By Weill Cornell MedicineJanuary 13, 20252 Comments6 Mins Read

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A new study by Weill Cornell Medicine and the Boyce Thompson Institute reveals that the body produces a molecule, BA-MCY, which counteracts gut microbes’ signals to regulate bile acid production, balancing fat metabolism and cholesterol levels. This discovery could lead to new treatments for metabolic disorders and highlights the role of dietary fiber in supporting this balance. Credit: SciTechDaily.com

Researchers discovered that the body and gut microbes jointly regulate fat metabolism using BA-MCY, a molecule that balances bile acid production. This discovery could lead to new treatments for metabolic diseases and emphasizes the role of diet in health.

Beneficial gut microbes and the human body work together to fine-tune fat metabolism and cholesterol levels, according to a recent preclinical study conducted by researchers at Weill Cornell Medicine and the Boyce Thompson Institute at Cornell University’s Ithaca campus.

The human body has evolved alongside gut-residing beneficial microbes, collectively known as the microbiota. This co-evolution has fostered a symbiotic relationship where the microbes assist in digesting food and absorbing essential nutrients critical for both the host’s survival and the microbes’ sustenance.

A key aspect of this collaboration is the production of bioactive molecules that facilitate food breakdown and nutrient absorption by the host.

One of the most important groups of such molecules are termed bile acids (also known as ‘bile’) which are produced from cholesterol in the liver and then delivered to the intestine where they promote fat digestion.Lipid accumulation in a murine model of fatty liver disease, visualized by color-enhanced lipid droplets (pink) in liver tissue (green). Superimposed chemical structure of a newly discovered bile acid conjugate. Credit: Image courtesy of Dr. Mohammad Arifuzzaman, Dr. Christopher Parkhurst, Dr. Frank Schroeder, and Dr. David Artis.

Scientists have known for some time that gut bacteria modify bile acids into a form that stimulates a receptor called FXR, which reduces bile production. The new study, published Jan. 8 in Nature, reveals that an enzyme produced by intestinal cells converts bile acids into a different form that has the opposite effect. This altered form, called bile acid-methylcysteamine (BA–MCY), inhibits FXR to promote bile production and help boost fat metabolism.

“Our study reveals there is a dialogue occurring between the gut microbes and the body that is vital for regulating bile acid production,” said co-corresponding author Dr. David Artis, director of the Jill Roberts Institute for Research in Inflammatory Bowel Disease and the Friedman Center for Nutrition and Inflammation and the Michael Kors Professor in Immunology at Weill Cornell Medicine.

Bile Acids as Signaling Molecules

Bile acids help the digestive system break down fats into forms the body can take up and use. “But it now has become clear that bile acids are more than just digestive aids; they act as signaling molecules, regulating cholesterol levels, fat metabolism, and more,” said co-corresponding author Dr. Frank Schroeder, a professor at the Boyce Thompson Institute and a professor in the Department of Chemistry and Chemical Biology in the College of Arts and Sciences at Cornell University. “They do all this by binding to FXR, which acts like a traffic light, controlling cholesterol metabolism and bile acid production to avoid excess buildup.”

Now the cross-campus collaboration between the laboratories of Dr. Schroeder and Dr. Artis has revealed the host body’s role in this fundamental biological process. The study was co-led by Dr. Tae Hyung Won, a former postdoctoral associate in Dr. Schroeder’s laboratory and now assistant professor at Cha University in Korea; Dr. Christopher Parkhurst, an instructor of medicine at Weill Cornell Medicine, working in Dr. Artis’s lab; and Dr. Mohammad Arifuzzaman, an assistant professor of immunology in medicine at Weill Cornell Medicine.

The multidisciplinary collaboration between Drs. Artis and Schroeder has successfully merged the biomedical disciplines of immunology, chemical biology and host-microbiota interactions. In this study, they used a technique called untargeted metabolomics to identify all the molecules produced by mice with and without gut microbes. By comparing the two, they were able to distinguish which molecules were made by the gut microbes and which were produced by the body. BA-MCYs stood out as molecules that were produced by the mice but were nevertheless dependent on the presence of gut microbes.

