Ureña J, Fernández-Chacón R, Benot A R, Alvarez de Toledo G A, López-Barneo J
Departamento de Fisiología Médica y Biofísica, Universidad de Sevilla, Facultad de Medicina, Spain.
Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):10208-11. doi: 10.1073/pnas.91.21.10208.
We have investigated the changes of cytosolic [Ca2+] and the secretory activity in single glomus cells dispersed from rabbit carotid bodies during exposure to solutions with variable O2 tension (Po2). In normoxic conditions (Po2 = 145 mmHg; 1 mmHg = 133 Pa), intracellular [Ca2+] was 58 +/- 29 nM, and switching to low Po2 (between 10 and 60 mmHg) led to a reversible increase of [Ca2+] up to 800 nM. The response to hypoxia completely disappeared after removal of external Ca2+ or with the addition of 0.2 mM Cd2+ to the external solution. These same solutions also abolished both the Ca2+ current of the cells and the increase of internal [Ca2+] elicited by high external K+. Elevations of cytosolic [Ca2+] in response to hypoxia or to direct membrane depolarization elicited the release of dopamine, which was detected by amperometric techniques. Dopamine secretion occurred in episodes of spike-like activity that appear to represent the release from single secretory vesicles. From the mean charge of well-resolved secretory events, we estimated the average number of dopamine molecules per vesicle to be approximately 140,000, a value about 15 times smaller than a previous estimate in chromaffin granules of adrenomedullary cells. These results directly demonstrate in a single-cell preparation the secretory response of glomus cells to hypoxia. The data indicate that the enhancement of cellular excitability upon exposure to low Po2 results in Ca2+ entry through voltage-gated channels, which leads to an increase in intracellular [Ca2+] and exocytotic transmitter release.
我们研究了从兔颈动脉体分离出的单个球旁细胞在暴露于不同氧张力(Po2)溶液时胞质[Ca2+]的变化和分泌活性。在常氧条件下(Po2 = 145 mmHg;1 mmHg = 133 Pa),细胞内[Ca2+]为58±29 nM,切换到低Po2(10至60 mmHg之间)会导致[Ca2+]可逆性增加至800 nM。去除细胞外Ca2+或在细胞外溶液中添加0.2 mM Cd2+后,对低氧的反应完全消失。这些相同的溶液也消除了细胞的Ca2+电流以及高细胞外K+引起的细胞内[Ca2+]增加。低氧或直接膜去极化引起的胞质[Ca2+]升高引发了多巴胺的释放,这是通过安培技术检测到的。多巴胺分泌以尖峰样活动的形式出现,似乎代表单个分泌囊泡的释放。根据分辨良好的分泌事件的平均电荷,我们估计每个囊泡中多巴胺分子的平均数约为140,000,该值比先前对肾上腺髓质细胞嗜铬颗粒的估计值小约15倍。这些结果在单细胞制备中直接证明了球旁细胞对低氧的分泌反应。数据表明,暴露于低Po2时细胞兴奋性增强导致Ca2+通过电压门控通道进入,从而导致细胞内[Ca2+]增加和递质的胞吐释放。