Joana Poejo , Nadiia I. Gumerova , Annette Rompel , Ana M. Mata , Manuel Aureliano , Carlos Gutierrez-Merino
{"title":"揭示 Preyssler 型多氧钨酸盐对嘌呤能 P2 受体的激动特性","authors":"Joana Poejo , Nadiia I. Gumerova , Annette Rompel , Ana M. Mata , Manuel Aureliano , Carlos Gutierrez-Merino","doi":"10.1016/j.jinorgbio.2024.112640","DOIUrl":null,"url":null,"abstract":"<div><p>The Preyssler-type polyoxotungstate ({P<sub>5</sub>W<sub>30</sub>}) belongs to the family of polyanionic metal-oxides formed by group V and VI metal ions, such as V, Mo and W, commonly known as polyoxometalates (POMs). POMs have demonstrated inhibitory effect on a significant number of ATP-binding proteins <em>in vitro</em>. Purinergic P2 receptors, widely expressed in eukaryotic cells, contain extracellularly oriented ATP-binding sites and play many biological roles with health implications. In this work, we use the immortalized mouse hippocampal neuronal HT-22 cells in culture to study the effects of {P<sub>5</sub>W<sub>30</sub>} on the cytosolic Ca<sup>2+</sup> concentration. Changes in cytosolic Ca<sup>2+</sup> concentration were monitored using fluorescence microscopy of HT-22 cells loaded with the fluorescent Ca<sup>2+</sup> indicator Fluo3. <sup>31</sup>P-Nuclear magnetic resonance measurements of {P<sub>5</sub>W<sub>30</sub>} indicate its stability in the medium used for cytosolic Ca<sup>2+</sup> measurements for over 30 min. The findings reveal that addition of {P<sub>5</sub>W<sub>30</sub>} to the extracellular medium induces a sustained increase of the cytosolic Ca<sup>2+</sup> concentration within minutes. This Ca<sup>2+</sup> increase is triggered by extracellular Ca<sup>2+</sup> entry into the cells and is dose-dependent, with a half-of-effect concentration of 0.25 ± 0.05 μM {P<sub>5</sub>W<sub>30</sub>}. In addition, after the {P<sub>5</sub>W<sub>30</sub>}-induced cytosolic Ca<sup>2+</sup> increase, the transient Ca<sup>2+</sup> peak induced by extracellular ATP is reduced up to 100% with an apparent half-of-effect concentration of 0.15 ± 0.05 μM {P<sub>5</sub>W<sub>30</sub>}. Activation of metabotropic purinergic P2 receptors affords about 80% contribution to the increase of Fluo3 fluorescence elicited by {P<sub>5</sub>W<sub>30</sub>} in HT-22 cells, whereas ionotropic receptors contribute, at most, with 20%. These results suggest that {P<sub>5</sub>W<sub>30</sub>} could serve as a novel agonist of purinergic P2 receptors.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling the agonistic properties of Preyssler-type Polyoxotungstates on purinergic P2 receptors\",\"authors\":\"Joana Poejo , Nadiia I. Gumerova , Annette Rompel , Ana M. Mata , Manuel Aureliano , Carlos Gutierrez-Merino\",\"doi\":\"10.1016/j.jinorgbio.2024.112640\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The Preyssler-type polyoxotungstate ({P<sub>5</sub>W<sub>30</sub>}) belongs to the family of polyanionic metal-oxides formed by group V and VI metal ions, such as V, Mo and W, commonly known as polyoxometalates (POMs). POMs have demonstrated inhibitory effect on a significant number of ATP-binding proteins <em>in vitro</em>. Purinergic P2 receptors, widely expressed in eukaryotic cells, contain extracellularly oriented ATP-binding sites and play many biological roles with health implications. In this work, we use the immortalized mouse hippocampal neuronal HT-22 cells in culture to study the effects of {P<sub>5</sub>W<sub>30</sub>} on the cytosolic Ca<sup>2+</sup> concentration. Changes in cytosolic Ca<sup>2+</sup> concentration were monitored using fluorescence microscopy of HT-22 cells loaded with the fluorescent Ca<sup>2+</sup> indicator Fluo3. <sup>31</sup>P-Nuclear magnetic resonance measurements of {P<sub>5</sub>W<sub>30</sub>} indicate its stability in the medium used for cytosolic Ca<sup>2+</sup> measurements for over 30 min. The findings reveal that addition of {P<sub>5</sub>W<sub>30</sub>} to the extracellular medium induces a sustained increase of the cytosolic Ca<sup>2+</sup> concentration within minutes. This Ca<sup>2+</sup> increase is triggered by extracellular Ca<sup>2+</sup> entry into the cells and is dose-dependent, with a half-of-effect concentration of 0.25 ± 0.05 μM {P<sub>5</sub>W<sub>30</sub>}. In addition, after the {P<sub>5</sub>W<sub>30</sub>}-induced cytosolic Ca<sup>2+</sup> increase, the transient Ca<sup>2+</sup> peak induced by extracellular ATP is reduced up to 100% with an apparent half-of-effect concentration of 0.15 ± 0.05 μM {P<sub>5</sub>W<sub>30</sub>}. Activation of metabotropic purinergic P2 receptors affords about 80% contribution to the increase of Fluo3 fluorescence elicited by {P<sub>5</sub>W<sub>30</sub>} in HT-22 cells, whereas ionotropic receptors contribute, at most, with 20%. These results suggest that {P<sub>5</sub>W<sub>30</sub>} could serve as a novel agonist of purinergic P2 receptors.</p></div>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-06-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0162013424001648\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0162013424001648","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
Unveiling the agonistic properties of Preyssler-type Polyoxotungstates on purinergic P2 receptors
The Preyssler-type polyoxotungstate ({P5W30}) belongs to the family of polyanionic metal-oxides formed by group V and VI metal ions, such as V, Mo and W, commonly known as polyoxometalates (POMs). POMs have demonstrated inhibitory effect on a significant number of ATP-binding proteins in vitro. Purinergic P2 receptors, widely expressed in eukaryotic cells, contain extracellularly oriented ATP-binding sites and play many biological roles with health implications. In this work, we use the immortalized mouse hippocampal neuronal HT-22 cells in culture to study the effects of {P5W30} on the cytosolic Ca2+ concentration. Changes in cytosolic Ca2+ concentration were monitored using fluorescence microscopy of HT-22 cells loaded with the fluorescent Ca2+ indicator Fluo3. 31P-Nuclear magnetic resonance measurements of {P5W30} indicate its stability in the medium used for cytosolic Ca2+ measurements for over 30 min. The findings reveal that addition of {P5W30} to the extracellular medium induces a sustained increase of the cytosolic Ca2+ concentration within minutes. This Ca2+ increase is triggered by extracellular Ca2+ entry into the cells and is dose-dependent, with a half-of-effect concentration of 0.25 ± 0.05 μM {P5W30}. In addition, after the {P5W30}-induced cytosolic Ca2+ increase, the transient Ca2+ peak induced by extracellular ATP is reduced up to 100% with an apparent half-of-effect concentration of 0.15 ± 0.05 μM {P5W30}. Activation of metabotropic purinergic P2 receptors affords about 80% contribution to the increase of Fluo3 fluorescence elicited by {P5W30} in HT-22 cells, whereas ionotropic receptors contribute, at most, with 20%. These results suggest that {P5W30} could serve as a novel agonist of purinergic P2 receptors.