In biology, how cells die is as important as how they live. Cell death provides a counterbalance to cell division, maintaining the proper number of cells throughout an organism’s lifetime. Gaining a better understanding of how cells die is also important for cancer research. It can teach us how the body naturally fends off cancer — by preventing runaway cell growth — as well as point to new ways to target and kill tumor cells.
The lab of Sloan Kettering Institute cell biologist Michael Overholtzer explores the mechanisms of different kinds of cell death. More than a decade ago, while studying breast cancer cells, he was the first to observe a type of cell death called entosis, in which one cell engulfs and kills another.
In a study published in March 2019 in Cell Reports, Dr. Overholtzer described for the first time the role of entosis in the development of a tiny worm called C. elegans. The discovery is significant because until now very little has been known about the role that entosis plays in natural developmental processes.
“Understanding cell death in normal development can provide new clues about how it works and why it evolved,” says Dr. Overholtzer, who was recently named dean of the Gerstner Sloan Kettering Graduate School of Biomedical Sciences. “We hope this research will help us find ways to harness it for cancer treatment.”
Characterizing Different Kinds of Cell Death
The most well-studied form of cell death is called apoptosis. Apoptosis is a type of programmed cell death sometimes likened to cellular suicide, in which a cell breaks down in a regulated, systematic fashion. Apoptosis can occur in response to cell damage, but it’s also a normal part of development in embryos. For example, apoptosis in the hands and feet allows individual fingers and toes to form, by killing cells in the spaces in between them.
In the March 2019 study, the researchers focused on the development of the gastrointestinal and reproductive tracts of the C. elegans worm, a popular lab model for studying development. Research from a team at Rockefeller University had suggested that forms of cell death other than apoptosis were important in the formation of parts of the worm’s body. Dr. Overholtzer’s team decided to continue this line of inquiry.
In particular, the researchers looked at the role of cell death in the formation of the cloaca, the dual-purpose orifice at the hind end of worms, as well as many other organisms, from which excrement is discharged. In males, it is also where sperm are released. It turns out that entosis is vital to ensuring that the genital tract connects to the cloaca. Without it, male worms are sterile.
A Mysterious Process
Unlike apoptosis, entosis requires two cells. It might sound more like a murder than a suicide, but cells that undergo death by entosis still have a death wish. They actually burrow themselves into the other cell, where they are broken down and eaten.
“This is a really enigmatic process,” Dr. Overholtzer says. “Why would a cell decide to do this? It turns out that in the worm, it’s required for normal development.”
In the C. elegans embryo, a type of cell called a linker cell pulls the developing genital tract into the cloaca. The linker cell then burrows into another cell, where it is destroyed by entosis. Destruction of the linker cell creates an opening that allows sperm to enter the cloaca.
“There’s an ongoing question in biology, which is, ’Where do all these different cell death programs come from and why do they exist?’” he notes. “For entosis, this study demonstrates that a process observed initially in breast cancer cells also has a role in normal development.”
Further research will focus on figuring out whether entosis contributes to other developmental processes, as well as molecular changes in the cell that lead to death by entosis. The researchers also plan to study a piece of the linker cell that is left behind after the cell undergoes entosis, called the lobe. “These pieces stick around for a long time, so we think they may have some purpose,” Dr. Overholtzer concludes.Back to top