La Claire J W
Exp Cell Res. 1983 Apr 15;145(1):63-9. doi: 10.1016/s0014-4827(83)80008-1.
The cytoplasm (with its organelles) of intact cells of Ernodesmis verticillata (Chlorophyta) can be induced to contract in the presence of calcium ionophores and phenothiazine antipsychotics. The cell contents mimic wound-healing contraction if a combination of 10 microM A23187 and 10 microM chlorpromazine (or trifluoperazine) is present in a Ca2+-containing medium. The average incubation time is approx. 50 min for contraction. It is imperative that only fresh solutions of ionophores and phenothiazines are used, because stock solutions only 3 h old virtually double the response time of these cells. Separately, neither the ionophore nor the phenothiazines will induce contraction. The addition of 1.0 mM La3+ completely prevents induction of motility. With trifluoperazine, equimolar X-537A will substitute for A23187, but it takes three times as long to induce contraction. Motility cannot be induced in Ca2+-free media (containing 5.0 mM EGTA). It therefore appears that Ca2+ fluxes are responsible for triggering wound contraction in these giant algal cells. An influx of calcium ions from the external medium is suggested as being at least partially involved.
在钙离子载体和吩噻嗪类抗精神病药物存在的情况下,轮状扁藻(绿藻门)完整细胞的细胞质(及其细胞器)可被诱导收缩。如果在含钙培养基中存在10微摩尔A23187和10微摩尔氯丙嗪(或三氟拉嗪)的组合,细胞内容物会模拟伤口愈合收缩。收缩的平均孵育时间约为50分钟。必须仅使用离子载体和吩噻嗪的新鲜溶液,因为仅3小时的储备溶液实际上会使这些细胞的反应时间加倍。单独使用时,离子载体或吩噻嗪都不会诱导收缩。添加1.0毫摩尔La3+可完全阻止运动性的诱导。对于三氟拉嗪,等摩尔的X-537A可替代A23187,但诱导收缩所需的时间是其三倍。在无钙培养基(含有5.0毫摩尔乙二醇双(2-氨基乙基醚)四乙酸)中不能诱导运动性。因此,似乎钙离子通量负责触发这些大型藻类细胞的伤口收缩。有人认为,至少部分涉及从外部介质中流入钙离子。