How cell number and cellular properties of blood-banked red blood cells of different cell ages decline during storage
Numerous studies have suggested that transfusion of red blood cells (RBCs) stored over a long period of time may induce harmful effects due to storage-induced lesions. However, the underlying mechanisms responsible for this damage have not been identified. Furthermore, it is unclear why and how up t...
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description | Numerous studies have suggested that transfusion of red blood cells (RBCs) stored over a long period of time may induce harmful effects due to storage-induced lesions. However, the underlying mechanisms responsible for this damage have not been identified. Furthermore, it is unclear why and how up to 30% of long-stored RBCs disappear from the circulation within 24 hours after transfusion. The aim of this study was to determine how the cell number of RBCs of different ages changes during storage and how these cells undergo cumulative structural and functional changes with storage time.
We used Percoll centrifugation to fractionate the RBCs in blood bank stored RBC units into different aged sub-populations and then measured the number of intact cells in each sub-population as well the cells' biomechanical and biochemical parameters as functions of the storage period. We found that the RBC units stored for ≤ 14 days could be separated into four fractions: the top or young cell fraction, two middle fractions, and the lower or old fraction. However, after 14 days of storage, the cell number and cellular properties declined rapidly whereby the units stored for 21 days only exhibited the three lower fractions and not the young fraction. The cell number within a unit stored for 21 days decreased by 23% compared to a fresh unit and the cells that were lost had hemolyzed into harmful membrane fragments, microparticles, and free hemoglobin. All remaining cells exhibited cellular properties similar to those of senescent cells.
In RBC units stored for greater than 14 days, there were fewer intact cells with no healthy cells present, as well as harmful membrane fragments, microparticles, and free hemoglobin. Therefore, transfusion of these stored units would not likely help patients and may induce a series of clinical problems. |
doi_str_mv | 10.1371/journal.pone.0105692 |
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We used Percoll centrifugation to fractionate the RBCs in blood bank stored RBC units into different aged sub-populations and then measured the number of intact cells in each sub-population as well the cells' biomechanical and biochemical parameters as functions of the storage period. We found that the RBC units stored for ≤ 14 days could be separated into four fractions: the top or young cell fraction, two middle fractions, and the lower or old fraction. However, after 14 days of storage, the cell number and cellular properties declined rapidly whereby the units stored for 21 days only exhibited the three lower fractions and not the young fraction. The cell number within a unit stored for 21 days decreased by 23% compared to a fresh unit and the cells that were lost had hemolyzed into harmful membrane fragments, microparticles, and free hemoglobin. All remaining cells exhibited cellular properties similar to those of senescent cells.
In RBC units stored for greater than 14 days, there were fewer intact cells with no healthy cells present, as well as harmful membrane fragments, microparticles, and free hemoglobin. Therefore, transfusion of these stored units would not likely help patients and may induce a series of clinical problems.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0105692</identifier><identifier>PMID: 25167052</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Age ; Biology and Life Sciences ; Biomechanics ; Biomedical engineering ; Blood ; Blood banks ; Blood cells ; Blood Preservation - methods ; Blood transfusion ; Cell number ; Cellular Senescence - physiology ; Centrifugation ; Critical care ; Damage detection ; Engineering ; Erythrocyte Count ; Erythrocyte Transfusion ; Erythrocytes ; Erythrocytes - cytology ; Fragments ; Hemoglobin ; Hemoglobins ; Humans ; Laboratory animals ; Lesions ; Medicine ; Medicine and Health Sciences ; Microparticles ; Mortality ; Properties (attributes) ; Proteomics ; Rheology ; Storage ; Structure-function relationships ; Surgery ; Time Factors ; Transfusion</subject><ispartof>PloS one, 2014-08, Vol.9 (8), p.e105692</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Tuo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Tuo et al 2014 Tuo et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-99d6754bb38885bfc51755caeb302f84f96e6e740619f26245b828c41101ee193</citedby><cites>FETCH-LOGICAL-c659t-99d6754bb38885bfc51755caeb302f84f96e6e740619f26245b828c41101ee193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148343/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148343/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25167052$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Lam, Wilbur</contributor><creatorcontrib>Tuo, Wei-Wei</creatorcontrib><creatorcontrib>Wang, Di</creatorcontrib><creatorcontrib>Liang, Wen-Jing</creatorcontrib><creatorcontrib>Huang, Yao-Xiong</creatorcontrib><title>How cell number and cellular properties of blood-banked red blood cells of different cell ages decline during storage</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Numerous studies have suggested that transfusion of red blood cells (RBCs) stored over a long period of time may induce harmful effects due to storage-induced lesions. However, the underlying mechanisms responsible for this damage have not been identified. Furthermore, it is unclear why and how up to 30% of long-stored RBCs disappear from the circulation within 24 hours after transfusion. The aim of this study was to determine how the cell number of RBCs of different ages changes during storage and how these cells undergo cumulative structural and functional changes with storage time.
