Eder C, Klee R, Heinemann U
Department of Neurophysiology, Institute of Physiology, Humboldt University, D 10117 Berlin, Germany.
J Neurosci. 1998 Sep 15;18(18):7127-37. doi: 10.1523/JNEUROSCI.18-18-07127.1998.
A stretch-activated Cl- current (ICl) was investigated in cultured murine microglia using the whole-cell configuration of the patch-clamp technique. After application of membrane stretch, a Cl- current appeared within seconds, and its amplitude increased further within 3-8 min. ICl underwent rundown, which was prevented by addition of 4 mM ATP to the intracellular perfusing solution. The stretch-activated Cl- current exhibited outward rectification and did not show any voltage-dependent gating. Lowering the concentration of extracellular Cl- from 142 to 12 mM by equimolar substitution of Cl- with gluconate shifted the reversal potential of ICl by 41.6 +/- 1.8 mV in the depolarizing direction. 4, 4'-Diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS) and 4-acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid (SITS) blocked ICl in a voltage- and time-dependent manner. At a test potential of +40 mV, a half-maximal blockade at 16.1 microM DIDS and at 71.0 microM SITS was determined for ICl. At a concentration of 200 microM, 5-nitro-2-(3-phenylpropylamino)benzoic acid or flufenamic acid blocked ICl by 88% and 75%, respectively. Each of these four Cl- channel blockers reversibly inhibited the ramification process of microglia, whereas blockers of voltage-gated Na+ and K+ channels did not affect the transformation of microglia from their ameboid into the ramified phenotype. It is suggested that in microglia functional stretch-activated Cl- channels are required for the induction of ramification but not for maintaining the ramified shape.
采用膜片钳技术的全细胞模式,对培养的小鼠小胶质细胞中的牵张激活氯离子电流(ICl)进行了研究。施加细胞膜牵张后,数秒内出现氯离子电流,其幅度在3 - 8分钟内进一步增加。ICl会衰减,向细胞内灌流液中添加4 mM ATP可防止这种衰减。牵张激活的氯离子电流表现出外向整流特性,且未显示出任何电压依赖性门控。通过用葡萄糖酸盐等摩尔替代氯离子,将细胞外氯离子浓度从142 mM降至12 mM,使ICl的反转电位向去极化方向移动了41.6±1.8 mV。4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)和4-乙酰氨基-4'-异硫氰基芪-2,2'-二磺酸(SITS)以电压和时间依赖性方式阻断ICl。在测试电位为+40 mV时,测定ICl在16.1 microM DIDS和71.0 microM SITS时达到半数最大阻断。在浓度为200 microM时,5-硝基-2-(3-苯丙基氨基)苯甲酸或氟芬那酸分别阻断ICl达88%和75%。这四种氯离子通道阻滞剂中的每一种都可逆地抑制小胶质细胞的分支过程,而电压门控钠通道和钾通道阻滞剂不影响小胶质细胞从阿米巴样形态转变为分支状形态。提示在小胶质细胞中,功能性牵张激活氯离子通道是诱导分支所必需的,但不是维持分支状形态所必需的。