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 |
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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 & 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. Conclusion These findings may be useful for understanding the role of stromal cells in homing and engraftment of HSCs.</description><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Antigens, CD34 - analysis</subject><subject>Antigens, Differentiation - analysis</subject><subject>Bone Marrow</subject><subject>Cell Communication</subject><subject>Chemotaxis, Leukocyte - physiology</subject><subject>Coculture Techniques</subject><subject>Fetal Blood - cytology</subject><subject>Graft Survival</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic Stem Cells - chemistry</subject><subject>Hematopoietic Stem Cells - classification</subject><subject>Hematopoietic Stem Cells - physiology</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - physiology</subject><subject>Mice</subject><subject>Mice, Inbred NOD</subject><subject>Mice, SCID</subject><subject>Receptors, CXCR4 - biosynthesis</subject><subject>Receptors, CXCR4 - genetics</subject><subject>Solubility</subject><subject>Stromal Cells - physiology</subject><subject>Transplantation, Heterologous</subject><subject>Up-Regulation - physiology</subject><subject>Wnt Proteins - antagonists & inhibitors</subject><subject>Wnt Proteins - biosynthesis</subject><subject>Wnt Proteins - genetics</subject><issn>0301-472X</issn><issn>1873-2399</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2O1DAQhS0EYpqBGyDkFbuEcuI4zgYJNX8jtYTEjzQ7y7ErtJvE7rETYG7AmiNyEhy6JSQ2rEqqeu-V_RUhjxmUDJh4dijx-3GPU1kByBJ4CdDeIRsm27qo6q67SzZQAyt4W11fkAcpHQCgaTq4Ty6YbEQFbbchN1d-xqjN7IKn39y8p_tl0p6mOYZJj9TgOCaKfq-9wUS319v3nObFEVNaLdrbPP0c9TBP6GcaBmpCtLQfQ7B05_yvHz_p9mXN1_on7CG5N-gx4aNzvSSfXr_6uH1b7N69udq-2BWm7thcDMD7XrfSWGmtaY2QlenB5qYYWrCd6XsmLB9aKauq4Vqwum-wNUYL4Gyo6kvy9JR7jOFmwTSryaX1BdpjWJISHW-EFHUW8pPQxJBSxEEdo5t0vFUM1IpaHdQJtVpRK-Aqo862J-f8pZ_Q_jWd2WbB85MA8y-_OowqGYcZo3URzaxscP_b8G-AGZ13Ro9f8BbTISzRZ4KKqVQpUB_Wc6_XBgnAWsnq3_wTqaw</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Kobune, Masayoshi</creator><creator>Kawano, Yutaka</creator><creator>Takahashi, Sho</creator><creator>Takada, Kohichi</creator><creator>Murase, Kazuyuki</creator><creator>Iyama, Satosi</creator><creator>Sato, Tsutomu</creator><creator>Takimoto, Rishu</creator><creator>Niitsu, Yoshiro</creator><creator>Kato, Junji</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20080901</creationdate><title>Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells</title><author>Kobune, Masayoshi ; 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 & 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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