Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2010-9-3
pubmed:abstractText
During responses against viruses and malignancies, naive CD8 T lymphocytes expand to form both short-lived effector cells and a population containing cells with the potential to be long-lived and participate in memory responses (memory precursor effector cells). The strength of antigenic, costimulatory, and cytokine signals during responses impacts the magnitude and type of CD8 populations formed. In vitro studies have revealed that the tyrosine phosphatase Src homology region 2 domain-containing phosphatase-1 (SHP-1) regulates signal transduction from receptors on T cells including the TCR, helping set the activation threshold, and therefore may shape responses of mature CD8 T cells in vivo. Analysis of CD8 T cells from motheaten mice, which are globally deficient in SHP-1, proved problematic due to cell-extrinsic effects of SHP-1 deficiency in non-T cells on CD8 T cells. Therefore, a conditional knockout of SHP-1 in mature single-positive T cells was developed to analyze cell-intrinsic consequences of complete and partial SHP-1 deficiency on CD8 T cell responses to acute viral infection. The results demonstrated that SHP-1 has disparate effects on subpopulations of responding cells, limiting the magnitude and quality of primary and secondary responses by reducing the number of short-lived effector cells generated without affecting the size of the memory precursor effector cell pool that leads to formation of long-term memory.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1550-6606
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
185
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3256-67
pubmed:dateRevised
2011-9-19
pubmed:meshHeading
pubmed-meshheading:20696858-Animals, pubmed-meshheading:20696858-CD8-Positive T-Lymphocytes, pubmed-meshheading:20696858-Cell Differentiation, pubmed-meshheading:20696858-Cell Line, pubmed-meshheading:20696858-Cell Survival, pubmed-meshheading:20696858-Cricetinae, pubmed-meshheading:20696858-Down-Regulation, pubmed-meshheading:20696858-Growth Inhibitors, pubmed-meshheading:20696858-Immunologic Memory, pubmed-meshheading:20696858-Lymphocyte Depletion, pubmed-meshheading:20696858-Mice, pubmed-meshheading:20696858-Mice, Inbred C57BL, pubmed-meshheading:20696858-Mice, Knockout, pubmed-meshheading:20696858-Mice, Transgenic, pubmed-meshheading:20696858-Protein Tyrosine Phosphatase, Non-Receptor Type 6, pubmed-meshheading:20696858-Stem Cells, pubmed-meshheading:20696858-T-Lymphocyte Subsets, pubmed-meshheading:20696858-T-Lymphocytes, Cytotoxic
pubmed:year
2010
pubmed:articleTitle
SHP-1 in T cells limits the production of CD8 effector cells without impacting the formation of long-lived central memory cells.
pubmed:affiliation
Department of Immunology, School of Medicine, University of Washington, Seattle, WA 98195- 6425, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural