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钙在莱茵衣藻交配反应中的作用。

The role of calcium in the Chlamydomonas reinhardtii mating reaction.

作者信息

Goodenough U W, Shames B, Small L, Saito T, Crain R C, Sanders M A, Salisbury J L

机构信息

Department of Biology, Washington University, St. Louis, Missouri 63130.

出版信息

J Cell Biol. 1993 Apr;121(2):365-74. doi: 10.1083/jcb.121.2.365.

Abstract

The mating reaction of Chlamydomonas reinhardtii entails a rapid series of cell-cell interactions leading to cell fusion. We have demonstrated (Pasquale, S. M., and U. Goodenough. 1987. J. Cell Biol. 105:2279-2293) that cAMP plays a key role in this process: gametic flagellar adhesion elicits a sharp increase in intracellular cAMP, and presentation of dibutyryl-cAMP to unmated gametes elicits all known mating responses. The present study evaluates the role of Ca2+ in this system. We document that the mating-induced increase in cAMP, and hence the mating responses themselves, are blocked by a variety of drugs known to interfere with Ca(2+)-sensitive processes. These data suggest that Ca(2+)-mediated events may couple adhesion to the generation of cAMP. Such events, however, appear to be localized to the flagellar membrane; we find no evidence for the mating-related increase in cytosolic free Ca2+ that has been postulated by others. Indeed, by monitoring the length of the Ca(2+)-sensitive centrin-containing nucleus-basal body connector, we show that cytosolic free Ca2+ levels, if anything, decrease in response to cAMP signaling. We confirm a previous report that Ca2+ levels increase in the mating medium, but document that this represents a response to augmented cAMP levels and not a prelude. Finally, we show that IP3 levels remain constant throughout the mating reaction. These results are discussed in terms of the various signal transduction systems that have now been identified in Chlamydomonas.

摘要

莱茵衣藻的交配反应涉及一系列快速的细胞间相互作用,最终导致细胞融合。我们已经证明(帕斯夸莱,S.M.,和U.古德诺夫。1987年。《细胞生物学杂志》105:2279 - 2293),环磷酸腺苷(cAMP)在这一过程中起关键作用:配子鞭毛粘附引发细胞内cAMP急剧增加,向未交配的配子提供二丁酰环磷腺苷(dibutyryl-cAMP)会引发所有已知的交配反应。本研究评估了钙离子(Ca2+)在该系统中的作用。我们记录到,已知干扰Ca(2+)敏感过程的多种药物会阻断交配诱导的cAMP增加,进而阻断交配反应本身。这些数据表明,Ca(2+)介导的事件可能将粘附与cAMP的产生联系起来。然而,此类事件似乎局限于鞭毛膜;我们没有发现其他人所假设的与交配相关的胞质游离Ca2+增加的证据。事实上,通过监测对Ca(2+)敏感的含中心蛋白的核-基体连接体的长度,我们发现,胞质游离Ca2+水平如果有变化的话,是对cAMP信号作出反应而降低。我们证实了之前的一份报告,即交配培养基中Ca2+水平会升高,但记录表明这是对升高的cAMP水平的反应,而非前奏。最后,我们表明在整个交配反应过程中肌醇三磷酸(IP3)水平保持恒定。我们根据目前在衣藻中已确定的各种信号转导系统对这些结果进行了讨论。

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