A pure population of lung alveolar epithelial type II cells derived from human embryonic stem cells

被引:159
作者
Wang, Dachun
Haviland, David L.
Burns, Alan R.
Zsigmond, Eva
Wetsel, Rick A.
机构
[1] Univ Texas, Hlth Sci Ctr, Brown Fdn Inst Mol Med Prevent Human Dis, Res Ctr Immunol & Autoimmune Dis, Houston, TX 77030 USA
[2] Univ Texas, Hlth Sci Ctr, Brown Fdn Inst Mol Med Prevent Human Dis, Dev Biol Lab, Houston, TX 77030 USA
[3] Univ Texas, Sch Med, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Med, Cardiovasc Sci Sect, Houston, TX 77030 USA
关键词
complement; differentiation; surfactant proteins; alpha-1-antitrypsin; cystic fibrosis transmembrane conductance receptor;
D O I
10.1073/pnas.0700052104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alveolar epithelial type II (ATII) cells are small, cuboidal cells that constitute approximate to 60% of the pulmonary alveolar epithelium. These cells are crucial for repair of the injured alveolus by differentiating into alveolar epithelial type I cells. ATII cells derived from human ES (hES) cells are a promising source of cells that could be used therapeutically to treat distal lung diseases. We have developed a reliable transfection and culture procedure, which facilitates, via genetic selection, the differentiation of hES cells into an essentially pure (> 99%) population of ATII cells (hES-ATII). Purity, as well as biological features and morphological characteristics of normal ATII cells, was demonstrated for the hES-ATII cells, including lamellar body formation, expression of surfactant proteins A, B, and C, a-l-antitrypsin, and the cystic fibrosis transmembrane conductance receptor, as well as the synthesis and secretion of complement proteins C3 and C5. Collectively, these data document the successful generation of a pure population of ATII cells derived from hES cells, providing a practical source of ATII cells to explore in disease models their potential in the regeneration and repair of the injured alveolus and in the therapeutic treatment of genetic diseases affecting the lung.
引用
收藏
页码:4449 / 4454
页数:6
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