Halachmi D, Eilam Y
Department of Bacteriology, Hebrew University, Hadassah Medical School, Jerusalem, Israel.
FEBS Lett. 1993 Jan 18;316(1):73-8. doi: 10.1016/0014-5793(93)81739-m.
Cytosolic Ca2+ concentrations ([Ca2+]i) were determined in haploid and diploid cells of Saccharomyces cerevisiae, loaded with indo-1 and exposed to media containing a range of Ca2+ concentrations. [Ca2+]i homeostasis was maintained at the 100-150 nM level in cells which were pre-incubated with glucose and exposed to 0.1 microM-10 mM Ca2+ in the medium. Slightly higher levels of [Ca2+]i were determined in cells exposed to 50 mM Ca2+. Pre-incubation with metabolic inhibitors instead of glucose caused a reduction in cellular ATP levels and an impaired [Ca2+]i homeostasis; [Ca2+]i reached 800 nM in cells exposed to 10 mM CaCl2. Cells of the delta vma4 mutant strain, with no functional vacuolar H(+)-ATPase, had elevated levels of [Ca2+]i, reaching 1.8 microM when pre-incubated with glucose and exposed to 10 mM CaCl2. Higher levels of [Ca2+]i were measured in the mutant cells which were pre-incubated with metabolic inhibitors. This result indicates the central role of the vacuoles in maintaining [Ca2+]i-homeostasis and suggests the presence of an additional non-vacuolar ATP-requiring mechanism which contributes to keeping [Ca2+]i at low levels.
测定了酿酒酵母单倍体和二倍体细胞中的胞质钙离子浓度([Ca2+]i),这些细胞加载了indo-1并暴露于含有一系列钙离子浓度的培养基中。在预先用葡萄糖孵育并暴露于培养基中0.1微摩尔/升 - 10毫摩尔/升钙离子的细胞中,[Ca2+]i稳态维持在100 - 150纳摩尔水平。暴露于50毫摩尔/升钙离子的细胞中测定的[Ca2+]i水平略高。用代谢抑制剂而非葡萄糖进行预孵育导致细胞ATP水平降低以及[Ca2+]i稳态受损;暴露于10毫摩尔/升氯化钙的细胞中[Ca2+]i达到800纳摩尔。缺乏功能性液泡H(+)-ATP酶的δvma4突变株细胞的[Ca2+]i水平升高,在用葡萄糖预孵育并暴露于10毫摩尔/升氯化钙时达到1.8微摩尔。在用代谢抑制剂预孵育的突变细胞中测得更高水平的[Ca2+]i。这一结果表明液泡在维持[Ca2+]i稳态中起核心作用,并提示存在一种额外的非液泡需ATP机制,该机制有助于将[Ca2+]i维持在低水平。