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Updated: May 12, 2026

Generation of 3D Whole Lung Organoids from Induced Pluripotent Stem Cells for Modeling Lung Developmental Biology and Disease
Published on: April 12, 2021
Major enzymes controlling the androgenic pressure in the developing lung
Yves Tremblay1, Pierre R Provost
1Reproduction Axis, Perinatal and Child Health, Rm T-1-49, CHUQ Research Center, Canada; Department of Obstetrics/Gynecology & Reproduction, Faculty of Medicine, Laval University, Québec City, Québec, Canada; Centre de Recherche en Biologie de la Reproduction (CRBR), Laval University, Québec City, Québec, Canada.
Androgens influence neonatal respiratory distress syndrome (RDS) and bronchopulmonary dysplasia (BPD). The developing lung metabolizes androgens via specific enzymes, offering potential pharmaceutical targets for lung maturation.
Area of Science:
- Neonatal physiology
- Endocrinology
- Pulmonary development
Background:
- Sex differences exist in neonatal respiratory distress syndrome (RDS) and bronchopulmonary dysplasia (BPD) incidence and severity.
- Androgens are implicated in RDS and suspected in BPD, with the developing lung actively metabolizing these hormones.
Purpose of the Study:
- To review major androgen-metabolizing enzymes in the developing lung.
- To explore the role of these enzymes in lung development and potential therapeutic applications.
Main Methods:
- Review of scientific literature on androgen metabolism in developing lungs (human and mouse).
- Focus on key enzymes like AKR1C3/Akr1c6, HSD17B2, and Akr1c14.
- Examination of lung development stages, including canalicular and saccular/alveolar phases.
Main Results:
- The developing lung expresses enzymes for both androgen synthesis (e.g., AKR1C3/Akr1c6) and inactivation (e.g., HSD17B2).
- Akr1c14 (3α-HSD) expression increases significantly with developmental time.
- Androgen metabolism is linked to surfactant synthesis (RDS) and lung structure development (BPD).
Conclusions:
- Androgen-metabolizing enzymes in the developing lung are crucial regulators of lung maturation.
- These enzymes represent potential pharmaceutical targets for accelerating lung maturation and treating neonatal lung diseases.
- Androgens exert both beneficial and detrimental effects on lung development, modulated by steroidogenic enzymes.
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