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第二信使系统对受体相互作用和激活的竞争:对组织特异性反应和疾病治疗的影响。

Competition by second messenger systems for receptor interaction and activation: implications for tissue-specific responses and disease therapy.

作者信息

Crouch M F, Frew I J, Simson L, Davy D A

机构信息

Molecular Signalling Group, John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1997 Aug;24(8):632-8. doi: 10.1111/j.1440-1681.1997.tb02104.x.

DOI:10.1111/j.1440-1681.1997.tb02104.x
PMID:9269540
Abstract
  1. At any one instant, most receptors are now recognized to be able to stimulate multiple signal transduction pathways in a cell when activated by an appropriate hormone. These different signalling pathways appear to allow for distinct cellular responses, such as cell proliferation, differentiation, and shape change. 2. In addition, many different types of cell will possess the same type of receptor. Therefore, for a hormone to be able to transmit differential signals to the various cell types able to respond to it, cells must discriminate the stimulus at some point. Such discrimination would seem to be an absolute requirement to allow a tissue-specific response to an identical initial stimulus. In theory, this specificity could occur at many points in the receptor signal transduction cascade, including cytosolic receptor coupling systems and tissue/cell-specific responsive genes. 3. The present paper summarizes our work and that of others which has determined some of the coupling systems of G-protein-coupled receptors and tyrosine kinase receptors and how these systems may be interacting. 4. In addition to these theoretical considerations, a potential therapeutic strategy underlies the ability of receptors to couple to more than one signal transduction system. If a response to a hormone were, for example, either cell proliferation or cell morphological change or differentiation and separate receptor-coupled signalling systems were responsible for these effects, pharmacological intervention may allow the transfer from one signalling system to another. If such a change allowed a permanent change to the differentiated phenotype, this could potentially form the basis of a signal-based cancer therapy.
摘要
  1. 现在人们认识到,在任何一个时刻,大多数受体在被适当的激素激活时,都能够在细胞内刺激多种信号转导途径。这些不同的信号通路似乎能引发不同的细胞反应,如细胞增殖、分化和形态改变。2. 此外,许多不同类型的细胞会拥有相同类型的受体。因此,一种激素若要能够向能够对其作出反应的各种细胞类型传递不同的信号,细胞必须在某个环节对刺激进行区分。这种区分似乎是对相同初始刺激产生组织特异性反应的绝对必要条件。理论上,这种特异性可能发生在受体信号转导级联反应的许多环节,包括胞质受体偶联系统和组织/细胞特异性反应基因。3. 本文总结了我们和其他人的工作,这些工作确定了一些G蛋白偶联受体和酪氨酸激酶受体的偶联系统,以及这些系统可能是如何相互作用的。4. 除了这些理论上的考虑之外,受体能够与不止一个信号转导系统偶联这一特性还潜在地构成了一种治疗策略的基础。例如,如果对一种激素的反应是细胞增殖、细胞形态改变或分化,且不同的受体偶联信号系统分别负责这些效应,那么药物干预可能会实现从一种信号系统向另一种信号系统的转变。如果这种转变能使细胞表型发生永久性改变,那么这可能会成为一种基于信号的癌症治疗方法的基础。

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