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Combined Cellular Thermometry Reveals That Salmonella typhimurium Warms Macrophages by Inducing a Pyroptosis-like
Leyang Wu1,2, Feng Chen3, Xiaoyao Chang1
1State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing210023, China.
Abstract:
The attenuated Salmonella typhimurium VNP20009, enriched in tumors, is known to have antitumor effects and recruit macrophages. Little is known, however, about whether VNP will lead to specific changes in macrophages, e.g., cell temperature. Here, using a real-time wireless multicell thermometry system, we reported for the first time that VNP20009 increases the macrophage temperature by 0.2 °C. Nigericin, recognized as an inducer of pyroptosis, was found to induce macrophage warming. Moreover, the ΔsipD-VNP20009 strain failed to induce macrophage pyroptosis and simultaneously failed to warm macrophages, and the Gsdmd-/- macrophages that were unable to achieve pyroptosis were no longer warmed following VNP20009 induction. These results suggested that the occurrence of macrophage pyroptosis is the key to VNP20009-mediated cell warming. With the aid of a single-cell thermometry system, it was further confirmed that cell warming occurred in pyroptosis-like macrophages. Cellular warming was not detected after the induction of pyroptosis in macrophages with loss of mitochondrial biological function, suggesting a critical role of mitochondria in warming. Moreover, we found that VNP20009 caused local tumor temperature increases. The local tumor warming induced by VNP20009 was significantly reduced after macrophage clearance. Notably, this temperature increase contributed to M1-type polarization. These findings expanded our knowledge of the cellular biological changes induced by the strain on macrophages, as well as the biochemical phenomena accompanying pyroptosis, and provide a reference for the study of biochemical signals transduced to biothermal signals with a combined cell-level temperature detector.
Insights
Salmonella typhimurium VNP20009 increases macrophage temperature via pyroptosis, a process involving mitochondria. This bacterial strain also causes localized tumor warming, promoting M1 macrophage polarization.
Area of Science:
- Immunology
- Microbiology
- Biophysics
Background:
- Salmonella typhimurium VNP20009 exhibits antitumor properties and recruits macrophages.
- The specific cellular changes, such as temperature shifts, induced by VNP20009 in macrophages are not well understood.
Purpose of the Study:
- To investigate the effect of VNP20009 on macrophage cell temperature.
- To elucidate the mechanism underlying VNP20009-induced cellular temperature changes and its relation to pyroptosis and tumor microenvironment.
Main Methods:
- Real-time wireless multicell thermometry system for measuring macrophage temperature.
- Utilized VNP20009, ΔsipD-VNP20009 strains, and Gsdmd-/- macrophages to study pyroptosis.
- Single-cell thermometry and assessment of mitochondrial function.
Main Results:
- VNP20009 significantly increased macrophage temperature by 0.2 °C.
- Macrophage pyroptosis, induced by VNP20009 and nigericin, was directly linked to cellular warming.
- Mitochondria play a critical role in VNP20009-induced cellular warming, and tumor warming was reduced upon macrophage clearance, correlating with M1 polarization.
Conclusions:
- Macrophage pyroptosis is the key mediator of VNP20009-induced cellular warming.
- Mitochondria are essential for the biothermal signal transduction during pyroptosis.
- VNP20009-induced tumor warming influences macrophage polarization, offering insights into bacterial-host interactions and biothermal signaling.
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