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Calcium May Be the Key to Slowing Down Aging

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Summary

Researchers at UVA Health discovered that improper calcium signaling in immune cell mitochondria drives chronic inflammation, leading to age-related ailments. Targeting tissue-resident macrophages with drugs could prevent neurodegenerative diseases, offering new therapeutic strategies for cardiometabolic and neurodegenerative conditions.

Key takeaways

    • Improper calcium signaling in immune cell mitochondria drives chronic inflammation, accelerating aging and causing age-related ailments like heart disease and brain disorders.
    • UVA Health researchers found that age-related loss of calcium uptake in immune cells called macrophages leads to harmful inflammation ("inflammaging").
    • Targeting tissue-resident macrophages with appropriate drugs could prevent age-associated neurodegenerative diseases, providing new therapeutic strategies for cardiometabolic and neurodegenerative conditions.

    A key driver of chronic inflammation

    School of Medicine researchers have discovered a key driver of chronic inflammation that accelerates aging. That finding could let us slow the clock to live longer, healthier lives, and may allow us to prevent age-related conditions such as deadly heart disease and devastating brain disorders that rob us of our faculties.


    So what drives this harmful inflammation? The answer is improper calcium signaling in the mitochondria of certain immune cells. Mitochondria are the power generators in all cells, and they rely heavily on calcium signaling.

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    The UVA Health researchers, led by Bimal N. Desai, PhD, found that the mitochondria in the immune cells called macrophages lose their ability to take up and use calcium with age. This, the researchers show, leads to chronic inflammation responsible for many of the ailments that afflict our later years.


    The researchers believe that increasing calcium uptake by the mitochondrial macrophages could prevent the harmful inflammation and its terrible effects. Because macrophages reside in all organs of our bodies, including the brain, targeting such “tissue-resident macrophages” with appropriate drugs may allow us to slow age-associated neurodegenerative diseases.


    “I think we have made a key conceptual breakthrough in understanding the molecular underpinnings of age-associated inflammation,” said Desai, of UVA’s Department of Pharmacology and UVA’s Carter Immunology Center. “This discovery illuminates new therapeutic strategies to interdict the inflammatory cascades that lie at the heart of many cardiometabolic and neurodegenerative diseases.”

    The Inflammation of Aging – ‘Inflammaging’

    Macrophages are white blood cells that play critical roles in our immune systems and, in turn, our good health. They swallow up dead or dying cells, allowing our bodies to remove cellular debris, and patrol for pathogens and other foreign invaders. In this latter role, they act as important sentries for our immune systems, calling for help from other immune cells as needed.


    Scientists have known that macrophages become less effective with age, but it has been unclear why. Desai’s new discovery suggests answers.


    Desai and his team say their research has identified a “keystone” mechanism responsible for age-related changes in the macrophages. These changes, the scientists believe, make the macrophages prone to chronic, low-grade inflammation at the best of times. And when the immune cells are confronted by an invader or tissue damage, they can become hyperactive. This drives what is known as “inflammaging” – chronic inflammation that drives aging.


    Further, the UVA Health scientists suspect that the mechanism they have discovered will hold true not just for macrophages but for many other related immune cells generated in the bone marrow. That means we may be able to stimulate the proper functioning of those cells as well, potentially giving our immune systems a big boost in old age, when we become more susceptible to disease.

    Next Steps

    Fixing “inflammaging” won’t be as simple as taking a calcium supplement. The problem is not a shortage of calcium so much as the macrophages’ inability to use it properly. But Desai’s new discovery has pinpointed the precise molecular machinery involved in this process, so we should be able to discover ways to stimulate this machinery in aging cells.


    “This highly interdisciplinary research effort, at the interface of computational biology, immunology, cell biology and biophysics, wouldn’t have been possible without the determination of Phil Seegren, the graduate student who spearheaded this ambitious project,” Desai said. “Now, moving forward, we need an equally ambitious effort to figure out the wiring that controls this mitochondrial process in different types of macrophages and then manipulate that wiring in creative ways for biomedical impact.”  


    Reference: Seegren PV, Harper LR, Downs TK, et al. Reduced mitochondrial calcium uptake in macrophages is a major driver of inflammaging. Nat Aging. 2023;3(7):796-812. doi: 10.1038/s43587-023-00436-8


    This article has been republished from the following materials. Article summaries may be generated using fact-checked AI models. Note: material may have been edited for length and content. For further information, please contact the cited source.