Loading…
Lung cells from neonates show a mesenchymal stem cell phenotype
Mesenchymal stem cells have been isolated from adult bone marrow, peripheral blood, adipose tissue, trabecular bone, articular synovium, and bronchial submucosa. We hypothesized that the lungs of premature infants undergoing mechanical ventilation contain fibroblast-like cells with features of mesen...
Saved in:
Published in: | American journal of respiratory and critical care medicine 2007-06, Vol.175 (11), p.1158-1164 |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 1164 |
container_issue | 11 |
container_start_page | 1158 |
container_title | American journal of respiratory and critical care medicine |
container_volume | 175 |
creator | HENNRICK, Kenneth T KEETON, Angela G THANNICKAL, Victor J HERSHENSON, Marc B NANUA, Suparna KIJEK, Theresa G GOLDSMITH, Adam M SAJJAN, Umadevi S BENTLEY, J. Kelley LAMA, Vibha N MOORE, Bethany B SCHUMACHER, Robert E |
description | Mesenchymal stem cells have been isolated from adult bone marrow, peripheral blood, adipose tissue, trabecular bone, articular synovium, and bronchial submucosa.
We hypothesized that the lungs of premature infants undergoing mechanical ventilation contain fibroblast-like cells with features of mesenchymal stem cells.
Tracheal aspirate fluid from mechanically ventilated, premature (< 30 wk gestation) infants 7 days old or younger was obtained from routine suctioning and plated on plastic culture dishes.
A total of 11 of 20 patients studied demonstrated fibroblast-like cells, which were identified as early as 6 hours after plating. Cells were found to express the mesenchymal stem cell markers STRO-1, CD73, CD90, CD105, and CD166, as well as CCR2b, CD13, prolyl 4-hydroxylase, and alpha-smooth muscle actin. Cells were negative for the hematopoietic and endothelial cell markers CD11b, CD31, CD34, or CD45. Tracheal aspirate monocyte chemoattractant protein-1/CCL2 levels were ninefold higher in aspirates in which fibroblast-like cells were found, and cells demonstrated chemotaxis in response to monocyte chemoattractant protein. Placement of cells into appropriate media resulted in adipogenic, osteogenic, and myofibroblastic differentiation. Patients from whom mesenchymal stem cells were isolated tended to require more days of mechanical ventilation and supplemental oxygen.
Together, these data demonstrate that tracheal aspirate fluid from premature, mechanically ventilated infants contains fibroblasts with cell markers and differentiation potential typically found in mesenchymal stem cells. |
doi_str_mv | 10.1164/rccm.200607-941OC |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_70512713</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70512713</sourcerecordid><originalsourceid>FETCH-LOGICAL-p266t-24bbdc4b366a5b523cab5578af5974a0d49e89f52c15f802af9834ef0487523e3</originalsourceid><addsrcrecordid>eNpd0E1LxDAQgOEgiuvXD_AiQdBb10kyaZKTyOIXLHhR8FbSbOLu0rS1aZH991ZdETzNHB6GlyHklMGUsRyvOufilAPkoDKD7Gm2Qw6YFDJDo2B33EGJDNG8TshhSmsAxjWDfTJhSgiOGg_I9Xyo36jzVZVo6JpIa9_UtveJpmXzQS2NPvnaLTfRVjT1Pn5b2i593fSb1h-TvWCr5E-284i83N0-zx6y-dP94-xmnrU8z_uMY1kuHJYiz60sJRfOllIqbYM0Ci0s0HhtguSOyaCB22C0QB8AtRq1F0fk8udu2zXvg099EVfpK8WOwUMqFEjGFRMjPP8H183Q1WNbwYyRJteoRnS2RUMZ_aJou1W03ab4_csILrbAJmer0NnardKf0xq0QRCfHIdxWg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>199596847</pqid></control><display><type>article</type><title>Lung cells from neonates show a mesenchymal stem cell phenotype</title><source>Freely Accessible Journals</source><source>EZB Electronic Journals Library</source><creator>HENNRICK, Kenneth T ; KEETON, Angela G ; THANNICKAL, Victor J ; HERSHENSON, Marc B ; NANUA, Suparna ; KIJEK, Theresa G ; GOLDSMITH, Adam M ; SAJJAN, Umadevi S ; BENTLEY, J. Kelley ; LAMA, Vibha N ; MOORE, Bethany B ; SCHUMACHER, Robert E</creator><creatorcontrib>HENNRICK, Kenneth T ; KEETON, Angela G ; THANNICKAL, Victor J ; HERSHENSON, Marc B ; NANUA, Suparna ; KIJEK, Theresa G ; GOLDSMITH, Adam M ; SAJJAN, Umadevi S ; BENTLEY, J. Kelley ; LAMA, Vibha N ; MOORE, Bethany B ; SCHUMACHER, Robert E</creatorcontrib><description>Mesenchymal stem cells have been isolated from adult bone marrow, peripheral blood, adipose tissue, trabecular bone, articular synovium, and bronchial submucosa.