We used Percoll centrifugation to fractionate the RBCs in blood bank stored RBC units into different aged sub-populations and then measured the number of intact cells in each sub-population as well the cells' biomechanical and biochemical parameters as functions of the storage period. We found that the RBC units stored for ≤ 14 days could be separated into four fractions: the top or young cell fraction, two middle fractions, and the lower or old fraction. However, after 14 days of storage, the cell number and cellular properties declined rapidly whereby the units stored for 21 days only exhibited the three lower fractions and not the young fraction. The cell number within a unit stored for 21 days decreased by 23% compared to a fresh unit and the cells that were lost had hemolyzed into harmful membrane fragments, microparticles, and free hemoglobin. All remaining cells exhibited cellular properties similar to those of senescent cells.
In RBC units stored for greater than 14 days, there were fewer intact cells with no healthy cells present, as well as harmful membrane fragments, microparticles, and free hemoglobin. Therefore, transfusion of these stored units would not likely help patients and may induce a series of clinical problems.</description><subject>Age</subject><subject>Biology and Life Sciences</subject><subject>Biomechanics</subject><subject>Biomedical engineering</subject><subject>Blood</subject><subject>Blood banks</subject><subject>Blood cells</subject><subject>Blood Preservation - methods</subject><subject>Blood transfusion</subject><subject>Cell number</subject><subject>Cellular Senescence - physiology</subject><subject>Centrifugation</subject><subject>Critical care</subject><subject>Damage detection</subject><subject>Engineering</subject><subject>Erythrocyte Count</subject><subject>Erythrocyte Transfusion</subject><subject>Erythrocytes</subject><subject>Erythrocytes - cytology</subject><subject>Fragments</subject><subject>Hemoglobin</subject><subject>Hemoglobins</subject><subject>Humans</subject><subject>Laboratory animals</subject><subject>Lesions</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Microparticles</subject><subject>Mortality</subject><subject>Properties (attributes)</subject><subject>Proteomics</subject><subject>Rheology</subject><subject>Storage</subject><subject>Structure-function relationships</subject><subject>Surgery</subject><subject>Time Factors</subject><subject>Transfusion</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl2L1DAUhoso7rr6D0QLguDFjEmbpOmNsCzqDiws-HUb0uSkkzWTzCatH__ezEx3mYKClND25HnfnLyconiO0RLXDX57E8bopVtug4clwoiytnpQnOK2rhasQvXDo--T4klKNwjRmjP2uDipKGYNotVpMV6Gn6UC50o_bjqIpfR6_z86GcttDFuIg4VUBlN2LgS96KT_DrqMee0Le3q_r60xEMEPB0PZZ5kG5ayHUo_R-r5MQ4i5_rR4ZKRL8Gx6nxVfP7z_cnG5uLr-uLo4v1ooRtth0baaNZR0Xc05p51RFDeUKgldjSrDiWkZMGgIYrg1FasI7XjFFcEYYYB8-7Pi5cF360ISU2JJYEo5RghjmonVgdBB3ohttBsZf4sgrdgXQuyFzAEoByIfDw3NISIiCWEgjSKcawwVzh1WLHu9m04buw1olZOI0s1M5zverkUffgiCCa9JnQ1eTQYx3I6Qhn-0PFG9zF1Zb0I2UxublDgnuGENw2TXzPIvVH40bKzKM2Nsrs8Eb2aCzAzwa-jlmJJYff70_-z1tzn7-ohdg3TDOgU3Djb4NAfJAVQxpBTB3CeHkdiN_F0aYjfyYhr5LHtxnPq96G7G6z-3G_uW</recordid><startdate>20140828</startdate><enddate>20140828</enddate><creator>Tuo, Wei-Wei</creator><creator>Wang, Di</creator><creator>Liang, Wen-Jing</creator><creator>Huang, Yao-Xiong</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140828</creationdate><title>How cell number and cellular properties of blood-banked red blood cells of different cell ages decline during storage</title><author>Tuo, Wei-Wei ; Wang, Di ; Liang, Wen-Jing ; Huang, Yao-Xiong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c659t-99d6754bb38885bfc51755caeb302f84f96e6e740619f26245b828c41101ee193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age</topic><topic>Biology and Life Sciences</topic><topic>Biomechanics</topic><topic>Biomedical