Research Snapshot: Novel discovery describes mechanisms of wound detection in body

Model of epithelial wound detection. Destroyed cells at the center of wounds release proteases, cleaving extracellular pro-Gbp into its active form, which diffuses to distal cells to activate a calcium response through the receptor Mthl10.
Model of epithelial wound detection. Destroyed cells at the center of wounds release proteases, cleaving extracellular pro-Gbp into its active form, which diffuses to distal cells to activate a calcium response through the receptor Mthl10.

By Aaron Conley

THE IDEA

A new study from Vanderbilt University researchers has established a novel way to understand how the body discovers and responds to wounds. The research was led by graduate student James O’Connor and Professor Andrea Page-McCaw in the Department of Cell and Developmental Biology, and Shane Hutson, chair of the Department of Physics and Astronomy and professor of physics and biological sciences.

Aaron Stevens
Aaron Stevens
Andrea Page-McCaw
Andrea Page-McCaw
James O'Connor
James O’Connor

Cells that cover the body and its organs, known as epithelial cells, must be able to heal wounds, as they are uniquely subjected to all kinds of insults and abrasions. “When these cells detect a wound nearby, they change their behaviors,” said Page-McCaw. “They transition from stationary, nondividing, noninvasive cells to cells that migrate, divide and invade.” This also describes the behaviors of cancer cells, which adopt wound-healing behaviors without any wound.

The trans-institutional team of scientists started by looking into the earliest known response of epithelial cells to a nearby wound: an increase in calcium levels. This increase typically occurs within a minute of wounding.

“We were able to connect the response of these cells directly to the cellular damage inherent in wounding,” Page-McCaw said. “We found that wounds destroy cells, causing them to leak or even burst, and some of their contents gets out. Outside of cells, tissues have a detector molecule ready to sense these cellular contents. When they do, proteases in the cellular contents chop up the detector molecule into smaller pieces, which spread to nearby cells. This activates receptors on the cells’ surfaces, giving them the information that a wound is nearby.”

The multidisciplinary collaboration with Hutson’s lab brought the convergence of experimental biology and theoretical mathematical modeling together. “James O’Connor led the experiments,” Page-McCaw said, “and we worked collaboratively with the Hutson lab to analyze the data quantitatively. Aaron Stevens, graduate student in the Hutson lab, generated a mathematical model that showed this scenario is plausible if the cells release their contents slowly, rather than all at once. This finding was an interesting aspect that we had not noticed, but we were able to go back and see evidence for such a slow release.”

WHY IT MATTERS

Successful and efficient wound healing is an important aspect of bodily recovery from trauma or surgery. This research brings us closer to a full mechanistic understanding of how wounds are recognized by epithelial cells and how this leads to wound healing. A foundational understanding of this behavior is essential to developing therapeutics that can address this health issue.

Slow wound healing time can be caused by many factors, leading to infection and declining health. Healogics, the nation’s leading provider of advanced wound care, sponsors an annual Wound Care Awareness Week in June that recognizes the “nearly 7 million people in the United States living with a nonhealing wound.” Healogics notes that “the prevalence of chronic wounds is growing in tandem with an aging population and increasing rates of diseases, such as diabetes and heart disease.”

Additionally, by figuring out how to downregulate these wound-healing behaviors in combination with other cancer interventions, this work offers insights that could help combat cancer’s adoption of this mechanism.

WHAT’S NEXT

Shane Hutson
Shane Hutson

Page-McCaw and Hutson will focus on how cells use the information they receive about the presence of a wound, specifically how the information is encoded in the calcium signal dynamics and then converted into migration, proliferation and changes in cell- and tissue-level mechanics. “Now that we have a solid understanding of how the presence of a wound is first signaled to nearby cells, we can ask a lot of interesting follow-up questions,” said Hutson. “How much information is present in those signals? Can cells interpret the signals to know how large the wound is or how far they are from the wound? Do they use the way the dynamic signals change with time to make that measurement? What are the detailed mechanisms by which the signals then get turned into cellular actions?” Through those and other questions, this research will contribute to a stronger foundational understanding of cell behavior that can be translated to impact human health.

FUNDING

This work was supported by the National Institute of General Medical Sciences, the National Institute of Arthritis and Musculoskeletal and Skin Diseases, the National Institute of Cancer, the National Institute of Child Health and Human Development, and the American Heart Association.

GO DEEPER

The article “Proteolytic activation of Growth-Blocking Peptides triggers calcium responses through the GPCR Mthl10 during epithelial wound detection” was published in the journal Developmental Cell on July 16.

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