Direct Comparison by Limiting Dilution Analysis of Long-Term Culture-Initiating Cells in Human Bone Marrow, Umbilical Cord Blood, and Blood Stem Cells
Limiting-dilution analysis of long-term culture-initiating cells (LTCIC) is a quantitative method of estimating hematopoietic stem cell activity in clinical samples. We compared the numbers of LTCIC in bone marrow (BM), umbilical cord blood, and blood progenitor cells (obtained from patients with so...
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Veröffentlicht in: | Blood 1994-12, Vol.84 (11), p.3653-3659 |
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description | Limiting-dilution analysis of long-term culture-initiating cells (LTCIC) is a quantitative method of estimating hematopoietic stem cell activity in clinical samples. We compared the numbers of LTCIC in bone marrow (BM), umbilical cord blood, and blood progenitor cells (obtained from patients with solid tumors at leukapheresis after mobilization with induction chemotherapy and filgrastim administration), using a two-stage long-term culture system and a limiting-dilution technique, scoring cobblestone areas of greater than 15 hematopoietic cells weekly for up to 8 weeks. Samples were obtained from 30 normal BMs, 20 human umbilical cords, and 32 leukapheresis products. Direct comparison of LTCIC in the three sources showed that the median proportions of cells generating hematopoietic foci from unfractionated mononuclear cells at 5 and 8 weeks, respectively, were 1:13,314 and 1:33,949 for BM, 1:12,506 and 1:34,546 for umbilical cord blood, and 1:10,302 and 1:12,891 for leukapheresis product. The estimated proportions of LTCIC from unfractionated mononuclear cells and CD34+ cells were similar in experiments with leukapheresis product. Leukapheresis product was superior to umbilical cord blood and cord blood to BM at 5 and 8 weeks of culture (P = .01). In two-stage long-term cultures, more colonies per flask and CD34+ cells were found in assays of leukapheresis product than in BM or umbilical cord blood cultures (P= .0005). Results obtained by this simplified limiting-dilution analysis correlated well with standard long-term cultures and can be used as a measure of the stem cell population. These data suggest that the incidence of putative stem cells in leukapheresis product and umbilical cord blood are at least comparable with that of BM. |
doi_str_mv | 10.1182/blood.V84.11.3653.bloodjournal84113653 |
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Michael ; Ryder, David ; Testa, Nydia G.</creator><creatorcontrib>Pettengell, Ruth ; Luft, Thomas ; Henschler, Reinhard ; Hows, Jill M. ; Dexter, T. Michael ; Ryder, David ; Testa, Nydia G.</creatorcontrib><description>Limiting-dilution analysis of long-term culture-initiating cells (LTCIC) is a quantitative method of estimating hematopoietic stem cell activity in clinical samples. We compared the numbers of LTCIC in bone marrow (BM), umbilical cord blood, and blood progenitor cells (obtained from patients with solid tumors at leukapheresis after mobilization with induction chemotherapy and filgrastim administration), using a two-stage long-term culture system and a limiting-dilution technique, scoring cobblestone areas of greater than 15 hematopoietic cells weekly for up to 8 weeks. Samples were obtained from 30 normal BMs, 20 human umbilical cords, and 32 leukapheresis products. Direct comparison of LTCIC in the three sources showed that the median proportions of cells generating hematopoietic foci from unfractionated mononuclear cells at 5 and 8 weeks, respectively, were 1:13,314 and 1:33,949 for BM, 1:12,506 and 1:34,546 for umbilical cord blood, and 1:10,302 and 1:12,891 for leukapheresis product. The estimated proportions of LTCIC from unfractionated mononuclear cells and CD34+ cells were similar in experiments with leukapheresis product. Leukapheresis product was superior to umbilical cord blood and cord blood to BM at 5 and 8 weeks of culture (P = .01). In two-stage long-term cultures, more colonies per flask and CD34+ cells were found in assays of leukapheresis product than in BM or umbilical cord blood cultures (P= .0005). Results obtained by this simplified limiting-dilution analysis correlated well with standard long-term cultures and can be used as a measure of the stem cell population. These data suggest that the incidence of putative stem cells in leukapheresis product and umbilical cord blood are at least comparable with that of BM.