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首页> 外文期刊>The Journal of Physiology >Swelling- and cAMP-activated Cl- currents in isolated rat carotid body type I cells.
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Swelling- and cAMP-activated Cl- currents in isolated rat carotid body type I cells.

机译:分离的大鼠颈动脉I型细胞中的溶胀和cAMP激活的Cl电流。

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1. In the whole-cell configuration of the patch clamp technique, isolated rat carotid body type I cells exhibited reversible activation of Cl- currents during cell swelling effected by hypotonic extracellular solutions. 2. Hypotonic solutions evoked outwardly rectifying, non-inactivating currents which showed time-independent activation. The reversal potential (E(rev)) for the hypotonically evoked current was 1.6 +/- 0.6 mV (n = 26). Reduction of extracellular Cl- from 133 to 65.5 mM caused a shift in E(rev) of +14.7 +/- 0.4 mV (n = 5). 3. The swelling-activated Cl- current could not activate when ATP was omitted from the patch pipette or when substituted for the non-hydrolysable ATP analogues 5'-adenylylimidodiphosphate, AMP-PNP (2 mM) or beta, gamma-methylene-adenosine 5'-triphosphate. AMP-PCP (2 mM). The current also failed to activate in the absence of free intracellular Ca2+. 4. The swelling-activated Cl- current was sensitive to blockade by the Cl- channel blockers niflumic acid (300 microM) and 4,4'-diisothiocyanatostilbene-2, 2'-disulphonic acid (DIDS; 200 microM), although the blockade by DIDS was voltage dependent. 5. A similar, non-inactivating, outwardly rectifying Cl- current was evoked by the inclusion of cAMP (200 microM) in the patch pipette. This current could be inhibited by niflumic acid (300 microM), DIDS (200 microM) and hypertonic solutions, and was virtually abolished in the absence of intracellular ATP. 6. In conclusion, carotid body type I cells possess Cl- currents activated by cell swelling and rises in intracellular cAMP concentration. These currents may be involved in cell volume regulation, blood volume and osmolarity regulation and the response of the type I cell to chemostimuli.
机译:1.在膜片钳技术的全细胞配置中,低渗性细胞外溶液影响的细胞膨胀过程中,分离的大鼠颈动脉I型细胞表现出可逆的Cl电流激活。 2.低渗溶液引起向外整流的非灭活电流,显示出与时间无关的激活作用。低渗诱发电流的反向电位(E(rev))为1.6 +/- 0.6 mV(n = 26)。细胞外Cl-从133降低到65.5 mM,导致E(rev)的变化为+14.7 +/- 0.4 mV(n = 5)。 3.当从贴片移液器中省略ATP或代替不可水解的ATP类似物5'-adelylylimidodiphosphate,AMP-PNP(2 mM)或β,γ-亚甲基-腺苷时,溶胀激活的Cl电流无法激活。 5'-三磷酸。 AMP-PCP(2毫米)。在缺乏游离细胞内Ca 2+的情况下,电流也未能激活。 4.溶胀激活的Cl-电流对Cl-通道阻滞剂尼氟酸(300 microM)和4,4'-二异硫氰基苯乙烯2,2'-二磺酸(DIDS; 200 microM)的阻滞敏感,尽管被阻滞DIDS的电压取决于电压。 5.通过在贴片移液器中加入cAMP(200 microM)可以诱发类似的,非灭活的,向外整流的Cl-电流。该电流可被尼氟酸(300 microM),DIDS(200 microM)和高渗溶液抑制,并且在没有细胞内ATP的情况下实际上已被消除。 6.总之,颈动脉I型细胞具有被细胞肿胀激活的Cl电流,并增加了细胞内cAMP的浓度。这些电流可能参与细胞体积调节,血容量和渗透压调节以及I型细胞对化学趋化因子的反应。

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