Oudega M, Rosano C, Sadi D, Wood P M, Schwab M E, Hagg T
The Miami Project to Cure Paralysis, University of Miami School of Medicine, Miami, FL 33136, USA.
Neuroscience. 2000;100(4):873-83. doi: 10.1016/s0306-4522(00)00350-x.
Neutralization of the myelin-associated neurite growth inhibitors NI-35 and NI-250 by IN-1 antibodies can promote axonal regeneration of several types of central nervous neurons. Here, we investigated in adult rats whether IN-1 can promote regeneration of ascending sensory axons across a peripheral nerve bridge back into the spinal cord. IN-1 was administered by hybridoma cells injected in the cerebral cortex or thoracic cord, its presence confirmed in tissue sections and cerebrospinal fluid, and its effectiveness demonstrated in co-cultures of oligodendrocytes and sensory neurons. With a two week infusion of control vehicle into the dorsal spinal cord 3 mm rostral to the nerve graft, only 3+/-2% of the anterogradely labeled sensory fibers present at the rostral end of the nerve graft had grown up to 0.5 mm, but not farther into the spinal cord. A similar limited extent of regeneration was seen with IN-1 or with infusion of Dantrolene, an inhibitor of NI-35/250 activity in vitro. With infusion of nerve growth factor rostral to the nerve graft, 40% of the fibers at the rostral end of the graft were found at 0.5 mm, 34% at 1 mm, 24% at 2 mm and 14% at 3 mm (the infusion site) into the spinal cord. Treatment with IN-l antibodies did not enhance the growth-promoting effects of nerve growth factor. We suggest that the neurite growth inhibitors NI-35 or NI-250 do not play a major inhibitory role in the regeneration of the ascending sensory fibers across a nerve bridge and back into the spinal cord of the adult rat.
IN-1抗体对髓磷脂相关神经突生长抑制剂NI-35和NI-250的中和作用可促进几种中枢神经神经元的轴突再生。在此,我们研究了在成年大鼠中,IN-1是否能促进上升的感觉轴突通过周围神经桥再生回到脊髓。通过将杂交瘤细胞注射到大脑皮层或胸段脊髓来给予IN-1,在组织切片和脑脊液中证实其存在,并在少突胶质细胞和感觉神经元的共培养中证明其有效性。在神经移植头端3毫米处向脊髓背侧注入对照载体两周,在神经移植头端存在的顺行标记感觉纤维中,只有3±2%生长到了0.5毫米,但没有进一步长入脊髓。使用IN-1或注入丹曲林(一种体外NI-35/250活性抑制剂)时,也观察到了类似的有限再生程度。在神经移植头端注入神经生长因子后,在移植头端的纤维中,40%在0.5毫米处被发现,34%在1毫米处,24%在2毫米处,14%在3毫米(注入部位)处进入脊髓。用IN-1抗体治疗并没有增强神经生长因子的促生长作用。我们认为,神经突生长抑制剂NI-35或NI-250在成年大鼠上升的感觉纤维通过神经桥再生回到脊髓的过程中并不起主要抑制作用。