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Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes
Total calcium content, determined by atomic absorption spectroscopy, Ca2+ influx, and cytosolic free Ca2+ concentration ([Ca]1), estimated by a method involving the incorporation of a Ca2+ chelator (Quin 2), were measured in erythrocytes from β-thalassemic (β-thal) and hemoglobin C (CC) patients. El...
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Published in: | Blood 1987-09, Vol.70 (3), p.804-808 |
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description | Total calcium content, determined by atomic absorption spectroscopy, Ca2+ influx, and cytosolic free Ca2+ concentration ([Ca]1), estimated by a method involving the incorporation of a Ca2+ chelator (Quin 2), were measured in erythrocytes from β-thalassemic (β-thal) and hemoglobin C (CC) patients. Elevation of the total calcium content was observed in the cells from all patients, particularly in CC and splenectomized β-thal. However, [Ca]1 was within the normal range (-25 nmol/L) in all the pathologic cells. Ca2+ influx in CC cells and in cells from nonsplenectomized β-thal patients was also within the same range as that observed in control erythrocytes. In cells from splenectomized β-thal patients, the kinetic of 45Ca influx was biphasic, indicating the existence of two pools of exchangeable Ca2+. Density fractionation of the cells from one splenec- tomized β-thal patient showed that the rapid pool corresponded to the lightest cell fraction, which was also found to have the highest calcium content. The dense cells exhibited a normal Ca2+ influx as well as a smaller increase in total calcium content. It is suggested that, as in sickle cell anemia, the excess of Ca2+ in β-thal cells is not free in the cytoplasm but trapped within endocytic vacuoles, especially in a population of abnormal cells that are normally removed by the spleen. In CC patients, who have a functional spleen, a different mechanism could be responsible for the calcium retention. In conclusion, the present results demonstrate that in these two cases of hemolytic anemia associated with high calcium content, Ca2+ permeability and the level of cytosolic Ca2+ are normal.© 1987 by Grune & Stratton, Inc.0006-4971/87/7003-0031$3.00/0 |
doi_str_mv | 10.1182/blood.V70.3.804.804 |
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Elevation of the total calcium content was observed in the cells from all patients, particularly in CC and splenectomized β-thal. However, [Ca]1 was within the normal range (-25 nmol/L) in all the pathologic cells. Ca2+ influx in CC cells and in cells from nonsplenectomized β-thal patients was also within the same range as that observed in control erythrocytes. In cells from splenectomized β-thal patients, the kinetic of 45Ca influx was biphasic, indicating the existence of two pools of exchangeable Ca2+. Density fractionation of the cells from one splenec- tomized β-thal patient showed that the rapid pool corresponded to the lightest cell fraction, which was also found to have the highest calcium content. The dense cells exhibited a normal Ca2+ influx as well as a smaller increase in total calcium content. It is suggested that, as in sickle cell anemia, the excess of Ca2+ in β-thal cells is not free in the cytoplasm but trapped within endocytic vacuoles, especially in a population of abnormal cells that are normally removed by the spleen. In CC patients, who have a functional spleen, a different mechanism could be responsible for the calcium retention. In conclusion, the present results demonstrate that in these two cases of hemolytic anemia associated with high calcium content, Ca2+ permeability and the level of cytosolic Ca2+ are normal.© 1987 by Grune & Stratton, Inc.0006-4971/87/7003-0031$3.00/0</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V70.3.804.804</identifier><identifier>PMID: 3620701</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adenosine Triphosphate - blood ; Anemias. Hemoglobinopathies ; Biological and medical sciences ; Calcium - blood ; Cell Membrane Permeability ; Cytosol - metabolism ; Diseases of red blood cells ; Erythrocytes - metabolism ; Hematologic and hematopoietic diseases ; Hemoglobin C Disease - blood ; Humans ; Medical sciences ; Osmolar Concentration ; Thalassemia - blood</subject><ispartof>Blood, 1987-09, Vol.70 (3), p.804-808</ispartof><rights>1987 American Society of Hematology</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2754-1948284666921d3796826b5867d0ab9301642ea7a2d07a680bf2551e9baacac23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006497120786702$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7404700$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3620701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rhoda, M.D.</creatorcontrib><creatorcontrib>Galacteros, F.</creatorcontrib><creatorcontrib>Beuzard, Y.</creatorcontrib><creatorcontrib>Giraud, F.</creatorcontrib><title>Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes</title><title>Blood</title><addtitle>Blood</addtitle><description>Total calcium content, determined by atomic absorption spectroscopy, Ca2+ influx, and cytosolic free Ca2+ concentration ([Ca]1), estimated by a method involving the incorporation of a Ca2+ chelator (Quin 2), were measured in erythrocytes from β-thalassemic (β-thal) and hemoglobin C (CC) patients. Elevation of the total calcium content was observed in the cells from all patients, particularly in CC and splenectomized β-thal. However, [Ca]1 was within the normal range (-25 nmol/L) in all the pathologic cells. Ca2+ influx in CC cells and in cells from nonsplenectomized β-thal patients was also within the same range as that observed in control erythrocytes. In cells from splenectomized β-thal patients, the kinetic of 45Ca influx was biphasic, indicating the existence of two pools of exchangeable Ca2+. Density fractionation of the cells from one splenec- tomized β-thal patient showed that the rapid pool corresponded to the lightest cell fraction, which was also found to have the highest calcium content. The dense cells exhibited a normal Ca2+ influx as well as a smaller increase in total calcium content. It is suggested that, as in sickle cell anemia, the excess of Ca2+ in β-thal cells is not free in the cytoplasm but trapped within endocytic vacuoles, especially in a population of abnormal cells that are normally removed by the spleen. In CC patients, who have a functional spleen, a different mechanism could be responsible for the calcium retention. In conclusion, the present results demonstrate that in these two cases of hemolytic anemia associated with high calcium content, Ca2+ permeability and the level of cytosolic Ca2+ are normal.