Protein needed to fight Cancer

To slay the larger cancer cell they are attached to, the two smaller killer T cells release protein bombs. 

Immune cells blast infections and cancer with protein ‘bombs’

By Mitch Leslie May. 7, 2020 , 2:00 PM


Our immune system’s killer T cells earn their name. They destroy infected and cancerous cells, and now, research reveals new details about how they do it. The cells bombard their targets with protein “bombs” packed with deadly chemicals.

The study “is clearly a significant step forward in refining our knowledge” about how these immune sentinels take out dangerous cells, says immunologist David Masopust of the University of Minnesota Medical School.

One of a killer T cell’s most important weapons is perforin, a protein that punctures the outer membrane of the target cell. Enzymes called granzymes that the T cell also releases can then pour in and trigger the victim to commit suicide. Whether killer T cells just squirt out granzymes and perforin or rely on specialized structures to transport the lethal molecules to the target cell has not been clear.

To find out, immunologist Michael Dustin of the University of Oxford and colleagues tracked molecules spilled by attacking killer T cells. Their results, reported today in Science, suggest the cells package the molecules into containers the team calls supramolecular attack particles, or SMAPs. By analyzing the payloads of these bombs, the scientists discovered that SMAPs contain not just perforin and granzymes, but also more than 280 other kinds of proteins.

For a closer look at SMAPs’ structure, the researchers turned to a type of superresolution imaging known as direct stochastic optical reconstruction microscopy, which can pinpoint individual molecules. Cells release some types of small particles that are swaddled in lipids, but SMAPs sport a protein coat and harbor granzyme and perforin in their core. Instead of just leaking perforin and granzymes, killer T cells fashion a complex receptacle to deliver them, the researchers conclude.

To simulate the interactions between killer T cells and their victims, Dustin and his team placed the T cells on a double layer of lipids that is similar to the membrane that encloses cells. SMAPs rapidly showed up on the membrane, suggesting the T cells began to discharge them after latching on.

When the researchers plucked the killer T cells off the surface, some SMAPs remained behind. Like molecular mines, they could kill cells for up to 1 day, the team reports. Studies going back as far as the 1980s may have detected signs of SMAPs, Dustin says, but until recently researchers didn’t have the imaging technology to probe their structure.

Immunologist Christopher Mody of the University of Calgary says the paper deserves credit for “suggesting a new paradigm” for how perforin and granzymes converge at the target cell’s membrane. However, he cautions that the authors have not demonstrated whether killer T cells make and then release SMAPs or release the components, which then assemble into SMAPs at the target.

SMAPs’ complex contents suggest they may also have other functions, Dustin says. For example, the particles contain molecules that attract immune cells and manipulate their behavior, hinting that communication could be one of their roles. “We know they are important for killing, but we suspect it’s more than that,” Dustin says.

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