Long non-coding RNA may play a key role in cardiovascular disease

Through utilization of genetically modified high-risk atherosclerotic mice, a research team from Brigham and Women's Hospital identified and characterized Macrophage-Associated Atherosclerosis lncRNA Sequence (MAARS), which is expressed specifically in macrophages in atherosclerotic plaques and contributes to the progression of the disease. Results are published in Nature Communications.

"We hypothesized, given the unknown role of lncRNAs, that some may be highly expressed in the blood vessel wall during the process of atherosclerosis," said Mark Feinberg, MD, senior author and member of the Brigham's Division of Cardiovascular Medicine. "We want to identify who these actors are, what they are doing, and how we can understand their function in a way that provides a foundation for future therapeutic opportunities."

Feinberg and colleagues used genetically modified mice prone to atherosclerosis and placed them on a high cholesterol diet, which boosted their cholesterol to 500-1,000 units, up from a normal level of around 200 units. The mice were observed on their high cholesterol diet for 12 weeks, then placed on a normal diet and observed while their cholesterol levels returned to normal. Researchers isolated the innermost lining of the blood vessel walls of these mice and sent the samples for RNA sequencing to identify the presence of lncRNAs.

Among the list of present lncRNAs was MAARS, which piqued the interest of researchers with its specificity to macrophages and expression pattern. As atherosclerosis developed in the mice over the initial 12 weeks, the presence of MAARS increased 270-fold; once fed normal diets, the presence of MAARS decreased from its heightened expression by 60 percent. Targeted interruption of MAARS's function reduced atherosclerotic lesion formation by 52 percent by decreasing macrophage cell death and increasing efferocytosis -- the clearance of dead cellular debris -- from these lesions. These effects were largely independent of effects on circulating cholesterol.

Researchers found an important relationship between MAARS and an RNA-binding protein known as HuR. In the vessel wall, MAARS interacts with HuR, which plays a critical role in cell death. If MAARS is deliberately inhibited, HuR is released from the nucleus into the cytoplasm and the macrophages continue their cleaning. This chain of events leads to more active macrophages able to clean up more plaque and debris produced by atherosclerosis.

"lncRNAs play a really important role in cardiovascular disease," said Feinberg. "We had no idea what we were going to find, and we ended up identifying a lncRNA that has a crucial role in macrophages and pathways that could have therapeutic potential. We are shedding light on new players in old signaling pathways. It is so exciting to add more nuance to this area of research, since that means future studies will have that much more to work with."

This work was supported by the National Institutes of Health (HL115141, HL134849, HL148207, HL148355, HL153356), the American Heart Association (18SFRN33900144 and 20SFRN35200163, 18POST34030395), the Arthur K. Watson Charitable Trust, the Dr. Ralph and Marian Falk Medical Research Trust, a Sarnoff Cardiovascular Research Foundation Fellowship, and the Swiss National Science Foundation (P2BEP3_162063).