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Functionalization of Atomic Force Microscope Cantilevers with Single-T Cells or Single-Particle for Immunological Single-Cell Force Spectroscopy
Published on: July 10, 2019
Detection of lipopolysaccharide induced inflammatory responses in RAW264.7 macrophages using atomic force microscope
Jiang Pi1, Ting Li1, Jianxin Liu1
1State Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau 000853, China.
Abstract:
In recent years, LPS activated RAW264.7 cells are widely used as an in vitro inflammatory model for the screen of effective anti-inflammation drugs and the investigation of exact anti-inflammation mechanism of these drugs. But up to now, there are few data about the effect of LPS on the morphology, especially on the membrane ultrastructure and bio-mechanical properties of RAW264.7 macrophages. In this work, the topographical and biophysical changes of RAW264.7 macrophages upon LPS stimulation are detected by high resolution atomic force microscopy (AFM). The AFM results suggested that LPS activated RAW264.7 macrophages changed to be much bigger than control cells with some holes emerged on cell surface. The size of membrane protein clusters and the roughness of membrane significantly increased after LPS exposure. In addition, the AFM force measurement results demonstrated that LPS stimulation increased the adhesion force of RAW264.7 macrophages, and also increased the stiffness of RAW264.7 macrophages, which were attributed to the re-distribution of intracellular F-actin structures induced by LPS. These findings suggested that LPS stimulation could also induce the pathophysiological changes of RAW264.7 macrophages, which would benefit our understanding of the inflammatory processes in macrophages upon pathogen stimulation at nano-scale.
Insights
Lipopolysaccharide (LPS) stimulation significantly alters RAW264.7 macrophage morphology and mechanics. This study reveals nanoscale changes in cell surface, adhesion, and stiffness following LPS exposure.
Area of Science:
- Cell Biology
- Biophysics
- Immunology
Background:
- RAW264.7 cells stimulated with lipopolysaccharide (LPS) are a common in vitro model for anti-inflammatory drug screening.
- Limited data exists on LPS-induced morphological and biomechanical changes in these macrophages.
Purpose of the Study:
- To investigate the topographical and biophysical alterations in RAW264.7 macrophages stimulated by LPS.
- To understand the nanoscale changes in cell surface, adhesion, and stiffness.
Main Methods:
- High-resolution Atomic Force Microscopy (AFM) was employed to analyze topographical and force measurements.
- RAW264.7 macrophages were stimulated with LPS to induce inflammatory responses.
Main Results:
- LPS-activated macrophages exhibited increased size and surface roughness, with emergent holes.
- Significant increases in membrane protein cluster size, adhesion force, and cell stiffness were observed.
- These changes were linked to the LPS-induced redistribution of intracellular F-actin.
Conclusions:
- LPS stimulation induces significant pathophysiological changes in RAW264.7 macrophages at the nanoscale.
- These findings enhance the understanding of inflammatory processes in macrophages upon pathogen stimulation.
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