Genes associated with adult axon regeneration promoted by olfactory ensheathing cells: a new role for matrix metalloproteinase 2.
J Neurosci, 2006/5/17;26(20):5347-59.
Pastrana E[1], Moreno-Flores MT, Gurzov EN, Avila J, Wandosell F, Diaz-Nido J
Affiliations
PMID: 16707787
Impact factor: 6.709
Abstract
The molecular mechanisms used by olfactory ensheathing cells (OECs) to promote repair in the damaged adult mammalian CNS remain unknown. Thus, we used microarrays to analyze three OEC populations with different capacities to promote axonal regeneration in cultured rat retinal neurons. Gene expression in "long-term cultured OECs" that do not stimulate adult axonal outgrowth was compared with that of "primary olfactory ensheathing cells" and the immortalized OEC cell line TEG3. In this way, we identified a number of candidate genes that might play a role in promoting adult axonal regeneration. Among these genes, it was striking that both the matrix metalloproteinase 2 (MMP2) and an inhibitor of this protease were represented. The disruption of MMP2 activity in TEG3 cells impaired their capacity to trigger axon regeneration in cultured adult retinal neurons. Furthermore, the MMP2 protein was detected in grafts of OECs that elicited robust axonal regeneration in the injured spinal cord of adult rats in vivo. These data suggest that MMP2 does indeed participate in adult axonal regeneration induced by OECs.
MeSH terms
Animals; Animals, Newborn; Brain Tissue Transplantation; Cell Culture Techniques; Cell Line, Transformed; Cells, Cultured; Coculture Techniques; Enzyme Inhibitors; Gene Expression Regulation; Growth Cones; Male; Matrix Metalloproteinase 2; Matrix Metalloproteinase Inhibitors; Nerve Regeneration; Neuroglia; Neuronal Plasticity; Olfactory Bulb; Oligonucleotide Array Sequence Analysis; Rats; Rats, Wistar; Retinal Ganglion Cells; Spinal Cord; Spinal Cord Injuries
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