© 1987 by Grune & Stratton, Inc.0006-4971/87/7003-0031$3.00/0</description><subject>Adenosine Triphosphate - blood</subject><subject>Anemias. Hemoglobinopathies</subject><subject>Biological and medical sciences</subject><subject>Calcium - blood</subject><subject>Cell Membrane Permeability</subject><subject>Cytosol - metabolism</subject><subject>Diseases of red blood cells</subject><subject>Erythrocytes - metabolism</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hemoglobin C Disease - blood</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Osmolar Concentration</subject><subject>Thalassemia - blood</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNp9kMFu1DAURS0EKkPbL0BIXiA2KMOzndjJgkUVFVqpAhZtt9aL84YaJfFgZyrlt_gQvglPZ9Qliycv7rlX1mHsrYC1ELX81A0h9Ot7A2u1rqHc3wu2EpWsCwAJL9kKAHRRNka8Zm9S-gUgSiWrE3aitAQDYsVSi_Ij_0FxJOz84OeF49TzdplDCoN3_Clvw-RomiPOPkz8IhL_FmZ-PW7RR-q5n_jfP8XtAw6YEo25td-4ojH8HEKX05ZfxmV-iMEtM6Uz9mqDQ6Lz43vK7r5c3rZXxc33r9ftxU3hpKnKQjRlLetSa91I0SvT6Frqrqq16QG7RoHQpSQ0KHswqGvoNrKqBDUdokMn1Sn7cNjdxvB7R2m2o0-OhgEnCrtkjdGVUlWdQXUAXQwpRdrYbfQjxsUKsHvV9km1zaqtslnz_nLr3XF-143UP3eObnP-_phjcjhsIk7Op2fMlFAagIx9PmCUVTx6ijY5T9l3n9262fbB__cb_wBr1Zw_</recordid><startdate>198709</startdate><enddate>198709</enddate><creator>Rhoda, M.D.</creator><creator>Galacteros, F.</creator><creator>Beuzard, Y.</creator><creator>Giraud, F.</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198709</creationdate><title>Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes</title><author>Rhoda, M.D. ; Galacteros, F. ; Beuzard, Y. ; Giraud, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2754-1948284666921d3796826b5867d0ab9301642ea7a2d07a680bf2551e9baacac23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Adenosine Triphosphate - blood</topic><topic>Anemias. Hemoglobinopathies</topic><topic>Biological and medical sciences</topic><topic>Calcium - blood</topic><topic>Cell Membrane Permeability</topic><topic>Cytosol - metabolism</topic><topic>Diseases of red blood cells</topic><topic>Erythrocytes - metabolism</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hemoglobin C Disease - blood</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Osmolar Concentration</topic><topic>Thalassemia - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rhoda, M.D.</creatorcontrib><creatorcontrib>Galacteros, F.</creatorcontrib><creatorcontrib>Beuzard, Y.</creatorcontrib><creatorcontrib>Giraud, F.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rhoda, M.D.</au><au>Galacteros, F.</au><au>Beuzard, Y.</au><au>Giraud, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1987-09</date><risdate>1987</risdate><volume>70</volume><issue>3</issue><spage>804</spage><epage>808</epage><pages>804-808</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Total calcium content, determined by atomic absorption spectroscopy, Ca2+ influx, and cytosolic free Ca2+ concentration ([Ca]1), estimated by a method involving the incorporation of a Ca2+ chelator (Quin 2), were measured in erythrocytes from β-thalassemic (β-thal) and hemoglobin C (CC) patients. Elevation of the total calcium content was observed in the cells from all patients, particularly in CC and splenectomized β-thal. However, [Ca]1 was within the normal range (-25 nmol/L) in all the pathologic cells. Ca2+ influx in CC cells and in cells from nonsplenectomized β-thal patients was also within the same range as that observed in control erythrocytes. In cells from splenectomized β-thal patients, the kinetic of 45Ca influx was biphasic, indicating the existence of two pools of exchangeable Ca2+. Density fractionation of the cells from one splenec- tomized β-thal patient showed that the rapid pool corresponded to the lightest cell fraction, which was also found to have the highest calcium content. The dense cells exhibited a normal Ca2+ influx as well as a smaller increase in total calcium content. It is suggested that, as in sickle cell anemia, the excess of Ca2+ in β-thal cells is not free in the cytoplasm but trapped within endocytic vacuoles, especially in a population of abnormal cells that are normally removed by the spleen. In CC patients, who have a functional spleen, a different mechanism could be responsible for the calcium retention. In conclusion, the present results demonstrate that in these two cases of hemolytic anemia associated with high calcium content, Ca2+ permeability and the level of cytosolic Ca2+ are normal.© 1987 by Grune & Stratton, Inc.0006-4971/87/7003-0031$3.00/0</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>3620701</pmid><doi>10.1182/blood.V70.3.804.804</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - blood Anemias. Hemoglobinopathies Biological and medical sciences Calcium - blood Cell Membrane Permeability Cytosol - metabolism Diseases of red blood cells Erythrocytes - metabolism Hematologic and hematopoietic diseases Hemoglobin C Disease - blood Humans Medical sciences Osmolar Concentration Thalassemia - blood |
title | Ca2+ Permeability and Cytosolic Ca2+ Concentration Are Not Impaired in β-Thalassemic and Hemoglobin C Erythrocytes |
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