ライフサイエンスコーパス: latex bead

1 bortus 2308, live Escherichia coli HB101, or latex beads).

2 hagocytosis of M. tuberculosis or TDM-coated latex beads.

3 of particulate substances such as zymosan or latex beads.

4 icroruby dextran amine, or rhodamine labeled latex beads.

5 er systems such as colloidal gold or colored latex beads.

6 y their internalisation of 1 mum fluorescent latex beads.

7 d standards such as proteins and polystyrene latex beads.

8 the binding of neutrophils to albumin-coated latex beads.

9 y decreasing (85%) binding of ROS but not of latex beads.

10 was lower than for heat-killed organisms or latex beads.

11 es but also phagocytosable chitosan and even latex beads.

12 ulation with chitin but not with chitosan or latex beads.

13 ion was similar to the rate for phagocytosed latex beads.

14 ed by motors driving tethered cells or 1-mum latex beads.

15 reatment did not affect uptake of IgG-coated latex beads.

16 agocytosis of apoptotic neutrophils, but not latex beads.

17 ch as viruses, pathogenic bacteria, and even latex beads.

18 served following ingestion of oxidized OS or latex beads.

19 cules with monoclonal antibodies adsorbed to latex beads.

20 dvanced glycation end product-BSA-conjugated latex beads.

21 -8) and increasing phagocytosis of opsonized latex beads.

22 mosan, and mannan (a mannose polymer)-coated latex beads (1 microm) at 1, 10, or 100 microg/ml.

23 crom beta-glucan particles, laminarin-coated latex beads, 1 microm latex beads, 50 to 100 microm chit

24 labeled with a fluorescent antibody [2] or a latex bead [5], are seen to move longitudinally down the

25 cles, laminarin-coated latex beads, 1 microm latex beads, 50 to 100 microm chitin particles, or 50 to

26 inding of unopsonized particles (e.g., TiO2, latex beads; 63 +/- 5 and 67 +/- 4% inhibition, respecti

27 g of unopsonized particles (TiO2, Fe2O3, and latex beads; 66 +/- 5, 77 +/- 2, and 85 +/- 2% inhibitio

28 oad), while the second motor rotated a small latex bead (a light load).

29 o the same degree that phagosomes containing latex beads acquired these markers after 1.5 h of infect

30 or bR did not occur around neutrally charged latex beads acting as cell surrogates, demonstrating tha

31 urified SOF N-terminal peptide could promote latex bead adherence to HEp-2 cells and inhibit GAS inva

32 e, with the microcantilever technique, where latex beads affixed on silicon cantilevers were used as

33 an immunochromatographic assay (ICGA), and a latex bead agglutination assay (LBAA).

34 osable dichlorodihydrofluorescein-conjugated latex beads and cyclic hydroxylamines with differing mem

35 nthesized alpha-1,2-trimannose cap sugars on latex beads and demonstrated that C57BL/6 mice coinocula

36 We illustrate this by using two sizes of latex beads and demonstrating the simultaneous detection

37 agocytic uptake of serum-coated or -uncoated latex beads and E. coli However, consistent with previou

38 een fibrinogen molecules covalently bound to latex beads and either wild-type alphaIIbbeta3 molecules

39 slowed the motility of phagosomes containing latex beads and endogenous pigment granules.

40 Phagocytosis of latex beads and Escherichia coli bacteria was also not a

41 up, agglutination of Gal(alpha1-4)Gal-coated latex beads and human or sheep erythrocytes, and hemolys

42 nts, the Tfp of immobilized bacteria bind to latex beads and retract, pulling beads from the tweezers

43 uction; and in vitro capacity to phagocytose latex beads and to migrate toward the chemokine (C-C mot

44 polymerized from the surface of mDia1-coated latex beads, and deformed by manipulating both ends thro

45 th increased uptake of Ig-opsonized targets, latex beads, and fluid phase markers, and it was accompa

46 ntibacterial activity during phagocytosis of latex beads, and this too was dependent in large part on

47 the ingestion process, cells were exposed to latex beads at 15-20 degrees C, which allows engulfment

48 ts, up-converting phosphor technologies, and latex beads, between others) in LFBs.

49 n (90-226 emm1::km) was greatly reduced, and latex beads bound to M1 protein were readily internalize

50 Latex beads bound to the cell surface move in a myosin I

51 re stably attached to 1 mum (bacteria-sized) latex beads, but not directly linked to each other, in c

52 uMC generate ROS upon exposure to IgG-coated latex beads by 5-LO and COX; and ROS appear to have no s

53 Preferential uptake of latex beads by follicle-associated epithelium indicates

54 observation that soon after phagocytosis of latex beads by M phi, cell surface expression of HSA rap

55 uptake of nonpathogenic Escherichia coli and latex beads by nonphagocytic mammalian cells.

