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生长抑制性细胞外基质蛋白还通过降低钙电导和增加钾电导来抑制电活动。

Growth-inhibiting extracellular matrix proteins also inhibit electrical activity by reducing calcium and increasing potassium conductances.

作者信息

Vargas J, De-Miguel F F

机构信息

Departamento de Biofísica, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Apartado postal 70-253, C.P. 04510, D.F., Mexico.

出版信息

Neuroscience. 2009 Jan 23;158(2):592-601. doi: 10.1016/j.neuroscience.2008.10.006. Epub 2008 Oct 10.

Abstract

Inhibitionof neurite sprouting and electrical activity by extracellular matrix (ECM) glycoproteins was studied during neurite regeneration by using anterior pagoda (AP) neurons of the leech. Adult isolated neurons were plated in culture inside ganglion capsules, which among many ECM proteins, contain a group of inhibitory peanut lectin- (PNA) binding glycoproteins. These proteins inhibit neurite production and contribute to the formation of a bipolar outgrowth pattern by AP neurons. Addition of PNA lectin to the culture medium to block the inhibitory effects of ECM glycoproteins induced an increase of neurite sprouting, the loss of the bipolar pattern, and also an increase in the amplitude and duration of action potentials evoked by intracellular current injection. PNA lectin had independent effects on neurite sprouting and electrical activity, since there was no correlation between the total neurite length and the amplitude of the action potentials. Moreover, action potentials were increased by the presence of PNA lectin even in neurons that did not grow. The changes induced by PNA lectin on the active conductances underlying the action potentials were estimated by quantitative model simulations. We predict that the increases in the amplitude and duration of the action potential induced by PNA lectin were due to an increase in a calcium conductance and a reduction in the delayed rectifier potassium conductance. Our results suggest that inhibitory ECM glycoproteins may use independent signaling pathways to inhibit neurite sprouting and electrical activity. These proteins affect the action potential by changing the proportion of inward and outward active conductances.

摘要

利用水蛭前宝塔(AP)神经元,研究了细胞外基质(ECM)糖蛋白在神经突再生过程中对神经突萌发和电活动的抑制作用。将成年分离神经元接种在神经节囊内进行培养,在许多ECM蛋白中,神经节囊含有一组抑制性花生凝集素(PNA)结合糖蛋白。这些蛋白抑制神经突生成,并有助于AP神经元形成双极生长模式。向培养基中添加PNA凝集素以阻断ECM糖蛋白的抑制作用,可诱导神经突萌发增加、双极模式丧失,以及通过细胞内电流注入诱发的动作电位的幅度和持续时间增加。PNA凝集素对神经突萌发和电活动具有独立作用,因为总神经突长度与动作电位幅度之间没有相关性。此外,即使在不生长的神经元中,PNA凝集素的存在也会增加动作电位。通过定量模型模拟估计了PNA凝集素对动作电位基础上的主动电导的影响。我们预测,PNA凝集素诱导的动作电位幅度和持续时间的增加是由于钙电导增加和延迟整流钾电导降低。我们的结果表明,抑制性ECM糖蛋白可能使用独立的信号通路来抑制神经突萌发和电活动。这些蛋白通过改变内向和外向主动电导的比例来影响动作电位。

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