We hypothesized that the lungs of premature infants undergoing mechanical ventilation contain fibroblast-like cells with features of mesenchymal stem cells.
Tracheal aspirate fluid from mechanically ventilated, premature (< 30 wk gestation) infants 7 days old or younger was obtained from routine suctioning and plated on plastic culture dishes.
A total of 11 of 20 patients studied demonstrated fibroblast-like cells, which were identified as early as 6 hours after plating. Cells were found to express the mesenchymal stem cell markers STRO-1, CD73, CD90, CD105, and CD166, as well as CCR2b, CD13, prolyl 4-hydroxylase, and alpha-smooth muscle actin. Cells were negative for the hematopoietic and endothelial cell markers CD11b, CD31, CD34, or CD45. Tracheal aspirate monocyte chemoattractant protein-1/CCL2 levels were ninefold higher in aspirates in which fibroblast-like cells were found, and cells demonstrated chemotaxis in response to monocyte chemoattractant protein. Placement of cells into appropriate media resulted in adipogenic, osteogenic, and myofibroblastic differentiation. Patients from whom mesenchymal stem cells were isolated tended to require more days of mechanical ventilation and supplemental oxygen.
Together, these data demonstrate that tracheal aspirate fluid from premature, mechanically ventilated infants contains fibroblasts with cell markers and differentiation potential typically found in mesenchymal stem cells.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.200607-941OC</identifier><identifier>PMID: 17332484</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>5'-Nucleotidase - metabolism ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Antibodies ; Antigens, CD - metabolism ; Biological and medical sciences ; Biomarkers ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Body fat ; Bone marrow ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Cartilage ; Cell Adhesion ; Cell Adhesion Molecules, Neuronal - metabolism ; Cell Differentiation ; Cell Movement ; Cells, Cultured ; Chemokine CCL2 - metabolism ; Disease Progression ; Endoglin ; Enzyme-Linked Immunosorbent Assay ; Fetal Proteins - metabolism ; Fibroblasts ; Fibroblasts - pathology ; Flow Cytometry ; Humans ; Immunoblotting ; Immunohistochemistry ; Infant, Newborn ; Infant, Premature ; Intensive care medicine ; Lung - pathology ; Lung diseases ; Medical sciences ; Mesenchymal Stromal Cells - metabolism ; Mesenchymal Stromal Cells - pathology ; Phenotype ; Premature babies ; Premature birth ; Proteins ; Receptors, Cell Surface - metabolism ; Respiration, Artificial ; Respiratory distress syndrome ; Respiratory Distress Syndrome, Newborn - genetics ; Respiratory Distress Syndrome, Newborn - pathology ; Respiratory Distress Syndrome, Newborn - therapy ; Retrospective Studies ; Smooth muscle ; Stem cells ; Telangiectasia, Hereditary Hemorrhagic ; Thy-1 Antigens - metabolism ; Trachea - pathology ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Ventilators</subject><ispartof>American journal of respiratory and critical care medicine, 2007-06, Vol.175 (11), p.1158-1164</ispartof><rights>2007 INIST-CNRS</rights><rights>Copyright American Thoracic Society Jun 1, 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18808940$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17332484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HENNRICK, Kenneth T</creatorcontrib><creatorcontrib>KEETON, Angela G</creatorcontrib><creatorcontrib>THANNICKAL, Victor J</creatorcontrib><creatorcontrib>HERSHENSON, Marc B</creatorcontrib><creatorcontrib>NANUA, Suparna</creatorcontrib><creatorcontrib>KIJEK, Theresa G</creatorcontrib><creatorcontrib>GOLDSMITH, Adam M</creatorcontrib><creatorcontrib>SAJJAN, Umadevi S</creatorcontrib><creatorcontrib>BENTLEY, J. Kelley</creatorcontrib><creatorcontrib>LAMA, Vibha N</creatorcontrib><creatorcontrib>MOORE, Bethany B</creatorcontrib><creatorcontrib>SCHUMACHER, Robert E</creatorcontrib><title>Lung cells from neonates show a mesenchymal stem cell phenotype</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>Mesenchymal stem cells have been isolated from adult bone marrow, peripheral blood, adipose tissue, trabecular bone, articular synovium, and bronchial submucosa.
