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来自海绵Reniera sarai的聚合烷基吡啶鎓盐(聚APS)形成的不可逆和可逆孔道。

Irreversible and reversible pore formation by polymeric alkylpyridinium salts (poly-APS) from the sponge Reniera sarai.

作者信息

McClelland D, Evans R M, Abidin I, Sharma S, Choudhry F Z, Jaspars M, Sepcić K, Scott R H

机构信息

Department of Biomedical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD.

出版信息

Br J Pharmacol. 2003 Aug;139(8):1399-408. doi: 10.1038/sj.bjp.0705374.

Abstract
  1. In this study, we investigated the electrophysiological actions of a high molecular weight fraction, predominantly containing two polymeric 1,3-alkylpyridinium salts (poly-APS) of 5.5 and approximately 19 kDa isolated from the marine sponge Reniera sarai. The biological properties of poly-APS are of particular interest because this preparation may be used to deliver macromolecules into the intracellular environment without producing long-term damage to cells. Poly-APS (50-0.05 micro g ml(-1)) was applied to cultured dorsal root ganglion neurones or HEK 293 cells and changes in cell membrane properties were measured using whole-cell patch-clamp recording and fura-2 Ca(2+) imaging. 2. Poly-APS (50 micro g ml(-1)) evoked irreversible depolarisations in membrane potential and reductions in input resistance. However, doses of 5 micro g ml(-1) and less produced reversible effects on these cell membrane characteristics and on Ca(2+) permeability. 3. At 0.05 micro g ml(-1), poly-APS could robust transient increases in Ca(2+) permeability without damaging the neurones or subsequently attenuating Ca(2+) entry through voltage-activated channels. 4. Bathing cells in NaCl-based extracellular medium containing 1.5 mM zinc attenuated the irreversible and reversible effects of poly-APS on membrane properties (membrane potential, input resistance and whole-cell currents). In both DRG neurones and HEK 293 cells, zinc attenuated Ca(2+) entry evoked by poly-APS. These effects of zinc were only observed if zinc was continually present during poly-APS application. However, zinc failed to attenuate the actions of poly-APS if it was applied after the sponge toxin preparation had evoked changes in membrane properties. 5. In conclusion, the pore-forming preparation poly-APS can have dose-dependent interactions with cell membranes and at low doses these can be reversible. Additionally, the interactions between poly-APS and cell membranes could be attenuated by zinc.
摘要
  1. 在本研究中,我们研究了从海海绵Reniera sarai中分离出的一种高分子量组分的电生理作用,该组分主要含有两种聚合的1,3 - 烷基吡啶鎓盐(聚 - APS),分子量分别为5.5 kDa和约19 kDa。聚 - APS的生物学特性特别令人感兴趣,因为这种制剂可用于将大分子递送至细胞内环境而不会对细胞造成长期损害。将聚 - APS(50 - 0.05μg ml⁻¹)应用于培养的背根神经节神经元或HEK 293细胞,并使用全细胞膜片钳记录和fura - 2 Ca²⁺成像测量细胞膜特性的变化。2. 聚 - APS(50μg ml⁻¹)引起膜电位不可逆的去极化以及输入电阻降低。然而,5μg ml⁻¹及更低剂量对这些细胞膜特性和Ca²⁺通透性产生可逆影响。3. 在0.05μg ml⁻¹时,聚 - APS可使Ca²⁺通透性强劲短暂增加,而不会损伤神经元或随后减弱通过电压激活通道的Ca²⁺内流。4. 将细胞置于含有1.5 mM锌的基于NaCl的细胞外培养基中孵育,可减弱聚 - APS对膜特性(膜电位、输入电阻和全细胞电流)的不可逆和可逆影响。在背根神经节神经元和HEK 293细胞中,锌均可减弱聚 - APS引起的Ca²⁺内流。仅当在应用聚 - APS期间持续存在锌时,才会观察到锌的这些作用。然而,如果在海绵毒素制剂引起膜特性变化后应用锌,则锌无法减弱聚 - APS的作用。5. 总之,形成孔道的制剂聚 - APS可与细胞膜发生剂量依赖性相互作用,且在低剂量时这些相互作用是可逆的。此外,锌可减弱聚 - APS与细胞膜之间的相互作用。

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