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细胞内腺嘌呤核苷酸对大鼠胰腺β细胞中容量敏感阴离子通道的调节作用。

Regulation of a volume-sensitive anion channel in rat pancreatic beta-cells by intracellular adenine nucleotides.

作者信息

Miley H E, Brown P D, Best L

机构信息

School of Biological Sciences, University of Manchester, Oxford Road, Manchester M13 9PT, UK.

出版信息

J Physiol. 1999 Mar 1;515 ( Pt 2)(Pt 2):413-7. doi: 10.1111/j.1469-7793.1999.413ac.x.

Abstract
  1. The patch-clamp technique in the whole-cell configuration was used to measure the effects of intracellular adenine nucleotides on activity of the volume-sensitive anion channel in single, isolated rat pancreatic beta-cells. 2. In the absence of intracellular nucleotides, swelling of cells with a hypertonic pipette solution failed to activate the conductance. Addition of ATP over the range 2-10 mM maintaining the same degree of hypertonicity caused a progressive activation of the conductance. An increase in ATP produced a similar activation of the conductance in non-swollen cells, albeit with reduced current amplitudes. 3. Activation of the conductance was also observed in the presence of ATPgammaS, adenylyl imidophosphate (AMP-PNP), ADP, diadenosine tetraphosphate and GTPgammaS. Neither ADP nor GDPbetaS inhibited activation of the conductance by ATP. 4. It is concluded that activity of the beta-cell volume-sensitive anion channel can be modulated by changes in intracellular concentrations of ATP within the physiological concentration range by a mechanism that does not require nucleotide hydrolysis. Activity of the channel does not appear to be modulated by a G protein-coupled mechanism.
摘要
  1. 采用全细胞模式的膜片钳技术,测定细胞内腺嘌呤核苷酸对单个分离的大鼠胰腺β细胞中容量敏感型阴离子通道活性的影响。2. 在没有细胞内核苷酸的情况下,用高渗微管溶液使细胞肿胀未能激活该电导。在保持相同高渗程度的情况下,加入2 - 10 mM范围内的ATP会导致电导逐渐激活。ATP增加也会在未肿胀细胞中产生类似的电导激活,尽管电流幅度减小。3. 在存在ATPγS、腺苷酰亚胺二磷酸(AMP - PNP)、ADP、二腺苷四磷酸和GTPγS的情况下,也观察到了电导的激活。ADP和GDPβS均未抑制ATP对电导的激活。4. 得出的结论是,β细胞容量敏感型阴离子通道的活性可通过生理浓度范围内细胞内ATP浓度的变化进行调节,其机制不需要核苷酸水解。该通道的活性似乎不受G蛋白偶联机制的调节。

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Glucose-induced swelling in rat pancreatic beta-cells.葡萄糖诱导的大鼠胰腺β细胞肿胀
J Physiol. 1997 Oct 1;504 ( Pt 1)(Pt 1):191-8. doi: 10.1111/j.1469-7793.1997.00191.x.

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