Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells

Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− C...

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Veröffentlicht in:Experimental hematology 2008-09, Vol.36 (9), p.1121-1131
Hauptverfasser: Kobune, Masayoshi, Kawano, Yutaka, Takahashi, Sho, Takada, Kohichi, Murase, Kazuyuki, Iyama, Satosi, Sato, Tsutomu, Takimoto, Rishu, Niitsu, Yoshiro, Kato, Junji
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container_end_page 1131
container_issue 9
container_start_page 1121
container_title Experimental hematology
container_volume 36
creator Kobune, Masayoshi
Kawano, Yutaka
Takahashi, Sho
Takada, Kohichi
Murase, Kazuyuki
Iyama, Satosi
Sato, Tsutomu
Takimoto, Rishu
Niitsu, Yoshiro
Kato, Junji
description Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− CD34− stem cells, do not engraft well in bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. In this study, we examined the effect of human stromal interactions on the properties of CB Lin− CD34− cells. Materials and Methods CD34 and CXCR4 expression on fresh CB Lin− CD34− cells and CB Lin− CD34− cells cocultured with human stromal cells were analyzed. Homing activity and engraftment of these cells were assessed using NOD/SCID mice. In an attempt to identify the stromal CXCR4-inducing factor, CB Lin− CD34− cells were cocultured with a noncontact culture system in the presence of several inhibitors. Result Coculture with human stromal cells induced expression of CD34 and CXCR4 on CB Lin− CD34− cells. CXCR4 expression on CB Lin− CD34− cells was induced even in the noncontact culture condition, suggesting that this CXCR4-inducing factor is soluble. Moreover, CXCR4 induction was inhibited by the soluble Wnt inhibitor DKK1. Furthermore, these cells acquired homing activity and engrafted in the BM of NOD/SCID mice after intravenous injection. Conclusion These findings may be useful for understanding the role of stromal cells in homing and engraftment of HSCs.
doi_str_mv 10.1016/j.exphem.2008.04.007
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Hence, some populations of HSCs, including cord blood (CB) Lin− CD34− stem cells, do not engraft well in bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. In this study, we examined the effect of human stromal interactions on the properties of CB Lin− CD34− cells. Materials and Methods CD34 and CXCR4 expression on fresh CB Lin− CD34− cells and CB Lin− CD34− cells cocultured with human stromal cells were analyzed. Homing activity and engraftment of these cells were assessed using NOD/SCID mice. In an attempt to identify the stromal CXCR4-inducing factor, CB Lin− CD34− cells were cocultured with a noncontact culture system in the presence of several inhibitors. Result Coculture with human stromal cells induced expression of CD34 and CXCR4 on CB Lin− CD34− cells. CXCR4 expression on CB Lin− CD34− cells was induced even in the noncontact culture condition, suggesting that this CXCR4-inducing factor is soluble. Moreover, CXCR4 induction was inhibited by the soluble Wnt inhibitor DKK1. Furthermore, these cells acquired homing activity and engrafted in the BM of NOD/SCID mice after intravenous injection. Conclusion These findings may be useful for understanding the role of stromal cells in homing and engraftment of HSCs.</description><identifier>ISSN: 0301-472X</identifier><identifier>EISSN: 1873-2399</identifier><identifier>DOI: 10.1016/j.exphem.2008.04.007</identifier><identifier>PMID: 18562079</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Advanced Basic Science ; Animals ; Antigens, CD34 - analysis ; Antigens, Differentiation - analysis ; Bone Marrow ; Cell Communication ; Chemotaxis, Leukocyte - physiology ; Coculture Techniques ; Fetal Blood - cytology ; Graft Survival ; Hematology, Oncology and Palliative Medicine ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells - chemistry ; Hematopoietic Stem Cells - classification ; Hematopoietic Stem Cells - physiology ; Humans ; Intercellular Signaling Peptides and Proteins - physiology ; Mice ; Mice, Inbred NOD ; Mice, SCID ; Receptors, CXCR4 - biosynthesis ; Receptors, CXCR4 - genetics ; Solubility ; Stromal Cells - physiology ; Transplantation, Heterologous ; Up-Regulation - physiology ; Wnt Proteins - antagonists &amp; inhibitors ; Wnt Proteins - biosynthesis ; Wnt Proteins - genetics</subject><ispartof>Experimental hematology, 2008-09, Vol.36 (9), p.1121-1131</ispartof><rights>ISEH - Society for Hematology and Stem Cells</rights><rights>2008 ISEH - Society for Hematology and Stem Cells</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-f04bba78cd8ddc7c682cb0d4bb6f70d9cbb16d4f7882254a613b5e7cca6041f23</citedby><cites>FETCH-LOGICAL-c391t-f04bba78cd8ddc7c682cb0d4bb6f70d9cbb16d4f7882254a613b5e7cca6041f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.exphem.2008.04.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18562079$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobune, Masayoshi</creatorcontrib><creatorcontrib>Kawano, Yutaka</creatorcontrib><creatorcontrib>Takahashi, Sho</creatorcontrib><creatorcontrib>Takada, Kohichi</creatorcontrib><creatorcontrib>Murase, Kazuyuki</creatorcontrib><creatorcontrib>Iyama, Satosi</creatorcontrib><creatorcontrib>Sato, Tsutomu</creatorcontrib><creatorcontrib>Takimoto, Rishu</creatorcontrib><creatorcontrib>Niitsu, Yoshiro</creatorcontrib><creatorcontrib>Kato, Junji</creatorcontrib><title>Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells</title><title>Experimental hematology</title><addtitle>Exp Hematol</addtitle><description>Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− CD34− stem cells, do not engraft well in bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. In