Characterization of distal airway stem-like cells expressing N-terminally truncated p63 and thyroid transcription factor-1 in the human lung

被引:21
作者
Tanaka, Yusuke [1 ,2 ]
Yamaguchi, Miki [1 ]
Hirai, Sachie [1 ]
Sumi, Toshiyuki [1 ,2 ]
Tada, Makoto [1 ,3 ]
Saito, Atsushi [2 ]
Chiba, Hirofumi [2 ]
Kojima, Takashi [4 ]
Watanabe, Atsushi [3 ]
Takahashi, Hiroki [2 ]
Sakuma, Yuji [1 ]
机构
[1] Sapporo Med Univ, Res Inst Frontier Med, Dept Mol Med, Sch Med, Sapporo, Hokkaido, Japan
[2] Sapporo Med Univ, Dept Resp Med & Allergol, Sch Med, Sapporo, Hokkaido, Japan
[3] Sapporo Med Univ, Dept Thorac Surg, Sch Med, Sapporo, Hokkaido, Japan
[4] Sapporo Med Univ, Res Inst Frontier Med, Dept Cell Sci, Sch Med, Sapporo, Hokkaido, Japan
基金
日本学术振兴会;
关键词
Lung; Distal airway stem cell (DASC); Delta Np63; Thyroid transcription factor 1 (TTF-1); 3D culture; EPITHELIAL-MESENCHYMAL TRANSITION; IDIOPATHIC PULMONARY-FIBROSIS; BASAL-CELLS; ADENOCARCINOMA CELLS; ADULT LUNG; REGENERATION; TTF-1; IDENTIFICATION; POPULATIONS; CARCINOMA;
D O I
10.1016/j.yexcr.2018.09.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Distal airway stem cells (DASCs) in the mouse lung can differentiate into bronchioles and alveoli. However, it remains unclear whether the same stem cells exist in the human lung. Here, we found that human lung epithelial (HuL) cells, derived from normal, peripheral lung tissue, in monolayer, mostly express both the N-terminally truncated isoform of p63 (Delta Np63), a marker for airway basal cells, and thyroid transcription factor-1 (TTF-1), a marker for alveolar epithelial cells, even though these two molecules are usually expressed in a mutually exclusive way. Three-dimensionally cultured HuL cells differentiated to form bronchiole-like and alveolus-like organoids. We also uncovered a few bronchiolar epithelial cells expressing both Delta Np63 and TTF-1 in the human lung, suggesting that these cells are the cells of origin for HuL cells. Taken together, Delta Np63 + TTF-1(+) peripheral airway epithelial cells are possibly the human counterpart of mouse DASCs and may offer potential for future regenerative medicine.
引用
收藏
页码:141 / 149
页数:9
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