Bamber B A, Masters B A, Hoyle G W, Brinster R L, Palmiter R D
Department of Biochemistry, University of Washington, Seattle 98195.
Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):7839-43. doi: 10.1073/pnas.91.17.7839.
Leukemia inhibitory factor (LIF) is a cytokine growth factor that induces rat sympathetic neurons to switch their neurotransmitter phenotype from noradrenergic to cholinergic in vitro. To test whether LIF can influence neuronal differentiation in vivo, we generated transgenic mice that expressed LIF in pancreatic islets under the control of the insulin promoter and evaluated the neurotransmitter phenotype of the pancreatic sympathetic innervation. We also used the insulin promoter to coexpress nerve growth factor in the islets, which greatly increased the density of sympathetic innervation and facilitated analysis of the effects of LIF. Our data demonstrate that tyrosine hydroxylase and catecholamines declined and choline acetyltransferase increased in response to LIF. We conclude that LIF can induce neurotransmitter switching of sympathetic neurons in vivo.
白血病抑制因子(LIF)是一种细胞因子生长因子,在体外可诱导大鼠交感神经元将其神经递质表型从去甲肾上腺素能转变为胆碱能。为了测试LIF是否能在体内影响神经元分化,我们构建了在胰岛素启动子控制下在胰岛中表达LIF的转基因小鼠,并评估了胰腺交感神经支配的神经递质表型。我们还利用胰岛素启动子在胰岛中共表达神经生长因子,这极大地增加了交感神经支配的密度,并便于分析LIF的作用。我们的数据表明,酪氨酸羟化酶和儿茶酚胺减少,而胆碱乙酰转移酶因LIF而增加。我们得出结论,LIF可在体内诱导交感神经元的神经递质转换。