Immune Cell Isolation from Murine Intestine for Antibody Array Analysis

Author(s):  
Joshua A. Owens ◽  
Rheinallt M. Jones
2005 ◽  
Vol 382 (1-2) ◽  
pp. 128-133 ◽  
Author(s):  
Mineo Watanabe ◽  
Wei Guo ◽  
Shiping Zou ◽  
Shinichi Sugiyo ◽  
Ronald Dubner ◽  
...  

2010 ◽  
Vol 27 ◽  
pp. S74
Author(s):  
A. Holm ◽  
W. Wu ◽  
H.S. Slaastad ◽  
L. Goullart ◽  
D. Carrillo

2014 ◽  
Vol 403 (1-2) ◽  
pp. 79-86 ◽  
Author(s):  
Weidong Jiang ◽  
Ying Qing Mao ◽  
Ruochun Huang ◽  
Chaohui Duan ◽  
Yun Xi ◽  
...  

2011 ◽  
Vol 34 (5) ◽  
pp. 387-397 ◽  
Author(s):  
Denise M. Newsom ◽  
H. Denny Liggitt ◽  
Katherine O’Rourke ◽  
Dongyue Zhuang ◽  
David A. Schneider ◽  
...  

Oncogene ◽  
2007 ◽  
Vol 26 (29) ◽  
pp. 4216-4225 ◽  
Author(s):  
S J Moschos ◽  
A P Smith ◽  
M Mandic ◽  
C Athanassiou ◽  
K Watson-Hurst ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0246989
Author(s):  
Syed K. Rafi ◽  
Jeremy P. Goering ◽  
Adam J. Olm-Shipman ◽  
Lauren A. Hipp ◽  
Nicholas J. Ernst ◽  
...  

Topiramate is an anti-epileptic drug that is commonly prescribed not just to prevent seizures but also migraine headaches, with over 8 million prescriptions dispensed annually. Topiramate use during pregnancy has been linked to significantly increased risk of babies born with orofacial clefts (OFCs). However, the exact molecular mechanism of topiramate teratogenicity is unknown. In this study, we first used an unbiased antibody array analysis to test the effect of topiramate on human embryonic palatal mesenchyme (HEPM) cells. This analysis identified 40 differentially expressed proteins, showing strong connectivity to known genes associated with orofacial clefts. However, among known OFC genes, only TGFβ1 was significantly upregulated in the antibody array analysis. Next, we validated that topiramate could increase expression of TGFβ1 and of downstream target phospho-SMAD2 in primary mouse embryonic palatal mesenchyme (MEPM) cells. Furthermore, we showed that topiramate treatment of primary MEPM cells increased expression of SOX9. SOX9 overexpression in chondrocytes is known to cause cleft palate in mouse. We propose that topiramate mediates upregulation of TGFβ1 signaling through activation of γ-aminobutyric acid (GABA) receptors in the palate. TGFβ1 and SOX9 play critical roles in orofacial morphogenesis, and their abnormal overexpression provides a plausible etiologic molecular mechanism for the teratogenic effects of topiramate.


2008 ◽  
Vol 8 (2) ◽  
pp. 245-257 ◽  
Author(s):  
Weiwei Wu ◽  
Heidi Slåstad ◽  
Daniel de la Rosa Carrillo ◽  
Tom Frey ◽  
Geir Tjønnfjord ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Xue Mei Fan ◽  
Chun Lian Huang ◽  
Yi Ming Wang ◽  
Ning Li ◽  
Qiong Lin Liang ◽  
...  

Objective. Cytokines are essential promoters in the pathogenesis of diabetic nephropathy (DN) in type 2 diabetes. The following study investigates the adjustment mechanism of Tangshen formula (TSF) on cytokine expressions in db/db mice (DN animal model). Materials and Methods. Db/db mice were randomly divided into three groups. The treated groups were orally administered with TSF and losartan for 12 weeks. Biochemical and histological examinations were determined at 8 and 12 weeks posttreatment, while the cytokine antibody array analysis was applied to analyze the expression of 144 cytokines in kidney tissues at the end of the 12th week posttreatment. Results. TSF significantly reduced urinary albumin excretion and the levels of blood glucose, cholesterol, triglyceride, creatinine, and urea nitrogen. Furthermore, a significant decrease in glomerulus and mesangial area, as well as the downregulation of 24 cytokines and upregulated expressions of 5 cytokines, was found in the TSF-treated mice. Conclusions. The present study reveals that TSF could ameliorate the metabolic anomalies and renal injury in db/db mice. One of the important mechanisms for treatment of DN using the treatment of TSF is the control of the JAK/STAT signaling pathway via regulation of IL-2, IL-6, IL-13, Il-15, and IFN-γ expression.


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