The Guanosine-Adenosine Mechanism

鸟苷-腺苷机制

• 批准号: 8499412
• 负责人: EDWIN Kerry JACKSON
• 金额: $ 36.3万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-07-01 至 2016-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8499412
• 关键词: Adenosine; Biological; Biological Models; Blood Vessels; Blushing; Brain; Cell Surface Receptors; Cell physiology; Cells; Cellular Stress; Cyclic AMP; Cyclic GMP; Data; Enzymes; Evolution; Guanine; Guanosine; Heart; High Pressure Liquid Chromatography; Immune system; Injury; Kidney Diseases; Lung; Measures; Mediating; Metabolism; Physiological; Physiological Processes; Play; Purines; Role; Smooth Muscle Myocytes; Stress; Testing; Tissues; Vasodilation; analog; cell type; extracellular; in vivo; kidney cell; liquid chromatography mass spectrometry; purine; receptor; research study; response; response to injury; uptake

DESCRIPTION (provided by applicant): Adenosine and guanosine are naturally-occurring and structurally similar purines. Moreover, naturally- occurring cyclic analogues of adenosine and guanosine are involved in similar physiological processes (e.g., both cAMP and cGMP mediate vasodilation). Strangely, at first blush it would seem that evolution broke the symmetry between adenosine and guanosine by bestowing cells with adenosine, but not guanosine, receptors. Thus the standard view is that adenosine serves as a physiological regulator of cellular function via activation of its own cell-surface receptors, while guanosine is merely an idle bystander. The purpose of this application is to challenge this received view by proposing that guanosine also plays an important role in cellular physiology, not via its own receptors but rather by engaging a powerful collaborative mechanism involving adenosine. In this regard, we hypothesize that extracellular guanosine is THE major physiological determinant of extracellular levels of adenosine because guanosine blocks the disposition of adenosine from the extracellular compartment allowing greater activation of adenosine cell-surface receptors due to increased extracellular adenosine levels. We refer to this guanosine-adenosine interaction as the GUANOSINE- ADENOSINE MECHANISM. Our pilot experiments strongly suggest that our hypothesis is correct. In preglomerular vascular smooth muscle cells (a model system for microvascular smooth muscle cells) we observe that for any given amount of adenosine added to cells, the extracellular concentrations of adenosine [as measured by high performance liquid chromatography-mass spectrometry (LC-MS/MS)] are more than 10- fold higher when guanosine is also added to the cells. We also find that cellular stress/injury increases extracellular levels of BOTH guanosine and adenosine. Moreover, we find that guanosine PROFOUNDLY augments the biological effects of adenosine in vivo! These findings suggest that extracellular guanosine, by blocking the disposition of extracellular adenosine, is the most important physiological determinant of extracellular levels of adenosine yet discovered. We propose to test the existence of, the mechanism of and the importance of the Guanosine-Adenosine Mechanism with the following six Specific Aims: Aim 1 - To determine the existence of the Guanosine-Adenosine Mechanism in vascular and renal cell types; Aim 2 - To determine whether the Guanosine-Adenosine Mechanism is mediated directly by guanosine or indirectly by conversion of guanosine to guanine; Aim 3 - To determine whether the Guanosine-Adenosine Mechanism involves inhibition by guanosine of enzymes involved in adenosine metabolism; Aim 4 - To determine whether the Guanosine-Adenosine Mechanism involves inhibition by guanosine of transporters involved in adenosine uptake; Aim 5 - To determine whether the Guanosine-Adenosine Mechanism importantly contributes to elevated extracellular levels of adenosine following cellular stress with energy depletion; and Aim 6 - To determine whether the Guanosine-Adenosine Mechanism amplifies the effects of adenosine in vivo.

描述（由申请人提供）：腺苷和鸟苷是天然存在的结构相似的嘌呤。此外，腺苷和鸟苷的天然环状类似物也参与类似的生理过程（例如，cAMP和cGMP都介导血管舒张）。奇怪的是，乍一看，进化似乎通过赋予细胞腺苷受体而不是鸟苷受体而打破了腺苷和鸟苷之间的对称性。因此，标准的观点是腺苷通过激活其自身的细胞表面受体作为细胞功能的生理调节剂，而鸟苷仅仅是一个无所事事的旁观者。本应用的目的是通过提出鸟苷在细胞生理学中也发挥重要作用，而不是通过其自身的受体，而是通过涉及腺苷的强大协作机制来挑战这一公认的观点。在这方面，我们假设胞外鸟苷是胞外腺苷水平的主要生理决定因素，因为鸟苷阻断了腺苷从胞外腔室的处置，允许由于胞外腺苷水平增加而使腺苷细胞表面受体更大的活化。我们把这种鸟苷-腺苷相互作用称为鸟苷-腺苷机制。我们的初步实验有力地表明我们的假设是正确的。在肾小球前血管平滑肌细胞（微血管平滑肌细胞的模型系统）中，我们观察到，对于任何给定量的腺苷添加到细胞中，当鸟苷也添加到细胞中时，腺苷的细胞外浓度[通过高效液相色谱-质谱（LC-MS/MS）测量]高出10倍以上。我们还发现细胞应激/损伤增加了鸟苷和腺苷的细胞外水平。此外，我们发现鸟苷在体内极大地增强了腺苷的生物学效应！这些发现表明，胞外鸟苷通过阻断胞外腺苷的处置，是目前发现的胞外腺苷水平的最重要的生理决定因素。我们提出以下六个具体目的来检验鸟苷-腺苷机制的存在、机制和重要性：目的1 -确定鸟苷-腺苷机制在血管和肾细胞类型中的存在；目的2 -确定鸟苷-腺苷机制是由鸟苷直接介导还是通过鸟苷转化为鸟嘌呤间接介导；目的3 -确定鸟苷-腺苷机制是否涉及鸟苷对参与腺苷代谢的酶的抑制；目的4 -确定鸟苷-腺苷机制是否涉及鸟苷对参与腺苷摄取的转运蛋白的抑制；目的5 -确定鸟苷-腺苷机制是否对能量耗竭的细胞应激后细胞外腺苷水平升高起重要作用；目的6 -确定鸟苷-腺苷机制是否在体内放大了腺苷的作用。