How cells get used to the familiar
Peer-Reviewed Publication
Updates every hour. Last Updated: 6-May-2025 02:09 ET (6-May-2025 06:09 GMT/UTC)
Up until recently, habituation — a simple form of learning — was deemed the exclusive domain of complex organisms with brains and nervous systems, such as worms, insects, birds, and mammals. But a new study, published Nov. 19 in Current Biology, offers compelling evidence that even tiny single-cell creatures such as ciliates and amoebae, as well as the cells in our own bodies, could exhibit habituation akin to that seen in more complex organisms with brains.
Researchers have found that coronaviruses like SARS-CoV-2 contain genes that appear important for viral survival even though they don’t produce a working protein. Their work investigating how these mystery genes evolve could help forecast which variants might be more dangerous.
Researchers explain how individual cells are capable of rudimentary forms of learning previously thought exclusive to organisms with brains. By using mathematical simulations, they demonstrate that cells can adjust their responses to repeated stimuli through simple molecular circuits which could be a type of cellular ‘memory’, effectively helping cells "remember" and "learn" from experience. The findings could represent an important shift in how we view the fundamental units of life. If single cells can “remember," it could also help explain how cancer cells develop resistance to chemotherapy or how bacteria become resistant to antibiotics.
For the sixth time: Konstanz pioneer in collective behaviour research honoured as one of the most influential researchers of our time.
Cell-to-cell communication through nanosized particles, working as messengers and carriers, can now be analyzed in a whole new way, thanks to a new method involving CRISPR gene-editing technology. The particles, known as small extracellular vesicles (sEVs), play an important role in the spread of disease and as potential drug carriers. The newly developed system, named CIBER, enables thousands of genes to be studied at once, by labeling sEVs with a kind of RNA “barcode.” With this, researchers hope to find what factors are involved in sEV release from host cells. This will help advance our understanding of basic sEV biology and may aid in the development of new treatments for diseases, such as cancer.