Murphy M, Dutton R, Koblar S, Cheema S, Bartlett P
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Parkville, Victoria, Australia.
Prog Neurobiol. 1997 Aug;52(5):355-78. doi: 10.1016/s0301-0082(97)00020-8.
A number of different cytokines, each initially characterized on the basis of very different biological activities, all have very similar signalling pathways and share a similar tertiary structure. These cytokines include leukaemia inhibitory factor, ciliary neuronotrophic factor, oncostatin M, growth-promoting activity and cardiotrophin 1. They all have been found to regulate a number of properties of cells of the developing and mature nervous system in vitro and thus are neuroregulatory cytokines. The actions of these cytokines include regulation of neurotransmitter phenotype, differentiation of neuronal precursor cells both in the peripheral nervous system and in the spinal cord, survival of differentiated neurons, and regulation of development of both astrocytes and oligodendrocytes. In addition, studies in animal models show that these factors can rescue sensory and motor neurons from axotomy-induced cell death, which suggests that they can act as trauma factors for injured neurons. Analysis of the expression patterns of the different neuroregulatory cytokines and their receptors reveals that the receptors are expressed throughout nervous system development and following trauma, whereas the cytokines show temporal and spatial specific expression patterns. This is consistent with the idea that specific cytokines have specific roles in neural development and repair, but that their signalling pathways are shared. The phenotypes of the receptor knockouts show clear deficits in nervous system development, indicating a crucial role for LIF receptor signalling. Knockouts of individual cytokines are less dramatic, but LIF and CNTF knockouts do reveal deficits in maintenance of motor neurons or following trauma. Thus, whereas LIF and CNTF have clear roles in maintenance and following trauma, it is unclear which of the cytokines is involved in nervous system development. In clinical terms, these findings add further support to the use of these cytokines in nervous system trauma and disease.
许多不同的细胞因子,最初是根据非常不同的生物学活性来表征的,它们都具有非常相似的信号通路并共享相似的三级结构。这些细胞因子包括白血病抑制因子、睫状神经营养因子、制瘤素M、生长促进活性因子和心肌营养素1。它们都已被发现在体外调节发育中和成熟神经系统细胞的多种特性,因此是神经调节性细胞因子。这些细胞因子的作用包括调节神经递质表型、外周神经系统和脊髓中神经元前体细胞的分化、分化神经元的存活以及星形胶质细胞和少突胶质细胞发育的调节。此外,动物模型研究表明,这些因子可以挽救轴突切断诱导的感觉和运动神经元细胞死亡,这表明它们可以作为受损神经元的创伤因子。对不同神经调节性细胞因子及其受体表达模式的分析表明,受体在整个神经系统发育过程中和创伤后均有表达,而细胞因子则表现出时空特异性表达模式。这与特定细胞因子在神经发育和修复中具有特定作用,但它们的信号通路是共享的观点一致。受体基因敲除的表型在神经系统发育中显示出明显的缺陷,表明LIF受体信号传导具有关键作用。单个细胞因子的基因敲除影响较小,但LIF和CNTF基因敲除确实揭示了运动神经元维持或创伤后存在缺陷。因此,虽然LIF和CNTF在维持和创伤后有明确作用,但尚不清楚哪些细胞因子参与神经系统发育。从临床角度来看,这些发现进一步支持了这些细胞因子在神经系统创伤和疾病中的应用。