OECs. We then investigated whether motility could be up-regulated<br />
by pharmacological agents. So far, we found no evidence that glial migration is<br />
regulated by cGMP or cAMP signaling, but activating PKC enhances motility. Further<br />
experiments address the improved neurite outgrowth of human model (NT2)<br />
neurons in a co-culture system with OECs and SCs. The cell culture experiments using<br />
canine OECs and SCs serve to evaluate the potential therapeutic impact of the three<br />
glial cell types for repair of spinal cord injuries in a large animal model.<br />
This study was supported by a DFG grant (FG 1103, BI 262/16-1)<br />
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