{"title":"通过介导的外排限制细胞碘离子空间","authors":"G. Salvatore , M. Salvatore , J. Wolff","doi":"10.1016/0926-6585(66)90305-0","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. The movements of I<sup>−</sup> and other anions in Ehrlich ascites tumor cells were studied as a model to explain the restricted anion space of certain cells.</p></span></li><li><span>2.</span><span><p>2. At 38° all the anions tested (I<sup>−</sup>, Br<sup>−</sup>, ReO<sub>4</sub><sup>−</sup>, WO<sub>4</sub><sup>2−</sup>) penetrate only one-quarter of the cell volume. For I<sup>−</sup> this value, constant up to 6 h, is independent of the anion concentration in the medium from less than 1 μM to 0.124 M and is insensitive to anions that inhibit thyroidal I<sup>−</sup> transport competitively.</p></span></li><li><span>3.</span><span><p>3. At 4° the restriction of the I<sup>−</sup> (and Br<sup>−</sup>) compartments (but not that of ReO<sub>4</sub><sup>−</sup> or WO<sub>4</sub><sup>2−</sup>) is abolished and the I<sup>−</sup> space approaches the water content of the cell. Upon exposure of the cold-loaded cells to 38°, a net efflux of the halide is observed until the steady-state value of one-quarter of the cell volume is again attained.</p></span></li><li><span>4.</span><span><p>4. The temperature-dependent efflux of I<sup>−</sup> is sensitive to various metabolic inhibitors, but, in ascites fluid, at a rather high concentration.</p></span></li><li><span>5.</span><span><p>5. Cardiac glycosides and quinidine markedly decrease the ability of ascites cells to restrict the anion space. The same effect is produced by nucleoside triphosphates, particularly ATP, ITP and UTP.</p></span></li><li><span>6.</span><span><p>6. The behavior of I<sup>−</sup> and Na<sup>+</sup> was compared under identical conditions. Although certain similarities exist, a number of differences were noted.</p></span></li><li><span>7.</span><span><p>7. The evidence presented is consistent with the hypothesis that the halide restriction in ascites cells is due to a metabolism-dependent efflux.</p></span></li></ul></div>","PeriodicalId":100158,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis","volume":"120 3","pages":"Pages 383-394"},"PeriodicalIF":0.0000,"publicationDate":"1966-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6585(66)90305-0","citationCount":"6","resultStr":"{\"title\":\"Restriction of cellular iodide space by mediated efflux\",\"authors\":\"G. Salvatore , M. Salvatore , J. Wolff\",\"doi\":\"10.1016/0926-6585(66)90305-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p></p><ul><li><span>1.</span><span><p>1. The movements of I<sup>−</sup> and other anions in Ehrlich ascites tumor cells were studied as a model to explain the restricted anion space of certain cells.</p></span></li><li><span>2.</span><span><p>2. At 38° all the anions tested (I<sup>−</sup>, Br<sup>−</sup>, ReO<sub>4</sub><sup>−</sup>, WO<sub>4</sub><sup>2−</sup>) penetrate only one-quarter of the cell volume. For I<sup>−</sup> this value, constant up to 6 h, is independent of the anion concentration in the medium from less than 1 μM to 0.124 M and is insensitive to anions that inhibit thyroidal I<sup>−</sup> transport competitively.</p></span></li><li><span>3.</span><span><p>3. At 4° the restriction of the I<sup>−</sup> (and Br<sup>−</sup>) compartments (but not that of ReO<sub>4</sub><sup>−</sup> or WO<sub>4</sub><sup>2−</sup>) is abolished and the I<sup>−</sup> space approaches the water content of the cell. Upon exposure of the cold-loaded cells to 38°, a net efflux of the halide is observed until the steady-state value of one-quarter of the cell volume is again attained.</p></span></li><li><span>4.</span><span><p>4. The temperature-dependent efflux of I<sup>−</sup> is sensitive to various metabolic inhibitors, but, in ascites fluid, at a rather high concentration.</p></span></li><li><span>5.</span><span><p>5. Cardiac glycosides and quinidine markedly decrease the ability of ascites cells to restrict the anion space. The same effect is produced by nucleoside triphosphates, particularly ATP, ITP and UTP.</p></span></li><li><span>6.</span><span><p>6. The behavior of I<sup>−</sup> and Na<sup>+</sup> was compared under identical conditions. Although certain similarities exist, a number of differences were noted.</p></span></li><li><span>7.</span><span><p>7. The evidence presented is consistent with the hypothesis that the halide restriction in ascites cells is due to a metabolism-dependent efflux.</p></span></li></ul></div>\",\"PeriodicalId\":100158,\"journal\":{\"name\":\"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis\",\"volume\":\"120 3\",\"pages\":\"Pages 383-394\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1966-07-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6585(66)90305-0\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0926658566903050\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926658566903050","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Restriction of cellular iodide space by mediated efflux
1.
1. The movements of I− and other anions in Ehrlich ascites tumor cells were studied as a model to explain the restricted anion space of certain cells.
2.
2. At 38° all the anions tested (I−, Br−, ReO4−, WO42−) penetrate only one-quarter of the cell volume. For I− this value, constant up to 6 h, is independent of the anion concentration in the medium from less than 1 μM to 0.124 M and is insensitive to anions that inhibit thyroidal I− transport competitively.
3.
3. At 4° the restriction of the I− (and Br−) compartments (but not that of ReO4− or WO42−) is abolished and the I− space approaches the water content of the cell. Upon exposure of the cold-loaded cells to 38°, a net efflux of the halide is observed until the steady-state value of one-quarter of the cell volume is again attained.
4.
4. The temperature-dependent efflux of I− is sensitive to various metabolic inhibitors, but, in ascites fluid, at a rather high concentration.
5.
5. Cardiac glycosides and quinidine markedly decrease the ability of ascites cells to restrict the anion space. The same effect is produced by nucleoside triphosphates, particularly ATP, ITP and UTP.
6.
6. The behavior of I− and Na+ was compared under identical conditions. Although certain similarities exist, a number of differences were noted.
7.
7. The evidence presented is consistent with the hypothesis that the halide restriction in ascites cells is due to a metabolism-dependent efflux.