by Nancy Fliesler, Children's Hospital Boston

ROS and TLR3 signaling mediates the "eat-me" and "don't eat me" signals that determine stem cell clonal selection by macrophages. Credit: Science (2024). DOI: 10.1126/science.adn1629

Blood stem cells, which give rise to all of our blood cell types, undergo a quality assurance process after they're born. As the lab of Leonard Zon, MD, director of the Stem Cell Research program at Boston Children's, has documented, immune cells known as macrophages interact with each newly born cell. They engulf and eat any diseased or mutated stem cells, cued by a surface molecule called calreticulin, while encouraging healthy stem cells to divide and proliferate.

Now, studying zebrafish, researchers in the Zon Lab show that calreticulin—the "eat-me" signal—can be induced on blood stem cells in several ways, as can a complementary "don't-eat-me" signal the lab identified, beta-2-microglobulin (B2m).

They also found ways to manipulate the two signals, potentially preventing mutant, cancerous stem-cell populations or "clones" from taking over. Their findings are published in the journal Science.

"We want to educate macrophages to take out the mutant stem cells," says Zon, who is also affiliated with the Dana-Farber/Boston Children's Cancer and Blood Disorders Center. "They do take out the mutants periodically, but they're not efficient, and a cancer can overwhelm the system. This could be a whole new way of treating blood cancers like leukemia."

Finding the signals of blood stem cells

To better understand the eat-me signals origins, Zon and colleagues screened a panel of 1,200 chemicals in human cells. They found 93 compounds that induced production of calreticulin on their surface.

Just over half of the compounds induced calreticulin by increasing cellular levels of reactive oxygen species (ROS), known indicators of cellular stress. But the remaining compounds induced calreticulin through pathways that did not involve ROS. Live zebrafish assays, using live imaging and cellular barcoding techniques, revealed that macrophages killed the stem cells with increased ROS, allowing the rest to proliferate.

Separately, the team conducted a whole-genome CRISPR screen in human leukemic cells. They knocked out more than 10,000 genes to identify those that influenced whether macrophages killed blood stem cells or let them live. Together with the chemical screen and the genomic approach, the findings suggested there might be an active don't-eat-me signal.

The experiments pointed to the gene encoding TLR3, a receptor in the innate immune system. Macrophages killed more blood stem cells when it was knocked out. When TLR3 signaling was left intact, B2m—the don't-eat-me signal—went to the cell surface.

"When we made fish without B2m, more blood stem cells were engulfed and eliminated," says Cecilia Pessoa Rodrigues, Ph.D., of the Zon Lab and Harvard Stem Cell Institute, first author on the Science paper.

The team found another key player: repetitive RNA elements. These elements are scattered around the genome, and the body normally tries to suppress them. Zon's team showed that de-repressing these elements with methylation inhibitors triggered the TLR3 gene and increased B2m expression on the cell surface, enabling more blood stem cells to survive.

Tipping blood stem cells away from cancer

This work points to several prospects for controlling blood cancers by tweaking blood stem cells' balance of calreticulin (the eat-me signal) and B2m (the don't-eat-me signal). Drugs boosting calreticulin on the cell surface could possibly be combined with an antibody blocking either B2m or TLR3. Or either approach might work on its own.

The Zon Lab is now screening for drugs that create an eat-me signal in mutant stem cells but not in normal stem cells and drugs that would remove mutant clones of cells as a new treatment for preleukemia and leukemia.

In addition to treating cancer, Zon envisions using these approaches to treat clonal hematopoiesis. In this precancerous condition, which becomes more common as people age, acquired mutations can cause mutant blood stem cell populations to multiply faster than others, eventually taking up a large share of a person's blood cells.

"I think you can manipulate the system in multiple ways to get rid of bad stem cell clones and keep good clones," Zon says. "Getting rid of mutant clones could prevent cancer down the road."

More information: Cecilia Pessoa Rodrigues et al, Transcripts of repetitive DNA elements signal to block phagocytosis of hematopoietic stem cells, Science (2024). DOI: 10.1126/science.adn1629

Journal information: Science 

Provided by Children's Hospital Boston