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A target for improving recovery from lung injury

By: Katherine Unger Baillie | Kbaillie@Upenn.Edu | 215-898-9194 Date: Dec 14, 2022
Image of basal cells in a damaged lung one year after injury
A team from Penn Vet found that, even a year after lung injury, basal cells—marked in green and red and normally found in the airway—could be found deeper in the lung, where gas-exchange cells typically reside. Believed to contribute to impaired lung function, this ectopic growth could be redirected by blocking the activity of the protein p63, a potential therapeutic target. (Image: Aaron Weiner)

After a severe bout with a respiratory illness like flu, COVID, or RSV some patients’ lungs never fully recover. In these cases, scientists have seen cells normally found in the upper airway growing deep in the lungs, where gas-exchange cells should be. While this regrowth may serve as a patch for the damage, the out-of-place cells, known as basal cells, don’t promote the same respiratory functions, and a reduction in lung capacity may result.

Yet these basal cells possess the ability to mature into gas-exchange cells, given the right prompts. In a new study in Cell Reports by a team from Penn’s School of Veterinary Medicine, genetic and environmental tweaks to basal cells caused them to become gas-exchange cells, known as alveolar cells, in the lungs of mice who survived a flu infection. 

Andrew Vaughan, PhD, Penn Vet
Dr. Andrew Vaughan

Uncovering the factors responsible for inappropriate lung-tissue regeneration may point the way toward new, druggable targets for encouraging a more functional regrowth of lung tissue down the line, the researchers say.

“With severe acute respiratory distress syndrome, as some people develop from the flu or COVID, what you see at the tissue level is diffuse alveolar damage,” says Andrew Vaughan, an assistant professor at Penn Vet and senior author on the study. “You get these basal cells growing ectopically in the alveoli, and that seems to be a contributor to long-term loss of function.”

“These cells were doing their job quite well; they were just doing it in the wrong place,” says Aaron Weiner, a doctoral student in Vaughan’s group and the lead author on the study. “We were able to show that these basal cells could maintain some plasticity and capitalized on that plasticity to get them to differentiate into alveolar cells.”

Aaron Weiner

Early evidence of basal cell plasticity came from work Vaughan had done during his postdoctoral research, revealing that basal cells, while typically destined to become airway cells, held a capacity—albeit very limited—to become alveolar type 2 (AT2) cells, which produce surfactant and generate gas-exchanging type 1 cells, playing a key role in ensuring proper lung function.

Weiner took that understanding and paired it with additional background information related to the protein p63, expressed in many tissues and known as a master regulator of basal cell identity. Previous research on other types of tissue that also contain basal cells demonstrated that, when p63 activity was blocked, the cells take on the characteristics of mature cells in whatever tissue they reside in. “So, for example, if you’re in skin, you differentiate into more superficial skin cells,” says Weiner.

To test this in respiratory cells, the researchers asked what happens when p63 is deleted from these lung basal cells, both in mice and in cell culture. They found that taking some of these cells and putting them in growth conditions that mimicked the upper airway prompted them to become airway cells. But when the cells were grown in more alveolar-like conditions, they became provocatively similar to AT2 cells.

The team reasoned that by removing p63, basal cells appeared open to receiving cues from their local environment to become the “right” cell type. They found the same seemed to be true in mice that had experienced a lung injury. By transplanting basal cells that lacked p63 from mice that had lung injury from a flu infection into genetically normal controls that also had a lung injury, they were able to see that alveolar cells arose from the transplanted basal cells, enmeshed in the lining of the lungs—the epithelial tissue—of the recipient mice.

“These became the actual gas exchanging cells of the epithelium,” Weiner says.

“They were almost indistinguishable from the native epithelium,” Vaughan adds, only able to be identified by a lineage-tracing marker implanted in the transplanted cells.

Digging deeper into the mechanism by which p63 deletion enabled a greater plasticity in basal cell maturation, Vaughan, Weiner, and the team performed analyses to look for patterns in gene expression and epigenetic changes associated with the presence of the protein. Among the signals they uncovered was a tendency for cells lacking p63 to have more activation of markers associated with alveolar cell pathways and a repression of basal cell characteristics, such as those associated with the ability to migrate.

“There was a general shift toward a more distal lung, or alveolar state,” Vaughan says.

In other words, the researchers believe p63 may “lock in” basal cells to take on the characteristics of upper airways. When that “lock” is removed, they regain the ability to be more flexible and develop into alveolar cells.

Vaughan, Weiner, and others are already following up on leads from the study, exploring, for example, a means of specifically “turning off” p63 in alveolar cells after injury, so airway cells and other cell types that also express p63 would not be affected.

“There might be a short-term emergency benefit to having basal cells cover up these damaged parts of the lung tissue, so this is probably not a strategy that would be used during acute infection,” Vaughan says. “But you can imagine, given what we’ve seen with long COVID and how a loss of lung function can persist, that treating with a drug that guides these cells to take on an alveolar identity, as patients start to get over that acute phase and maybe for months after, could be valuable.”

Andrew E. Vaughan is an assistant professor in the Department of Biomedical Sciences at the University of Pennsylvania School of Veterinary Medicine.

Aaron I. Weiner is a Ph.D. candidate in the Vaughan laboratory at Penn’s School of Veterinary Medicine.

Weiner and Vaughan’s coauthors on the paper were Penn Vet’s Gan Zhao, Hanna M. Zayas, Nicolas P. Holcomb, Stephanie Adams-Tzivelekidis, Joanna Wong, Maria E. Gentile, Dyuthi Reddy, Joey Wei, Gargi Palashikar, and Kwaku Quansah. 

The study was supported by the National Institutes of Health (grants HL153539, HL164350, and 1F31HL15259701A1) and the Lisa Dean Moseley Foundation.

About Penn Vet

Ranked among the top ten veterinary schools worldwide, the University of Pennsylvania School of Veterinary Medicine (Penn Vet) is a global leader in veterinary education, research, and clinical care. Founded in 1884, Penn Vet is the first veterinary school developed in association with a medical school. The school is a proud member of the One Health initiative, linking human, animal, and environmental health.

Penn Vet serves a diverse population of animals at its two campuses, which include extensive diagnostic and research laboratories. Ryan Hospital in Philadelphia provides care for dogs, cats, and other domestic/companion animals, handling more than 34,600 patient visits a year. New Bolton Center, Penn Vet’s large-animal hospital on nearly 700 acres in rural Kennett Square, PA, cares for horses and livestock/farm animals. The hospital handles more than 6,200 patient visits a year, while our Field Services have gone out on more than 5,500 farm service calls, treating some 18,700 patients at local farms. In addition, New Bolton Center’s campus includes a swine center, working dairy, and poultry unit that provide valuable research for the agriculture industry.