4.8 Article

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

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0700052104

Keywords

complement; differentiation; surfactant proteins; alpha-1-antitrypsin; cystic fibrosis transmembrane conductance receptor

Funding

  1. NHLBI NIH HHS [R01 HL074333, R01 HL 070537, R21 HL102833, R01 HL070537, R01 HL 074333] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI025011, R01 AI 025011] Funding Source: Medline

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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.

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