Akabas M H
Department of Medicine, College of Physicians & Surgeons, Columbia University, New York, New York 10032.
Int Rev Neurobiol. 1990;32:241-79. doi: 10.1016/s0074-7742(08)60585-1.
The application of new techniques to the study of taste cells has revealed much about both the basic physiology of these cells and also about the mechanisms of taste transduction. The taste cells are electrically excitable cells with a variety of voltage-dependent ion currents. These ionic currents have an important role in the transduction of salt taste in mammals and frogs. In mudpuppies different ion channels are involved in the transduction of acidic-sour stimuli. The role of ion currents in the transduction of sweet taste is less clear. Some proposed mechanisms suggest an important role for ion currents and others suggest that the transduction process may be a biochemical event involving cell surface receptors and intracellular second messengers, possibly cAMP. The transduction of bitter taste seems to be a biochemical event involving cell surface receptors and intracellular second messengers in the inositol trisphosphate pathway. Thus, one cannot talk about "the mechanism" of taste transduction. Different taste modalities are transduced by different mechanisms. A corollary to this is that taste cells are not a homogeneous population of cells. In order to provide animals with the ability to discriminate between different taste modalities the taste cells consist of distinct subpopulations of cells based on their primary taste modality. The primary taste modality in a given cell is determined by the receptors and transduction mechanism(s) expressed in that cell. Evidence suggests that modality-specific receptors are expressed in a segregated manner in distinct subpopulations of taste cells. Secondary responses observed in gustatory axons may arise due to a lack of absolute specificity in the transduction processes and nonspecific effects of low pH and high ionic strength and osmolarity on the taste cells. An interesting area for future work will be to elucidate the mechanism(s) by which basal cells become committed to a given taste modality and how the gustatory neurons influence this process of differentiation. The involvement of the gustatory neurons is critical as they must synapse with taste cells of the correct taste modality to preserve the integrity of the information transferred to the CNS. This process of synaptogenesis is presumably mediated by the expression of taste-modality-specific, cell surface antigens on the basolateral domain of a taste cell and receptors on the appropriate neurons, but much work will be necessary to elucidate this process.(ABSTRACT TRUNCATED AT 400 WORDS)
将新技术应用于味觉细胞研究,已揭示了许多有关这些细胞的基本生理学以及味觉转导机制的信息。味觉细胞是具有多种电压依赖性离子电流的电兴奋性细胞。这些离子电流在哺乳动物和青蛙的盐味转导中起重要作用。在泥螈中,不同的离子通道参与酸 - 酸味刺激的转导。离子电流在甜味转导中的作用尚不清楚。一些提出的机制表明离子电流起重要作用,而另一些则表明转导过程可能是涉及细胞表面受体和细胞内第二信使(可能是环磷酸腺苷)的生化事件。苦味转导似乎是涉及细胞表面受体和肌醇三磷酸途径中细胞内第二信使的生化事件。因此,不能简单地谈论味觉转导的“机制”。不同的味觉模式通过不同的机制进行转导。由此得出的一个推论是,味觉细胞不是同质的细胞群体。为了使动物能够区分不同的味觉模式,味觉细胞根据其主要味觉模式由不同的细胞亚群组成。给定细胞中的主要味觉模式由该细胞中表达的受体和转导机制决定。有证据表明,模式特异性受体以分离的方式在不同亚群的味觉细胞中表达。在味觉轴突中观察到的次级反应可能是由于转导过程中缺乏绝对特异性以及低pH值、高离子强度和渗透压对味觉细胞的非特异性影响所致。未来研究的一个有趣领域将是阐明基底细胞如何确定为给定的味觉模式,以及味觉神经元如何影响这一分化过程。味觉神经元的参与至关重要,因为它们必须与正确味觉模式的味觉细胞形成突触,以保持传递到中枢神经系统的信息的完整性。这种突触形成过程大概是由味觉细胞基底外侧区域上味觉模式特异性细胞表面抗原和适当神经元上的受体的表达介导的,但要阐明这一过程还需要做很多工作。(摘要截选至400字)