Stem cell mobilization by hyperbaric oxygen
1 Institute for Environmental Medicine and Departments of 2 Emergency Medicine, 3 Surgery, and 4 Physiology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania Submitted 19 August 2005 ; accepted in final form 7 November 2005 We hypothesized that exposure to hyperbaric oxygen (HBO...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2006-04, Vol.290 (4), p.H1378-H1386 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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creator | Thom, Stephen R Bhopale, Veena M Velazquez, Omaida C Goldstein, Lee J Thom, Lynne H Buerk, Donald G |
description | 1 Institute for Environmental Medicine and Departments of 2 Emergency Medicine, 3 Surgery, and 4 Physiology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania
Submitted 19 August 2005
; accepted in final form 7 November 2005
We hypothesized that exposure to hyperbaric oxygen (HBO 2 ) would mobilize stem/progenitor cells from the bone marrow by a nitric oxide (·NO) -dependent mechanism. The population of CD34 + cells in the peripheral circulation of humans doubled in response to a single exposure to 2.0 atmospheres absolute (ATA) O 2 for 2 h. Over a course of 20 treatments, circulating CD34 + cells increased eightfold, although the overall circulating white cell count was not significantly increased. The number of colony-forming cells (CFCs) increased from 16 ± 2 to 26 ± 3 CFCs/100,000 monocytes plated. Elevations in CFCs were entirely due to the CD34 + subpopulation, but increased cell growth only occurred in samples obtained immediately posttreatment. A high proportion of progeny cells express receptors for vascular endothelial growth factor-2 and for stromal-derived growth factor. In mice, HBO 2 increased circulating stem cell factor by 50%, increased the number of circulating cells expressing stem cell antigen-1 and CD34 by 3.4-fold, and doubled the number of CFCs. Bone marrow ·NO concentration increased by 1,008 ± 255 nM in association with HBO 2 . Stem cell mobilization did not occur in knockout mice lacking genes for endothelial ·NO synthase. Moreover, pretreatment of wild-type mice with a ·NO synthase inhibitor prevented the HBO 2 -induced elevation in stem cell factor and circulating stem cells. We conclude that HBO 2 mobilizes stem/progenitor cells by stimulating ·NO synthesis.
nitric oxide; CD34; CD133; CXCR4; cKit; colony-forming cells; progenitor cells
Address for reprint requests and other correspondence: S. R. Thom, Institute for Environmental Medicine, Univ. of Pennsylvania, 1 John Morgan Bldg., 3620 Hamilton Walk, Philadelphia, PA 19104-6068 (e-mail: sthom{at}mail.med.upenn.edu ) |
doi_str_mv | 10.1152/ajpheart.00888.2005 |
format | Article |
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Submitted 19 August 2005
; accepted in final form 7 November 2005
We hypothesized that exposure to hyperbaric oxygen (HBO 2 ) would mobilize stem/progenitor cells from the bone marrow by a nitric oxide (·NO) -dependent mechanism. The population of CD34 + cells in the peripheral circulation of humans doubled in response to a single exposure to 2.0 atmospheres absolute (ATA) O 2 for 2 h. Over a course of 20 treatments, circulating CD34 + cells increased eightfold, although the overall circulating white cell count was not significantly increased. The number of colony-forming cells (CFCs) increased from 16 ± 2 to 26 ± 3 CFCs/100,000 monocytes plated. Elevations in CFCs were entirely due to the CD34 + subpopulation, but increased cell growth only occurred in samples obtained immediately posttreatment. A high proportion of progeny cells express receptors for vascular endothelial growth factor-2 and for stromal-derived growth factor. In mice, HBO 2 increased circulating stem cell factor by 50%, increased the number of circulating cells expressing stem cell antigen-1 and CD34 by 3.4-fold, and doubled the number of CFCs. Bone marrow ·NO concentration increased by 1,008 ± 255 nM in association with HBO 2 . Stem cell mobilization did not occur in knockout mice lacking genes for endothelial ·NO synthase. Moreover, pretreatment of wild-type mice with a ·NO synthase inhibitor prevented the HBO 2 -induced elevation in stem cell factor and circulating stem cells. We conclude that HBO 2 mobilizes stem/progenitor cells by stimulating ·NO synthesis.