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V84.11.3653.bloodjournal84113653</identifier><identifier>PMID: 7524745</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Animal cells ; Antigens, CD - analysis ; Antigens, CD34 ; Biological and medical sciences ; Blood Cell Count ; Blood Cells ; Bone Marrow Cells ; Cell Count ; Cell cultures. Hybridization. Fusion ; Cells, Cultured ; Colony-Forming Units Assay - methods ; Fetal Blood - cytology ; Fundamental and applied biological sciences. Psychology ; Hematopoietic Stem Cells ; Humans ; Infant, Newborn ; Leukapheresis ; Molecular and cellular biology</subject><ispartof>Blood, 1994-12, Vol.84 (11), p.3653-3659</ispartof><rights>1994 American Society of Hematology</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-c332e62b24a12854676d193dbd87e18c3c9f3be5af605eb98f2a5d3abda1e65b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3364594$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7524745$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pettengell, Ruth</creatorcontrib><creatorcontrib>Luft, Thomas</creatorcontrib><creatorcontrib>Henschler, Reinhard</creatorcontrib><creatorcontrib>Hows, Jill M.</creatorcontrib><creatorcontrib>Dexter, T. Michael</creatorcontrib><creatorcontrib>Ryder, David</creatorcontrib><creatorcontrib>Testa, Nydia G.</creatorcontrib><title>Direct Comparison by Limiting Dilution Analysis of Long-Term Culture-Initiating Cells in Human Bone Marrow, Umbilical Cord Blood, and Blood Stem Cells</title><title>Blood</title><addtitle>Blood</addtitle><description>Limiting-dilution analysis of long-term culture-initiating cells (LTCIC) is a quantitative method of estimating hematopoietic stem cell activity in clinical samples. We compared the numbers of LTCIC in bone marrow (BM), umbilical cord blood, and blood progenitor cells (obtained from patients with solid tumors at leukapheresis after mobilization with induction chemotherapy and filgrastim administration), using a two-stage long-term culture system and a limiting-dilution technique, scoring cobblestone areas of greater than 15 hematopoietic cells weekly for up to 8 weeks. Samples were obtained from 30 normal BMs, 20 human umbilical cords, and 32 leukapheresis products. Direct comparison of LTCIC in the three sources showed that the median proportions of cells generating hematopoietic foci from unfractionated mononuclear cells at 5 and 8 weeks, respectively, were 1:13,314 and 1:33,949 for BM, 1:12,506 and 1:34,546 for umbilical cord blood, and 1:10,302 and 1:12,891 for leukapheresis product. The estimated proportions of LTCIC from unfractionated mononuclear cells and CD34+ cells were similar in experiments with leukapheresis product. Leukapheresis product was superior to umbilical cord blood and cord blood to BM at 5 and 8 weeks of culture (P = .01). In two-stage long-term cultures, more colonies per flask and CD34+ cells were found in assays of leukapheresis product than in BM or umbilical cord blood cultures (P= .0005). Results obtained by this simplified limiting-dilution analysis correlated well with standard long-term cultures and can be used as a measure of the stem cell population. These data suggest that the incidence of putative stem cells in leukapheresis product and umbilical cord blood are at least comparable with that of BM.</description><subject>Animal cells</subject><subject>Antigens, CD - analysis</subject><subject>Antigens, CD34</subject><subject>Biological and medical sciences</subject><subject>Blood Cell Count</subject><subject>Blood Cells</subject><subject>Bone Marrow Cells</subject><subject>Cell Count</subject><subject>Cell cultures. Hybridization. Fusion</subject><subject>Cells, Cultured</subject><subject>Colony-Forming Units Assay - methods</subject><subject>Fetal Blood - cytology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hematopoietic Stem Cells</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Leukapheresis</subject><subject>Molecular and cellular biology</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkctu1TAQhi0EKofCIyB5gVg1wddclm1KaaWDQKJla9nOpHKV2Ac7KTovwvPic1FX3XRlz8zvf8bzIVRSUlLasC9mDKEvfzcihyWvJC_3mYewRK_HRlC6S75CKypZUxDCyGu0IoRUhWhr-ha9S-mBECo4kyfopJZM1EKu0L9LF8HOuAvTRkeXgsdmi9ducrPz9_jSjcvscvI8N9kml3AY8Dr4--IW4oS7ZZyXCMWNz3K9f9HBOCbsPL5eJu3xRfCAv-sYw98zfDcZNzqrx9wu9vhi94EzrP3xin_NMB0M3qM3gx4TfDiep-ju6uttd12sf3y76c7XhZVEzIXlnEHFDBOaskaKqq562vLe9E0NtLHctgM3IPVQEQmmbQamZc-16TWFShp-ij4ffDcx_FkgzWpyyeYJtIewJFVXddvWdZuFVwehjSGlCIPaRDfpuFWUqB0gtcehMqAcqh0L9RygbPTx2HExE_RPNkciuf7pWNcpb2qI2luXnmScV0K2Ist-HmSQt_PoIKpkHXgL_Z6n6oN76WT_ASTtvcY</recordid><startdate>19941201</startdate><enddate>19941201</enddate><creator>Pettengell, Ruth</creator><creator>Luft, Thomas</creator><creator>Henschler, Reinhard</creator><creator>Hows, Jill M.</creator><creator>Dexter, T. Michael</creator><creator>Ryder, David</creator><creator>Testa, Nydia G.