ライフサイエンスコーパス: phagocytosis

1 d N297D/S298A-IYG optimally drove tumor cell phagocytosis.

2 ecific, as opposed to general alterations in phagocytosis.

3 rform the critical physiological function of phagocytosis.

4 of interrelationships between chemotaxis and phagocytosis.

5 s essential for effector functions including phagocytosis.

6 This caused a disruption of Fc-binding and phagocytosis.

7 FcgammaRIIIA dimers were the main drivers of phagocytosis.

8 e in the optical force arises independent of phagocytosis.

9 ot resting macrophages following silica bead phagocytosis.

10 LMO1 preferentially regulated LC3-associated phagocytosis.

11 ncentrations and deterioration in neutrophil phagocytosis.

12 ctor 1-alpha and was essential for increased phagocytosis.

13 d many strategies to resist opsonization and phagocytosis.

14 y out functions that are analogous to animal phagocytosis.

15 eta-amyloid (Abeta) clearance independent of phagocytosis.

16 toskeletal processes required for macrophage phagocytosis.

17 etal remodeling as a way to block macrophage phagocytosis.

18 undergo complex, multiphasic changes during phagocytosis.

19 (POS) through a multistep process resembling phagocytosis.

20 n gliomas by internalizing the virus through phagocytosis.

21 lar material internalized by endocytosis and phagocytosis.

22 f neutrophils under conditions that preclude phagocytosis.

23 C5 split product needed for upregulation of phagocytosis.

24 The antibodies raised were found to promote phagocytosis.

25 tor-signaling is not essential for bacterial phagocytosis.

26 ts were limited to Fcgamma receptor-mediated phagocytosis.

27 ut also to detect and retain bacteria during phagocytosis.

28 tions in macrophages, namely TNF release and phagocytosis.

29 le expression, and capacity for professional phagocytosis.

30 o alter host actin dynamics and thus cripple phagocytosis.

31 by cancer cells directly protected them from phagocytosis.

32 ors and by up-regulating monocyte/macrophage phagocytosis.

33 ed the ability of RAW 264.7 cells to perform phagocytosis.

34 thus promotes hyper-inflammation and weakens phagocytosis.

35 creased survival in whole human blood due to phagocytosis.

36 irming that trogocytosis occurs, rather than phagocytosis.

37 , transgene-expressing cells from microglial phagocytosis.

38 ling, reactive oxygen species production and phagocytosis.

39 in cooperation and independently to mediate phagocytosis.

40 vation including nitric oxide production and phagocytosis.

41 e or reactive oxygen species production, and phagocytosis.

42 ed siRNA, using glucan particles taken up by phagocytosis.

43 inflammation and antibody-dependent cellular phagocytosis.

44 ular cytotoxicity, and Ab-dependent cellular phagocytosis.

45 CaMK4 recapitulated the observed defects in phagocytosis.

46 m pathways, and inhibited cell migration and phagocytosis.

47 and to discriminate between trogocytosis and phagocytosis.

48 ing proliferation, survival, clustering, and phagocytosis.

49 rotein alpha (SIRPalpha) controls macrophage phagocytosis.

50 bp gene, as a strong regulator of microglial phagocytosis.

51 After phagocytosis, A. fumigatus conidia rapidly escaped from

52 eads to cellular effector functions, such as phagocytosis, Ab-dependent cellular cytotoxicity, and cy

53 Phagocytosis activity of blood-borne macrophages decreas

54 Opsonic phagocytosis activity was strongly associated (hazard ra

55 t 4, 12, and 18 months of age for macrophage phagocytosis activity, ocular histological changes, and

56 3, CD4bs, and gp41 for Ab-dependent cellular phagocytosis (ADCP) activity, implicated in protective i

57 ses by enhancing antibody-dependent cellular phagocytosis (ADCP) in xenograft models.

58 Antibody-dependent cell-mediated phagocytosis (ADCP) was rarely detected during AIM (4 of

59 ether they can mediate Ab-dependent cellular phagocytosis (ADCP), which is an important element of an

60 cord microglia lacking ABCD1 are primed for phagocytosis, affecting neurons within an altered metabo

61 Phagocytosis after myocardial infarction (MI) is a prere

62 cytes and keratinocytes were used to examine phagocytosis and bacterial invasion, respectively.

