A new way to detect infection
Dr. Andrea Puhar and her team at The Laboratory for Molecular Infection Medicine Sweden (MIMS) at Umeå University, discovered that gut cells sense harmful bacteria through the mechanical force exerted on their cell surface during bacterial invasion. A protein called PIEZO1, which is able to sense mechanical signals, is necessary to detect invading bacteria. Activation of PIEZO1 during infection triggers a protective immune response. The study is now published in the scientific journal Cell Reports.
Note: this article originally appeard on the MIMS website https://www.mims.umu.se/news-events/2104-a-new-way-to-detect-infection.html
The immune system typically detects microbes through the chemical interaction of characteristic microbial molecules binding to dedicated cellular receptors. Activation of these receptors indicates the presence of specific types of microbes and regulates the immune response. A group of scientists at MIMS, which is based at Umeå University, Sweden, together with their collaborators, has now discovered that the detection of physical forces produced by bacterial infection can initiate the immune response.
Some harmful intestinal bacteria can breach the boundaries that separate the tissue from its surrounding environment. This initiates an inflammatory immune response that protects the body. During the invasion process, these trespassing microbes induce characteristic protrusions called ruffles on the surface of intestinal cells. The protrusions push against the cell surface, wrap around the bacteria and eventually take them up into the cell. These cellular movements produce mechanical force that results in changes in cell surface tension. The new study shows that cells sense these changes in surface tension as a signal for infection. The mechanical signal is detected by the action of a mechanosensor protein, PIEZO1.
“PIEZO1 is distributed all over the surface of intestinal cells like a net and functions as an alarm system that is activated at sites of bacterial invasion. Following PIEZO1 activation, infected cells send out alert signals that start the immune response. Our findings shine light on a new mode of sensing infection: while it was known before that cells have a “sense of smell” to chemically detect infection, we now show that they also have a “sense of touch” by physically detecting force changes”, says Andrea Puhar, lead author of the study.
In an earlier study, the authors discovered that intestinal epithelial cells secrete a molecule called ATP when they are infected with certain bacteria, such as the Gram-negative pathogens Shigella and Salmonella. Intestinal epithelial cells act as immune sentinels as they form a barrier to the gut lumen, where many beneficial microbes reside but at the same time harmful microbes start infection after ingestion. The authors showed that during bacterial infection extracellular ATP acts as a danger signal that causes acute intestinal inflammation, a protective immune response (Puhar et al., Immunity 39, 1121-1131, December 12, 2013).
How ATP secretion starts during infection was not known. Using Shigella and the Gram-positive intestinal pathogen Listeria along with pharmacological and genetic manipulation, the authors now show that different types of bacteria are able to trigger ATP secretion, provided they are invasive, a trait restricted to some pathogens but not found in beneficial gut microbes. Furthermore, using sterile beads of bacterial size that are taken up by cells, they showed that imitating the process of ruffle formation and the mechanical stimuli occurring during bacterial entry is sufficient to trigger ATP secretion. They found that the inherently mechanosensitive plasma membrane cation channel PIEZO1, which is known to sense changes in lipid bilayer tension, is necessary to induce ATP secretion during bacterial invasion via Ca2+ influx and, in addition, induces protective gene expression programmes.
“When I found that genetic inactivation of PIEZO1 abolished ATP secretion during bacterial invasion of intestinal epithelial cells, we had really strong proof that PIEZO1 was important to mechanically sensing infection and we were so excited. Then, using live-cell microscopy, my colleague Dorothee Langenbach, a postdoc in the team, showed that PIEZO1-dependent Ca2+ influx coincides with plasma membrane ruffle formation as bacteria are taken up into cells, and everything came together”, says Lalitha Tadala, PhD student in the Puhar lab and first author of the paper.
“Mechanical sensing of bacterial invasion, one of the first steps of infection, allows early immune detection and triggers a superfast immune response, which provides a strong evolutionary advantage in the never-ending struggle between dangerous microbes and our immune system. This mode of immune detection makes it possible to specifically react to invasive pathogens but is not activated by the beneficial bacteria inhabiting the gut. It will be interesting to see whether other types of pathogens that induce similar mechanical changes during infection are detected by PIEZO1 and whether the pathway is dysregulated during inflammatory diseases. This will determine if in the future we can exploit it to treat infectious or inflammatory diseases”, adds Andrea Puhar.
About the publication
Lalitha Tadala, Dorothee Langenbach, Mirjam Dannborg, Ramón Cervantes-Rivera, Atin Sharma, Kevin Vieth, Lisa M. Rieckmann, Alkwin Wanders, David A. Cisneros, Andrea Puhar (2022) Infection-induced membrane ruffling initiates danger and immune signaling via the mechanosensor PIEZO1. Cell Reports 40, 111173
Read the full scientific article: https://doi.org/10.1016/j.celrep.2022.111173
For more information, please contact
Andrea Puhar
Group leader at MIMS, Umeå
Research Fellow at the Department of Molecular Biology, Umeå University, Umeå
andrea.puhar@umu.se
+46-90-785 33 51
https://www.mims.umu.se/groups/andrea-puhar.html
https://www.umu.se/en/staff/andrea-puhar/
Nóra Lehotai,
Project coordinator and responsible for communications
MIMS, Umeå University, Umeå
nora.lehotai@umu.se
Umeå University
Umeå University is one of Sweden’s largest institutions of higher education with over 36,000 students and 4,000 faculty and staff. The university is home to a wide range of high-quality education programmes and world-class research in a number of fields. Umeå University was also where the revolutionary gene-editing tool CRISPR-Cas9 was discovered that has been awarded the Nobel Prize in Chemistry.
At Umeå University, distances are short. The university's unified campus encourages academic meetings, an exchange of ideas and interdisciplinary co-operation, and promotes a dynamic and open culture in which students and staff rejoice in the success of others.
The Laboratory for Molecular Infection Medicine Sweden, MIMS
MIMS is the Swedish Node of the Nordic EMBL Partnership for Molecular Medicine, hosted at Umeå University, where MIMS is affiliated with the Faculty of Medicine and the Faculty of Science and Technology and closely connected to the University Hospital of Umeå. Affiliated scientists across Sweden concentrate on understanding how viruses, bacteria and parasites cause disease and how their hosts respond to infection. MIMS brings together researchers from many disciplines to answer important and fundamental questions of infection biology. At the regional and national level MIMS contributes to and benefits from state-of-the-art research infrastructures in imaging, genomics and structural biology.