Instituto de Biologia y Medicina Experimental-CONICET, Laboratorio de Bioquimica Neuroendócrina, Obligado 2490, 1428, Buenos Aires, Argentina.
Cell Mol Neurobiol. 2010 Jan;30(1):123-35. doi: 10.1007/s10571-009-9437-8. Epub 2009 Aug 20.
In the Wobbler mouse, a mutation in the Vps54 gene is accompanied by motoneuron degeneration and astrogliosis in the cervical spinal cord. Previous work has shown that these abnormalities are greatly attenuated by progesterone treatment of clinically afflicted Wobblers. However, whether progesterone is effective at all disease stages has not yet been tested. The present work used genotyped (wr/wr) Wobbler mice at three periods of the disease: early progressive (1-2 months), established (5-8 months) or late stages (12 months) and age-matched wildtype controls (NFR/NFR), half of which were implanted with a progesterone pellet (20 mg) for 18 days. In untreated Wobblers, degenerating vacuolated motoneurons were initially abundant, experienced a slight reduction at the established stage and dramatically diminished during the late period. In motoneurons, the cholinergic marker choline acetyltransferase (ChAT) was reduced at all stages of the Wobbler disease, whereas hyperexpression of the growth-associated protein (GAP43) mRNA preferentially occurred at the early progressive and established stages. Progesterone therapy significantly reduced motoneuron vacuolation, enhanced ChAT immunoreactive perikarya and reduced the hyperexpression of GAP43 during the early progressive and established stages. At all stage periods, untreated Wobblers showed high density of glial fibrillary acidic protein (GFAP)+ astrocytes and decreased number of glutamine synthase (GS) immunostained cells. Progesterone treatment down-regulated GFAP+ astrocytes and up-regulated GS+ cell number. These data reinforced the usefulness of progesterone to improve motoneuron and glial cell abnormalities of Wobbler mice and further showed that therapeutic benefit seems more effective at the early progressive and established periods, rather than on advance stages of spinal cord neurodegeneration.
在摇摆鼠中,Vps54 基因突变伴随着颈脊髓运动神经元变性和星形胶质细胞增生。先前的工作表明,孕酮治疗临床上受影响的摇摆鼠可大大减轻这些异常。然而,孕酮是否在所有疾病阶段都有效尚未得到测试。本研究使用三种疾病阶段的基因分型(wr/wr)摇摆鼠:早期进行性(1-2 个月)、已建立(5-8 个月)或晚期(12 个月)和年龄匹配的野生型对照(NFR/NFR),其中一半植入孕酮丸(20mg)18 天。在未治疗的摇摆鼠中,最初大量出现变性空泡化运动神经元,在已建立的阶段略有减少,在晚期阶段急剧减少。在运动神经元中,胆碱能标记物胆碱乙酰转移酶(ChAT)在摇摆鼠疾病的所有阶段都减少,而生长相关蛋白(GAP43)mRNA 的过度表达则优先发生在早期进行性和已建立的阶段。孕酮治疗显著减少运动神经元空泡化,增强 ChAT 免疫反应性胞体,并减少早期进行性和已建立阶段 GAP43 的过度表达。在所有阶段,未治疗的摇摆鼠表现出高密 GFAP+星形胶质细胞和减少的谷氨酰胺合成酶(GS)免疫染色细胞数。孕酮治疗下调 GFAP+星形胶质细胞并上调 GS+细胞数。这些数据强化了孕酮改善摇摆鼠运动神经元和神经胶质细胞异常的有效性,并进一步表明治疗益处在早期进行性和已建立的阶段更为有效,而不是在脊髓神经退行性变的晚期阶段。