Red flags: Necroptosis and pyroptosis
These are the violent kinds, and they helped expand the cell death repertoire beyond apoptosis and necrosis. They’re often engaged when cells have been hijacked by viruses or other infectious agents. Rather than be reduced to virus factories, they kill themselves. These cells go down waving big red flags, in the form of chemicals they release to alert the immune system to come in and save their neighbors.
In a 1998 study, a team disabled the ability of cells grown in dishes to undergo apoptosis, and the cells still died. But they did it in a messy way that came to be called necroptosis for its mix of apoptosis and necrosis features. As with necrosis, the cells and their organelles swell up and then the outer membrane ruptures. Necroptosis is a handy backup mechanism because some infectious agents can disable apoptosis.
Then there’s pyroptosis, first observed in 1992 among white blood cells infected with dysentery bacteria and christened in 2001. This is “the screaming, alarm-ringing pro-inflammatory death of a potentially dangerous cell,” the namers wrote. As with necroptosis, cells swell up. They activate enzymes that poke holes in the cell membrane, so their contents leak out, calling up an immune response.
Whether from pyroptosis or necroptosis, that immune response is needed to activate the body’s defenses against infection, such as the fever that cooks invaders, says Kanneganti, who coauthored an article about molecules involved in cell death in the 2020 Annual Review of Immunology. But if too many cells die or the immune system gets stuck in the “on” position, that can lead to ongoing inflammation or autoimmune disease.
Mix and match: PANoptosis
Immune cells, too, may need to die in the case of infection, inflammation or even cancer. As Kanneganti’s group investigated this process, they noticed an alternate mode of death that incorporated elements of apoptosis, necroptosis and pyroptosis. Using the first letter of each classic type, they dubbed it PANoptosis. Since then, researchers have found this hybrid death method in other kinds of cells, too.
In PANoptosis, the cell assembles a big protein machine called the PANoptosome. This activates enzymes to puncture the cell’s membranes. As it dies, the cell releases red-flag molecules that tell other immune cells there’s a problem.
Why do cells need so many ways to achieve the same fatal end? Cells probably evolved these different options during an arms race with disease-causing microbes, Kanneganti surmises. The microbes, aiming to survive, may try to turn off cell death. But if the cell has a wide menu of death mechanisms, it can commit suicide in another manner, sacrificing itself to thwart the pathogen.
Kamikaze killing: NETosis
Immune cells may sacrifice themselves even more dramatically, in a kamikaze action that takes out surrounding pathogens too. This sensational act is the purview of white blood cells called neutrophils, which patrol areas of infection and swallow invaders.
But sometimes the infectious agents are too large, or too numerous, to devour. The neutrophils switch tactics and vomit their own DNA over the pathogen, ensnaring the invaders in a kind of genomic net. It’s called NETosis (for neutrophil extracellular traps). Other cells then dispose of the entangled pathogens.
On occasion, the net-throwing cell is already dying or dead as this takes place, making it a zombie cell committing one final, altruistic act, says immunologist Ben Croker, who studies the phenomenon at the University of California San Diego School of Medicine.
Death metal: Cuproptosis and ferroptosis
While cancer cells seem ominous, they are, in fact, quite vulnerable to death, says Todd Golub, a cancer biologist at the Broad Institute in Cambridge, Massachusetts. “The key,” he adds, “is to find the right triggers.”
Golub’s group found a trigger in drugs that ferry copper into cells. The team is still working out how that makes the cells croak in a process they christened cuproptosis in 2022.
Iron, too, can be deadly to cancer cells, as chemical biologist Brent Stockwell at Columbia University in New York discovered. In addition to tumors, normal cells in the brain, liver and kidneys appear to be particularly susceptible to this form of cell death, which he named ferroptosis in 2012. Researchers have also observed ferroptosis in a wide range of organisms, even yeast and plants, says Stockwell, who cowrote a description of the key features of ferroptosis in the 2019 Annual Review of Cancer Biology.
Stockwell and other researchers are working to identify drugs or special diets that would activate ferroptosis to combat cancer, or block it to protect cells from dying in diseases such as Alzheimer’s.
Eat me: Entosis
Overholtzer, while studying breast cancer cells in the early 2000s, noticed something weird: cancer cells burrowing into other cells. He and his lab supervisor dubbed the phenomenon entosis in 2007.
The invading cell winds up enclosed in a big, membranous bubble. It may starve and undergo apoptosis, or be killed by the surrounding cell. Then the outer cell digests its remains.
But sometimes, weirdly, it survives and pops out of the cell to live independently again. Noting this, some researchers have proposed that entosis gives cancer cells a way to temporarily hide out from the immune system or cancer drugs.
There’s still plenty to learn about cell deaths, and there are probably death modes still awaiting discovery, Golub speculates.
Ultimately, the study of life requires the investigation of cell death. As the Japanese author Haruki Murakami wrote, “Death exists, not as the opposite but as a part of life.”
This article originally appeared in Knowable Magazine, a nonprofit publication dedicated to making scientific knowledge accessible to all. Sign up for Knowable Magazine’s newsletter.
Knowable Magazine, 2024. DOI: 10.1146/knowable-092324-1 (About DOIs)
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