engineering</topic><topic>Blood</topic><topic>Blood banks</topic><topic>Blood cells</topic><topic>Blood Preservation - methods</topic><topic>Blood transfusion</topic><topic>Cell number</topic><topic>Cellular Senescence - physiology</topic><topic>Centrifugation</topic><topic>Critical care</topic><topic>Damage detection</topic><topic>Engineering</topic><topic>Erythrocyte Count</topic><topic>Erythrocyte Transfusion</topic><topic>Erythrocytes</topic><topic>Erythrocytes - cytology</topic><topic>Fragments</topic><topic>Hemoglobin</topic><topic>Hemoglobins</topic><topic>Humans</topic><topic>Laboratory animals</topic><topic>Lesions</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Microparticles</topic><topic>Mortality</topic><topic>Properties (attributes)</topic><topic>Proteomics</topic><topic>Rheology</topic><topic>Storage</topic><topic>Structure-function relationships</topic><topic>Surgery</topic><topic>Time Factors</topic><topic>Transfusion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tuo, Wei-Wei</creatorcontrib><creatorcontrib>Wang, Di</creatorcontrib><creatorcontrib>Liang, Wen-Jing</creatorcontrib><creatorcontrib>Huang, Yao-Xiong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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However, the underlying mechanisms responsible for this damage have not been identified. Furthermore, it is unclear why and how up to 30% of long-stored RBCs disappear from the circulation within 24 hours after transfusion. The aim of this study was to determine how the cell number of RBCs of different ages changes during storage and how these cells undergo cumulative structural and functional changes with storage time.
We used Percoll centrifugation to fractionate the RBCs in blood bank stored RBC units into different aged sub-populations and then measured the number of intact cells in each sub-population as well the cells' biomechanical and biochemical parameters as functions of the storage period. We found that the RBC units stored for ≤ 14 days could be separated into four fractions: the top or young cell fraction, two middle fractions, and the lower or old fraction. However, after 14 days of storage, the cell number and cellular properties declined rapidly whereby the units stored for 21 days only exhibited the three lower fractions and not the young fraction. The cell number within a unit stored for 21 days decreased by 23% compared to a fresh unit and the cells that were lost had hemolyzed into harmful membrane fragments, microparticles, and free hemoglobin. All remaining cells exhibited cellular properties similar to those of senescent cells.
In RBC units stored for greater than 14 days, there were fewer intact cells with no healthy cells present, as well as harmful membrane fragments, microparticles, and free hemoglobin. Therefore, transfusion of these stored units would not likely help patients and may induce a series of clinical problems.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25167052</pmid><doi>10.1371/journal.pone.0105692</doi><oa>free_for_read</oa></addata></record> |
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subjects | Age Biology and Life Sciences Biomechanics Biomedical engineering Blood Blood banks Blood cells Blood Preservation - methods Blood transfusion Cell number Cellular Senescence - physiology Centrifugation Critical care Damage detection Engineering Erythrocyte Count Erythrocyte Transfusion Erythrocytes Erythrocytes - cytology Fragments Hemoglobin Hemoglobins Humans Laboratory animals Lesions Medicine Medicine and Health Sciences Microparticles Mortality Properties (attributes) Proteomics Rheology Storage Structure-function relationships Surgery Time Factors Transfusion |
title | How cell number and cellular properties of blood-banked red blood cells of different cell ages decline during storage |
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