We hypothesized that the lungs of premature infants undergoing mechanical ventilation contain fibroblast-like cells with features of mesenchymal stem cells.
Tracheal aspirate fluid from mechanically ventilated, premature (< 30 wk gestation) infants 7 days old or younger was obtained from routine suctioning and plated on plastic culture dishes.
A total of 11 of 20 patients studied demonstrated fibroblast-like cells, which were identified as early as 6 hours after plating. Cells were found to express the mesenchymal stem cell markers STRO-1, CD73, CD90, CD105, and CD166, as well as CCR2b, CD13, prolyl 4-hydroxylase, and alpha-smooth muscle actin. Cells were negative for the hematopoietic and endothelial cell markers CD11b, CD31, CD34, or CD45. Tracheal aspirate monocyte chemoattractant protein-1/CCL2 levels were ninefold higher in aspirates in which fibroblast-like cells were found, and cells demonstrated chemotaxis in response to monocyte chemoattractant protein. Placement of cells into appropriate media resulted in adipogenic, osteogenic, and myofibroblastic differentiation. Patients from whom mesenchymal stem cells were isolated tended to require more days of mechanical ventilation and supplemental oxygen.
Together, these data demonstrate that tracheal aspirate fluid from premature, mechanically ventilated infants contains fibroblasts with cell markers and differentiation potential typically found in mesenchymal stem cells.</description><subject>5'-Nucleotidase - metabolism</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antibodies</subject><subject>Antigens, CD - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Body fat</subject><subject>Bone marrow</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Cartilage</subject><subject>Cell Adhesion</subject><subject>Cell Adhesion Molecules, Neuronal - metabolism</subject><subject>Cell Differentiation</subject><subject>Cell Movement</subject><subject>Cells, Cultured</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Disease Progression</subject><subject>Endoglin</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fetal Proteins - metabolism</subject><subject>Fibroblasts</subject><subject>Fibroblasts - pathology</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Intensive care medicine</subject><subject>Lung - pathology</subject><subject>Lung diseases</subject><subject>Medical sciences</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Mesenchymal Stromal Cells - pathology</subject><subject>Phenotype</subject><subject>Premature babies</subject><subject>Premature birth</subject><subject>Proteins</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Respiration, Artificial</subject><subject>Respiratory distress syndrome</subject><subject>Respiratory Distress Syndrome, Newborn - genetics</subject><subject>Respiratory Distress Syndrome, Newborn - pathology</subject><subject>Respiratory Distress Syndrome, Newborn - therapy</subject><subject>Retrospective Studies</subject><subject>Smooth muscle</subject><subject>Stem cells</subject><subject>Telangiectasia, Hereditary Hemorrhagic</subject><subject>Thy-1 Antigens - metabolism</subject><subject>Trachea - pathology</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Ventilators</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpd0E1LxDAQgOEgiuvXD_AiQdBb10kyaZKTyOIXLHhR8FbSbOLu0rS1aZH991ZdETzNHB6GlyHklMGUsRyvOufilAPkoDKD7Gm2Qw6YFDJDo2B33EGJDNG8TshhSmsAxjWDfTJhSgiOGg_I9Xyo36jzVZVo6JpIa9_UtveJpmXzQS2NPvnaLTfRVjT1Pn5b2i593fSb1h-TvWCr5E-284i83N0-zx6y-dP94-xmnrU8z_uMY1kuHJYiz60sJRfOllIqbYM0Ci0s0HhtguSOyaCB22C0QB8AtRq1F0fk8udu2zXvg099EVfpK8WOwUMqFEjGFRMjPP8H183Q1WNbwYyRJteoRnS2RUMZ_aJou1W03ab4_csILrbAJmer0NnardKf0xq0QRCfHIdxWg</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>HENNRICK, Kenneth T</creator><creator>KEETON, Angela G</creator><creator>THANNICKAL, Victor J</creator><creator>HERSHENSON, Marc B</creator><creator>NANUA, Suparna</creator><creator>KIJEK, Theresa G</creator><creator>GOLDSMITH, Adam M</creator><creator>SAJJAN, Umadevi S</creator><creator>BENTLEY, J. Kelley</creator><creator>LAMA, Vibha N</creator><creator>MOORE, Bethany B</creator><creator>SCHUMACHER, Robert E</creator><general>American Lung Association</general><general>American Thoracic Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20070601</creationdate><title>Lung cells from neonates show a mesenchymal stem cell phenotype</title><author>HENNRICK, Kenneth T ; KEETON, Angela G ; THANNICKAL, Victor J ; HERSHENSON, Marc B ; NANUA, Suparna ; KIJEK, Theresa G ; GOLDSMITH, Adam M ; SAJJAN, Umadevi S ; BENTLEY, J. Kelley ; LAMA, Vibha N ; MOORE, Bethany B ; SCHUMACHER, Robert E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-24bbdc4b366a5b523cab5578af5974a0d49e89f52c15f802af9834ef0487523e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>5'-Nucleotidase - metabolism</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Antibodies</topic><topic>Antigens, CD - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</topic><topic>Body fat</topic><topic>Bone marrow</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cartilage</topic><topic>Cell Adhesion</topic><topic>Cell Adhesion Molecules, Neuronal - metabolism</topic><topic>Cell Differentiation</topic><topic>Cell Movement</topic><topic>Cells, Cultured</topic><topic>Chemokine CCL2 - metabolism</topic><topic>Disease Progression</topic><topic>Endoglin</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fetal Proteins - metabolism</topic><topic>Fibroblasts</topic><topic>Fibroblasts - pathology</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>Infant, Newborn</topic><topic>Infant, Premature</topic><topic>Intensive care medicine</topic><topic>Lung - pathology</topic><topic>Lung diseases</topic><topic>Medical sciences</topic><topic>Mesenchymal Stromal Cells - metabolism</topic><topic>Mesenchymal Stromal Cells - pathology</topic><topic>Phenotype</topic><topic>Premature babies</topic><topic>Premature birth</topic><topic>Proteins</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Respiration, Artificial</topic><topic>Respiratory distress syndrome</topic><topic>Respiratory Distress Syndrome, Newborn - genetics</topic><topic>Respiratory Distress Syndrome, Newborn - pathology</topic><topic>Respiratory Distress Syndrome, Newborn - therapy</topic><topic>Retrospective Studies</topic><topic>Smooth muscle</topic><topic>Stem cells</topic><topic>Telangiectasia, Hereditary Hemorrhagic</topic><topic>Thy-1 Antigens - metabolism</topic><topic>Trachea - pathology</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HENNRICK, Kenneth T</creatorcontrib><creatorcontrib>KEETON, Angela G</creatorcontrib><creatorcontrib>THANNICKAL, Victor J</creatorcontrib><creatorcontrib>HERSHENSON, Marc B</creatorcontrib><creatorcontrib>NANUA, Suparna</creatorcontrib><creatorcontrib>KIJEK, Theresa G</creatorcontrib><creatorcontrib>GOLDSMITH, Adam M</creatorcontrib><creatorcontrib>SAJJAN, Umadevi S</creatorcontrib><creatorcontrib>BENTLEY, J. Kelley</creatorcontrib><creatorcontrib>LAMA, Vibha N</creatorcontrib><creatorcontrib>MOORE, Bethany B</creatorcontrib><creatorcontrib>SCHUMACHER, Robert E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</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>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HENNRICK, Kenneth T</au><au>KEETON, Angela G</au><au>THANNICKAL, Victor J</au><au>HERSHENSON, Marc B</au><au>NANUA, Suparna</au><au>KIJEK, Theresa G</au><au>GOLDSMITH, Adam M</au><au>SAJJAN, Umadevi S</au><au>BENTLEY, J. Kelley</au><au>LAMA, Vibha N</au><au>MOORE, Bethany B</au><au>SCHUMACHER, Robert E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lung cells from neonates show a mesenchymal stem cell phenotype</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>175</volume><issue>11</issue><spage>1158</spage><epage>1164</epage><pages>1158-1164</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Mesenchymal stem cells have been isolated from adult bone marrow, peripheral blood, adipose tissue, trabecular bone, articular synovium, and bronchial submucosa.
We hypothesized that the lungs of premature infants undergoing mechanical ventilation contain fibroblast-like cells with features of mesenchymal stem cells.
Tracheal aspirate fluid from mechanically ventilated, premature (< 30 wk gestation) infants 7 days old or younger was obtained from routine suctioning and plated on plastic culture dishes.
A total of 11 of 20 patients studied demonstrated fibroblast-like cells, which were identified as early as 6 hours after plating. Cells were found to express the mesenchymal stem cell markers STRO-1, CD73, CD90, CD105, and CD166, as well as CCR2b, CD13, prolyl 4-hydroxylase, and alpha-smooth muscle actin. Cells were negative for the hematopoietic and endothelial cell markers CD11b, CD31, CD34, or CD45. Tracheal aspirate monocyte chemoattractant protein-1/CCL2 levels were ninefold higher in aspirates in which fibroblast-like cells were found, and cells demonstrated chemotaxis in response to monocyte chemoattractant protein. Placement of cells into appropriate media resulted in adipogenic, osteogenic, and myofibroblastic differentiation. Patients from whom mesenchymal stem cells were isolated tended to require more days of mechanical ventilation and supplemental oxygen.
Together, these data demonstrate that tracheal aspirate fluid from premature, mechanically ventilated infants contains fibroblasts with cell markers and differentiation potential typically found in mesenchymal stem cells.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>17332484</pmid><doi>10.1164/rccm.200607-941OC</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1073-449X |
ispartof | American journal of respiratory and critical care medicine, 2007-06, Vol.175 (11), p.1158-1164 |
issn | 1073-449X 1535-4970 |
language | eng |
recordid | cdi_proquest_miscellaneous_70512713 |
source | Freely Accessible Journals; EZB Electronic Journals Library |
subjects | 5'-Nucleotidase - metabolism Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Antibodies Antigens, CD - metabolism Biological and medical sciences Biomarkers Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis Body fat Bone marrow Bone marrow, stem cells transplantation. Graft versus host reaction Cartilage Cell Adhesion Cell Adhesion Molecules, Neuronal - metabolism Cell Differentiation Cell Movement Cells, Cultured Chemokine CCL2 - metabolism Disease Progression Endoglin Enzyme-Linked Immunosorbent Assay Fetal Proteins - metabolism Fibroblasts Fibroblasts - pathology Flow Cytometry Humans Immunoblotting Immunohistochemistry Infant, Newborn Infant, Premature Intensive care medicine Lung - pathology Lung diseases Medical sciences Mesenchymal Stromal Cells - metabolism Mesenchymal Stromal Cells - pathology Phenotype Premature babies Premature birth Proteins Receptors, Cell Surface - metabolism Respiration, Artificial Respiratory distress syndrome Respiratory Distress Syndrome, Newborn - genetics Respiratory Distress Syndrome, Newborn - pathology Respiratory Distress Syndrome, Newborn - therapy Retrospective Studies Smooth muscle Stem cells Telangiectasia, Hereditary Hemorrhagic Thy-1 Antigens - metabolism Trachea - pathology Transfusions. Complications. Transfusion reactions. Cell and gene therapy Ventilators |
title | Lung cells from neonates show a mesenchymal stem cell phenotype |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T19%3A02%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lung%20cells%20from%20neonates%20show%20a%20mesenchymal%20stem%20cell%20phenotype&rft.jtitle=American%20journal%20of%20respiratory%20and%20critical%20care%20medicine&rft.au=HENNRICK,%20Kenneth%20T&rft.date=2007-06-01&rft.volume=175&rft.issue=11&rft.spage=1158&rft.epage=1164&rft.pages=1158-1164&rft.issn=1073-449X&rft.eissn=1535-4970&rft_id=info:doi/10.1164/rccm.200607-941OC&rft_dat=%3Cproquest_pubme%3E70512713%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p266t-24bbdc4b366a5b523cab5578af5974a0d49e89f52c15f802af9834ef0487523e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=199596847&rft_id=info:pmid/17332484&rfr_iscdi=true |