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细胞内游离钙增加会诱导离体耳蜗外毛细胞发生周向收缩。

Increasing intracellular free calcium induces circumferential contractions in isolated cochlear outer hair cells.

作者信息

Dulon D, Zajic G, Schacht J

机构信息

Kresge Hearing Research Institute, University of Michigan, Ann Arbor 48109.

出版信息

J Neurosci. 1990 Apr;10(4):1388-97. doi: 10.1523/JNEUROSCI.10-04-01388.1990.

Abstract

The relationship between intracellular free calcium and the motile responses of outer hair cells isolated from the guinea pig cochlea was examined. Calcium levels were modulated by the addition of the calcium ionophores ionomycin or A23187 to the incubation medium and monitored with the fluorescent calcium indicator fluo-3. In the presence of 1.25 mM external calcium, the application of either ionophore (10 microM) led to an increase in intracellular free calcium from 157 +/- 76 nM to 1200 +/- 500 nM within 30-60 sec. Concurrently, cells elongated by 1-2 microns, cell diameter decreased, and cell volume shrank by 269 +/- 220 microns 3 (5.0 +/- 4.1%). The reduction in diameter was most pronounced in the middle portion of the cell (4.4% +/- 4.2%), also evident in the apical region (3.1% +/- 4.8%) but not significant in the basal region near the nucleus. This response was observed in outer hair cells from basal and apical turns of the cochlea and was reversed when the cells were rinsed with calcium-free medium supplemented with 2 mM EGTA. Optical imaging of the cell membrane with the potentiometric dye 1-(3-sulfonatopropyl)-4-[beta] [2-(di-n-butylaminol)-6-naphthyl vinyl] pyridinium betaine during the elevation of intracellular calcium demonstrated features of contractility at the lateral cell membrane. A rise in intracellular calcium as well as the motile response was still observed after a 5-min exposure of the cells to a calcium-free solution (supplemented with 2 mM EGTA), indicating that the ionophore was also able to liberate calcium from intracellular sites. However, depletion of calcium stores through prolonged incubation of the cells in calcium-free medium (30-60 min) suppressed both the calcium signal and the cell response. The calmodulin inhibitors trifluoperazine and pimozide (30 microM) blocked the cell motility induced by ionomycin while they left the increase of intracellular calcium unaffected. These observations suggest that calcium-dependent circumferential contractions in outer hair cells are mediated by calmodulin. The application to the extracellular medium of putative neurotransmitters of the cochlear efferent system such as acetylcholine and GABA led to neither an increase in intracellular calcium nor a modification of cell shape. Therefore, these neurotransmitters may not be directly involved in calcium-induced contractions in outer hair cells. The circumferential contractions altered the stiffness of the plasma membrane and the turgor of the cell. Under normal conditions, changes in cell volume were inversely proportional to the osmotic pressure of the extracellular medium following van't Hoff's law.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

研究了豚鼠耳蜗分离出的外毛细胞内游离钙与运动反应之间的关系。通过向孵育培养基中添加钙离子载体离子霉素或A23187来调节钙水平,并用荧光钙指示剂Fluo-3进行监测。在存在1.25 mM细胞外钙的情况下,施加任何一种离子载体(10 μM)都会导致细胞内游离钙在30 - 60秒内从157±76 nM增加到1200±500 nM。同时,细胞伸长1 - 2微米,细胞直径减小,细胞体积缩小269±220立方微米(5.0±4.1%)。直径的减小在细胞中部最为明显(4.4%±4.2%),在顶端区域也很明显(3.1%±4.8%),但在靠近细胞核的基部区域不显著。在耳蜗基部和顶端转弯处的外毛细胞中都观察到了这种反应,当用补充有2 mM EGTA的无钙培养基冲洗细胞时,反应逆转。在用电位染料1 -(3 - 磺丙基)- 4 - [β] [2 -(二正丁氨基)- 6 - 萘基乙烯基]吡啶鎓甜菜碱对细胞膜进行光学成像时,在细胞内钙升高期间显示出侧细胞膜的收缩特征。在细胞暴露于无钙溶液(补充有2 mM EGTA)5分钟后,仍观察到细胞内钙的升高以及运动反应,这表明离子载体也能够从细胞内位点释放钙。然而,通过在无钙培养基中长时间孵育细胞(30 - 60分钟)耗尽钙储存会抑制钙信号和细胞反应。钙调蛋白抑制剂三氟拉嗪和匹莫齐特(30 μM)阻断了离子霉素诱导的细胞运动,而不影响细胞内钙的增加。这些观察结果表明,外毛细胞中钙依赖性的周向收缩是由钙调蛋白介导的。向细胞外培养基中施加耳蜗传出系统的假定神经递质,如乙酰胆碱和GABA,既不会导致细胞内钙增加,也不会改变细胞形状。因此,这些神经递质可能不直接参与外毛细胞中钙诱导的收缩。周向收缩改变了质膜的硬度和细胞的膨压。在正常条件下,细胞体积的变化与细胞外培养基的渗透压成反比,符合范特霍夫定律。(摘要截于400字)

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