2007
DOI: 10.1364/oe.15.011020
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The interaction of lipopolysaccharide with membrane receptors on macrophages pretreated with extract of Reishi polysaccharides measured by optical tweezers

Abstract: Lipopolysaccharide (LPS), one of the cell wall components of Gram-negative bacteria, is recognized by and interacted with receptors on macrophages. In this paper, we report the trapping of LPS-coated polystyrene particles via optical tweezers and measured its interaction with murine macrophages (J774A.1 cells) for cells pre-treated with extract of Reishi polysaccharides (EORP) vs. those without EORP treatment. Our experimental results indicate that the cellular affinity for LPS increases when the macrophage is… Show more

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Cited by 20 publications
(7 citation statements)
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“…Recently, Wei et al (2007) found that GLPS not only enhances the J774A.1 macrophage surface expression of TLR4 and CD14 as well as LPS binding and phagocytosis internalization, but it also reduces the adhesion time constant and increases the force constant of the binding interaction. Treatment with F3, an active ingredient of GLPS, increased the population of CD14 þ CD26 þ monocyte/macrophage in human umbilical cord blood mononuclear cells (Chien et al, 2004).…”
Section: Effect Of Glps On Macrophagesmentioning
confidence: 99%
“…Recently, Wei et al (2007) found that GLPS not only enhances the J774A.1 macrophage surface expression of TLR4 and CD14 as well as LPS binding and phagocytosis internalization, but it also reduces the adhesion time constant and increases the force constant of the binding interaction. Treatment with F3, an active ingredient of GLPS, increased the population of CD14 þ CD26 þ monocyte/macrophage in human umbilical cord blood mononuclear cells (Chien et al, 2004).…”
Section: Effect Of Glps On Macrophagesmentioning
confidence: 99%
“…To demonstrate that an interaction does exist between the bacterium and the substratum, the interaction force (represented by a force constant K bio ) between a single bacterium and the surrounding agar gel (0.2%) in LB was measured by oscillatory optical tweezers (Figure 3); similar techniques have been applied successfully to measure the interaction between biomolecules and mammalian cells [14], [15]. The mean value of K bio for strain BW25113 was 34.2±7.0 dyne/cm.…”
Section: Resultsmentioning
confidence: 99%
“…To measure the interaction of the bacterium with the surrounding LB agar gel in terms of the interaction force constant K bio , a previously described method [15] was modified. In brief, when bacteria grew to an appropriate density, the bacterial solution was dropped into LB-agar to make a final agar concentration at 0.2% (w/v).…”
Section: Methodsmentioning
confidence: 99%
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“…The cell culture chamber containing an objective heater (Bioptechs) is mounted on an inverted microscope (Olympus IX81). Combining optical tweezers with known optical spring constants as force sensors and phase-sensitive detection 24,[45][46][47] , we measure the viscoelasticity in living cells. Notably, since the cytoplasm has different optical properties from that of the medium, the optical spring constant used for measuring intracellular stiffness modulus would be corrected via the refractive index mismatching 24 .…”
Section: Methodsmentioning
confidence: 99%