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Oscillatory hyperpolarizations and resting membrane potentials of mouse fibroblast and macrophage cell lines.

机译:小鼠成纤维细胞和巨噬细胞细胞系的振荡超极化和静息膜电位。

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摘要

L cells (a mouse fibroblast cell line) and macrophages have been reported to exhibit slow oscillatory hyperpolarizations and relatively low membrane potentials, when measured with glass micro-electrodes. This paper describes the role of micro-electrode-induced leakage in these oscillations for L cells and a mouse macrophage cell line (P388D1). Both L cells and macrophages showed fast negative-going peak-shaped potential transients upon micro-electrode entry. This shows that the micro-electrode introduces a leakage conductance across the membrane. The peak values of these fast transients were less negative for L cells (-17 mV) than for macrophages (-39 mV), although their sustained resting membrane potentials were about equal (-13 mV). This indicates that the pre-impaled membrane potential of macrophages is more negative than that of L cells. Ionophoretic injection of Ca2+ into the P388D1 macrophages showed the existence of a Ca2+ -dependent hyperpolarizing conductance presumed to be involved in the oscillatory hyperpolarizations of L cells and macrophages. Cells increased in size by X-ray irradiation to reduce membrane input resistances were still found to be susceptible to micro-electrode-induced leakage. Impalement transients upon entry of a second electrode during a hyperpolarization evoked by a first electrode, were often step-shaped instead of peak-shaped due to the high membrane conductance associated with hyperpolarization. Since peak-shaped impalement transients were always seen with the first impalement both in oscillating and non-oscillating cells, oscillatory hyperpolarizations cannot be regarded as spontaneously occurring in the unperturbed cells but are induced by micro-electrode penetration. Since the hyperpolarizing response can be evoked by ionophoretic injection of Ca2+, and oscillatory as well as single hyperpolarizing responses are absent in a Ca2+ -free medium, it is concluded that the Ca2+ needed intracellularly to activate the hyperpolarizing responses enters the cell via the leakage pathway introduced by the measuring electrode.
机译:当用玻璃微电极测量时,L细胞(小鼠成纤维细胞系)和巨噬细胞显示出缓慢的振荡超极化和相对较低的膜电位。本文描述了微电极诱导的泄漏在L细胞和小鼠巨噬细胞系(P388D1)的这些振荡中的作用。 L细胞和巨噬细胞在微电极进入时均显示快速的负峰形电位瞬变。这表明微电极在膜上引入了漏电导。尽管它们持续的静息膜电位大约相等(-13 mV),但这些快速瞬变的峰值对L细胞(-17 mV)的负性要小于对巨噬细胞(-39 mV)的负性。这表明巨噬细胞的预先刺穿的膜电位比L细胞更负。 Ca2 +离子注入P388D1巨噬细胞表明存在依赖Ca2 +的超极化电导,推测其与L细胞和巨噬细胞的振荡超极化有关。仍然发现通过X射线辐照增加细胞大小以降低膜输入电阻,这些细胞仍然容易受到微电极引起的泄漏的影响。在由第一电极引起的超极化过程中,第二电极进入时的刺穿瞬变通常是阶梯形而不是峰形,这是由于与超极化相关的高膜电导。由于在振荡和非振荡电池中总是会出现峰形的瞬态瞬态现象,因此振荡超极化不能被认为是在不受干扰的细胞中自发发生,而是由微电极穿透引起的。由于可以通过离子注入Ca2 +引起超极化反应,并且在不含Ca2 +的培养基中不存在振荡以及单个超极化反应,因此得出结论,细胞内激活超极化反应所需的Ca2 +通过泄漏途径进入细胞。由测量电极引入。

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