Taking look at inner working of cells to see how they respond to heat stress

Imagine the life of a yeast cell, floating around the kitchen in a spore that eventually lands on a bowl of grapes.

Life is good: food for days, at least until someone notices the rotting fruit and throws them out. But then the sun shines through a window, the section of the counter where the bowl is sitting heats up, and suddenly life gets uncomfortable for the humble yeast. When temperatures get too high, the cells shut down their normal processes to ride out the stressful conditions and live to feast on grapes on another, cooler day.

This “heat shock response” of cells is a classic model of biological adaptation, part of the fundamental processes of life—conserved in creatures from single-celled yeast to humans—that allow our cells to adjust to changing conditions in their environment. For years, scientists have focused on how different genes respond to heat stress to understand this survival technique.

Now, thanks to the innovative use of advanced imaging techniques, researchers at the University of Chicago are getting an unprecedented look at the inner machinery of cells to see how they respond to heat stress.

“Adaptation is a hidden superpower of the cells,” said Asif Ali, a postdoctoral researcher at UChicago who specializes in capturing images of cellular processes. "They don’t have to use this superpower all the time, but once they’re stuck in a harsh condition, suddenly, there's no way out. So, they employ this as a survival strategy.”

How cells adapt

Ali works in the lab of David Pincus, assistant professor of molecular genetics and cell biology at UChicago, where their team studies study how cells adapt to stressful and complex environments, including the heat shock response.

In the new study, published Oct. 16 in Nature Cell Biology, they combined several new imaging techniques to show that in response to heat shock, cells employ a protective mechanism for their orphan ribosomal proteins – critical proteins for growth that are highly vulnerable to aggregation when normal cell processing shuts down – by preserving them within liquid-like condensates.

Once the heat shock subsides, these condensates get dispersed with the help of molecular chaperone proteins, facilitating integration of the orphaned proteins into functional mature ribosomes that can start churning out proteins again. This rapid restart of ribosome production allows the cell to pick back up where it left off without wasting energy.

The study also shows that cells unable to maintain the liquid state of these condensates don’t recover as quickly, falling behind by ten generations while they try to reproduce the lost proteins.

New cell biological technique

“Asif developed an entirely new cell biological technique that lets us visualize orphaned ribosomal proteins in cells in real time, for the first time,” Pincus said. “Like many innovations, it took a technological breakthrough to enable us to see a whole new biology that was invisible to us before but has always been going on in cells that we've been studying for years.”

Ribosomes are crucial machines inside the cytoplasm of all cells that read the genetic instructions on messenger RNA and build chains of amino acids that fold into proteins. Producing ribosomes to perform this process is energy intensive, so under conditions of stress like heat shock, it’s one of the first things a cell shuts down to conserve energy.

At any given time though, 50% of newly synthesized proteins inside a cell are ribosomal proteins that haven’t been completely translated yet. Up to a million ribosomal proteins are produced per minute in a cell, so if ribosome production shuts down, these millions of proteins could be left floating around unattended, prone to clumping together or folding improperly, which can cause problems down the line.

Instead of focusing on how genes behave during heat shock, Ali and Pincus wanted to look inside the machinery of cells to see what happens to these “orphaned” ribosomal proteins. For this, Ali used microscopes managed by the UChicago Integrated Light Microscopy Core, including a new tool called lattice light sheet 4D imaging that uses multiple sheets of laser light to create fully dimensional images of components inside living cells.

Because he wanted to focus on what was happening to just the orphaned proteins during heat shock, Ali also used a classic technique called “pulse labeling” with a modern twist: a special dye called a “HaloTag” to flag the newly synthesized orphan proteins.

Often when scientists want to track the activity of a protein inside a cell, they use a green fluorescent protein tag that glows bright green under a microscope. But since there are so many mature ribosomal proteins in a cell, using GFPs would just light up the whole cell. Instead, the pulse labelling with HaloTag dye allows researchers to light up just the newly created ribosomes and leave the mature ones dark.

‘Loosely affiliated biomolecular goo’

Using these combined imaging tools, the researchers saw that the orphaned proteins were collected into liquid-like droplets of material near the nucleolus (Pincus used the scientific term “loosely affiliated biomolecular goo”). These blobs were accompanied by molecular chaperones, proteins that usually assist the ribosomal production process by helping fold new proteins. In this case, the chaperones seemed to be “stirring” the collected proteins, keeping them in a liquid state and preventing them from clumping together.

This finding is intriguing, Pincus said, because many human diseases like cancer and neurodegenerative disorders are linked to misfolded or aggregated clumps of proteins. Once proteins get tangled together, they stay that way too, so this “stirring” mechanism seems to be another adaptation.

“I think a very plausible general definition for cellular health and disease is if things are liquid and moving around, you are in a healthy state, once things start to clog up and form these aggregates, that's pathology,” Pincus said. “We really think we're uncovering the fundamental mechanisms that might be clinically relevant, or at least, at the mechanistic heart of so many human diseases.”

Research was supported by the National Institutes of Health under award numbers R01 GM138689 and R35 GM144278, along with support from the Neubauer Family Foundation, and the National Science Foundation Quantum Leap Challenge Institute Quantum sensing for Biophysics and Bioengineering grant OMA-2121044. Additional authors include Rania Garde, Olivia C. Schaffer, Jared A. M. Bard, Kabir Husain, Samantha Keyport Kik, Kathleen A. Davis, Sofia Luengo-Woods, Maya G. Igarashi, D. Allan Drummond, and Allison H. Squires from the University of Chicago.

This story was adapted from the UChicago Biological Sciences Division website.