Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion

被引:19
作者
Cho, Jin Ah [1 ]
Park, Eunmi [2 ]
机构
[1] Boston Childrens Hosp, Div GI Cell Biol, Boston, MA USA
[2] Hannam Univ, Dept Food & Nutr, Taejon 305811, South Korea
关键词
Curcumin; Intestine; Anti-inflammatory response; NF-kappa B; Bacteria; EPITHELIAL-CELL LINE; NF-KAPPA-B; INDUCED COLITIS; INFLAMMATION; RATS; ACTIVATION; IL-1-BETA; KINASE; P38; ER;
D O I
10.4162/nrp.2015.9.2.117
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
BACKGROUND/OBJECTIVES: Curcumin, a major component of the Curcuma species, contains antioxidant and anti-inflammatory properties. Although it was found to induce apoptosis in cancer cells, the functional role of curcumin as well as its molecular mechanism in anti-inflammatory response, particularly in intestinal cells, has been less investigated. The intestine epithelial barrier is the first barrier and the most important location for the substrate coming from the lumen of the gut. SUBJECTS/METHODS: We administered curcumin treatment in the human intestinal epithelial cell lines, T84 and Caco-2. We examined endoplasmic reticulum (ER) stress response by thapsigargin, qPCR of XBP1 and BiP, electrophysiology by wild-type cholera toxin in the cells. RESULTS: In this study, we showed that curcumin treatment reduces ER stress and thereby decreases inflammatory response in human intestinal epithelial cells. In addition, curcumin confers protection without damaging the membrane tight junction or actin skeleton change in intestine epithelial cells. Therefore, curcumin treatment protects the gut from bacterial invasion via reduction of ER stress and anti-inflammatory response in intestinal epithelial cells. CONCLUSIONS: Taken together, our data demonstrate the important role of curcumin in protecting the intestine by modulating ER stress and inflammatory response post intoxication.
引用
收藏
页码:117 / 122
页数:6
相关论文
共 20 条
[1]
Short curcumin treatment modulates oxidative stress, arginase activity, aberrant crypt foci, and TGF-β1 and HES-1 transcripts in 1,2-dimethylhydrazine-colon carcinogenesis in mice [J].
Bounaama, Abdelkader ;
Djerdjouri, Bahia ;
Laroche-Clary, Audrey ;
Le Morvan, Valerie ;
Robert, Jacques .
TOXICOLOGY, 2012, 302 (2-3) :308-317
[2]
RETRACTED: The Unfolded Protein Response Element IRE1α Senses Bacterial Proteins Invading the ER to Activate RIG-I and Innate Immune Signaling (Retracted article. See vol. 23, pg. 571, 2018) [J].
Cho, Jin A. ;
Lee, Ann-Hwee ;
Platzer, Barbara ;
Cross, Benedict C. S. ;
Gardner, Brooke M. ;
De Luca, Heidi ;
Luong, Phi ;
Harding, Heather P. ;
Glimcher, Laurie H. ;
Walter, Peter ;
Fiebiger, Edda ;
Ron, David ;
Kagan, Jonathan C. ;
Lencer, Wayne I. .
CELL HOST & MICROBE, 2013, 13 (05) :558-569
[3]
NF-κB and the link between inflammation and cancer [J].
DiDonato, Joseph A. ;
Mercurio, Frank ;
Karin, Michael .
IMMUNOLOGICAL REVIEWS, 2012, 246 :379-400
[4]
Curcumin suppresses p38 mitogen-activated protein kinase activation, reduces IL-1β and matrix metalloproteinase-3 and enhances IL-10 in the mucosa of children and adults with inflammatory bowel disease [J].
Epstein, Jenny ;
Docena, Guillermo ;
MacDonald, Thomas T. ;
Sanderson, Ian R. .
BRITISH JOURNAL OF NUTRITION, 2010, 103 (06) :824-832
[5]
Homeostasis and Inflammation in the Intestine [J].
Garrett, Wendy S. ;
Gordon, Jeffrey I. ;
Glimcher, Laurie H. .
CELL, 2010, 140 (06) :859-870
[6]
Glimcher Laurie H, 2012, Cell, V148, P1077
[7]
Aberrant mucin assembly in mice causes endoplasmic reticulum stress and spontaneous inflammation resembling ulcerative colitis [J].
Heazlewood, Chad K. ;
Cook, Matthew C. ;
Eri, Rajaraman ;
Price, Gareth R. ;
Tauro, Sharyn B. ;
Taupin, Douglas ;
Thornton, David J. ;
Png, Chin Wen ;
Crockford, Tanya L. ;
Cornall, Richard J. ;
Adams, Rachel ;
Kato, Masato ;
Nelms, Keats A. ;
Hong, Nancy A. ;
Florin, Timothy H. J. ;
Goodnow, Christopher C. ;
McGuckin, Michael A. .
PLOS MEDICINE, 2008, 5 (03) :440-460
[8]
Curcumin and its Formulations: Potential Anti-Cancer Agents [J].
Ji, Jun-Ling ;
Huang, Xian-Feng ;
Zhu, Hai-Liang .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2012, 12 (03) :210-218
[9]
Jian YT, 2005, WORLD J GASTROENTERO, V11, P1747, DOI 10.3748/wjg.v11.i12.1747
[10]
The IκB kinase -: a bridge between inflammation and cancer [J].
Karin, Michael .
CELL RESEARCH, 2008, 18 (03) :334-342