Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/41989
Title: ZSWIM1: A novel biomarker in T helper cell differentiation.
Authors: Hogarth P.M.;Ko K.K.;Powell M.S.
Institution: (Ko, Powell, Hogarth) Centre for Biomedical Research, Burnet Institute, Melbourne 3004, VIC, Australia (Ko, Powell, Hogarth) Department of Pathology, University of Melbourne, Melbourne 3084, VIC, Australia (Powell) School of Public Health and Preventive Medicine, Monash University, Clayton 3168, VIC, Australia (Hogarth) Department of Immunology, Monash University, Melbourne 3004, VIC, Australia (Powell) Monash Centre for Health Research and Implementation Schoolof Public Health, Preventive Medicine, Monash University-in partnership with Monash Health Locked Bag 29, Clayton 3168, VIC, Australia
Issue Date: 25-Jun-2014
Copyright year: 2014
Publisher: Elsevier
Place of publication: Netherlands
Publication information: Immunology Letters. 160 (2) (pp 133-138), 2014. Date of Publication: August 2014.
Journal: Immunology Letters
Abstract: The effector memory CD4+ Th17 cells play critical roles in bacterial immunity and pathological inflammation in autoimmune conditions. ZSWIM1 is a gene encoding a protein of unknown function in leukocytes-but containing a zinc finger SWIM motif. In peripheral blood mononuclear cells, the expression of ZSWIM1 is highest in lymphocytes, and in particular shows greatest abundance in naive CD4+ T cells. Upon polarisation of naive CD4+ T cells, ZSWIM1 expression is retained in Th17 cells but is selectively down regulated in Th1 cells. Similarly in in vitro expanded effector memory CD4+ T cells, ZSWIM1 was more abundant in Th17 cells compared to Th1 or Th17 polyfunctional (Th17pf) cells, which produce IL-17A and IFNgamma. Although stimulation of cytokine production by PMA and ionomycin reduced ZSWIM1 expression, the relative differences in abundance between the cell types were maintained. The activation sensitive nature of ZSWIM1 expression suggests that it may play a novel role in the development or function of T helper cells. © 2014 Elsevier B.V.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.imlet.2014.01.016
PubMed URL: 24508175 [http://www.ncbi.nlm.nih.gov/pubmed/?term=24508175]
ISSN: 0165-2478
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/41989
Type: Article
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