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...

Full description

Saved in:
Bibliographic Details
Published in:American journal of respiratory and critical care medicine 2007-06, Vol.175 (11), p.1158-1164
Main Authors: 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
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 (&lt; 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&amp;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 (&lt; 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 &amp; Allied Health Database</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; 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 (&lt; 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