Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-3-15
pubmed:abstractText
HIV infection is characterized by gradual immune system collapse and hematopoietic dysfunction. We recently showed that HIV enters multipotent hematopoietic progenitor cells and establishes both active cytotoxic and latent infections that can be reactivated by myeloid differentiation. However, whether these multipotent progenitors include long-lived hematopoietic stem cells (HSCs) that could establish viral reservoirs for the life of the infected person remains unknown. Here we provide direct evidence that HIV targets long-lived HSCs and show that infected HSCs yield stable, multilineage engraftment in a xenograft model. Furthermore, we establish that the capacity to use the chemokine receptor CXCR4 for entry determines whether a virus will enter multipotent versus differentiated progenitor cells. Because HSCs live for the life span of the infected person and are crucial for hematopoietic health, these data may explain the poor prognosis associated with CXCR4-tropic HIV infection and suggest HSCs as long-lived cellular reservoirs of latent HIV.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/, http://linkedlifedata.com/resource/pubmed/grant/M01-RR000042, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-04A2, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-05, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-05S1, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-06, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-06S1, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-07, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-07S1, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-07S2, http://linkedlifedata.com/resource/pubmed/grant/R01 AI051192-08, http://linkedlifedata.com/resource/pubmed/grant/R21 AI086599-01, http://linkedlifedata.com/resource/pubmed/grant/R21 AI086599-02, http://linkedlifedata.com/resource/pubmed/grant/R56 AI051192-04
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1934-6069
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
17
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
223-34
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:21402361-Animals, pubmed-meshheading:21402361-Antigens, CD, pubmed-meshheading:21402361-Antigens, CD4, pubmed-meshheading:21402361-Cell Count, pubmed-meshheading:21402361-Cells, Cultured, pubmed-meshheading:21402361-Cloning, Molecular, pubmed-meshheading:21402361-Glycoproteins, pubmed-meshheading:21402361-Green Fluorescent Proteins, pubmed-meshheading:21402361-HIV Infections, pubmed-meshheading:21402361-HIV-1, pubmed-meshheading:21402361-Hematopoietic Stem Cell Transplantation, pubmed-meshheading:21402361-Hematopoietic Stem Cells, pubmed-meshheading:21402361-Host-Pathogen Interactions, pubmed-meshheading:21402361-Humans, pubmed-meshheading:21402361-Mice, pubmed-meshheading:21402361-Mice, Inbred NOD, pubmed-meshheading:21402361-Mice, SCID, pubmed-meshheading:21402361-Peptides, pubmed-meshheading:21402361-Receptors, CXCR4, pubmed-meshheading:21402361-Recombinant Proteins, pubmed-meshheading:21402361-Transplantation, Heterologous, pubmed-meshheading:21402361-Viral Load, pubmed-meshheading:21402361-Viral Plaque Assay, pubmed-meshheading:21402361-Viral Tropism, pubmed-meshheading:21402361-Virus Latency
pubmed:year
2011
pubmed:articleTitle
HIV-1 utilizes the CXCR4 chemokine receptor to infect multipotent hematopoietic stem and progenitor cells.
pubmed:affiliation
Graduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural