首页> 外文期刊>American Journal of Physiology >Volume changes and whole cell membrane currents activated during gradual osmolarity decrease in C6 glioma cells: contribution of two types of K+ channels.
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Volume changes and whole cell membrane currents activated during gradual osmolarity decrease in C6 glioma cells: contribution of two types of K+ channels.

机译:C6胶质瘤细胞的体积渗透压降低期间激活的体积变化和全细胞膜电流:两种K +通道的贡献。

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摘要

Volume changes and whole cell ionic currents activated by gradual osmolarity reductions (GOR) of 1.8 mosM/min were characterized in C6 glioma cells. Cells swell less in GOR than after sudden osmolarity reductions (SOR), the extent of swelling being partly Ca(2+) dependent. In nominally Ca(2+)-free conditions, GOR activated predominantly whole cell outward currents. Cells depolarized from the initial -79 mV to a steady state of -54 mV reached at 18% osmolarity reduction [hyposmolarity of -18% (H-18%)]. Recordings of Cl(-) and K(+) currents showed activation at H-3% of an outwardly rectifying Cl(-) current, with conductance of 1.6 nS, sensitive to niflumic acid and 5-nitro-2-(3-phenylpropylamino)benzoic acid, followed at H-18% by an outwardly rectifying K(+) current with conductance of 4.1 nS, inhibited by clofilium but insensitive to the typical K(+) channel blockers. With 200 nM Ca(2+) in the patch pipette, whole cell currents activated at H-3% and at H-13% cells depolarized from -77 to -63 mV. A K(+) current activated at H-1%, showing a rapid increase in conductance, suppressed by charybdotoxin and insensitive to clofilium. These results show the operation of two different K(+) channels in response to GOR in the same cell type, activated by Ca(2+) and osmolarity and with different osmolarity activation thresholds. Taurine and glutamate efflux, monitored by labeled tracers, showed delayed osmolarity thresholds of H-39 and H-33%, respectively. This observation clearly separates the Cl(-) and amino acid osmosensitive pathways. The delayed amino acid efflux may contribute to counteract swelling at more stringent osmolarity reductions.
机译:在C6胶质瘤细胞中表征了通过1.8 mosM / min的逐渐渗透压降低(GOR)激活的体积变化和全细胞离子电流。细胞的GOR溶胀比突然的摩尔渗透压降低(SOR)后少,肿胀程度部分取决于Ca(2+)。在名义上无Ca(2+)的条件下,GOR主要激活整个细胞的外向电流。从最初的-79 mV去极化到-54 mV的稳态去极化的细胞达到18%的渗透压降低[低渗透压为-18%(H-18%)]。 Cl(-)和K(+)电流的记录显示在向外整流的Cl(-)电流的H-3%处被激活,电导为1.6 nS,对尼氟酸和5-硝基-2-(3-苯基丙基氨基)敏感苯甲酸),然后在H-18%处以4.1 nS的电导率向外整流K(+)电流,该电流被clofilium抑制,但对典型的K(+)通道阻滞剂不敏感。用贴片移液器中的200 nM Ca(2+),全细胞电流在H-3%和H-13%时被激活,从-77极化到-63 mV。 K(+)电流在H-1%处激活,显示出电导的快速增加,受到甲藻毒素的抑制并且对氯菲芬不敏感。这些结果显示在相同的细胞类型中,两个不同的K(+)通道对GOR的响应,由Ca(2+)和渗透压激活,并具有不同的渗透压激活阈值。通过标记示踪剂监测的牛磺酸和谷氨酸外排分别显示出延迟的渗透压阈值H-39和H-33%。该观察清楚地分离了Cl(-)和氨基酸渗透敏感性途径。延迟的氨基酸外排可能有助于以更严格的渗透压降低来抵消肿胀。

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