In an article published in Gastroenterology, NOMIS Awardee Ronald M. Evans and colleagues report that a protein known as estrogen-related receptor gamma (ERR ɣ) is critical for preventing pancreatic auto-digestion in mice. Moreover, they discovered that people with pancreatitis have lower levels of ERR ɣ in cells affected by this inflammation.
Salk study points toward a potential new therapeutic target for pancreatitis and pancreatic cancer
LA JOLLA—Every day, your pancreas produces about one cup of digestive juices, a mixture of molecules that can break down the food you eat. But if these powerful molecules become activated before they make their way to the gut, they can damage the pancreas itself—digesting the very cells that created them, leading to the painful inflammation known as pancreatitis, and predisposing a person to pancreatic cancer.
Now, Salk scientists report in the journal Gastroenterology on April 21, 2022, that a protein known as estrogen-related receptor gamma (ERR ɣ) is critical for preventing pancreatic auto-digestion in mice. Moreover, they discovered that people with pancreatitis have lower levels of ERR ɣ in cells affected by this inflammation.
These findings suggest that new therapies aimed at regulating ERR ɣ activity could help prevent or treat pancreatitis and pancreatic cancer.
“Our finding provides new insight into both the basic biology of how pancreas cells function, and what might drive pancreatitis and pancreatic cancer,” says Professor Ronald Evans, director of Salk’s Gene Expression Laboratory, March of Dimes Chair in Molecular and Developmental Biology, and co-senior author of the study.
The pancreas is home to two main cell types with distinct functions: beta cells that release insulin to control blood sugar levels and acinar cells that produce digestive juices. Evans and his colleagues previously discovered that ERR ɣ helps pancreatic beta cells release insulin and might be useful as a treatment for diabetes. In follow-up studies, the team also discovered that mice lacking ERR ɣ developed severe pancreatitis.
To understand the role of ERR ɣ in pancreatic acinar cells, the researchers compared mice, as well as isolated cells, with and without the protein. They discovered ERR ɣ is required for the functioning of the acinar cells’ mitochondria—organelles that generate energy.
“Mitochondria have been known to be the major source of energy in acinar cells since the 1960s, but the factor that controls this vital energy production program in acinar cells has been a long-standing mystery,” says co-senior author Jae Myoung Suh of the Korea Advanced Institute of Science and Technology (KAIST), in South Korea.
Without ERR ɣ, acinar cells not only have dysregulated energy regulation but, as a result, incorrectly activate digestive enzymes to start auto-digestion.
“The mitochondria in these cells have to be particularly robust,” says Staff Scientist Michael Downes, a co-author of the new work. “If things go wrong, those digestive enzymes are activated and then auto-digestion of the pancreas begins.”
The group showed that not only did auto-digestion of pancreatic acinar cells begin in the absence of ERR ɣ, but so did cellular changes that indicate early pancreatic cancer.
The researchers next turned to data from patients with pancreatitis to determine whether the mouse and lab results are relevant to human disease. They compared pancreatitis biopsies with those collected from normal pancreatic cells—including healthy sections of the pancreas in the same patients. Cells affected by pancreatitis, they discovered, had lower levels of ERR ɣ.
“We examined data across multiple different locations and patient groups and found that ERR ɣ is very consistently decreasing with pancreatitis,” says co-first author Tae Gyu Oh, a bioinformatics analyst at Salk.
Oh and his colleagues went on to show that levels of 83 other genes, many of which are directly regulated by ERR ɣ, were also altered in the pancreatitis samples. Moreover, when they searched through the data from two large studies comparing gene expression in people, they discovered that some of those 83 genes are associated with rare types of inherited pancreatitis and pancreatic cancer.
“The fact that this was linked back to patients with chronic pancreatitis suggests that ERR ɣ is clinically relevant and could make a good drug target in the future,” says Evans.
The researchers are planning future studies to look in depth at the pre-cancerous changes that ERR ɣ dysregulation and pancreatitis lead to, as well as how drugs could help increase ERR ɣ to prevent or treat pancreatic diseases.
Other authors include Weiwei Fan, Sagar P. Bapat, Ye Zheng, Ruth T. Yu, Annette Atkins and Eiji Yoshihara of Salk; Jinhyuk Choi, Heewon Jung, Kun-Young Park, Hyemi Shin, Taehee Jo, Du-Seock Kang, Sujung Hong, and Pilhan Kim of KAIST; Dipanjan Chanda and In-Kyu Lee of Kyungpook National University Hospital; Jina Kim and Sung Jin Cho of Daegu-Gyeongbuk Medical Innovation Foundation; Moongi Ji and Man-Jeong Paik of Sunchon National University; Minkyo Jung and Ji Young Mun of Korea Brain Research Institute; Takashi Syoji of Kyoto University; Ayami Matsushima of Kyushu University; David C. Whitcomb, Phil Greer and Brandon Blobner of the University of Pittsburgh; Mark O. Goodarzi and Stephen J. Pandol of Cedars-Sinai Medical Center; Jerome I. Rotter of UCLA; Christopher Liddle of the University of Sydney; as well as the entire North American Pancreatitis Study 2 (NAPS2) Consortium.
Continue reading this Salk Institute release
Read the Gastroenterology publication: Estrogen-related receptor γ maintains pancreatic acinar cell function and identity by regulating cellular metabolism
Ronald M. Evans
Professor, director of Salk’s Gene Expression Laboratory and holder of the March of Dimes Chair in Molecular and Developmental Biology
Salk Institute for Biological Studies
The Science of Health: The Fundamental Mechanisms of Organ Communication
NOMIS RESEARCH PROJECT