Blood is a common medium through which invasive bacterial infections disseminate in the human body. neutrophil-bacteria assays allow flexible mechanistic studies and screening of interventional strategies. In standard neutrophil-bacteria assays, both the immune cells and microorganisms are typically interrogated in an exogenous, homogeneous, bulk fluid environment (e.g., culture media or bacterial broth in microtiter plates), lacking the relevant physicochemical factors in the heterogenous blood-tissue microenvironment (e.g., capillary bed) with single-cell confinement. Here we present an neutrophil-bacteria assay by leveraging an open microfluidic model known as "μ-Blood" that supports sub-microliter liquid microchannels with single-cell confinement. In this study we compare the exogenous and endogenous fluids including neutrophils in RPMI (standard suspension cell culture media) and whole blood in response to ( , a gram-positive, non-motile bacterium) in phosphate buffered saline (PBS), Mueller Hinton Broth (MHB), and human serum. Our results reveal a significant disparity between the exogenous and endogenous fluid microenvironments in the growth kinetics of bacteria, the spontaneous generation of capillary (i.e., Marangoni) flow, and the outcome of neutrophil intervention on the spreading bacteria.
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http://dx.doi.org/10.1101/2024.01.22.576723 | DOI Listing |
Cancer Cell
December 2024
Research Program in Systems Oncology, University of Helsinki, Helsinki, Finland; Department of Obstetrics and Gynecology, Department of Oncology, Clinical Trials Unit, Comprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland; iCAN Digital Precision Cancer Medicine Flagship, Helsinki, Finland; Institute for Molecular Medicine Finland, Helsinki Institute for Life Sciences, University of Helsinki, Helsinki, Finland. Electronic address:
Anti-tumor immunity is crucial for high-grade serous ovarian cancer (HGSC) prognosis, yet its adaptation upon standard chemotherapy remains poorly understood. Here, we conduct spatial and molecular characterization of 117 HGSC samples collected before and after chemotherapy. Our single-cell and spatial analyses reveal increasingly versatile immune cell states forming spatiotemporally dynamic microcommunities.
View Article and Find Full Text PDFActa Biomater
December 2024
Translational Tumor Engineering Laboratory, Department of Biomedical Engineering, National University of Singapore, Singapore 119276, Singapore; Cancer Science Institute, National University of Singapore, Singapore 117599, Singapore; The N.1 Institute for Health, National University of Singapore, Singapore 117456, Singapore. Electronic address:
Anal Chem
December 2024
Department of Biophysics, School of Basic Medical Sciences, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, China.
Micromachines (Basel)
November 2024
Department of Pure and Applied Physics, Graduate School of Advanced Science and Engineering, Waseda University, Tokyo 169-8555, Japan.
Wiring technology to control the length and direction of neurite outgrowth and to connect them is one of the most crucial development issues for forming single-cell-based neuronal networks. However, with current neurite wiring technology, it has been difficult to stop neurite extension at a specific length and connect it to other neurites without causing miswiring due to over-extension. Here, we examined a novel method of wiring neurites without miswiring by controlling the length of neurites in open-ended bending microchannel arrays connected beyond the maximum bending angle of neurite outgrowth.
View Article and Find Full Text PDFSmall
November 2024
Delft University of Technology, Delft, 2628 CD, The Netherlands.
Synchronization plays a crucial role in the dynamics of living organisms. Uncovering the mechanism behind it requires an understanding of individual biological oscillators and the coupling forces between them. Here, a single-cell assay is developed that studies rhythmic behavior in the motility of E.
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