“The BA-MCYs demonstrate a new paradigm: molecules that are not produced by the gut microbes but are still dependent on their presence,” co-first author Dr. Won said. Through a series of experiments, the investigators then showed how the body makes the BA-MCYs and how these molecules provide a way for the body to counteract the microbe’s signals to produce less bile acid, preventing the slowdown of cholesterol metabolism.

“This balancing act is crucial,” Dr. Schroeder said. “When gut bacteria produce lots of bile acids that strongly activate FXR, the body pushes back by making BA-MCYs, ensuring the bile acid system stays balanced.”

Potential Therapeutic Implications

The researchers also showed in their preclinical model that boosting BA-MCY levels helped reduce fat accumulation in the liver and that increasing intake of dietary fiber also enhanced BA-MCY production. “Importantly, BA-MCYs were also detected in human blood samples, indicating that a similar mechanism may occur in people,” Dr. Arifuzzaman added.

The results may suggest potential treatment targets for metabolic disorders, including fatty liver disease, high cholesterol, and obesity-related disorders. They also suggest that dietary approaches like boosting certain forms of fiber intake may help by supporting the body’s system of checks and balances. The next steps for the collaborators are learning more about how these processes are regulated and studying this type of microbe-gut crosstalk in different disease states.

The investigators suggested their study approach may also help researchers study the role of the gut microbiota in a wide range of diseases, from infection and chronic inflammation to obesity and cancer.

“Our paper is a roadmap to using untargeted metabolomics and chemistry to better understand how the dialogue between the gut microbiota and the body impacts a range of diseases,” Dr. Artis said.

Reference: “Host metabolism balances microbial regulation of bile acid signalling” by Tae Hyung Won, Mohammad Arifuzzaman, Christopher N. Parkhurst, Isabella C. Miranda, Bingsen Zhang, Elin Hu, Sanchita Kashyap, Jeffrey Letourneau, Wen-Bing Jin, Yousi Fu, Douglas V. Guzior, JRI Live Cell Bank, Robert A. Quinn, Chun-Jun Guo, Lawrence A. David, David Artis and Frank C. Schroeder, 8 January 2025, Nature.
DOI: 10.1038/s41586-024-08379-9

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Biology

Scientists Discover New Molecule That Boosts Fat Metabolism Naturally

By Weill Cornell MedicineJanuary 13, 20252 Comments6 Mins Read

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A new study by Weill Cornell Medicine and the Boyce Thompson Institute reveals that the body produces a molecule, BA-MCY, which counteracts gut microbes’ signals to regulate bile acid production, balancing fat metabolism and cholesterol levels. This discovery could lead to new treatments for metabolic disorders and highlights the role of dietary fiber in supporting this balance. Credit: SciTechDaily.com

Researchers discovered that the body and gut microbes jointly regulate fat metabolism using BA-MCY, a molecule that balances bile acid production. This discovery could lead to new treatments for metabolic diseases and emphasizes the role of diet in health.

Beneficial gut microbes and the human body work together to fine-tune fat metabolism and cholesterol levels, according to a recent preclinical study conducted by researchers at Weill Cornell Medicine and the Boyce Thompson Institute at Cornell University’s Ithaca campus.

The human body has evolved alongside gut-residing beneficial microbes, collectively known as the microbiota. This co-evolution has fostered a symbiotic relationship where the microbes assist in digesting food and absorbing essential nutrients critical for both the host’s survival and the microbes’ sustenance.

A key aspect of this collaboration is the production of bioactive molecules that facilitate food breakdown and nutrient absorption by the host.

One of the most important groups of such molecules are termed bile acids (also known as ‘bile’) which are produced from cholesterol in the liver and then delivered to the intestine where they promote fat digestion.Lipid accumulation in a murine model of fatty liver disease, visualized by color-enhanced lipid droplets (pink) in liver tissue (green). Superimposed chemical structure of a newly discovered bile acid conjugate. Credit: Image courtesy of Dr. Mohammad Arifuzzaman, Dr. Christopher Parkhurst, Dr. Frank Schroeder, and Dr. David Artis.

Scientists have known for some time that gut bacteria modify bile acids into a form that stimulates a receptor called FXR, which reduces bile production. The new study, published Jan. 8 in Nature, reveals that an enzyme produced by intestinal cells converts bile acids into a different form that has the opposite effect. This altered form, called bile acid-methylcysteamine (BA–MCY), inhibits FXR to promote bile production and help boost fat metabolism.

