News Release

Discovery of new heart failure trigger could change the way cardiovascular drugs are made

Researchers find that the switch between healthy and failing heart depends on the way one particular heart protein is activated -- important news for drug makers targeting the protein to treat cardiovascular disease

Peer-Reviewed Publication

Sanford Burnham Prebys

APJ's Yin-Yang Role in Cardiac Function

image: APJ's yin-yang role in cardiac function: the receptor APJ serves a dual function in heart health, depending on how it’s activated. While APJ enhances heart health upon binding the hormone apelin (green), APJ can also trigger heart enlargement and failure when it senses certain mechanical changes (red). view more 

Credit: Sanford-Burnham Medical Research Institute

LA JOLLA, Calif., July 18, 2012 – In their quest to treat cardiovascular disease, researchers and pharmaceutical companies have long been interested in developing new medicines that activate a heart protein called APJ. But researchers at Sanford-Burnham Medical Research Institute (Sanford-Burnham) and the Stanford University School of Medicine have now uncovered a second, previously unknown, function for APJ—it senses mechanical changes when the heart is in danger and sets the body on a course toward heart failure. This means that activating APJ could actually be harmful in some cases—potentially eye-opening information for some heart drug makers. The study appears July 18 in Nature.

"Just finding a molecule that activates APJ is not enough. What's important to heart failure is not if this receptor is 'on' or 'off,' but the way it's activated," said Pilar Ruiz-Lozano, Ph.D., who led the study. Ruiz-Lozano, formerly assistant professor at Sanford-Burnham, is now associate professor of pediatrics in the Stanford University School of Medicine and adjunct faculty member at Sanford-Burnham.

Stretching the heart

APJ is a receptor that sits on the cell surface in many organs, where it senses the external environment. When a hormone called apelin comes along and binds APJ, it sets off a molecular chain reaction that influences a number of cellular functions. Many previous studies have shown that apelin-APJ activity directs beneficial processes such as embryonic heart development, maintenance of normal blood pressure, and new blood vessel formation.

According to Ruiz-Lozano's latest study, however, APJ can also be activated a second, more harmful, way that doesn't involve apelin. In this pathway, APJ senses and responds to mechanical changes in the heart.

To better understand these mechanical changes, let's look at a person with high blood pressure. In this case, the person's heart has to work harder to pump the same amount of blood at the same rate as a healthy person. To meet the increased demand, individual heart muscle cells start making more proteins, making the cells bigger. Eventually, cell membranes stretch and each cell begins to pull away from its neighbor. This leads to an enlarged heart—a condition known as hypertrophy. In pathological (disease) conditions, hypertrophy can lead to heart failure.

APJ and heart failure

The best way to determine the role a protein plays in a particular cellular process is to see what happens when it's missing. To do this, Ruiz-Lozano's team, including co-first authors Maria Cecilia Scimia, Ph.D. and Cecilia Hurtado, Ph.D., used mice that lack APJ. Under everyday conditions, the APJ-deficient mice appeared perfectly normal. However, unlike their normal counterparts, the mice lacking APJ couldn't sense danger when their hearts enlarged. As a result, mice were actually healthier without APJ—none succumbed to heart failure.

"In other words, without APJ, ignorance is bliss—the heart doesn't sense the danger and so it doesn't activate the hypertrophic pathways that lead to heart failure," Ruiz-Lozano said. "This tells us that, depending on how it's done, activating APJ might make matters worse for heart disease patients."


This research was funded by a sponsored research agreement with Wyeth and the U.S. National Institutes of Health. The study was co-authored by Maria Cecilia Scimia, Sanford-Burnham; Cecilia Hurtado, Sanford-Burnham; Saugata Ray, Sanford-Burnham; Scott Metzler, Stanford University; Ke Wei, Sanford-Burnham; Jianming Wang, Sanford-Burnham; Chris E. Woods, Stanford University; Nicole H. Purcell, University of California, San Diego; Daniele Catalucci, National Research Council of Italy; Takashi Akasaka, Sanford-Burnham; Orlando F. Bueno, Wyeth Pharmaceutical; George P. Vlasuk, Wyeth Pharmaceutical; Perla Kaliman, The August Pi i Sunyer Biomedical Research Institute; Rolf Bodmer, Sanford-Burnham; Layton H. Smith, Sanford-Burnham; Euan Ashley, Stanford University; Mark Mercola, Sanford-Burnham; Joan Heller Brown, University of California, San Diego; and Pilar Ruiz-Lozano, Sanford-Burnham and Stanford University.

About Sanford-Burnham Medical Research Institute

Sanford-Burnham Medical Research Institute is dedicated to discovering the fundamental molecular causes of disease and devising the innovative therapies of tomorrow. The Institute consistently ranks among the top five organizations worldwide for its scientific impact in the fields of biology and biochemistry (defined by citations per publication) and currently ranks third in the nation in NIH funding among all laboratory-based research institutes. Sanford-Burnham utilizes a unique, collaborative approach to medical research and has established major research programs in cancer, neurodegeneration, diabetes, and infectious, inflammatory, and childhood diseases. The Institute is especially known for its world-class capabilities in stem cell research and drug discovery technologies. Sanford-Burnham is a U.S.-based, non-profit public benefit corporation, with operations in San Diego (La Jolla), California and Orlando (Lake Nona), Florida. For more information, news, and events, please visit us at

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