Please use this identifier to cite or link to this item: http://ktisis.cut.ac.cy/handle/10488/6990
Title: Leptin receptor expression and signaling in lymphocytes: kinetics during lymphocyte activation, role in lymphocyte survival, and response to high fat diet in mice
Authors: Papathanassoglou, Elizabeth 
El-Haschimi, Karim
Li, Xian Chang
Keywords: Immunology;Lymphocytes;Mice;Antigens;Cells
Issue Date: 2006
Publisher: The American Association of Immunologists
Source: Journal of immunology, 2006, Volume 176, Issue 12, Pages 7745-7752
Abstract: Leptin has direct effects not only on neuroendocrine function and metabolism, but also on T cell-mediated immunity. We report in this study that leptin receptor (ObR) is expressed on resting normal mouse CD4 +, CD8 +, B cells, and monocyte/macrophages. ObR expression is up-regulated following cell activation, but with different kinetics, in different lymphocyte subsets. Leptin binding to ObR results in increased STAT-3 activation in T cells, with a different activation pattern in resting vs anti-CD3 Ab stimulated T cells. Leptin also promotes lymphocyte survival in vitro by suppressing Fas-mediated apoptosis. B lymphocytes appear to be more susceptible to the antiapoptotic effects of leptin, and they show higher surface expression of ObR, compared with T cells. Moreover, CD4 + T cells isolated from ObR-deficient mice displayed a reduced proliferative response, compared with normal controls. Furthermore, ObR/STAT-3-mediated signaling in T lymphocytes is decreased in the diet-induced obese mouse model of obesity and leptin resistance. In summary, our findings show that the ObR is expressed on normal mouse lymphocyte subsets, that leptin plays a role in lymphocyte survival, and that leptin alters the ObR/STAT-3-mediated signaling in T cells. Taken together, our data further support the notion that nutritional status acting via leptin-dependent mechanisms may alter the nature and vigor of the immune response. Copyright
URI: http://ktisis.cut.ac.cy/handle/10488/6990
ISSN: 0022-1767 (print)
1550-6606 (online)
DOI: http://www.jimmunol.org/content/176/12/7745.full
Rights: © 2006 by The American Association of Immunologists, Inc
Type: Article
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