The Ability of Human Schwann Cell Grafts to Promote Regeneration in the Transected Nude Rat Spinal Cord

• Published in: Experimental neurology 1997-12, Vol.148 (2), p.502-522
• Main Authors: Guest, James D, Rao, Arundathi, Olson, Les, Bunge, Mary Bartlett, Bunge, Richard P
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Animals; anterograde tracing; Axonal Transport; Axons - physiology; Biological and medical sciences; Cauda Equina; Cerebrospinal fluid. Spinal cord. Spinal roots. Spinal nerves; Child; Child, Preschool; CNS regeneration; human Schwann cell transplantation; Humans; inflammation; Medical sciences; Middle Aged; Motor Activity; Nerve Fibers, Myelinated - physiology; Nerve Regeneration; Neurosurgery; Peripheral Nerves; propriospinal neurons; Rats; Rats, Nude; retrograde tracing; Schwann Cells - physiology; Schwann Cells - transplantation; Spinal Cord - pathology; Spinal Cord - physiology; Spinal Cord - physiopathology; Spinal Cord Injuries - pathology; Spinal Cord Injuries - physiopathology; Spinal Cord Injuries - surgery; spinal cord injury; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases; transition zone; Transplantation, Heterologous - methods; Transplantation, Heterologous - physiology
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1006/exnr.1997.6693

Advances in the purification and expansion of Schwann cells (SCs) from adult human peripheral nerve, together with biomaterials development, have made the construction of unique grafts with defined properties possible. We have utilized PAN/PVC guidance channels to form solid human SC grafts which can be transplanted either with or without the channel. We studied the ability of grafts placed with and without channels to support regeneration and to influence functional recovery; characteristics of the graft and host/graft interface were also compared. The T9–T10 spinal cord of nude rats was resected and a graft was placed across the gap; methylprednisolone was delivered acutely to decrease secondary injury. Channels minimized the immigration of connective tissue into grafts but contributed to some necrotic tissue loss, especially in the distal spinal cord. Grafts without channels contained more myelinated axons (x= 2129±785) vs (x=1442±514) and were larger in cross-sectional area (x=1.53±0.24 mm2) vs (x= 0.95±0.86 mm2). The interfaces formed between the host spinal cord and the grafts placed without channels were highly interdigitated and resembled CNS–PNS transition zones; chondroitin sulfate proteoglycans was deposited there. Whereas several neuronal populations including propriospinal, sensory, motoneuronal, and brainstem neurons regenerated into human SC grafts, only propriospinal and sensory neurons were observed to reenter the host spinal cord. Using combinations of anterograde and retrograde tracers, we observed regeneration of propriospinal neurons up to 2.6 mm beyond grafts. We estimate that 1% of the fibers that enter grafts reenter the host spinal cord by 45 days after grafting. Following retrograde tracing from the distal spinal cord, more labeled neurons were unexpectedly found in the region of the dextran amine anterograde tracer injection site where a marked inflammatory reaction had occurred. Animals with bridging grafts obtained modestly higher scores during open field [(x=8.2±0.35) vs (x=6.8±0.42),P=0.02] and inclined plane testing (x=38.6±0.542) vs (x= 36.3±0.53),P=0.006] than animals with similar grafts in distally capped channels. In summary, this study showed that in the nude rat given methylprednisolone in combination with human SC grafts, some regenerative growth occurred beyond the graft and a modest improvement in function was observed.