Notch2 Is Required for Inflammatory Cytokine-Driven Goblet Cell Metaplasia in the Lung

被引:196
作者
Danahay, Henry [1 ]
Pessotti, Angelica D. [2 ]
Coote, Julie [1 ]
Montgomery, Brooke E. [2 ]
Xia, Donghui [2 ]
Wilson, Aaron [2 ]
Yang, Haidi [2 ]
Wang, Zhao [2 ]
Bevan, Luke [1 ]
Thomas, Chris [2 ]
Petit, Stephanie [2 ]
London, Anne [3 ]
LeMotte, Peter [3 ]
Doelemeyer, Arno [4 ]
Velez-Reyes, German L. [2 ]
Bernasconi, Paula [2 ]
Fryer, Christy J. [2 ]
Edwards, Matt [1 ]
Capodieci, Paola [2 ]
Chen, Amy [2 ]
Hild, Marc [2 ]
Jaffe, Aron B. [2 ]
机构
[1] Novartis Inst BioMed Res, Resp Dis Area, Horsham RH12 5AB, W Sussex, England
[2] Novartis Inst BioMed Res, Dev & Mol Pathways, Cambridge, MA 02139 USA
[3] Novartis Inst BioMed Res, Novartis Biol Ctr, Cambridge, MA 02139 USA
[4] Novartis Inst BioMed Res, Discovery & Investigat Pathol, Cambridge, MA 02139 USA
来源
CELL REPORTS | 2015年 / 10卷 / 02期
关键词
MUCIN GENE-EXPRESSION; MUCOCILIARY DIFFERENTIATION; IN-VITRO; AIRWAY; INTERLEUKIN-13; ASTHMA; SURFACE; ADULTS; CLARA; MOUSE;
D O I
10.1016/j.celrep.2014.12.017
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The balance and distribution of epithelial cell types is required to maintain tissue homeostasis. A hallmark of airway diseases is epithelial remodeling, leading to increased goblet cell numbers and an overproduction of mucus. In the conducting airway, basal cells act as progenitors for both secretory and ciliated cells. To identify mechanisms regulating basal cell fate, we developed a screenable 3D culture system of airway epithelial morphogenesis. We performed a high-throughput screen using a collection of secreted proteins and identified inflammatory cytokines that specifically biased basal cell differentiation toward a goblet cell fate, culminating in enhanced mucus production. We also demonstrate a specific requirement for Notch2 in cytokine-induced goblet cell metaplasia in vitro and in vivo. We conclude that inhibition of Notch2 prevents goblet cell metaplasia induced by a broad range of stimuli and propose Notch2 neutralization as a therapeutic strategy for preventing goblet cell metaplasia in airway diseases.
引用
收藏
页码:239 / 252
页数:14
相关论文
共 46 条
[1]   HYPERSECRETION OF MUCIN IN RESPONSE TO INFLAMMATORY MEDIATORS BY GUINEA-PIG TRACHEAL EPITHELIAL-CELLS IN-VITRO IS BLOCKED BY INHIBITION OF NITRIC-OXIDE SYNTHASE [J].
ADLER, KB ;
FISCHER, BM ;
LI, HF ;
CHOE, NH ;
WRIGHT, DT .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 13 (05) :526-530
[2]  
[Anonymous], 1995, CELL MOL BIOL
[3]   Squamous metaplasia amplifies pathologic epithelial-mesenchymal interactions in COPD patients [J].
Araya, Jun ;
Cambier, Stephanie ;
Markovics, Jennifer A. ;
Wolters, Paul ;
Jablons, David ;
Hill, Arthur ;
Finkbeiner, Walter ;
Jones, Kirk ;
Broaddus, V. Courtney ;
Sheppard, Dean ;
Barzcak, Andrea ;
Xiao, Yuanyuan ;
Erle, David J. ;
Nishimura, Stephen L. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (11) :3551-3562
[4]   IL-13-induced changes in the goblet cell density of human bronchial epithelial cell cultures: MAP kinase and phosphatidylinositol 3-kinase regulation [J].
Atherton, HC ;
Jones, G ;
Danahay, H .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (03) :L730-L739
[5]   The cytokine network in asthma and chronic obstructive pulmonary disease [J].
Barnes, Peter J. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (11) :3546-3556
[6]   NOTCH TARGETS AND THEIR REGULATION [J].
Bray, Sarah ;
Bernard, Fred .
NOTCH SIGNALING, 2010, 92 :253-275
[7]   Stimulation of airway mucin gene expression by interleukin (IL)-17 through IL-6 paracrine/autocrine loop [J].
Chen, Y ;
Thai, P ;
Zhao, YH ;
Ho, YS ;
DeSouza, MM ;
Wu, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (19) :17036-17043
[8]   IL-17 in Severe Asthma Where Do We Stand? [J].
Chesne, Julie ;
Braza, Faouzi ;
Mahay, Guillaume ;
Brouard, Sophie ;
Aronica, Marc ;
Magnan, Antoine .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 190 (10) :1094-1101
[9]   Lebrikizumab Treatment in Adults with Asthma [J].
Corren, Jonathan ;
Lemanske, Robert F., Jr. ;
Hanania, Nicola A. ;
Korenblat, Phillip E. ;
Parsey, Merdad V. ;
Arron, Joseph R. ;
Harris, Jeffrey M. ;
Scheerens, Heleen ;
Wu, Lawren C. ;
Su, Zheng ;
Mosesova, Sofia ;
Eisner, Mark D. ;
Bohen, Sean P. ;
Matthews, John G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (12) :1088-1098
[10]  
Dabbagh K, 1999, J IMMUNOL, V162, P6233