56 hly scattering metal-coated polystyrene (PS) latex beads by using solvent-controlled heterocoagulatio

57 n molecule 1 (CD54) of EC was measured using latex beads coated with antibody to CD54 as a model for

58 Flow cytometry testing with latex beads coated with human leukocyte antigen (HLA) cl

59 By analyzing the internalization of latex beads coated with invasin derivatives, an addition

60 tent with a direct role of the minor pilins, latex beads coated with SpaB or SpaC protein bind specif

61 g Jurkat T cells as effectors and cell-sized latex beads coated with various antibodies as artificial

62 of adenovirus and transferrin-coated 100-nm latex beads compared to MH-S, a GM(+/+) AM cell line.

63 rganisms and by 280% in phagocytosis of FITC-latex beads compared to those that received the antisens

64 and a 65% reduction in phagocytosis of FITC-latex beads compared to those treated with the sense oli

65 These latex bead compartments (LBCs) are encased in membrane a

66 phagosomes but not in phagosomes containing latex beads conjugated with another protein.

67 Murine macrophages were pulsed with latex beads conjugated with OVA.

68 BFA inhibited macrophage processing of latex bead-conjugated Ag for presentation to T cells, su

69 eomic analysis of the membrane fraction from latex bead-containing (LBC) phagosomes isolated from mac

70 After 120 minutes of in vivo exposure, latex beads could be found in cervical lymph nodes.

71 igen and antibody immobilized on polystyrene latex beads (diameter, 0.109 +/- 0.0025 micron).

72 IgG-coated latex beads did stimulate ROS production in huMC, and in

73 MSU crystals, but not latex beads, directly bound recombinant soluble (s) CD14

74 es of the murine eye that ingest fluorescent latex beads do not migrate to regional lymph nodes.

75 ents, in comparison to phagosomes containing latex beads, do not readily interact with incoming endoc

76 at keratinocytes phagocytose melanosomes and latex beads equally well and that this phagocytic proces

77 during uptake of diverse targets, including latex beads, Escherichia coli, Salmonella typhimurium, a

78 Latex bead-exposed PEC were not more potent APC, and the

79 haped and non-biological samples, the use of latex beads for calibration can provide sufficient accur

80 endocytic pathway do not permit endocytosed latex beads from reaching terminal lysosomes in an anter

81 Phagocytosis of latex beads had no effect on the expression of thymosin

82 eas medium conditioned by Mphi phagocytizing latex beads had no proapoptotic effects upon neutrophils

83 In response to phagocytosis of latex beads, human embryonic kidney 293 cells synthesize

84 n not expressed by Pn, but not with 1-microm latex beads in adjuvant.

85 phoP(+) or phoP mutant Y. pestis strains or latex beads in J774A.1 macrophages.

86 ize in the vicinity of phagosomes containing latex beads in stimulated macrophages.

87 in vitro and opsonized particles (IgG-coated latex beads) in vitro and in vivo in intact mice.

88 OVA-conjugated latex beads, in addition to stimulating brisk proliferat

89 fluorescein isothiocyanate (FITC)-conjugated latex beads, indicating that alveolar macrophages from P

90 taken to examine the mechanisms that mediate latex bead-induced resistance to Acanthamoeba keratitis.

91 In contrast, IgG-coated latex bead-induced ROS production in human polymorphonuc

92 used to evaluate the role of neutrophils in latex-bead-induced protection against Acanthamoeba kerat

93 and determine the role of macrophages in the latex-bead-induced resistance.

94 ults indicate that intracorneal injection of latex beads induces a remarkable resistance to Acanthamo

95 Instillation of sterile 1.0 microM latex beads into the central corneal epithelium renders

96 ts of a retrograde tracer (usually rhodamine latex beads) into the superficial layers of the superior

97 icles (WGA-Au-HRP) or fluorescein-conjugated latex beads, into the LC labeled numerous (approximately

98 Latex bead labeling of peripheral blood Gr1(lo) monocyte

99 somes with phagosomes containing scintillant latex beads led to light emission in a reaction requirin

100 the giant vacuoles acquired large numbers of latex beads, M. tuberculosis, and avirulent L. pneumophi

101 o microscopy by tracking 10 mum, polystyrene latex beads mixed into the solution.

102 and LRG-47 localized to vacuoles containing latex beads, neither protein localized to vacuoles conta

103 was also stimulated by immune complex-coated latex beads or cross-linking of Abs specific for Fc gamm

104 Phagosomes containing latex beads or heat-killed M. tuberculosis, on the other

105 In contrast, phagosomes containing latex beads or heat-killed organisms appeared to be proc

106 s between micrometer sized particles, either latex beads or red blood cells (RBCs), create aggregates

107 CD103(+) DCs were able to ingest and traffic latex beads or soluble antigen.

108 the specific nature of phagosomes containing latex beads or wild-type S. typhimurium (viable or heat-

109 alpha-MSH, were conjugated to microspheres (latex beads) or macrospheres (polyamide beads) through a

110 albumin or ovalbumin), amino-functionalized latex beads, or dextran polymer and arrayed at the surfa

111 e optical labels such as gold nanoparticles, latex beads, or fluorescent nanoparticles to visualize t

112 administered i.p. 200 mg/kg GaAs crystals or latex beads, or vehicle.

113 Also analyzed were phagocytized black latex beads, phagocytized melanosomes pretreated to simu

114 during intracellular transport, we examined latex beads phagocytosed into living mammalian macrophag

115 ll line internalized fluid phase markers and latex beads (phagocytosis) at one-third the rate of cont

116 ding protein profiles of these vesicles with latex bead phagosomal compartments (LBC).