</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>19941201</creationdate><title>Direct Comparison by Limiting Dilution Analysis of Long-Term Culture-Initiating Cells in Human Bone Marrow, Umbilical Cord Blood, and Blood Stem Cells</title><author>Pettengell, Ruth ; Luft, Thomas ; Henschler, Reinhard ; Hows, Jill M. ; Dexter, T. Michael ; Ryder, David ; Testa, Nydia G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-c332e62b24a12854676d193dbd87e18c3c9f3be5af605eb98f2a5d3abda1e65b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animal cells</topic><topic>Antigens, CD - analysis</topic><topic>Antigens, CD34</topic><topic>Biological and medical sciences</topic><topic>Blood Cell Count</topic><topic>Blood Cells</topic><topic>Bone Marrow Cells</topic><topic>Cell Count</topic><topic>Cell cultures. Hybridization. Fusion</topic><topic>Cells, Cultured</topic><topic>Colony-Forming Units Assay - methods</topic><topic>Fetal Blood - cytology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hematopoietic Stem Cells</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Leukapheresis</topic><topic>Molecular and cellular biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pettengell, Ruth</creatorcontrib><creatorcontrib>Luft, Thomas</creatorcontrib><creatorcontrib>Henschler, Reinhard</creatorcontrib><creatorcontrib>Hows, Jill M.</creatorcontrib><creatorcontrib>Dexter, T. Michael</creatorcontrib><creatorcontrib>Ryder, David</creatorcontrib><creatorcontrib>Testa, Nydia G.</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>Pettengell, Ruth</au><au>Luft, Thomas</au><au>Henschler, Reinhard</au><au>Hows, Jill M.</au><au>Dexter, T. Michael</au><au>Ryder, David</au><au>Testa, Nydia G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct Comparison by Limiting Dilution Analysis of Long-Term Culture-Initiating Cells in Human Bone Marrow, Umbilical Cord Blood, and Blood Stem Cells</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1994-12-01</date><risdate>1994</risdate><volume>84</volume><issue>11</issue><spage>3653</spage><epage>3659</epage><pages>3653-3659</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Limiting-dilution analysis of long-term culture-initiating cells (LTCIC) is a quantitative method of estimating hematopoietic stem cell activity in clinical samples. We compared the numbers of LTCIC in bone marrow (BM), umbilical cord blood, and blood progenitor cells (obtained from patients with solid tumors at leukapheresis after mobilization with induction chemotherapy and filgrastim administration), using a two-stage long-term culture system and a limiting-dilution technique, scoring cobblestone areas of greater than 15 hematopoietic cells weekly for up to 8 weeks. Samples were obtained from 30 normal BMs, 20 human umbilical cords, and 32 leukapheresis products. Direct comparison of LTCIC in the three sources showed that the median proportions of cells generating hematopoietic foci from unfractionated mononuclear cells at 5 and 8 weeks, respectively, were 1:13,314 and 1:33,949 for BM, 1:12,506 and 1:34,546 for umbilical cord blood, and 1:10,302 and 1:12,891 for leukapheresis product. The estimated proportions of LTCIC from unfractionated mononuclear cells and CD34+ cells were similar in experiments with leukapheresis product. Leukapheresis product was superior to umbilical cord blood and cord blood to BM at 5 and 8 weeks of culture (P = .01). In two-stage long-term cultures, more colonies per flask and CD34+ cells were found in assays of leukapheresis product than in BM or umbilical cord blood cultures (P= .0005). Results obtained by this simplified limiting-dilution analysis correlated well with standard long-term cultures and can be used as a measure of the stem cell population. These data suggest that the incidence of putative stem cells in leukapheresis product and umbilical cord blood are at least comparable with that of BM.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>7524745</pmid><doi>10.1182/blood.V84.11.3653.bloodjournal84113653</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal cells Antigens, CD - analysis Antigens, CD34 Biological and medical sciences Blood Cell Count Blood Cells Bone Marrow Cells Cell Count Cell cultures. Hybridization. Fusion Cells, Cultured Colony-Forming Units Assay - methods Fetal Blood - cytology Fundamental and applied biological sciences. Psychology Hematopoietic Stem Cells Humans Infant, Newborn Leukapheresis Molecular and cellular biology |
title | Direct Comparison by Limiting Dilution Analysis of Long-Term Culture-Initiating Cells in Human Bone Marrow, Umbilical Cord Blood, and Blood Stem Cells |
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