It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
iNKT cells play a critical role in controlling the strength and character of adaptive and innate immune responses. Their unique functional characteristics are induced by a transcriptional program initiated by positive selection mediated by CD1d expressed by CD4+CD8+ (double positive, DP) thymocytes. Here, using a novel Vα14 TCR transgenic strain bearing greatly expanded numbers of CD24hiCD44loNKT cells, we examined transcriptional events in four immature thymic iNKT cell subsets. A transcriptional regulatory network approach identified transcriptional changes in proximal components of the TCR signalling cascade in DP NKT cells. Subsequently, positive and negative selection, and lineage commitment, occurred at the transition from DP NKT to CD4 NKT. Thus, this study introduces previously unrecognised steps in early NKT cell development, and separates the events associated with modulation of the T cell signalling cascade prior to changes associated with positive selection and lineage commitment.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 James Cook University, Molecular & Cell Biology, College of Public Health, Medical & Veterinary Sciences, The Science Place, Building 142, Townsville, Australia (GRID:grid.1011.1) (ISNI:0000 0004 0474 1797); Hai Duong Medical Technical University, Hai Duong, Viet Nam (GRID:grid.1011.1)
2 Central Queensland University, School of Medical and Applied Sciences, Rockhampton, Australia (GRID:grid.1023.0) (ISNI:0000 0001 2193 0854)
3 James Cook University, Molecular & Cell Biology, College of Public Health, Medical & Veterinary Sciences, The Science Place, Building 142, Townsville, Australia (GRID:grid.1011.1) (ISNI:0000 0004 0474 1797)
4 Federation University Australia, School of Science, Psychology and Sport, Ballarat, Australia (GRID:grid.1040.5) (ISNI:0000 0001 1091 4859); University of Melbourne, Peter Doherty Institute for Immunity and Infection, Parkville, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)