Scemes E, Spray D C
Department of Physiology, University of Sao Paulo, Brazil.
Glia. 1998 Sep;24(1):74-84.
When exposed to 20% and 35%, but not to 50% hyposmotic solutions, mouse astrocytes recovered their volume within a few minutes, which coincided with the activation of nonjunctional conductances. Conductance of gap junctions between astrocyte pairs also increased after exposure to a 35% hyposmotic shock; however, this effect began at 3 min after the shock, when cells had partially recovered their initial volumes. During the first minute of exposure to 20% and 35% hyposmotic stimuli, there was a transient monophasic increase in intracellular calcium levels; exposure to 50% hyposmotic solution led to intracellular Ca2+ oscillations. The differences in time courses of nonjunctional conductance changes, Ca2+ alterations, and intercellular coupling suggest that distinct second messenger pathways are involved in each response. The velocity of mechanically evoked calcium waves propagated among the astrocytes increased at 7.5 min after 35% hyposmotic shock. This increase was not seen with 20% or 50% hyposmotic stimuli and is not ascribable to the increase in junctional conductance because it was blocked by suramin, a P2 purinergic receptor antagonist. Given that the transduction pathways activated during cell swelling (e.g., generation of phospholipases, phosphokinases, arachidonic acid) exert inhibitory effects on astrocytic gap junctions (Giaume and McCarthy, 1996), it is proposed that the increased junctional conductance during hyposmotic shock is due to increased number of channels, perhaps triggered by the initial Ca2+ signals (Dolmetsch et al., 1997). As a functional consequence of the increased coupling and enhanced extracellular propagation of Ca2+ waves, spread of signaling molecules throughout the glial network is expected to be significantly enhanced during hyposmotic stress. The increased intercellular communication between mouse astrocytes in response to hyposmotic challenge thus occurs via both gap junction-dependent and -independent mechanisms and presumably provides neuroprotective effects following nervous system injury.
当暴露于20%和35%但不是50%的低渗溶液时,小鼠星形胶质细胞在几分钟内恢复其体积,这与非连接电导的激活同时发生。暴露于35%的低渗休克后,星形胶质细胞对之间的缝隙连接电导也增加;然而,这种效应在休克后3分钟开始,此时细胞已部分恢复其初始体积。在暴露于20%和35%的低渗刺激的第一分钟内,细胞内钙水平有短暂的单相增加;暴露于50%的低渗溶液导致细胞内Ca2+振荡。非连接电导变化、Ca2+改变和细胞间偶联的时间进程差异表明,每种反应涉及不同的第二信使途径。在35%的低渗休克后7.5分钟,机械诱发的钙波在星形胶质细胞间传播的速度增加。20%或50%的低渗刺激未观察到这种增加,并且这不能归因于连接电导的增加,因为它被P2嘌呤能受体拮抗剂苏拉明阻断。鉴于细胞肿胀期间激活的转导途径(例如磷脂酶、磷酸激酶、花生四烯酸的产生)对星形胶质细胞缝隙连接有抑制作用(吉奥姆和麦卡锡,1996年),有人提出低渗休克期间连接电导增加是由于通道数量增加,可能由初始Ca2+信号触发(多尔梅奇等人,1997年)。作为偶联增加和Ca2+波细胞外传播增强的功能结果,在低渗应激期间,信号分子在整个胶质网络中的传播预计会显著增强。因此,小鼠星形胶质细胞对低渗挑战的细胞间通讯增加是通过缝隙连接依赖性和非依赖性机制发生的,并且可能在神经系统损伤后提供神经保护作用。