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Scientists Discover Silent 'Scream' of Human Skin: A Breakthrough in Cellular Communication

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  1. menna omar

    menna omar Bronze Member

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    Scientists Discover the Silent 'Scream' of Human Skin: A Breakthrough in Cellular Communication

    Human skin, long known as a protective barrier against the external environment, has now revealed a hidden mechanism of communication that could significantly impact the field of medicine. For the first time, researchers have discovered that skin cells can "scream" to communicate with neighboring cells in response to injury. This discovery opens new doors for understanding how the body reacts to damage and offers potential for innovative medical technologies to accelerate healing.

    The Mystery of Skin Communication

    Until recently, it was believed that skin cells, specifically epithelial cells that line the outer layer of skin and organs, were relatively silent when it came to electrical communication. Unlike neurons that send rapid, short-lived bioelectrical signals across the body, epithelial cells were thought to be non-responsive in a similar way. However, a team of researchers from the University of Massachusetts Amherst, led by polymath Steve Granick and biomedical engineer Sun-Min Yu, uncovered a surprising and significant discovery: epithelial cells "scream" slowly and persistently when they experience injury, creating a long, slow electrical signal that spreads across large areas of the tissue.

    This discovery is revolutionary because it suggests that the body has additional layers of communication beyond the rapid responses of the nervous system. When these skin cells are injured, they send signals to their neighbors in a manner akin to a nerve impulse, but at a much slower rate — about 1,000 times slower. Granick compares it to a nerve’s electrical impulse but with a pace more similar to that of a slow-motion conversation between the cells.

    The Experiment: A Chip, Laser, and Electrical Signals

    To investigate this process, Granick and Yu designed a groundbreaking experiment. They created a system that allowed them to monitor the electrical activity of epithelial cells. The system consisted of a chip connected to around 60 electrodes, which were coated with a single layer of human keratinocytes, the primary cells that form the epidermis or outer skin layer. These keratinocytes were grown in a lab, providing a controlled environment for the study.

    The researchers used a laser to "sting" the skin layer, causing a localized injury. Then, the electrode array recorded the electrical responses from the cells in the affected area. What they observed was nothing short of astonishing: the epithelial cells communicated through electrical signals that propagated slowly across the tissue, reaching distances of up to hundreds of micrometers from the injury site.

    The Nature of the 'Scream'

    The electrical signals transmitted by the epithelial cells were slow, traveling at a speed of about 10 millimeters per second. This is in stark contrast to the fast electrical communication observed in neurons, which can transmit signals at speeds exceeding 100 meters per second. This slow, prolonged signaling is unlike anything previously recorded in the skin cells and could be crucial for the way the skin heals itself after injury.

    Interestingly, this communication process relies on ion channels, tiny pores in the cell membranes that allow the movement of charged ions such as calcium. The study revealed that these channels were especially sensitive to mechanical stimuli such as pressure or stretching, suggesting that they are activated by physical damage to the tissue. This mechanism is different from neurons, which rely on changes in voltage or chemical signals to transmit information.

    Moreover, the "screams" from the epithelial cells lasted much longer than the brief electrical signals of neurons. The communication between the cells could continue for up to five hours, allowing for an extended period of coordination across the damaged area. While the voltage of the epithelial signals was similar to that of neurons, the duration and nature of the signals highlighted a distinct form of communication suited for the slow, ongoing process of tissue repair.

    Implications for Medical Technology

    This new understanding of how epithelial cells communicate in response to injury has significant implications for medical technology. For example, the discovery could lead to the development of biomedical devices that mimic this slow cellular communication. Wearable sensors, electronic bandages, or bioelectronic devices could be created to monitor and stimulate this cellular activity, potentially speeding up the healing process of wounds and injuries.

    Researchers are still exploring the full range of factors involved in this process, such as the precise role of calcium ions in the signaling and whether other types of epithelial cells react differently. While much more work needs to be done, the initial findings offer a promising avenue for future research in wound healing and regenerative medicine.

    Yu, one of the lead researchers, explains, “Understanding these screams between wounded cells opens doors we didn’t know existed.” This breakthrough could mark the beginning of a new era in cellular communication research, one that has the potential to revolutionize the way we treat injuries, accelerate recovery, and develop innovative medical devices.

    Conclusion: A New Frontier in Cellular Communication

    The discovery of the "silent scream" of skin cells marks a major shift in our understanding of how the body communicates at the cellular level. It highlights the complexity of the body’s communication networks and the potential for using these signals to enhance medical treatment. As research continues, this discovery could pave the way for the development of new technologies that harness the body’s natural healing processes, making recovery from injuries faster, more efficient, and more effective than ever before.

    Learn more: https://www.pnas.org/doi/full/10.1073/pnas.2427123122
     

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