scientific image

Gut microbiome influences location of immune cells

Researchers at the Experimental and Clinical Research Center of Max Delbrück Center and Charité – Universitätsmedizin Berlin have found that microbial communities in the mouse GI tract are unevenly distributed, which influences immune cell populations. The work was published in “Gut Microbes.”

Researchers at the Experimental and Clinical Research Center of Max Delbrück Center and Charité – Universitätsmedizin Berlin (ECRC) have found that different anatomical sections of the gastrointestinal tracts of mice carry different compositions of microbial communities. Moreover, the specific makeup of the microbiota can influence the type and abundance of immune cells in any particular region. The study, which was published in “Gut Microbes,” maps the complex spatial organization of immune cells and microbial communities, providing a tool for studying the interaction between gut microbes and inflammatory diseases.

Previous research has hinted at the existence of “hotspots” along the GI tract where specific immune cells and microbes might interact more intensely. But no one had systematically investigated this across the entire gut, says Dr. Hendrik Bartolomaeus, in the Immune-Microbial Dynamics in Cardiorenal Disease lab of Dr. Nicola Wilck, and an author of the study. “We were motivated by a simple question: How are immune cells organized along the gut, and how does the microbiome influence this organization?”

Microbial communities shape the immune system

The researchers compared the GI tracts of germ-free mice with conventionally colonized mice by dissecting their intestines into segments, and then extracting microbial DNA. They used metagenomic sequencing to identify all the bacterial species present. Concurrently, they isolated immune cells from the segments and analyzed them using flow cytometry, a commonly used technique to identify and quantify different immune cell types based on specific cellular markers.

Images of the colons of conventional (left) and germ free (right) mice showing how bacterial colonization affects the distribution of immune cells along the mouse intestine. CD45 immune cells are show in red, CD3 immune cells are shown in yellow. Immune cells are concentrated close to the gut lumen, where bacterial colonization occurs. In germ free mice, this distribution is disturbed.

They found that not only did the microbial communities in the GI tract of conventional mice vary depending on location. But this also significantly influenced the distribution and type of immune cells found along the gut. For instance, adaptive immune cells, which are acquired after exposure to antigens – foreign substances that induce an immune response – were more prominent in the lower parts of the intestine, while innate immune cells were more abundant in the upper segments. This pattern was severely disturbed in germ-free mice, which lack bacterial antigens in their intestine.

Harithaa Anandakumar, PhD student and lead author of the study, then categorized the immune cells according to whether their presence and abundance is influenced only by location, by an interaction with the microbiota at that location, or both. She then created an app that summarizes the information. “We built a go-to app so that anyone who is interested in a specific immune cell type can look it up and see where it's most abundant in the gut and whether it is influenced by the microbiome, the location, or an interaction of both.”

Such a resource had been lacking, says Wilck, who is also a specialist at Charité’s Department of Nephrology and Medical Intensive Care. Now any scientist working with mouse models can use it. His own lab studies how immune cells travel from the gut into tissues and organs in various mouse models of disease. “We can now use this resource to study whether the immune cells we find in organs damaged by hypertension or kidney disease come from the gut,” he says.

Text: Gunjan Sinha

 

Further information

Literature

Harithaa Anandakumar, Ariana Rauch, Moritz Wimmer, et al. (2024): “Segmental Patterning of Microbiota and Immune Cells in the Murine Intestinal Tract.” Gut Microbes. DOI: 10.1080/19490976.2024.2398126

 

Photo for download

Caption: Images of the colons of conventional (left) and germ free (right) mice showing how bacterial colonization affects the distribution of immune cells along the mouse intestine. CD45 immune cells are show in red, CD3 immune cells are shown in yellow. Immune cells are concentrated close to the gut lumen, where bacterial colonization occurs. In germ free mice, this distribution is disturbed.

Credit: Ariana Rauch, Max Delbrück Center

 

Contacts:

Dr. Nicola Wilck
Group Leader of the Immune-Microbial Dynamics in Cardiorenal Disease lab
Experimental and Clinical Research Center
Max Delbrück Center, Charité – Universitätsmedizin Berlin
nicola.wilck@charite.de

Dr. Hendrik Bartolomaeus
Immune-Microbial Dynamics in Cardiorenal Disease lab
Experimental and Clinical Research Center
Max Delbrück Center, Charité – Universitätsmedizin Berlin
hendrik.bartolomaeus@mdc-berlin.de

Gunjan Sinha
Editor, Communications 
Max Delbrück Center 
+49 30 9406-2118
Gunjan.Sinha@mdc-berlin.de or presse@mdc-berlin.de

Max Delbrück Center

The Max Delbrück Center for Molecular Medicine in the Helmholtz Association (Max Delbrück Center) is one of the world’s leading biomedical research institutions. Max Delbrück, a Berlin native, was a Nobel laureate and one of the founders of molecular biology. At the locations in Berlin-Buch and Mitte, researchers from some 70 countries study human biology – investigating the foundations of life from its most elementary building blocks to systems-wide mechanisms. By understanding what regulates or disrupts the dynamic equilibrium of a cell, an organ, or the entire body, we can prevent diseases, diagnose them earlier, and stop their progression with tailored therapies. Patients should be able to benefit as soon as possible from basic research discoveries. This is why the Max Delbrück Center supports spin-off creation and participates in collaborative networks. It works in close partnership with Charité – Universitätsmedizin Berlin in the jointly-run Experimental and Clinical Research Center (ECRC), the Berlin Institute of Health (BIH) at Charité, and the German Center for Cardiovascular Research (DZHK). Founded in 1992, the Max Delbrück Center today employs 1,800 people and is 90 percent funded by the German federal government and 10 percent by the State of Berlin.