4.4 Article

Centrifugal migration of mesenchymal cells in embryonic lung

Journal

DEVELOPMENTAL DYNAMICS
Volume 237, Issue 3, Pages 750-757

Publisher

WILEY-LISS
DOI: 10.1002/dvdy.21462

Keywords

retrovirus; microinjection; alkaline phosphatase; smooth muscle; clonal analysis

Funding

  1. NHLBI NIH HHS [P01 HL060231-08, R01 HL044977-16, R01 HL044060-16, R01 HL044977, 2R01 HL44984, P01 HL060231, R01 HL044060, R01 HL044984] Funding Source: Medline

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Murine lung development begins at embryonic day (E) 9.5. Normal lung structure and function depend on the patterns of localization of differentiated cells. Pulmonary mesenchymal cell lineages have been relatively unexplored. Importantly, there has been no prior evidence of clonality of any lung cells. Herein we use a definitive genetic approach to demonstrate a common origin for proximal and distal pulmonary mesenchymal cells. A retroviral library with 3,400 unique inserts was microinjected into the airway lumen of E11.5 lung buds. After 7-11 days of culture, buds were stained for placental alkaline phosphatase (PLAP). Most PLAP+ cells are peribronchial smooth muscle cells, initially localized laterally near the hilum, then migrating down airways to the subpleural region. Laser-capture microdissection and polymerase chain reaction confirm the clonal identities of PLAP+ cells proximally and distally. Our observation of this fundamental process during lung development opens new avenues for investigation of maladaptive mesenchymal responses in lung diseases.

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