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肌肉衍生分化因子可增加大鼠中脑培养的多巴胺能神经元中酪氨酸羟化酶基因的表达及酶活性。

Muscle-derived differentiation factor increases expression of the tyrosine hydroxylase gene and enzyme activity in cultured dopamine neurons from the rat midbrain.

作者信息

Iacovitti L, Evinger M J, Stull N D

机构信息

Institute of Neuroscience, Hahnemann University Medical School, Philadelphia, PA 19102.

出版信息

Brain Res Mol Brain Res. 1992 Dec;16(3-4):215-22. doi: 10.1016/0169-328x(92)90228-4.

Abstract

Our earlier work demonstrated that certain populations of brain neurons which do not synthesize catecholamine (CA) neurotransmitters in vivo, will, when grown in culture with muscle-derived differentiation factor (MDF), unexpectedly express the gene for the CA biosynthetic enzyme tyrosine hydroxylase (TH). In this paper, we sought to determine whether MDF could also regulate TH expression in those neurons which normally synthesize CA neurotransmitters. Incubation of cultured dopamine neurons from the ventral midbrain with MDF elevated the levels of TH mRNA and TH enzyme activity 5- to 40-fold higher than that measured in control cultures. Sympathetic neurons were unaffected by a similar MDF treatment. Unlike the 2-day critical period for MDF-responsivity in non-CA neurons. CA neurons remained susceptible to MDF's influence over an extended developmental interval (E14-18), suggesting that MDF may be important for TH gene regulation in brain CA neurons even differentiation is complete. Because of these unique properties, MDF may provide a unique opportunity to explore ways in which the TH gene might be directly manipulated in these cell populations in order to correct the CA imbalances that occur in certain neurological diseases and disorders.

摘要

我们早期的研究表明,体内不合成儿茶酚胺(CA)神经递质的某些脑神经元群体,在与肌肉衍生分化因子(MDF)一起培养时,会意外地表达CA生物合成酶酪氨酸羟化酶(TH)的基因。在本文中,我们试图确定MDF是否也能调节那些正常合成CA神经递质的神经元中TH的表达。用MDF孵育来自腹侧中脑的培养多巴胺神经元,使TH mRNA水平和TH酶活性比对照培养物中测得的水平提高了5至40倍。交感神经元对类似的MDF处理没有反应。与非CA神经元中MDF反应性的2天关键期不同,CA神经元在延长的发育间隔(E14 - 18)内仍易受MDF的影响,这表明即使分化完成,MDF对脑CA神经元中TH基因的调控可能也很重要。由于这些独特的特性,MDF可能提供了一个独特的机会,来探索在这些细胞群体中直接操纵TH基因的方法,以纠正某些神经疾病和紊乱中出现的CA失衡。

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