The secret signals our organs send to repair tissues and slow ageing

New Scientist · Feb 2, 2026 · Collected from RSS

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Davide Bonazzi At first glance, it might not seem like people have much in common with deer. But a strange discovery about how their antlers regenerate is lifting the lid on the unseen ways that our bodies work, too. Biologist Chunyi Li, who has long studied deer in north-east China, noticed something odd that happened when the animals regrew their antlers each year. This regrowth coincided with healthier-looking animals that showed much faster healing of their wounds and less scarring, leading him to suspect that the regenerating antlers somehow promoted regeneration in the wider body. Li’s hunch was confirmed last year when he and his colleagues at Changchun Sci-Tech University in Jilin, China, found that the growing antlers release messages that tell other parts of the body to shift into regenerative wound-healing mode – evidence of a hitherto-hidden communication network that connects distant organs. This finding doesn’t apply only to deer. In recent years, researchers have discovered a web of chatter among the human body’s organs and tissues, even those we once thought were dull and inert. We now know that your fat and brain tissue converse to influence the speed at which you age, your skeleton sends information packets to the pancreas to control metabolism, and much more. By tapping into these communication networks, we may be able to develop radical new ways to boost our health and slow ageing – and some clinical trials of this approach are already under way. Crosstalk between organs These ongoing findings are emerging from the new field of inter-organ communication, which is building on the old physiological idea that organs function together as a greater whole. We have long known that information is transmitted around the body via nerve networks and hormones, but what is extraordinary about these latest discoveries is the growing diversity of ways in which organs and tissues “talk” to each other to coordinate their action. Indeed, inter-organ communication is now seen as critical machinery for controlling metabolism, ageing and overall health. The ageing process is orchestrated via “conversations” between different organs and tissuesChris Howes/Wild Places Photography/Alamy “I think we’ll suddenly see that organs are communicating in ways we didn’t know about,” says Irene Miguel-Aliaga at the Crick Institute in London. “And then if we find that, then we can see what goes wrong in disease.” The first clues that there might be more to some organs and tissues than first supposed arose in the mid-1990s, when researchers discovered that fat, or adipose tissue, makes a hormone called leptin, which helps control appetite and the body’s energy balance. This transformed our perception of fat: once seen as passive storage tissue, it is now thought of as a dynamic, vital organ. Since then, it has emerged that pretty much every organ or tissue is chipping in. One of the biggest surprises is bone, long thought of as a lifeless mechanical scaffold. In fact, we now know that bone functions as a sophisticated “endocrine” organ, secreting a hormone called osteocalcin that influences metabolism, male fertility and exercise performance. It even reaches the brain, where it reduces anxiety, improves spatial memory and enhances cognition. Boosting falling levels of osteocalcin may one day offer a way of tackling age-related decline in muscle and brain function. “ Osteoporosis isn’t the only condition that could benefit from intervening in inter-organ signalling: ageing itself could be a target “ The skeleton has its fingers in so many pies because the energetic cost of running it is exorbitant. To repair tiny fractures caused by mechanical stress, bone is constantly being broken down by cells called osteoclasts, and in turn constantly rebuilt by cells known as osteoblasts. “Bone health has to be connected to energy metabolism in a way that bone can grow, but not at the expense of the other organs and function,” says Gerard Karsenty at Columbia University in New York. This is why it has such a powerful influence on so many other organs and tissues. And, importantly, other organs talk back. One such organ is fat, which talks to bone via leptin. Back in 2002, it was discovered that fat sends signals to the brain, which responds in part by increasing nerve activity in the sympathetic nervous system, whose tendrils reach many organs, including bone. There, its nerve endings send signals to osteoblasts, reducing bone building and increasing bone destruction. This means that leptin signals from fat are a major regulator of bone mass. Our skeleton isn’t just a mechanical scaffold, but a dynamic organ that orchestrates many processes in the bodyMichael Heise/Unsplash Osteoporosis treatment A study from 2018 showed that these signals can be jammed with existing blood-pressure drugs known as beta-blockers, which inhibit stress hormones like