Image: Computer reconstruction of tissue structure around a nonadhesive region (black area).
Their study appears this week in an advance online edition of Nature Materials.
“We were trying to understand the basic relationship between collective cellular motions and collective cellular forces, as might occur during cancer cell invasion, for example. But in doing so we stumbled onto a phenomenon that was totally unexpected,” said senior author Jeffrey Fredberg, professor of bioengineering and physiology in the HSPH Department of Environmental Health and co-senior investigator of HSPH’s Molecular and Integrative Cellular Dynamics lab.
Biologists, engineers, and physicists worked together to shed light on collective cellular motion because it plays a key role in functions such as wound healing, organ development, and tumor growth. Using a technique called monolayer stress microscopy—which they invented themselves—they measured the forces affecting a single layer of moving epithelial cells. They examined the cells’ velocity and direction as well as traction—how some cells either pull or push themselves and thus force collective movement.
As they expected, the researchers found that when an obstacle was placed in the path of an advancing cell layer—in this case, a gel that provided no traction—the cells moved around it, tightly hugging the sides of the gel as they passed. However, the researchers also found something surprising—that the cells, in addition to moving forward, continued to pull themselves collectively back toward the gel, as if yearning to fill the unfilled space. The researchers dubbed this movement “kenotaxis,” from the Greek words “keno” (vacuum) and “taxis” (arrangement), because it seemed the cells were attempting to fill a vacuum.
This new finding could help researchers better understand cell behavior—and evaluate potential drugs to influence that behavior—in a variety of complex diseases, such as cancer, asthma, cardiovascular disease, developmental abnormalities, and glaucoma,” explains co-author Xavier Trepat, group leader at IBEC and ICREA research professor. “The findings could also help with tissue engineering and regenerative medicine, both of which rely on cell migration.”
In carcinomas, for instance—which represent 90% of all cancers and involve epithelial cells—the new information on cell movement could improve understanding of how cancer cells migrate through the body. Asthma research could also get a boost, because scientists think migration of damaged epithelial cells in the lungs are involved in the airway narrowing caused by the disease.
“Kenotaxis is a property of the cellular collective, not the individual cell,” says Jae Hun Kim, the study’s first author. “It was amazing to us that the cellular collective can organize to pull itself systematically in one direction while moving systematically in an altogether different direction.”
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Article reference: Jae Hun Kim, Xavier Serra-Picamal, Dhananjay T. Tambe, Enhua H. Zhou, Chan Young Park, Monirosadat Sadati, Jin-Ah Park, Ramaswamy Krishnan, Bomi Gweon, Emil Millet, James P. Butler, Xavier Trepat & Jeffrey J. Fredberg (2013). Propulsion and navigation within the advancing monolayer sheet. Nature Materials, advance online publication
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