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Pleiotrophin is a neurotrophic factor for spinal motor neurons

机译:促营养素是脊髓运动神经元的神经营养因子

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Regeneration in the peripheral nervous system is poor after chronic denervation. Denervated Schwann cells act as a "transient target" by secreting growth factors to promote regeneration of axons but lose this ability with chronic denervation. We discovered that the mRNA for pleiotrophin (PTN) was highly up-regulated in acutely denervated distal sciatic nerves, but high levels of PTN mRNA were not maintained in chronically denervated nerves. PTN protected spinal motor neurons against chronic excitotoxic injury and caused increased outgrowth of motor axons out of the spinal cord ex-plants and formation of "miniventral rootlets." In neonatal mice, PTN protected the facial motor neurons against cell death induced by deprivation from target-derived growth factors. Similarly, PTN significantly enhanced regeneration of myelinated axons across a graft in the transected sciatic nerve of adult rats. Our findings suggest a neurotrophic role for PTN that may lead to previously unrecognized treatment options for motor neuron disease and motor axonal regeneration.
机译:慢性神经支配后,外周神经系统再生不良。去神经支配的雪旺细胞通过分泌生长因子促进轴突再生而充当“瞬时靶标”,但由于慢性去神经支配而丧失了这种能力。我们发现,在急性神经支配的远端坐骨神经中,促神经营养素(PTN)的mRNA高度上调,但是在慢性神经支配的神经中,PTN mRNA的水平并未得到维持。 PTN保护脊髓运动神经元免受慢性兴奋性毒性损伤,并导致运动轴突从脊髓外植体中向外生长,并形成“小腹根”。在新生小鼠中,PTN保护面部运动神经元免于因剥夺目标来源的生长因子而引起的细胞死亡。同样,PTN显着增强了成年大鼠横断坐骨神经中移植物中髓鞘轴突的再生。我们的发现表明PTN具有神经营养作用,可能导致先前无法识别的运动神经元疾病和运动轴突再生治疗选择。

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