Xiaoyu Tan
University of Kansas
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Featured researches published by Xiaoyu Tan.
Journal of Immunology | 2007
Xiaoyu Tan; Suzanne Essengue; Jaya Talreja; Jeff Reese; Daniel J. Stechschulte; Kottarappat N. Dileepan
Although histamine plays an essential role in inflammation, its influence on cyclooxygenases (COX) and prostanoid homeostasis is not well understood. In this study, we investigated the effects of histamine on the expression of COX-1 and COX-2 and determined their contribution to the production of PGE2, prostacyclin (PGI2), and thromboxane A2 in human coronary artery endothelial cells (HCAEC). Incubation of HCAEC monolayers with histamine resulted in marked increases in the expression of COX-2 and production of PGI2 and PGE2 with no significant change in the expression of COX-1. Histamine-induced increases in PGI2 and PGE2 production were due to increased expression and function of COX-2 because gene silencing by small interfering RNA or inhibition of the catalytic activity by a COX-2 inhibitor blocked prostanoid production. The effects of histamine on COX-2 expression and prostanoid production were mediated through H1 receptors. In addition to the direct effect, histamine was found to amplify LPS-stimulated COX-2 expression and PGE2 and PGI2 production. In contrast, histamine did not stimulate thromboxane A2 production in resting or LPS-activated HCAEC. Histamine-induced increases in the production of PGE2 and PGI2 were associated with increased expression of mRNA encoding PGE2 and PGI2 synthases. The physiological role of histamine on the regulation of COX-2 expression in the vasculature is indicated by the findings that the expression of COX-2 mRNA, but not COX-1 mRNA, was markedly reduced in the aortic tissues of histidine decarboxylase null mice. Thus, histamine plays an important role in the regulation of COX-2 expression and prostanoid homeostasis in vascular endothelium.
American Journal of Physiology-heart and Circulatory Physiology | 2012
Donald D. Smith; Xiaoyu Tan; Vineesh V. Raveendran; Ossama Tawfik; Daniel J. Stechschulte; Kottarappat N. Dileepan
Mast cells are important cells of the immune system and are recognized as participants in the pathogenesis of atherosclerosis. In this study, we evaluated the role of mast cells on the progression of atherosclerosis and hepatic steatosis using the apolipoprotein E-deficient (ApoE(-/-)) and ApoE(-/-)/mast cell-deficient (Kit(W-sh/W-sh)) mouse models maintained on a high-fat diet. The en face analyses of aortas showed a marked reduction in plaque coverage in ApoE(-/-)/Kit(W-sh/W-sh) compared with ApoE(-/-) after a 6-mo regimen with no significant change noted after 3 mo. Quantification of intima/media thickness on hematoxylin and eosin-stained histological cross sections of the aortic arch revealed no significant difference between ApoE(-/-) and ApoE(-/-)/Kit(W-sh/W-sh) mice. The high-fat regimen did not induce atherosclerosis in either Kit(W-sh/W-sh) or wild-type mice. Mast cells with indications of degranulation were seen only in the aortic walls and heart of ApoE(-/-) mice. Compared with ApoE(-/-) mice, the serum levels of total cholesterol, low-density lipoprotein and high-density lipoprotein were decreased by 50% in ApoE(-/-)/Kit(W-sh/W-sh) mice, whereas no appreciable differences were noted in serum levels of triglycerides or very low density lipoprotein. ApoE(-/-)/Kit(W-sh/W-sh) mice developed significantly less hepatic steatosis than ApoE(-/-) mice after the 3-mo regimen. The analysis of Th1/Th2/Th17 cytokine profile in the sera revealed significant reduction of interleukin (IL)-6 and IL-10 in ApoE(-/-)/Kit(W-sh/W-sh) mice compared with ApoE(-/-) mice. The assessment of systemic generation of thromboxane A(2) (TXA(2)) and prostaglandin I(2) (PGI(2)) revealed significant decrease in the production of PGI(2) in ApoE(-/-)/Kit(W-sh/W-sh) mice with no change in TXA(2). The decrease in PGI(2) production was found to be associated with reduced levels of cyclooxygenase-2 mRNA in the aortic tissues. A significant reduction in T-lymphocytes and macrophages was noted in the atheromas of the ApoE(-/-)/Kit(W-sh/W-sh) mice. These results demonstrate the direct involvement of mast cells in the progression of atherosclerosis and hepatic steatosis.