“Our study reveals there is a dialogue occurring between the gut microbes and the body that is vital for regulating bile acid production,” said co-corresponding author Dr. David Artis, director of the Jill Roberts Institute for Research in Inflammatory Bowel Disease and the Friedman Center for Nutrition and Inflammation and the Michael Kors Professor in Immunology at Weill Cornell Medicine.

Bile Acids as Signaling Molecules

Bile acids help the digestive system break down fats into forms the body can take up and use. “But it now has become clear that bile acids are more than just digestive aids; they act as signaling molecules, regulating cholesterol levels, fat metabolism, and more,” said co-corresponding author Dr. Frank Schroeder, a professor at the Boyce Thompson Institute and a professor in the Department of Chemistry and Chemical Biology in the College of Arts and Sciences at Cornell University. “They do all this by binding to FXR, which acts like a traffic light, controlling cholesterol metabolism and bile acid production to avoid excess buildup.”

Now the cross-campus collaboration between the laboratories of Dr. Schroeder and Dr. Artis has revealed the host body’s role in this fundamental biological process. The study was co-led by Dr. Tae Hyung Won, a former postdoctoral associate in Dr. Schroeder’s laboratory and now assistant professor at Cha University in Korea; Dr. Christopher Parkhurst, an instructor of medicine at Weill Cornell Medicine, working in Dr. Artis’s lab; and Dr. Mohammad Arifuzzaman, an assistant professor of immunology in medicine at Weill Cornell Medicine.

The multidisciplinary collaboration between Drs. Artis and Schroeder has successfully merged the biomedical disciplines of immunology, chemical biology and host-microbiota interactions. In this study, they used a technique called untargeted metabolomics to identify all the molecules produced by mice with and without gut microbes. By comparing the two, they were able to distinguish which molecules were made by the gut microbes and which were produced by the body. BA-MCYs stood out as molecules that were produced by the mice but were nevertheless dependent on the presence of gut microbes.

“The BA-MCYs demonstrate a new paradigm: molecules that are not produced by the gut microbes but are still dependent on their presence,” co-first author Dr. Won said. Through a series of experiments, the investigators then showed how the body makes the BA-MCYs and how these molecules provide a way for the body to counteract the microbe’s signals to produce less bile acid, preventing the slowdown of cholesterol metabolism.

“This balancing act is crucial,” Dr. Schroeder said. “When gut bacteria produce lots of bile acids that strongly activate FXR, the body pushes back by making BA-MCYs, ensuring the bile acid system stays balanced.”

Potential Therapeutic Implications

The researchers also showed in their preclinical model that boosting BA-MCY levels helped reduce fat accumulation in the liver and that increasing intake of dietary fiber also enhanced BA-MCY production. “Importantly, BA-MCYs were also detected in human blood samples, indicating that a similar mechanism may occur in people,” Dr. Arifuzzaman added.

The results may suggest potential treatment targets for metabolic disorders, including fatty liver disease, high cholesterol, and obesity-related disorders. They also suggest that dietary approaches like boosting certain forms of fiber intake may help by supporting the body’s system of checks and balances. The next steps for the collaborators are learning more about how these processes are regulated and studying this type of microbe-gut crosstalk in different disease states.

The investigators suggested their study approach may also help researchers study the role of the gut microbiota in a wide range of diseases, from infection and chronic inflammation to obesity and cancer.

“Our paper is a roadmap to using untargeted metabolomics and chemistry to better understand how the dialogue between the gut microbiota and the body impacts a range of diseases,” Dr. Artis said.

Reference: “Host metabolism balances microbial regulation of bile acid signalling” by Tae Hyung Won, Mohammad Arifuzzaman, Christopher N. Parkhurst, Isabella C. Miranda, Bingsen Zhang, Elin Hu, Sanchita Kashyap, Jeffrey Letourneau, Wen-Bing Jin, Yousi Fu, Douglas V. Guzior, JRI Live Cell Bank, Robert A. Quinn, Chun-Jun Guo, Lawrence A. David, David Artis and Frank C. Schroeder, 8 January 2025, Nature.
DOI: 10.1038/s41586-024-08379-9

CholesterolFatGut