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Functional and structural effects of amyloid-β aggregate on Xenopus laevis oocytes.

机译:淀粉样β蛋白聚集体对非洲爪蟾卵母细胞的功能和结构影响。

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摘要

Xenopus laevis oocytes exposed to amyloid-β aggregate generated oscillatory electric activity (blips) that was recorded by two-microelectrode voltage-clamp. The cells exhibited a series of "spontaneous" blips ranging in amplitude from 3.8 ± 0.9 nA at the beginning of the recordings to 6.8 ± 1.7 nA after 15 min of exposure to 1 μM aggregate. These blips were similar in amplitude to those induced by the channel-forming antimicrobial agents amphotericin B (7.8 ± 1.2 nA) and gramicidin (6.3 ± 1.1 nA). The amyloid aggregate-induced currents were abolished when extracellular Ca(2+) was removed from the bathing solution, suggesting a central role for this cation in generating the spontaneous electric activity. The amyloid aggregate also affected the Ca(2+)-dependent Cl(-) currents of oocytes, as shown by increased amplitude of the transient-outward chloride current (T(out)) and the serum-activated, oscillatory Cl(-) currents. Electron microcopy revealed that amyloid aggregate induced the dissociation of the follicular cells that surround the oocyte, thus leading to a failure in the electro-chemical communication between these cells. This was also evidenced by the suppression of the oscillatory Ca(2+)-dependent ATP-currents, which require proper coupling between oocytes and the follicular cell layer. These observations, made using the X. laevis oocytes as a versatile experimental model, may help to understand the effects of amyloid aggregate on cellular communication.
机译:暴露于淀粉样蛋白β的非洲爪蟾卵母细胞产生振荡电活动(斑点),该活动由两个微电极电压钳记录。细胞显示出一系列“自发”斑点,幅度从记录开始时的3.8±0.9 nA到暴露于1μM聚集体15分钟后的6.8±1.7 nA。这些斑点的幅度与通道形成的抗菌剂两性霉素B(7.8±1.2 nA)和短杆菌肽(6.3±1.1 nA)诱导的斑点相似。当从沐浴液中去除细胞外Ca(2+)时,淀粉样蛋白聚集体诱导的电流被消除,表明该阳离子在产生自发电活动中的核心作用。淀粉样蛋白聚集体还影响卵母细胞的Ca(2+)依赖性Cl(-)电流,如瞬时向外氯化物电流(T(out))和血清激活的振荡性Cl(-)的幅度增加所显示潮流。电子显微镜显示淀粉样蛋白聚集体诱导卵母细胞周围的卵泡细胞解离,从而导致这些细胞之间的电化学通讯失败。这也可以通过抑制振荡的Ca(2+)依赖的ATP-电流来证明,这需要卵母细胞和滤泡细胞层之间的适当耦合。使用X. laevis卵母细胞作为通用实验模型进行的这些观察,可能有助于了解淀粉样蛋白聚集体对细胞通讯的影响。

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