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Cytokine-induced SOCS expression is inhibited by cAMP analogue: Impact on regeneration in injured retina

机译:cAMP类似物抑制细胞因子诱导的SOCS表达:对受损视网膜的再生的影响

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Injured adult retinal ganglion cells (RGCs) regrow axons into peripheral nerve (PN) grafted onto cut optic nerve. Survival and regeneration of RGCs is increased by intraocular injections of ciliary neurotrophic factor (CNTF) and axonal regeneration is further enhanced by co-injection of a cyclic AMP analogue (CPT-cAMP). Based on these data, and because cytokine signaling is negatively regulated by suppressor of cytokine signaling (SOCS) proteins, we set out to determine whether CNTF injections increase retinal SOCS expression and whether any changes are attenuated by co-injection with CPT-cAMP. Using quantitative PCR we found increased SOCS1, SOCS2 and SOCS3 mRNA levels at various times after a single CNTF injection. Expression remained high for many days. SOCS protein levels were also increased. In situ hybridization revealed that RGCs express SOCS3 mRNA, and SOCS expression in cultured RGCs was increased by CNTF. Co-injection of CPT-cAMP reduced CNTF induced expression of SOCS1 and SOCS3 mRNA and decreased SOCS3 protein expression. CNTF injection also transiently increased retinal leukemia inhibitory factor (LIF) expression, an effect that was also moderated by CPT-cAMP. We propose that, along with known reparative effects of elevated cAMP on neurons, reducing SOCS upregulation may be an additional way in which cyclic nucleotides augment cytokine-induced regenerative responses in the injured CNS.
机译:受伤的成人视网膜神经节细胞(RGCs)将轴突重新长入移植到切开的视神经上的周围神经(PN)中。眼内注射睫状神经营养因子(CNTF)可提高RGC的存活和再生能力,而共注射环状AMP类似物(CPT-cAMP)可进一步增强轴突再生能力。基于这些数据,并且由于细胞因子信号转导(SOCS)蛋白抑制因子对细胞因子信号的负调控,我们着手确定CNTF注射液是否会增加视网膜SOCS的表达,以及是否通过与CPT-cAMP共注射来减弱任何变化。使用定量PCR,我们发现在一次CNTF注射后的不同时间,SOCS1,SOCS2和SOCS3 mRNA水平增加。连续数天保持高表达。 SOCS蛋白水平也增加了。原位杂交表明,RGC表达SOCS3 mRNA,CNTF增加了培养的RGC中SOCS的表达。 CPT-cAMP的共同注射降低CNTF诱导的SOCS1和SOCS3 mRNA表达,并降低SOCS3蛋白表达。 CNTF注射还可以短暂增加视网膜白血病抑制因子(LIF)的表达,这种作用也可以通过CPT-cAMP缓解。我们提出,连同已知的cAMP升高对神经元的修复作用,减少SOCS上调可能是环状核苷酸增强受伤的CNS中细胞因子诱导的再生反应的另一种方式。

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