nitric oxide; CD34; CD133; CXCR4; cKit; colony-forming cells; progenitor cells
Address for reprint requests and other correspondence: S. R. Thom, Institute for Environmental Medicine, Univ. of Pennsylvania, 1 John Morgan Bldg., 3620 Hamilton Walk, Philadelphia, PA 19104-6068 (e-mail: sthom{at}mail.med.upenn.edu )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00888.2005</identifier><identifier>PMID: 16299259</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antigens, CD34 - metabolism ; Cell Movement - physiology ; Cell Proliferation ; Cells, Cultured ; Female ; Hematopoietic Stem Cells - cytology ; Hematopoietic Stem Cells - physiology ; Humans ; Hyperbaric Oxygenation - methods ; Male ; Mice ; Mice, Knockout ; Middle Aged ; Nitric Oxide - metabolism ; Oxygen - metabolism</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2006-04, Vol.290 (4), p.H1378-H1386</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-5d55576b93e1b7a1ccaef80119d17a9cc83e73f51bc04436cd4b9d41f57b96103</citedby><cites>FETCH-LOGICAL-c461t-5d55576b93e1b7a1ccaef80119d17a9cc83e73f51bc04436cd4b9d41f57b96103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16299259$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thom, Stephen R</creatorcontrib><creatorcontrib>Bhopale, Veena M</creatorcontrib><creatorcontrib>Velazquez, Omaida C</creatorcontrib><creatorcontrib>Goldstein, Lee J</creatorcontrib><creatorcontrib>Thom, Lynne H</creatorcontrib><creatorcontrib>Buerk, Donald G</creatorcontrib><title>Stem cell mobilization by hyperbaric oxygen</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 Institute for Environmental Medicine and Departments of 2 Emergency Medicine, 3 Surgery, and 4 Physiology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania
Submitted 19 August 2005
; accepted in final form 7 November 2005
We hypothesized that exposure to hyperbaric oxygen (HBO 2 ) would mobilize stem/progenitor cells from the bone marrow by a nitric oxide (·NO) -dependent mechanism. The population of CD34 + cells in the peripheral circulation of humans doubled in response to a single exposure to 2.0 atmospheres absolute (ATA) O 2 for 2 h. Over a course of 20 treatments, circulating CD34 + cells increased eightfold, although the overall circulating white cell count was not significantly increased. The number of colony-forming cells (CFCs) increased from 16 ± 2 to 26 ± 3 CFCs/100,000 monocytes plated. Elevations in CFCs were entirely due to the CD34 + subpopulation, but increased cell growth only occurred in samples obtained immediately posttreatment. A high proportion of progeny cells express receptors for vascular endothelial growth factor-2 and for stromal-derived growth factor. In mice, HBO 2 increased circulating stem cell factor by 50%, increased the number of circulating cells expressing stem cell antigen-1 and CD34 by 3.4-fold, and doubled the number of CFCs. Bone marrow ·NO concentration increased by 1,008 ± 255 nM in association with HBO 2 . Stem cell mobilization did not occur in knockout mice lacking genes for endothelial ·NO synthase. Moreover, pretreatment of wild-type mice with a ·NO synthase inhibitor prevented the HBO 2 -induced elevation in stem cell factor and circulating stem cells. We conclude that HBO 2 mobilizes stem/progenitor cells by stimulating ·NO synthesis.
nitric oxide; CD34; CD133; CXCR4; cKit; colony-forming cells; progenitor cells
Address for reprint requests and other correspondence: S. R. Thom, Institute for Environmental Medicine, Univ. of Pennsylvania, 1 John Morgan Bldg., 3620 Hamilton Walk, Philadelphia, PA 19104-6068 (e-mail: sthom{at}mail.med.upenn.edu )</description><subject>Animals</subject><subject>Antigens, CD34 - metabolism</subject><subject>Cell Movement - physiology</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Female</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Hematopoietic Stem Cells - physiology</subject><subject>Humans</subject><subject>Hyperbaric Oxygenation - methods</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Middle Aged</subject><subject>Nitric Oxide - metabolism</subject><subject>Oxygen - metabolism</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLFOwzAURS0EoqXwBUgoEwtK6xfHSSwmVFGKVImBMlu24zSukibYiWj4elJaKAuTh3fPfX4HoWvAYwAaTMS6zrWwzRjjJEnGAcb0BA37SeADJewUDTGJiB8BoQN04dwa94k4IudoAFHAWEDZEN29Nrr0lC4Kr6ykKcynaEy18WTn5V2trRTWKK_adiu9uURnmSicvjq8I_Q2e1xO5_7i5el5-rDwVRhB49OU0n6PZESDjAUoJXSWYACWQiyYUgnRMckoSIXDkEQqDSVLQ8hoLFkEmIzQ7b63ttV7q13DS-N2XxQbXbWOR3EcJmF_yQiRfVDZyjmrM15bUwrbccB854j_OOLfjvjOUU_dHOpbWer0yByk9IHJPpCbVf5hrOZ13jlTFdWqOzYGDPOQz4HESU_c_0_M2qJY6m3zi_4heZ1m5AuFOopN</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Thom, Stephen