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HERE
It is a cold, dark January here in the Northern Hemisphere.
Alas, every cell that lives will one day die, but typical cell death isn't disruptive, chaotic, or injurious.
In the early 1970s, researchers described a formal, highly controlled death process known as "apoptosis".
It is widespread across the tree of
life and regulated by the same genes in a diverse range of species,
from worms to mammals.
Crucially, apoptosis doesn't hurt the dying cell's neighbors:
The ability of cells to die in this way is critical for the survival of multicellular species.
In animals with nervous systems, for example, early development can be a violent time:
When apoptosis goes awry, it can lead to a slew of complications.
Cancer is composed of
cells
that should die but don't, while people with autoimmune diseases are
riddled with cells that should not die but do.
Researchers are continuing to unpack what it means for a
cell to live or die - and even to come back to life.
In one study, researchers found that 2 million years ago, the first eukaryotes - a cell type with complex organization, including a nucleus and mitochondria, like those that make up our bodies - likely already had the tools for apoptosis, inherited from simpler bacterial forebears.
It's still debated why exactly the process originated.
Some researchers speculate that
ancient bacteria may have used these tools as defenses from external
predators. Others propose that apoptosis evolved in single-celled
organisms as a method of self-sacrifice for the good of the
population, to prevent the spread of disease, for instance.
Under the right conditions, some cells that have undergone apoptosis can resurrect themselves in a process called anastasis, after the Greek word for "rising to life."
Just as apoptosis is a highly controlled process, so is anastasis; likewise, researchers have found anastasis in many different organisms, from fruit flies to rodents.
It may have evolved as a way to hit the brakes on
widespread apoptosis after severe but temporary stress, to limit
permanent tissue damage.
Most life on Earth is dormant:
But how?
One study identified a protein, called a hibernation factor, that "pulls the emergency brake" in cells in Arctic permafrost by halting the creation of new proteins.
Dormancy isn't unique to microbes:
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