{"title":"糖尿病神经再生中微管蛋白和神经丝表达改变和轴突生长受损","authors":"Gang Xu, C. Pierson, Y. Murakawa, A. Sima","doi":"10.1093/JNEN/61.2.164","DOIUrl":null,"url":null,"abstract":"Cytoskeletal protein expression in sensory neurons and sciatic nerve axonal growth were examined in type 1 diabetic BB/Wor rats after sciatic nerve crush injury. Diabetic male rats were subjected to sciatic nerve crush at 6 wk of diabetes. L4 and L5 dorsal root ganglia (DRG) mRNA expression of low and medium molecular weight neurofilaments (NF-L, NF-M), βII- and βIII-tubulin as well as protein expression of NF-L, NF-M, and β-tubulin were examined at various time points following crush injury and compared with age- and sex-matched non-diabetic BB/Wor rats. Steady state mRNA expression of NF-L, NF-M, βII- and βIII-tubulin were decreased in diabetic DRG. NF-L and NF-M proteins were also decreased in DRG of uncrushed diabetic animals. After crush injury, βII- and βIII-tubulin mRNA were upregulated in control animals at day 2 and day 6, respectively, and β-tubulin protein showed similarly increased expression after crush injury, while such upregulations did not occur in diabetic animals. Conversely, mRNA and protein expressions of NF-L, NF-M were downregulated to a lesser extent in diabetic animals compared to control rats. These changes were associated with impaired axonal elongation and caliber growth of regenerating fibers in diabetic rats. We propose that upregulation of tubulin has a negative feedback on NF expression in response to nerve injury, as seen in control rats. The absence of this upregulation in diabetic animals may impair its regulatory effect on NF expression and contribute to perturbed nerve regeneration seen in diabetic nerve.","PeriodicalId":14858,"journal":{"name":"JNEN: Journal of Neuropathology & Experimental Neurology","volume":"7 1","pages":"164–175"},"PeriodicalIF":0.0000,"publicationDate":"2002-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"52","resultStr":"{\"title\":\"Altered Tubulin and Neurofilament Expression and Impaired Axonal Growth in Diabetic Nerve Regeneration\",\"authors\":\"Gang Xu, C. Pierson, Y. Murakawa, A. Sima\",\"doi\":\"10.1093/JNEN/61.2.164\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cytoskeletal protein expression in sensory neurons and sciatic nerve axonal growth were examined in type 1 diabetic BB/Wor rats after sciatic nerve crush injury. Diabetic male rats were subjected to sciatic nerve crush at 6 wk of diabetes. L4 and L5 dorsal root ganglia (DRG) mRNA expression of low and medium molecular weight neurofilaments (NF-L, NF-M), βII- and βIII-tubulin as well as protein expression of NF-L, NF-M, and β-tubulin were examined at various time points following crush injury and compared with age- and sex-matched non-diabetic BB/Wor rats. Steady state mRNA expression of NF-L, NF-M, βII- and βIII-tubulin were decreased in diabetic DRG. NF-L and NF-M proteins were also decreased in DRG of uncrushed diabetic animals. After crush injury, βII- and βIII-tubulin mRNA were upregulated in control animals at day 2 and day 6, respectively, and β-tubulin protein showed similarly increased expression after crush injury, while such upregulations did not occur in diabetic animals. Conversely, mRNA and protein expressions of NF-L, NF-M were downregulated to a lesser extent in diabetic animals compared to control rats. These changes were associated with impaired axonal elongation and caliber growth of regenerating fibers in diabetic rats. We propose that upregulation of tubulin has a negative feedback on NF expression in response to nerve injury, as seen in control rats. The absence of this upregulation in diabetic animals may impair its regulatory effect on NF expression and contribute to perturbed nerve regeneration seen in diabetic nerve.\",\"PeriodicalId\":14858,\"journal\":{\"name\":\"JNEN: Journal of Neuropathology & Experimental Neurology\",\"volume\":\"7 1\",\"pages\":\"164–175\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"52\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JNEN: Journal of Neuropathology & Experimental Neurology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/JNEN/61.2.164\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JNEN: Journal of Neuropathology & Experimental Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/JNEN/61.2.164","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 52
摘要
观察1型糖尿病BB/Wor大鼠坐骨神经挤压损伤后感觉神经元细胞骨架蛋白表达及坐骨神经轴突生长情况。糖尿病雄性大鼠在糖尿病6周时进行坐骨神经压迫。在挤压损伤后的不同时间点检测L4和L5背根神经节(DRG)低、中分子量神经丝(NF-L、NF-M)、βII和β iii微管蛋白的mRNA表达以及NF-L、NF-M和β-微管蛋白的蛋白表达,并与年龄和性别匹配的非糖尿病BB/Wor大鼠进行比较。在糖尿病DRG中,NF-L、NF-M、βII-和β iii -微管蛋白mRNA的稳态表达降低。未压碎的糖尿病动物DRG中NF-L和NF-M蛋白也降低。挤压损伤后,对照组动物βII-和β iii -微管蛋白mRNA分别在第2天和第6天上调,β-微管蛋白表达在挤压损伤后也同样升高,而糖尿病动物没有出现这种上调。相反,与对照大鼠相比,糖尿病动物NF-L、NF-M的mRNA和蛋白表达下调程度较轻。这些变化与糖尿病大鼠再生纤维轴突伸长和直径生长受损有关。我们认为,在神经损伤时,微管蛋白的上调对NF表达有负反馈作用,正如在对照大鼠中看到的那样。在糖尿病动物中,这种上调的缺失可能会损害其对NF表达的调节作用,并导致糖尿病神经中神经再生的紊乱。
Altered Tubulin and Neurofilament Expression and Impaired Axonal Growth in Diabetic Nerve Regeneration
Cytoskeletal protein expression in sensory neurons and sciatic nerve axonal growth were examined in type 1 diabetic BB/Wor rats after sciatic nerve crush injury. Diabetic male rats were subjected to sciatic nerve crush at 6 wk of diabetes. L4 and L5 dorsal root ganglia (DRG) mRNA expression of low and medium molecular weight neurofilaments (NF-L, NF-M), βII- and βIII-tubulin as well as protein expression of NF-L, NF-M, and β-tubulin were examined at various time points following crush injury and compared with age- and sex-matched non-diabetic BB/Wor rats. Steady state mRNA expression of NF-L, NF-M, βII- and βIII-tubulin were decreased in diabetic DRG. NF-L and NF-M proteins were also decreased in DRG of uncrushed diabetic animals. After crush injury, βII- and βIII-tubulin mRNA were upregulated in control animals at day 2 and day 6, respectively, and β-tubulin protein showed similarly increased expression after crush injury, while such upregulations did not occur in diabetic animals. Conversely, mRNA and protein expressions of NF-L, NF-M were downregulated to a lesser extent in diabetic animals compared to control rats. These changes were associated with impaired axonal elongation and caliber growth of regenerating fibers in diabetic rats. We propose that upregulation of tubulin has a negative feedback on NF expression in response to nerve injury, as seen in control rats. The absence of this upregulation in diabetic animals may impair its regulatory effect on NF expression and contribute to perturbed nerve regeneration seen in diabetic nerve.