Regeneration of airway epithelial cells to study rare cell states in cystic fibrosis

被引:8
|
作者
Barbry, Pascal [1 ,2 ]
Cavard, Amelie [1 ,2 ]
Chanson, Marc [3 ,4 ]
Jaffe, Aron B. [5 ]
Plasschaert, Lindsey W. [5 ]
机构
[1] Univ Cote dAzur, Sophia Antipolis, France
[2] CNRS, Sophia Antipolis, France
[3] Univ Geneva, Dept Gynecol & Obstet, Fac Med, Geneva, Switzerland
[4] Univ Geneva, Dept Cell Physiol & Metab, Fac Med, Geneva, Switzerland
[5] Novartis Inst BioMed Res, Resp Dis, Cambridge, MA USA
基金
瑞士国家科学基金会;
关键词
Cellular models; RNA-seq; Repair; Airway epithelium; Cystic fibrosis; STEM-CELLS; SIGNALING CONTROLS; BASAL-CELLS; DIFFERENTIATION; REPAIR; LUNG; SEGREGATION; EXPRESSION; REGULATOR; DYNAMICS;
D O I
10.1016/j.jcf.2019.09.010
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Pathological remodeling of the airway epithelium is commonly observed in cystic fibrosis (CF). Thus, tissue repair is critical to restore integrity and maintenance of the epithelial barrier function. Epithelial repair is a multi-step process initiated by progenitor cell migration into the injured area, proliferation, and re-differentiation into all of the cell types that contribute to the function of a normal airway epithelium. Recent technological advances applied to relevant animal and cell injury models have helped in understanding the complexity of progenitor cell differentiation. This short review will introduce the current knowledge of the mechanisms regulating airway epithelial cell (AEC) regeneration and repair, with a focus on the specification of two rare cell types/states: ionocytes and deuterosomal cells. (C) 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:S42 / S46
页数:5
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