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白血病抑制因子在体内损害大鼠视觉皮层的结构和神经化学发育。

Leukemia inhibitory factor impairs structural and neurochemical development of rat visual cortex in vivo.

作者信息

Engelhardt Maren, di Cristo Graziella, Grabert Jochen, Patz Silke, Maffei Lamberto, Berardi Nicoletta, Wahle Petra

机构信息

Developmental Neurobiology, Faculty of Biology and Biotechnology, Ruhr-University Bochum, Germany; Institute of Neuroanatomy, Medical Faculty Mannheim, CBTM, Heidelberg University, Germany.

Institute of Neuroscience CNR, Pisa, Italy; CHU Sainte-Justine Research Center and Department of Pediatrics, Université de Montréal, Montreal, QC, Canada.

出版信息

Mol Cell Neurosci. 2017 Mar;79:81-92. doi: 10.1016/j.mcn.2016.12.008. Epub 2017 Jan 11.

Abstract

Minipump infusions into visual cortex in vivo at the onset of the critical period have revealed that the proinflammatory cytokine leukemia inhibitory factor (LIF) delays the maturation of thalamocortical projection neurons of the lateral geniculate nucleus, and tecto-thalamic projection neurons of the superior colliculus, and cortical layer IV spiny stellates and layer VI pyramidal neurons. Here, we report that P12-20 LIF infusion inhibits somatic maturation of pyramidal neurons and of all interneuron types in vivo. Likewise, DIV 12-20 LIF treatment in organotypic cultures prevents somatic growth GABA-ergic neurons. Further, while NPY expression is increased in the LIF-infused hemispheres, the expression of parvalbumin mRNA and protein, Kv3.1 mRNA, calbindin D-28k protein, and GAD-65 mRNA, but not of GAD-67 mRNA or calretinin protein is substantially reduced. Also, LIF treatment decreases parvalbumin, Kv3.1, Kv3.2 and GAD-65, but not GAD-67 mRNA expression in OTC. Developing cortical neurons are known to depend on neurotrophins. Indeed, LIF alters neurotrophin mRNA expression, and prevents the growth promoting action of neurotophin-4 in GABA-ergic neurons. The results imply that LIF, by altering neurotrophin expression and/or signaling, could counteract neurotrophin-dependent growth and neurochemical differentiation of cortical neurons.

摘要

在关键期开始时向视觉皮层进行微型泵体内输注,结果显示促炎细胞因子白血病抑制因子(LIF)会延迟外侧膝状体丘脑皮质投射神经元、上丘的顶盖-丘脑投射神经元、皮质第IV层棘状星形神经元和第VI层锥体神经元的成熟。在此,我们报告在P12 - 20进行LIF输注会在体内抑制锥体神经元和所有中间神经元类型的体细胞成熟。同样,在器官型培养物中进行DIV 12 - 20的LIF处理可阻止GABA能神经元的体细胞生长。此外,虽然在输注LIF的半球中NPY表达增加,但小白蛋白mRNA和蛋白、Kv3.1 mRNA、钙结合蛋白D - 28k蛋白以及GAD - 65 mRNA的表达显著降低,而GAD - 67 mRNA或钙视网膜蛋白的表达未降低。而且,LIF处理会降低器官型培养物中小白蛋白、Kv3.1、Kv3.2和GAD - 65的mRNA表达,但不会降低GAD - 67的mRNA表达。已知发育中的皮层神经元依赖神经营养因子。实际上,LIF会改变神经营养因子mRNA的表达,并阻止神经营养因子 - 4在GABA能神经元中的促生长作用。这些结果表明,LIF通过改变神经营养因子的表达和/或信号传导,可能会抵消皮层神经元依赖神经营养因子的生长和神经化学分化。

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