Coordinate interactions of cyclic nucleotide and phospholipid metabolizing pathways in calcium-dependent cellular processes.

S G Laychock
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引用次数: 19

Abstract

It is hoped that his review enables the reader to appreciate the complexities implicit in the interactions among Ca2+, cyclic nucleotides, and phospholipid-metabolizing pathways in cell signal transduction. The interactions are varied and intricate, often involving several levels of cell amplification mechanisms. Upsetting the balance of fatty acids in membrane phospholipids can have detrimental effects on adenylate cyclase. Thus, n - 3 fatty acid enrichment of phospholipids suppresses adenylate cyclase activity. The effects of significant alterations in dietary fatty acids, such as might occur with the current vogue for n - 3 eicosapentaenoic acid and docosahexaenoic acid (fish oil) dietary enrichment regimens, will need to be assessed more fully with regard to stimulus-induced changes in cyclic nucleotide production in various tissues. Since the n - 3 fatty acids have not been demonstrated to affect guanylate cyclase activity, dietary changes in certain of these fatty acids would not be expected to contribute to changes in cGMP generation as much as in cAMP production. Moreover, the ingestion of large quantities of these n - 3 fatty acids can alter the profile of cyclooxygenase and lipoxygenase products produced in cells. According to the paradigm developed in this article, changes in the metabolism of fatty acids are amplified by alterations in cyclic nucleotide production and phospholipase activities, with the eventual physiological impact predicated on the tissue type and the specific stimulus response. There appears to be a rather clear distinction between the regulatory properties of eicosanoids regarding adenylate and guanylate cyclase activities. Whereas prostaglandins often stimulate adenylate cyclase activity, they have little effect on guanylate cyclase activity. On the other hand, the HETE compounds seem to play an important role in guanylate cyclase regulation in certain cells. Moreover, arachidonic acid affects adenylate cyclase activity without prior peroxidation, whereas endoperoxides and hydroperoxides are more effective than arachidonic acid with regard to guanylate cyclase stimulation. However, in the intact cell there is a strong implication that the dual stimulation of guanylate cyclase by Ca2+ and fatty acid evokes optimal enzyme activity. An advantage of multidimensional response mechanisms in cells includes the ability to recognize different stimuli and to respond with specific, coordinated responses modulated in their intensity and/or duration by messenger interaction. Few cell types respond to receptor stimulation in an all-or-none fashion, and the "milieu interior" depends on specific, graded responses to the autonomic nervous system and endocrine stimuli.(ABSTRACT TRUNCATED AT 400 WORDS)

钙依赖性细胞过程中环核苷酸和磷脂代谢途径的协调相互作用。
希望他的评论能使读者理解细胞信号转导中Ca2+、环核苷酸和磷脂代谢途径之间相互作用的复杂性。相互作用是多样而复杂的,通常涉及几个层次的细胞扩增机制。破坏膜磷脂中脂肪酸的平衡会对腺苷酸环化酶产生不利影响。因此,磷脂的n - 3脂肪酸富集抑制腺苷酸环化酶活性。饮食脂肪酸显著改变的影响,例如当前流行的n - 3二十碳五烯酸和二十二碳六烯酸(鱼油)饮食富集方案,将需要更充分地评估刺激诱导的各种组织中环核苷酸产生的变化。由于n - 3脂肪酸尚未被证明会影响鸟苷酸环化酶的活性,因此饮食中某些脂肪酸的变化不会像影响cAMP的产生那样影响cGMP的产生。此外,大量摄入这些n - 3脂肪酸可以改变细胞中产生的环加氧酶和脂加氧酶产物的谱。根据本文发展的范式,脂肪酸代谢的变化被环核苷酸产生和磷脂酶活性的改变放大,最终的生理影响取决于组织类型和特定刺激反应。二十烷类化合物对腺苷酸和鸟苷酸环化酶活性的调控特性似乎有相当明显的区别。然而前列腺素经常刺激腺苷酸环化酶的活性,它们对鸟苷酸环化酶的活性几乎没有影响。另一方面,HETE化合物似乎在某些细胞的鸟苷酸环化酶调节中起重要作用。此外,花生四烯酸在没有事先过氧化的情况下影响腺苷酸环化酶的活性,而在刺激鸟苷酸环化酶方面,内过氧化物和氢过氧化物比花生四烯酸更有效。然而,在完整的细胞中,Ca2+和脂肪酸对鸟苷酸环化酶的双重刺激产生了最佳的酶活性。细胞中多维反应机制的一个优势包括能够识别不同的刺激,并通过信使相互作用调节其强度和/或持续时间,以特定的、协调的反应作出反应。很少有细胞类型会对受体刺激做出全有或全无的反应,而“环境内部”取决于对自主神经系统和内分泌刺激的特定、分级反应。(摘要删节为400字)
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