Immunology | 2011
Vineesh V. Raveendran; Xiaoyu Tan; Matthew E. Sweeney; Beth Levant; Joyce G. Slusser; Daniel J. Stechschulte; Kottarappat N. Dileepan
Summary Histamine is a well‐recognized modulator of vascular inflammation. We have shown that histamine, acting via H1 receptors (H1R), synergizes lipopolysaccharide (LPS)‐induced production of prostaglandin I2 (PGI2), PGE2 and interleukin‐6 (IL‐6) by endothelial cells. The synergy between histamine and LPS was partly attributed to histamine ‐induced expression of Toll‐like receptor 4 (TLR4). In this study, we examined whether LPS stimulates the H1R expression in human coronary artery endothelial cells (HCAEC) with resultant enhancement of histamine responsiveness. Incubation of HCAEC with LPS (10–1000 ng/ml) resulted in two‐fold to fourfold increases in H1R mRNA expression in a time‐dependent and concentration‐dependent fashion. In contrast, LPS treatment did not affect H2R mRNA expression. The LPS‐induced H1R mRNA expression peaked by 4 hr after LPS treatment and remained elevated above the basal level for 20–24 hr. Flow cytometric and Western blot analyses revealed increased expression of H1R protein in LPS‐treated cells. The specific binding of [3H]pyrilamine to H1R in membrane proteins from LPS‐treated HCAEC was threefold higher than the untreated cells. The LPS‐induced H1R expression was mediated through TLR4 as gene silencing by TLR4‐siRNA and treatment with a TLR4 antagonist inhibited the LPS effect. When HCAEC were pre‐treated with LPS for 24 hr, washed and challenged with histamine, 17‐, 10‐ and 15‐fold increases in PGI2, PGE2 and IL‐6 production, respectively, were noted. Histamine‐induced enhancement of the synthesis of PGI2, PGE2 and IL‐6 by LPS‐primed HCAEC was completely blocked by an H1R antagonist. The results demonstrate that LPS, through TLR4 activation, up‐regulates the expression and function of H1R and amplifies histamine‐induced inflammatory responses in HCAEC.
PLOS ONE | 2014
Vineesh V. Raveendran; Donald D. Smith; Xiaoyu Tan; Matthew E. Sweeney; Gregory A. Reed; Colleen A. Flynn; Ossama Tawfik; Ginger L. Milne; Kottarappat N. Dileepan
Although increased serum histamine levels and H1R expression in the plaque are seen in atherosclerosis, it is not known whether H1R activation is a causative factor in the development of the disease, or is a host defense response to atherogenic signals. In order to elucidate how pharmacological inhibition of histamine receptor 1 (H1R) signaling affects atherogenesis, we administered either cetirizine (1 and 4 mg/kg. b.w) or fexofenadine (10 and 40 mg/kg. b.w) to ApoE−/− mice maintained on a high fat diet for three months. Mice ingesting a low dose of cetirizine or fexofenadine had significantly higher plaque coverage in the aorta and cross-sectional lesion area at the aortic root. Surprisingly, the higher doses of cetirizine or fexofenadine did not enhance atherosclerotic lesion coverage over the controls. The low dose of fexofenadine, but not cetirizine, increased serum LDL cholesterol. Interestingly, the expression of iNOS and eNOS mRNA was increased in aortas of mice on high doses of cetirizine or fexofenadine. This may be a compensatory nitric oxide (NO)-mediated vasodilatory mechanism that accounts for the lack of increase in the progression of atherosclerosis. Although the administration of cetirizine did not alter blood pressure between the groups, there was a positive correlation between blood pressure and lesion/media ratio at the aortic root in mice receiving the low dose of cetirizine. However, this association was not observed in mice treated with the high dose of cetirizine or either doses of fexofenadine. The macrophages or T lymphocytes densities were not altered by low doses of H1-antihistamines, whereas, high doses decreased the number of macrophages but not T lymphocytes. The number of mast cells was decreased only in mice treated with low dose of fexofenadine. These results demonstrate that chronic ingestion of low therapeutic doses of cetirizine or fexofenadine enhance progression of atherosclerosis.
Journal of Physiology and Pharmacology | 2010
Donald D. Smith; Xiaoyu Tan; Ossama Tawfik; Ginger L. Milne; Daniel J. Stechschulte; Kottarappat N. Dileepan
Journal of Physiology and Pharmacology | 2011
Xiaoyu Tan; Ellen M. Poulose; Vineesh V. Raveendran; Bao Ting Zhu; Daniel J. Stechschulte; Kottarappat N. Dileepan
The FASEB Journal | 2008
Donald D. Smith; Xiaoyu Tan; Ossama Tawfik; Daniel J. Stechschulte; Kottarappat N. Dileepan
Journal of Immunology | 2009
Xiaoyu Tan; Ellen M. Poulose; Daniel J. Stechschulte; Kottarappat N. Dileepan
Journal of Immunology | 2011
Vineesh V. Raveendran; Xiaoyu Tan; Matthew E. Sweeney; Daniel J. Stechschulte; Kottarapat Dileepan
Journal of Immunology | 2011
Xiaoyu Tan; Greoge Cherian; Rachel Cherian; Daniel J. Stechschulte; Kottarappat N. Dileepan