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白血病抑制因子和睫状神经营养因子调节培养的交感神经元中毒蕈碱受体的表达。

Leukemia inhibitory factor and ciliary neurotrophic factor regulate expression of muscarinic receptors in cultured sympathetic neurons.

作者信息

Ludlam W H, Kessler J A

机构信息

Department of Neurology, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

Dev Biol. 1993 Feb;155(2):497-506. doi: 10.1006/dbio.1993.1047.

DOI:10.1006/dbio.1993.1047
PMID:8432402
Abstract

Regulation of muscarinic receptor expression was studied in cultured sympathetic neurons of the neonatal rat superior cervical ganglion (SCG). Leukemia inhibitory factor (LIF) and ciliary neurotrophic factor (CNTF), both previously shown to regulate neurotransmitter development in cultured SCG neurons (Yamamori et al., 1989; Saadat et al., 1989), were examined for effects on receptor expression. Exposure of SCG neurons to LIF or CNTF (5 ng/ml) prevented the normal developmental increase in muscarinic receptors as measured by whole cell binding of N-methyl[3H]scopolamine. Reduction in receptor binding was detected within 2 to 4 days of treatment, with a 65-80% reduction after 16 days. Scatchard analysis demonstrated a reduction in total receptor number (Bmax) with no significant change in receptor affinity (Kd). Concentrations of 1 ng/ml of either factor reduced receptor expression with near-maximal effectiveness at doses of 10 ng/ml. The decrease in muscarinic receptors was not blocked by atropine, indicating that it was not agonist induced. Treatment with LIF or CNTF did not affect the survival of cultured neurons. Further, effects on receptor expression were reversible after discontinuance of treatment. Finally, treatment with either factor increased overall protein synthesis, indicating the integrity of cellular metabolism of cultures and hence the specificity of the decrease in muscarinic receptor number. LIF and CNTF thus regulate receptor as well as neurotransmitter development and could therefore play a role during synaptogenesis in the developing nervous system.

摘要

在新生大鼠颈上神经节(SCG)培养的交感神经元中研究了毒蕈碱受体表达的调节。白血病抑制因子(LIF)和睫状神经营养因子(CNTF),先前均已证明可调节培养的SCG神经元中的神经递质发育(Yamamori等人,1989年;Saadat等人,1989年),研究了它们对受体表达的影响。将SCG神经元暴露于LIF或CNTF(5 ng/ml)可阻止毒蕈碱受体正常的发育性增加,这通过N-甲基[3H]东莨菪碱的全细胞结合来测量。在治疗的2至4天内检测到受体结合减少,16天后减少65-80%。Scatchard分析表明总受体数量(Bmax)减少,而受体亲和力(Kd)无显著变化。两种因子1 ng/ml的浓度均可降低受体表达,在10 ng/ml的剂量下具有接近最大的效果。毒蕈碱受体的减少未被阿托品阻断,表明这不是激动剂诱导的。用LIF或CNTF治疗不影响培养神经元的存活。此外,治疗停止后对受体表达的影响是可逆的。最后,用任何一种因子治疗均可增加总体蛋白质合成,表明培养物细胞代谢的完整性,因此毒蕈碱受体数量减少具有特异性。因此,LIF和CNTF调节受体以及神经递质的发育,因此可能在发育中的神经系统的突触形成过程中发挥作用。

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Leukemia inhibitory factor and ciliary neurotrophic factor regulate expression of muscarinic receptors in cultured sympathetic neurons.白血病抑制因子和睫状神经营养因子调节培养的交感神经元中毒蕈碱受体的表达。
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