Fibroblasts Genetically Modified to Produce BDNF Support Regrowth of Chronically Injured Serotonergic Axons
Open Access
- 1 December 2000
- journal article
- research article
- Published by SAGE Publications in Neurorehabilitation and Neural Repair
- Vol. 14 (4) , 311-317
- https://doi.org/10.1177/154596830001400407
Abstract
Cells genetically modified to release a variety of growth and/or neurotrophic factors have been used for transplantation into the injured spinal cord as a means to deliver therapeutic products. Axon growth into and through such transplants has been demonstrated after intervention after an acute injury. The present study examined their potential to support regeneration in a chronic injury condition. Five weeks after a cervical hemisection in adult rats, the lesion site was debrided of scar tissue and expanded in both rostral and caudal directions. Animals received a transplant of cultured normal fibroblasts (control) or fibroblasts genetically modified to produce brain-derived neurotrophic factor (BDNF). Six weeks later, animals were killed to determine the extent of growth of serotonergic axons into the transplant. Axons immunoreactive for serotonin (5-HT-ir) were found to cross the rostral interface of host spinal cord readily with either type of fibroblast cell transplant, but the number and density of 5-HT-ir axons extending into the BDNF-producing transplants was markedly greater than those in the control fibroblasts. Axons coursed in all directions among normal fibroblast transplants, whereas growth was more oriented along a longitudinal plane when BDNF was being released by the transplanted cells. The length of growth and the percentage of the transplant length occupied by 5-HT-ir axons were significantly greater in BDNF-producing transplants than in the normal fibroblasts. Many serotonergic axons approached the caudal end of the BDNF-producing cell transplants, although most failed to penetrate the host spinal cord distal to the lesion. These results indicate that whereas fibroblast cell transplants alone can support regrowth of axons from chronically injured supraspinal neurons, modification of these cells to produce BDNF results in a significant increase in the extent of growth into the transplant.Keywords
This publication has 23 references indexed in Scilit:
- Long-Distance Axonal Regeneration in the Transected Adult Rat Spinal Cord Is Promoted by Olfactory Ensheathing Glia TransplantsJournal of Neuroscience, 1998
- Transplants and Neurotrophic Factors Prevent Atrophy of Mature CNS Neurons after Spinal Cord InjuryExperimental Neurology, 1998
- Repair of Adult Rat Corticospinal Tract by Transplants of Olfactory Ensheathing CellsScience, 1997
- Changes occur in the ability to promote axonal regeneration as the post-injury period increasesNeuroReport, 1997
- Treatment of the Chronically Injured Spinal Cord with Neurotrophic Factors Can Promote Axonal Regeneration from Supraspinal NeuronsExperimental Neurology, 1997
- A Combination of BDNF and NT-3 Promotes Supraspinal Axonal Regeneration into Schwann Cell Grafts in Adult Rat Thoracic Spinal CordExperimental Neurology, 1995
- Axonal regeneration into Schwann cell‐seeded guidance channels grafted into transected adult rat spinal cordJournal of Comparative Neurology, 1995
- Demonstration of the potential for chronically injured neurons to regenerate axons into intraspinal peripheral nerve graftsExperimental Neurology, 1991
- Intraspinal transplantation of embyronic spinal cord tissue in neonatal and adult ratsJournal of Comparative Neurology, 1986
- Peripheral nerve autografts to the rat spinal cord: Studies with axonal tracing methodsBrain Research, 1982