Optic nerve regeneration within artificial Schwann cell graft in the adult rat

• Published in: Brain research bulletin 2001-06, Vol.55 (3), p.409-419
• Main Authors: NEGISHI, Hisanari, DEZAWA, Mari, OSHITARI, Toshiyuki, ADACHI-USAMI, Emiko
• Format: Article
• Language: English
• Subjects: Animals; Axons - physiology; Biological and medical sciences; Cell Survival - drug effects; Development. Senescence. Regeneration. Transplantation; Fundamental and applied biological sciences. Psychology; Immunohistochemistry; Male; Microscopy, Electron; Microscopy, Immunoelectron; Nerve Growth Factors - pharmacology; Nerve Regeneration; Nerve Tissue Proteins - metabolism; Optic Nerve - pathology; Optic Nerve - physiopathology; Optic Nerve - surgery; Rats; Rats, Wistar; Retinal Ganglion Cells - physiology; Schwann Cells - physiology; Schwann Cells - transplantation; Vertebrates: nervous system and sense organs
• ISSN: 0361-9230; 1873-2747
• DOI: 10.1016/s0361-9230(01)00534-2

We investigate whether an artificial graft made by cultured Schwann cell, extracellular matrix (ECM) and trophic factors can provide the environment for the regeneration of retinal ganglion cell (RGC) axons in adult rats. Six kinds of artificial grafts were used: ECM (control); ECM and Schwann cells; ECM, Schwann cells and either nerve growth factor, brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT-4); ECM, Schwann cells, BDNF and NT-4, combined with intravitreal injection of BDNF. The grafts were transplanted onto the transected optic nerve. RGC regeneration was evaluated by dil retrograde labeling, immunohistochemistry, and electron microscopy at 3 weeks post-operation. The degree of dil labeled RGC was approximately 2% for ECM alone, and 10% for ECM and Schwann cells (p < 0.01). The labeling increased to approximately 20% by administration of neurotrophins. The addition of intravitreous BDNF injection resulted in highest labeling percentage of 30%. Immunohistochemical study showed that axons were association with GAP-43 and cell adhesion molecules. Neurotrophin receptors (Trk-A and Trk-B) were detected in nerve fibers both in the retina and in the graft. Remyelination was seen by electron microscopic observation. These results demonstrate that the regeneration of RGC axons is induced with the use of cultured Schwann cells and ECM as promoting factors for regrowth. The degree of regeneration was significantly increased by neurotrophins in the grafts and in the vitreous.