adrenaline released by the sympathetic nervous system. So these drugs might be a cost-effective way of preventing bone loss in women after menopause and in older people more generally. Two clinical trials investigating this are currently under way. Osteoporosis isn’t the only condition that could benefit from intervening in inter-organ signalling: ageing itself could be a target. This springs from the surprising discovery in 2013 that a small region of the brain known as the hypothalamus appears to integrate conversations from multiple organs, and so acts as a high-order controller of ageing and, in turn, longevity. Shin-ichiro Imai at Washington University in St Louis, Missouri, whose team was one of the two that made the discovery, thinks of this orchestration as an entire interconnected system that maintains a stable function, or “robustness”. When this robustness falters, it results in ageing and physiological decline. “We need to integrate all the different pieces from all the different layers, like a molecular layer, cellular layer, tissue, organ layer, to understand the whole system,” he says. Longevity controller Imai and his colleagues have put many of these pieces together. For example, in 2024, they showed that a particular subset of neurons in the hypothalamus of mice talks to adipose tissue through the sympathetic nervous system, triggering the release of an enzyme essential for producing NAD+, a molecule that is vital to cellular metabolism and associated with longevity. When the researchers stimulated these neurons in old mice, the mice lived longer than control mice that didn’t receive this stimulation. “This is the first demonstration in mammals that manipulation of specific neurons really delays ageing and extends lifespan,” says Imai. Moreover, the 2024 study concluded that “these findings clearly demonstrate the importance of the inter-tissue communication… in mammalian aging and longevity control”. Other organs, including skeletal muscle and the small intestine, also converse with the hypothalamus. For instance, in unpublished work, Imai and his colleagues have identified the hormone used by skeletal muscle to communicate with this brain region. Each of these communication pathways operates independently but synergistically to maintain the overall system’s robustness, says Imai, which we can tap into in turn. So, rather than someone taking supplements to boost NAD+ in the hope of slowing down the ageing process – a strategy whose efficacy is still being investigated in humans – Imai proposed a new approach last year, which he terms “inter-organ communication management”. This would involve interventions to strengthen each of these brain-organ conversations simultaneously “as an anti-ageing preventative measure”, he says. “We are working to translate this idea to humans.” The body’s diverse languages To do this, we need to fully understand all the different communication systems that organs use to send messages around the body. We now know that organs use a bewildering smorgasbord of languages to communicate, not just the well-known routes of hormones and nerve action. These include metabolites, small molecules carrying information about energy status and cellular health, and new signaling molecules, such as those produced when skeletal muscles contract that act on many other tissues, including the brain and liver. New types of these messengers are constantly being uncovered, thanks to advances in analytical technologies. For instance, in January, researchers showed how a type of body fat called beige fat regulates blood pressure via a protein it produces called QSOX1, which helps control the stiffness of blood vessels. And a study from November last year found that cancer cells manipulate inter-organ signaling — in this case, via nerves — to undermine the immune response against them. But one of the most exciting discoveries in the field of inter-organ communication is the way that many of these factors are shunted around the body in mysterious bubble-like blobs known as extracellular vesicles (EVs), which our cells constantly shed. When they were first spotted in cells in the 1980s, researchers assumed the cells were just spitting out junk. But we now know there is a whole constellation of EVs of varying sizes, carrying a range of cargoes, from large vesicles bearing mitochondria (the energy engines of the cell) to smaller ones known as exosomes that carry tiny fragments of RNA called microRNAs, which can influence gene activity in recipient cells. Bubble-like blobs called extracelllular vesicles are a key way for organs to send messages around the bodyShutterstock/Juan Gaertner Here, too, new varieties of EVs are continually being unearthed, such as the discovery last year of particularly massive ones dubbed “blebbisomes”, which function as mobile communication centres. At the opposite end of the spectrum are the tiny exomeres and supemeres, both discovered in 2021, which aren’t encased in membrane. Plus, there are oncosomes, produced by cancer cells. All are emerging as im