63 DJ-1(-/-) macrophages exhibited enhanced phagocytosis and bactericidal activity in vitro, and ado

64 ranulation of primary granules and inhibited phagocytosis and bactericidal activity of neutrophils, w

65 and Alzheimer disease (AD) are defective in phagocytosis and degradation amyloid beta1-42 (Abeta1-42

66 C1q opsonization also increased phagocytosis and efferocytosis in macrophage foam cells.

67 Inhibiting phagocytosis and endosomal acidification in BMDCs or moD

68 However, CR3 phagocytosis and fibronectin haptotaxis, both integrin-d

69 ible roles of JN in RPE molecular transport, phagocytosis and formation of outer blood-retinal barrie

70 Yop proteins into the cytoplasm that prevent phagocytosis and generation of proinflammatory cytokines

71 I) are defective in amyloid-beta1-42 (Abeta) phagocytosis and have low resistance to apoptosis by Abe

72 decrease in the macrophage capacity for NTHi phagocytosis and increased nasopharyngeal bacterial load

73 ossibility that platelets enhance macrophage phagocytosis and intracellular killing of S. aureus In t

74 es further defined the connection between OS phagocytosis and ketogenesis in wild-type mice and mice

75 pathogens have developed strategies to evade phagocytosis and killing by neutrophils.

76 Phagocytosis and killing of NTHi by macrophages were eva

77 on pathogenic mechanism involving macrophage phagocytosis and microglial synaptic pruning, and raises

78 ount of consideration of the contribution of phagocytosis and other host defenses in the research for

79 Monocytes were studied for phagocytosis and oxidative burst.

80 eticulin, the mBiNE stimulated HER2-targeted phagocytosis and produced durable antitumour immune resp

81 Host mechanisms controlling fungal phagocytosis and replication remain obscure.

82 d, following a therapeutic dosage, activates phagocytosis and resolution signals in type 2 diabetes.

83 dogenous diabetic overexpression, activating phagocytosis and resolution signals.

84 show multimodal dynamics of PtdIns4P during phagocytosis and suggest that the phosphoinositide plays

85 ing processes we describe are LC3-associated phagocytosis and targeting by autophagy proteins, both o

86 s as ones that participate in B. burgdorferi phagocytosis and the resulting cytokine activation.

87 te M1-M2 phenotype that is optimal for Abeta phagocytosis and the stabilization of cognitive decline.

88 mechanisms by which these receptors mediate phagocytosis and to identify signaling pathways activate

89 rther show that specific cellular processes (phagocytosis and transendothelial migration) are enriche

90 Indeed, three antibodies displayed cellular phagocytosis and/or antibody-dependent cell-mediated cyt

91 tes play a central role in pathogen sensing, phagocytosis, and antigen presentation and consist of mu

92 tworks involved in lamellipodial protrusion, phagocytosis, and cell adhesion.

93 immune system involved in the opsonization, phagocytosis, and destruction of microorganisms infectin

94 Macrophage motility, phagocytosis, and differentiation in vivo are thus coupl

95 ) demonstrate decreased autophagy, augmented phagocytosis, and enhanced scavenger receptor (macrophag

96 Complement-mediated opsonization, phagocytosis, and immune stimulation are critical proces

97 onal survival, outgrowth, synaptogenesis and phagocytosis, and induce the death of neurons and oligod

98 urther enhances MFGE8 expression, aggravates phagocytosis, and leads to neuronal injury.

99 , upregulated molecular pathways involved in phagocytosis, and prevented the renal function decline a

100 lism as well as augmented size, granularity, phagocytosis, and respiratory burst.

101 epithelial macrophage projections, efficient phagocytosis, and stabilized enteroid barrier function r

102 ebbishields fused with immune cells to evade phagocytosis, and the resultant hybrid cells exhibited i

103 by necroptotic cells drives recognition and phagocytosis, and this may limit the inflammatory respon

104 n, antibody-dependent cellular cytotoxicity, phagocytosis, and virion capture).

105 species (ROS) production, degranulation, and phagocytosis are normal in the absence of STIM2, suggest

106 ts ligand Gas6, astrocytic genes involved in phagocytosis, are upregulated after acute sleep deprivat

107 MiR-142(-/-) neutrophils showed altered phagocytosis as a consequence of chemotactic behavior, i

108 EhRab35 is involved in the initial stage of phagocytosis as well as in the phagolysosomal biogenesis

109 WGA-Fc opsonization increased fungal phagocytosis, as well augmented the antifungal functions

110 infected erythrocytes (IE); however, current phagocytosis assays use IE collected from infected indiv

111 onfirmed by immunoblot analyses and in vitro phagocytosis assays.

112 We further found that the phagocytosis-associated protein MERTK was significantly

113 Lack of P2X7 receptor function reduced phagocytosis at all ages compared to wild-type mice.

114 y cytokines, miRNAs, and functions including phagocytosis, autophagy, and cell metabolism.

115 involvement of skin barrier and endocytosis/phagocytosis/autophagy, in addition to known innate and

116 rescence lifetimes would correlate well with phagocytosis because phagosomes become acidified and the

117 e T3S protein PcrV did not enhance bacterial phagocytosis but did enhance killing of the few bacteria

118 We hypothesized that myelin phagocytosis by astrocytes is an early event during lesi

119 We find that androgen regulates Sertoli cell phagocytosis by controlling expression of miR-471-5p and

120 exhibit delays in two processes that require phagocytosis by glial cells, the immune cells in the bra

121 le MER), a critical biomarker of compromised phagocytosis by innate macrophages.