this study, we examined the effect of human stromal interactions on the properties of CB Lin− CD34− cells. Materials and Methods CD34 and CXCR4 expression on fresh CB Lin− CD34− cells and CB Lin− CD34− cells cocultured with human stromal cells were analyzed. Homing activity and engraftment of these cells were assessed using NOD/SCID mice. In an attempt to identify the stromal CXCR4-inducing factor, CB Lin− CD34− cells were cocultured with a noncontact culture system in the presence of several inhibitors. Result Coculture with human stromal cells induced expression of CD34 and CXCR4 on CB Lin− CD34− cells. CXCR4 expression on CB Lin− CD34− cells was induced even in the noncontact culture condition, suggesting that this CXCR4-inducing factor is soluble. Moreover, CXCR4 induction was inhibited by the soluble Wnt inhibitor DKK1. Furthermore, these cells acquired homing activity and engrafted in the BM of NOD/SCID mice after intravenous injection. 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Kawano, Yutaka ; Takahashi, Sho ; Takada, Kohichi ; Murase, Kazuyuki ; Iyama, Satosi ; Sato, Tsutomu ; Takimoto, Rishu ; Niitsu, Yoshiro ; Kato, Junji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-f04bba78cd8ddc7c682cb0d4bb6f70d9cbb16d4f7882254a613b5e7cca6041f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Antigens, CD34 - analysis</topic><topic>Antigens, Differentiation - analysis</topic><topic>Bone Marrow</topic><topic>Cell Communication</topic><topic>Chemotaxis, Leukocyte - physiology</topic><topic>Coculture Techniques</topic><topic>Fetal Blood - cytology</topic><topic>Graft Survival</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic Stem Cells - chemistry</topic><topic>Hematopoietic Stem Cells - classification</topic><topic>Hematopoietic Stem Cells - physiology</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - physiology</topic><topic>Mice</topic><topic>Mice, Inbred NOD</topic><topic>Mice, SCID</topic><topic>Receptors, CXCR4 - biosynthesis</topic><topic>Receptors, CXCR4 - genetics</topic><topic>Solubility</topic><topic>Stromal Cells - physiology</topic><topic>Transplantation, Heterologous</topic><topic>Up-Regulation - physiology</topic><topic>Wnt Proteins - antagonists &amp; inhibitors</topic><topic>Wnt Proteins - biosynthesis</topic><topic>Wnt Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobune, Masayoshi</creatorcontrib><creatorcontrib>Kawano, Yutaka</creatorcontrib><creatorcontrib>Takahashi, Sho</creatorcontrib><creatorcontrib>Takada, Kohichi</creatorcontrib><creatorcontrib>Murase, Kazuyuki</creatorcontrib><creatorcontrib>Iyama, Satosi</creatorcontrib><creatorcontrib>Sato, Tsutomu</creatorcontrib><creatorcontrib>Takimoto, Rishu</creatorcontrib><creatorcontrib>Niitsu, Yoshiro</creatorcontrib><creatorcontrib>Kato, Junji</creatorcontrib><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>Experimental hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobune, Masayoshi</au><au>Kawano, Yutaka</au><au>Takahashi, Sho</au><au>Takada, Kohichi</au><au>Murase, Kazuyuki</au><au>Iyama, Satosi</au><au>Sato, Tsutomu</au><au>Takimoto, Rishu</au><au>Niitsu, Yoshiro</au><au>Kato, Junji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells</atitle><jtitle>Experimental hematology</jtitle><addtitle>Exp Hematol</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>36</volume><issue>9</issue><spage>1121</spage><epage>1131</epage><pages>1121-1131</pages><issn>0301-472X</issn><eissn>1873-2399</eissn><abstract>Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− CD34− stem cells, do not engraft well in bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. In this study, we examined the effect of human stromal interactions on the properties of CB Lin− CD34− cells. Materials and Methods CD34 and CXCR4 expression on fresh CB Lin− CD34− cells and CB Lin− CD34− cells cocultured with human stromal cells were analyzed. Homing activity and engraftment of these cells were assessed using NOD/SCID mice. In an attempt to identify the stromal CXCR4-inducing factor, CB Lin− CD34− cells were cocultured with a noncontact culture system in the presence of several inhibitors. Result Coculture with human stromal cells induced expression of CD34 and CXCR4 on CB Lin− CD34− cells. CXCR4 expression on CB Lin− CD34− cells was induced even in the noncontact culture condition, suggesting that this CXCR4-inducing factor is soluble. Moreover, CXCR4 induction was inhibited by the soluble Wnt inhibitor DKK1. Furthermore, these cells acquired homing activity and engrafted in the BM of NOD/SCID mice after intravenous injection. Conclusion These findings may be useful for understanding the role of stromal cells in homing and engraftment of HSCs.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>18562079</pmid><doi>10.1016/j.exphem.2008.04.007</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Advanced Basic Science
Animals
Antigens, CD34 - analysis
Antigens, Differentiation - analysis
Bone Marrow
Cell Communication
Chemotaxis, Leukocyte - physiology
Coculture Techniques
Fetal Blood - cytology
Graft Survival
Hematology, Oncology and Palliative Medicine
Hematopoietic Stem Cell Transplantation
Hematopoietic Stem Cells - chemistry
Hematopoietic Stem Cells - classification
Hematopoietic Stem Cells - physiology
Humans
Intercellular Signaling Peptides and Proteins - physiology
Mice
Mice, Inbred NOD
Mice, SCID
Receptors, CXCR4 - biosynthesis
Receptors, CXCR4 - genetics
Solubility
Stromal Cells - physiology
Transplantation, Heterologous
Up-Regulation - physiology
Wnt Proteins - antagonists & inhibitors
Wnt Proteins - biosynthesis
Wnt Proteins - genetics
title Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells
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