R</creator><creator>Bhopale, Veena M</creator><creator>Velazquez, Omaida C</creator><creator>Goldstein, Lee J</creator><creator>Thom, Lynne H</creator><creator>Buerk, Donald G</creator><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>20060401</creationdate><title>Stem cell mobilization by hyperbaric oxygen</title><author>Thom, Stephen R ; Bhopale, Veena M ; Velazquez, Omaida C ; Goldstein, Lee J ; Thom, Lynne H ; Buerk, Donald G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-5d55576b93e1b7a1ccaef80119d17a9cc83e73f51bc04436cd4b9d41f57b96103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Antigens, CD34 - metabolism</topic><topic>Cell Movement - physiology</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Female</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Hematopoietic Stem Cells - physiology</topic><topic>Humans</topic><topic>Hyperbaric Oxygenation - methods</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Middle Aged</topic><topic>Nitric Oxide - metabolism</topic><topic>Oxygen - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thom, Stephen R</creatorcontrib><creatorcontrib>Bhopale, Veena M</creatorcontrib><creatorcontrib>Velazquez, Omaida C</creatorcontrib><creatorcontrib>Goldstein, Lee J</creatorcontrib><creatorcontrib>Thom, Lynne H</creatorcontrib><creatorcontrib>Buerk, Donald G</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>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thom, Stephen R</au><au>Bhopale, Veena M</au><au>Velazquez, Omaida C</au><au>Goldstein, Lee J</au><au>Thom, Lynne H</au><au>Buerk, Donald G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stem cell mobilization by hyperbaric oxygen</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>290</volume><issue>4</issue><spage>H1378</spage><epage>H1386</epage><pages>H1378-H1386</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>1 Institute for Environmental Medicine and Departments of 2 Emergency Medicine, 3 Surgery, and 4 Physiology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania
Submitted 19 August 2005
; accepted in final form 7 November 2005
We hypothesized that exposure to hyperbaric oxygen (HBO 2 ) would mobilize stem/progenitor cells from the bone marrow by a nitric oxide (·NO) -dependent mechanism. The population of CD34 + cells in the peripheral circulation of humans doubled in response to a single exposure to 2.0 atmospheres absolute (ATA) O 2 for 2 h. Over a course of 20 treatments, circulating CD34 + cells increased eightfold, although the overall circulating white cell count was not significantly increased. The number of colony-forming cells (CFCs) increased from 16 ± 2 to 26 ± 3 CFCs/100,000 monocytes plated. Elevations in CFCs were entirely due to the CD34 + subpopulation, but increased cell growth only occurred in samples obtained immediately posttreatment. A high proportion of progeny cells express receptors for vascular endothelial growth factor-2 and for stromal-derived growth factor. In mice, HBO 2 increased circulating stem cell factor by 50%, increased the number of circulating cells expressing stem cell antigen-1 and CD34 by 3.4-fold, and doubled the number of CFCs. Bone marrow ·NO concentration increased by 1,008 ± 255 nM in association with HBO 2 . Stem cell mobilization did not occur in knockout mice lacking genes for endothelial ·NO synthase. Moreover, pretreatment of wild-type mice with a ·NO synthase inhibitor prevented the HBO 2 -induced elevation in stem cell factor and circulating stem cells. We conclude that HBO 2 mobilizes stem/progenitor cells by stimulating ·NO synthesis.
nitric oxide; CD34; CD133; CXCR4; cKit; colony-forming cells; progenitor cells
Address for reprint requests and other correspondence: S. R. Thom, Institute for Environmental Medicine, Univ. of Pennsylvania, 1 John Morgan Bldg., 3620 Hamilton Walk, Philadelphia, PA 19104-6068 (e-mail: sthom{at}mail.med.upenn.edu )</abstract><cop>United States</cop><pmid>16299259</pmid><doi>10.1152/ajpheart.00888.2005</doi></addata></record> |
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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Antigens, CD34 - metabolism Cell Movement - physiology Cell Proliferation Cells, Cultured Female Hematopoietic Stem Cells - cytology Hematopoietic Stem Cells - physiology Humans Hyperbaric Oxygenation - methods Male Mice Mice, Knockout Middle Aged Nitric Oxide - metabolism Oxygen - metabolism |
title | Stem cell mobilization by hyperbaric oxygen |
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