Universal tool for tracking cell-to-cell interactions

One of the fundamental goals of basic biology is understanding how diverse cell types work in concert to form tissues, organs, and organ systems. Recent efforts to catalog the different cell types in every tissue in our bodies are a step in the right direction, but only one piece of the puzzle. The great mystery of how those cells communicate with one another remains unsolved.

The LIPSTIC technology can track the physical interactions between cells, such as a dendritic cell activating T cells.

Now, a new paper in Nature describes uLIPSTIC, a tool capable of laying the groundwork for a dynamic map tracking the physical interactions between different cells—the elusive cellular interactome. The authors have been perfecting the technology since 2018 and the latest iteration can in principle allow researchers to directly observe any cell-to-cell interaction in vivo.

“With uLIPSTIC we can ask how cells work together, how they communicate, and what messages they transfer,” says Rockefeller’s Gabriel D. Victora. “That’s where biology resides.”

Kiss-and-run

Ever since single-cell mRNA sequencing came into its own, researchers have been scrambling to connect the dots and explain how diverse cells unite to form tissue. Several methods of cataloging cell-to-cell interactions have already emerged, but all have considerable shortcomings. Early efforts that involved direct observation under a microscope failed to retrieve interacting cells for further analysis; subsequent attempts leaned on advanced imaging techniques that intuit how cells might interact based on their structure and proximity to other cells. No approach captured true physical interactions and signal exchange between cell membranes.

Enter LIPSTIC, an innovative approach from the Victora lab that involved labeling cellular structures that touch when two cells make fleeting, “kiss-and-run” contact before parting ways. The labels ensured that, if one cell “kissed” another, it would leave a mark akin to a lipstick, enabling easy identification and quantification of physical interactions between cells.

Originally, the platform had narrow applications. Victora and colleagues designed LIPSTIC to record a very specific kind of cell-to-cell interaction between T cells and B cells, a major focus of their lab. Other researchers, however, began clamoring for a version of LIPSTIC that would work on other cellular interactions too. “We could have tailored a LIPSTIC for every type of interaction,” Victora says. “But why not try to make a universal version, instead?”

Mapping every interaction

In the original version of LIPSTIC, a “donor” cell uses an enzyme borrowed from bacteria to place a labeled peptide tag onto the surface of an “acceptor” cell upon contact—the biochemical equivalent of applying lipstick to one cell and looking for a kiss print on another. That method required knowing exactly how the “kiss” would occur, identifying molecules the donor cell uses to interact with recipient cells and painstakingly forcing the tags onto those molecules. But over time the team discovered that dousing the cells with a high volume of enzyme and its target would ensure that any interaction that one cell had with another cell would be tracked just as efficiently.

“If you cram partner cells with enough enzyme and target, you can make any any cell pair capable of LISPTIC labeling without needing to know in advance what molecules these cells will use for their interaction,” Victora says.

The result was uLIPSTIC, a universal platform not bound by foreknowledge of molecules, ligands, or receptors. Scientists can now theoretically smear uLIPSTIC on any cell, without preconceived notions of how it would interact with its environment, and observe physical cell-to-cell interactions. To demonstrate the power of the platform, the team showed that uLIPSTIC could expand beyond LIPSTIC’s narrow repertoire of B cells and T cells to track how dendritic cells kickstart the body’s immune response against tumors and food allergens.

“The reception to uLIPSTIC has been great,” says Sandra Nakandakari-Higa, a PhD student in the Victora lab and lead author on the paper. “We’re already getting a lot of inquiries from other labs about how they can adapt our system to their models.”

The team hopes to eventually use uLIPSTIC to discover the receptor-ligand pairs key to cellular interactions, in an effort to better understand how cells unite into tissue at the molecular level. Eventually, the team envisions uLIPSTIC as a key tool in the effort to generate comprehensive atlases describing how cells interact to form tissue—a key to the long-awaited interactome.

This article is republished from the Rockefeller University website. Read the original here.