117 diminished EEA1 recruitment to newly formed latex bead phagosomes and blocked phagosomal acquisition

118 of translocation of SK1G82D and SK1S225A to latex bead phagosomes were indistinguishable from those

119 osis H37Rv, inhibited recruitment of EEA1 to latex bead phagosomes, and diminished their maturation.

120 ced acquisition of late endocytic markers by latex bead phagosomes, demonstrating an essential role o

121 a decrease in EEA1 colocalization with model latex bead phagosomes, which normally acquire EEA1 and s

122 er demonstrated by converse experiments with latex bead phagosomes.

123 cytochalasin D prevented iNOS recruitment to latex bead phagosomes.

124 xin 4 and transferrin receptor on PIM-coated latex bead phagosomes.

125 Latex beads preferentially bound to a subpopulation of c

126 ILC3s can take up latex beads, process protein antigen, and consequently p

127 actor (prfA) mutants of L. monocytogenes, or latex beads produced mss1 expression levels similar to t

128 e the opsonophagocytic uptake of ClfA-coated latex beads, protect against an intravenous challenge in

129 Neutrophil depletion did not abrogate the latex beads' protective effect.

130 crophagicidal drug clodronate eliminated the latex beads' protective effect.

131 Plasma membrane tethers formed by latex beads pull back on the beads with a force that was

132 The uptake of latex beads showed that M-cell function was similar in a

133 is factor alpha/fibrinogen, immunoglobulin G latex beads, Staphylococcus aureus, formyl-methionyl-leu

134 Engulfment of the apoptotic bodies, but not latex beads, stimulated Kupffer cell generation of death

135 ced by both live and fixed parasites but not latex beads, suggesting that PS expression was parasite

136 es ingest less apoptotic thymocytes (but not latex beads) than wild-type macrophages, and this defect

137 ling forces to human neutrophils adhering to latex beads that were coated with antibodies to CD62L (L

138 osomes were specifically labeled with 800-nm latex beads that were conjugated with streptavidin and A

139 , having been tethered to glass or marked by latex beads, the rotation of the internal components has

140 In fibroblasts plated on collagen-coated latex beads there are large increases of [Ca(2+)]i, time

141 nce was examined by assessing the binding of latex beads to neutrophils.

142 or beta1 integrin antibodies immobilized on latex beads to promote integrin aggregation.

143 ic binding of synthetic Le(x), conjugated to latex beads, to gastric tissue.

144 Latex bead treatment did not affect adherence of trophoz

145 Latex bead treatment induced a significant infiltration

146 In vitro experiments examined the effect of latex bead treatment on the capacity of A. castellanii t

147 Model phagosomes harboring latex beads undergo a coordinated Rab5-Rab7 exchange, wh

148 gn, target exosomes were firstly captured by latex beads via aldimine condensation, followed by bio-r

149 Phagocytosis of 4- micro m latex beads was also impaired in mAM cells as determined

150 The colocalization of iNOS with ingested latex beads was an actin-dependent process, since treatm

151 killed M.tb, live Staphylococcus aureus, or latex beads was associated with translocation of cytosol

152 mycobacterial antigens covalently coupled to latex beads was chloroquine insensitive.

153 ated epithelium, transcytosis of fluorescent latex beads was evaluated with confocal microscopy.

154 ocytosis of opsonized bacteria particles and latex beads was observed upon incubation of murine macro

155 of intimin, when purified and immobilized on latex beads, was sufficient to trigger A/E lesions on pr

156 , biocytin, fluorogold, and rhodamine-linked latex beads), we have shown that, as in other avian grou

157 Latex beads were coated with a recombinant fragment cont

158 Fluorescent latex beads were coated with fibronectin (FN), collagen

159 Fluorescent 0.2-microm polystyrene latex beads were either instilled into the conjunctival

160 In contrast, heat-killed organisms and latex beads were in acidic vacuoles which contained the

161 flammatory agents were also stimulatory, but latex beads were ineffective, indicating that microbial

162 Within 20 minutes of an in vivo exposure, latex beads were internalized by the follicle-associated

163 that infection and LPS were stimulatory but latex beads were not.

164 The rates of phagocytosis of bacteria and latex beads were significantly higher in Rap1 WT(+) and

165 The 100-nm latex beads were surface-modified with the temperature-s

166 Negatively charged, 500 nm latex beads were used in multiple-particle tracking expe

167 acids was inefficient at promoting entry of latex beads, whereas dimerization of this derivative by

168 tion arrest, and model phagosomes containing latex beads, which follow the normal pathway of maturati

169 tics and the ability to bind and translocate latex beads, which make it indistinguishable from antige

170 Unlike the model phagosomes containing latex beads, which transiently recruited EEA1, mycobacte

171 athogen mimics (namely glycodendrimer-coated latex beads with acid-labile linkers) were synthesized.

172 Coating of latex beads with the major mycobacterial cell envelope g

173 We have used fluorescent latex beads, with or without covalently conjugated OVA,