Li M, Sendtner M, Smith A
Centre for Genome Research, University of Edinburgh, UK.
Nature. 1995 Dec 14;378(6558):724-7. doi: 10.1038/378724a0.
Development and maintenance of the mammalian nervous system is dependent upon neurotrophic cytokines. One class of neurotrophic factor acts through receptor complexes involving the low-affinity leukaemia inhibitory factor receptor subunit (LIF-R). Members of this family of cytokines, such as ciliary neurotrophic factor (CNTF) and leukaemia inhibitory factor (LIF), have profound effects on the survival and maintenance of motor neurons. Recently it was reported that mice lacking LIF-R die shortly after birth unlike mice lacking CNTF or LIF which are viable. Here we describe histopathological analyses of lifr mutants that reveal a loss > 35% of facial motor neurons, 40% of spinal motor neurons and 50% of neurons in the nucleus ambiguus. These findings point to the existence of a ligand for LIF-R that is required for the normal development of motor neurons in both brainstem nuclei and spinal cord.
哺乳动物神经系统的发育和维持依赖于神经营养细胞因子。一类神经营养因子通过涉及低亲和力白血病抑制因子受体亚基(LIF-R)的受体复合物发挥作用。这类细胞因子家族的成员,如睫状神经营养因子(CNTF)和白血病抑制因子(LIF),对运动神经元的存活和维持有深远影响。最近有报道称,缺乏LIF-R的小鼠在出生后不久就会死亡,这与缺乏CNTF或LIF且能存活的小鼠不同。在此,我们描述了对lifr突变体的组织病理学分析,结果显示面部运动神经元损失超过35%,脊髓运动神经元损失40%,疑核中的神经元损失50%。这些发现表明,存在一种LIF-R的配体,它是脑干核和脊髓中运动神经元正常发育所必需的。