Understanding lung development and the signals provided by the embryonic environment are of great relevance to public health. A better knowledge of the cues that guide proper lung growth and the process that forms a highly branched, specialized structure will shed light on the causes of improper development. Congenital disorders, such as pulmonary hypoplasia, or insufficient lung growth, result when embryological processes go awry. Improper development may also predispose to adult conditions such as asthma. The goal of this project is to elucidate the dynamic processes involved in lung development and determine the dependence on neural stimulation for lung growth. The quail is an amniote with similar development to mammals, and it is much more accessible for genetic labeling experiments to study embryogenesis. Confocal and two-photon imaging of transgenic quail lungs that have multiple cellular structures labeled in different colors will be used to dynamically illustrate early lung development. The importance of neural stimulation for lung growth and branching will be measured by modulating neural inputs to the lungs and assessing growth and cell fate. These studies will contribute insight into the dynamics of lung development and what regulates the process. Such knowledge may lead to interventions to rescue congenital disorders, treat asthma, guide efforts to engineer replacement tissue, or stimulate lung repair following injury in adults.

Public Health Relevance

Project Narrative Increasing our knowledge of the factors that direct the proper embryological development of the lung has great implications for improving public health. Understanding how the lung develops will help clarify the causes that underlie congenital disorders and may lead to new interventions for infant respiratory conditions and chronic syndromes such as asthma. Better insight into how the lungs form may also facilitate tissue engineering or the ability to stimulate lung repair following injury.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
1F30HL110723-01
Application #
8203512
Study Section
Special Emphasis Panel (ZRG1-F10A-S (20))
Program Officer
Colombini-Hatch, Sandra
Project Start
2011-09-30
Project End
2016-09-29
Budget Start
2011-09-30
Budget End
2012-09-29
Support Year
1
Fiscal Year
2011
Total Cost
$46,800
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Bower, Danielle V; Lansdale, Nick; Navarro, Sonia et al. (2017) SERCA directs cell migration and branching across species and germ layers. Biol Open 6:1458-1471
Bower, Danielle V; Lee, Hyung-Kook; Lansford, Rusty et al. (2014) Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission. BMC Biol 12:92
Han, Chao; Pang, Shuo; Bower, Danielle V et al. (2013) Wide field-of-view on-chip Talbot fluorescence microscopy for longitudinal cell culture monitoring from within the incubator. Anal Chem 85:2356-60