Using a four-dimensional microscopy technique, researchers at Vanderbilt University and Vanderbilt University Medical Center have created of mouse lung tissue grown in the laboratory. What they have learned has been nothing short of groundbreaking.
“For the first time, we’ve been able to live-image the lung as it forms, and quantify and measure those cellular movements that come together to make an organ with a surface area large enough for gas exchange,” said , MD, associate professor of Pediatrics and Cell and Developmental Biology.
The group’s findings, published Feb. 24 as the cover article in , the journal of the American Society of Clinical Investigation, represent a significant step toward improved treatment and prevention of bronchopulmonary dysplasia (BPD), which occurs in about 50% of infants born two to four months prematurely.
“If we can understand how the lung forms, then we have a blueprint for how to grow new lungs after injury,” said the paper’s first author, Nick Negretti, PhD, a senior post-doctoral fellow in the who co-led the research.
“Mice have an extraordinary ability to repair the lung,” said Sucre, the paper’s senior author, who directs the Biodevelopmental Origins of Lung Disease () Center at VUMC. “I want to give babies the superpower of the mouse.”
Premature babies with BPD require oxygen and mechanical ventilation in the early days after birth to help them breathe. Oxygen therapy is a double-edged sword, however, because it also can damage delicate lung tissue.
Though many premature babies can be weaned off the ventilator after a few days, they are at increased risk for developing serious breathing problems later in life, including chronic obstructive pulmonary disease.
Respiration — the exchange of oxygen for carbon dioxide — occurs in the alveoli of the lungs across a fragile basement membrane between epithelial cells and blood vessels. According to the traditional view of lung development, ingrowing septa (dividers) emerge from a layer of epithelial, endothelial and mesenchymal cells to divide airspaces into the alveoli.
But when the researchers imaged slices of living neonatal mouse lung over three days, a different view emerged, one of a ballooning outgrowth of epithelial cells supported by a ring of myofibroblasts, or cells that promote tissue formation.
The innovative technology implemented by the Sucre lab allows for testing and identification of the specific molecules and pathways that guide this process. It also is a discovery tool for drugs that can promote tissue regeneration after injury.
Sucre said her lab is “keen to understand … what are the pathways in the resilient (mouse) lung that can repair it after infection and injury? How do we bottle that?”
Citation: “Epithelial outgrowth through mesenchymal rings drives alveologenesis.” .
The study was supported in part by National Institutes of Health grants T32 HL094296, K08 HL143051, R01 HL158556, K08 HL130595, R01 HL153246, R01 HL145372, P01 HL092470, R01 HL163195, R03 HL154287, K08 HL133484, and R01 HL157373, and by the Francis Family Foundation, the Chan Zuckerberg Initiative Imaging Scientists Program, and a Vanderbilt University Trans-Institutional Programs (TIPs) Award.
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Credit: Vanderbilt University Medical Center
Caption: Illustration: Alveolar epithelial cells (cyan) bud from mesenchymal rings of myofibroblasts and other cells (magenta). Image credit: Nick Negretti, PhD, and Jennifer Sucre, MD.

Credit: Vanderbilt University Medical Center
Caption: From left, Nick Negretti, PhD, Bryan Millis, PhD, Jennifer Sucre, MD, and Chris Jetter co-led a research team that achieved a new view of lung development —one that could improve outcomes for premature babies. (photo by Donn Jones)
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