122 omplement on the bacterial surface, promoted phagocytosis by macrophages and neutrophils, and protect

123 ed protein response and improve amyloid-beta phagocytosis by macrophages of patients with mild cognit

124 Phagocytosis by macrophages plays a critical role in can

125 esis of this study was that active Abeta1-42 phagocytosis by macrophages prevents brain amyloidosis a

126 ng Pf phage, P. aeruginosa was less prone to phagocytosis by macrophages than bacteria not producing

127 al-3 to bind and opsonize the live cells for phagocytosis by microglia.

128 to CD47-mediated protection of exosomes from phagocytosis by monocytes and macrophages.

129 eath of the neutrophils and their subsequent phagocytosis by monocytes and macrophages.

130 diator, resolvin D1, in vitro increase Abeta phagocytosis by Mvarphis of patients with MCI.

131 on of neutrophils in the nerve, and elevated phagocytosis by neutrophils.

132 sed survival compared with WT bacteria after phagocytosis by neutrophils.

133 riments, we could not detect any significant phagocytosis by purified PMNs of anti-CD20-opsonized CLL

134 und that MARCO was involved in C. neoformans phagocytosis by resident pulmonary macrophages and DC.

135 Both phenotypes are linked to impaired phagocytosis by specialized phagocytes: Sertoli cells an

136 Pharmacological inhibition of ATG-dependent phagocytosis by the cardiac glycoside neriifolin, an inh

137 h serum components and undergoes substantial phagocytosis by the reticuloendothelial system, causing

138 ut not A53T pMac, show significantly reduced phagocytosis capability and this can be phenocopied by a

139 CDCC) and complement-dependent cell-mediated phagocytosis (CDCP) by immunological effector molecules

140 rives evasion of chromosomal instability and phagocytosis checkpoints by apoptotic cancer stem cells.

141 oid cells, including inflammatory responses, phagocytosis, chemokine secretion, and proangiogenic act

142 nd MEK/ERK pathways in the regulation of RPE phagocytosis, confirmed by immunoblot analyses and in vi

143 Failure of phagocytosis could be induced experimentally by incubati

144 zation, antibodies mediate functions such as phagocytosis, cytotoxicity, and maintenance of immune ho

145 Because LC3-associated phagocytosis delivers cargo for degradation, the contrib

146 new phagocyte functions after apoptotic cell phagocytosis demonstrates the enormity of ways to mediat

147 hare mechanistic pathways for chemotaxis and phagocytosis; Dictyostelium chemotax toward bacteria and

148 k underscore the physiologic significance of phagocytosis during tissue injury.

149 ovel linkage between genomic instability and phagocytosis evasion that is coordinated by the blebbish

150 ability, blebbishield emergency program, and phagocytosis evasion to offer poor prognosis.

151 ximal epitope, whereas Ab-dependent cellular phagocytosis favored an epitope positioned further away.

152 zheimer's disease and MCI, possess effective phagocytosis for Abeta and protect homeostasis of the br

153 oideum This social amoeba kills bacteria via phagocytosis for nutrient acquisition at its single-cell

154 ne-rod dystrophy, while interfering with the phagocytosis function of RPE associated with down-regula

155 ange of actin-dependent functions, including phagocytosis, granule exocytosis, and migration.

156 As a result, understanding the mechanisms of phagocytosis has been an area of great interest in the f

157 ctions of CD36 in parasite sequestration and phagocytosis have been clearly defined, less is known ab

158 receptors that participate in B. burgdorferi phagocytosis have been reported, including the scavenger

159 RPE phagocytosis helps maintain the viability of photorecept

160 e defined the core signature of macrophages, phagocytosis imprinted a distinct antiinflammatory profi

161 ere we report a primitive form of artificial phagocytosis in a binary community of synthetic protocel

162 K) cell activity and neutrophil and monocyte phagocytosis in a concentration- and species-dependent m

163 ABCD1 in microglial activity toward neuronal phagocytosis in cell culture.

164 ll pathogenicity, and identify ATG-dependent phagocytosis in DCs as a key regulator in driving autoim

165 ired protein enzymes allowing the control of phagocytosis in macrophages.

166 to an increase in the initial efficiency of phagocytosis in milk.

167 enhancing clearance of debris via macrophage phagocytosis in multiple tumor types.

168 al role of NLRP3 in modulating autophagy and phagocytosis in neutrophils and suggest that therapies s

169 should be targeted to modulate autophagy and phagocytosis in neutrophils to control bacterial burden

170 solution markers CD163+CD206], and Abeta1-42 phagocytosis in patients initially diagnosed as having M

171 tween plant and animal PCD is the absence of phagocytosis in plants.

172 bined results indicated that early stages of phagocytosis in the RPE are mainly characterized by pron

173 The regulatory mechanisms underlying phagocytosis in the RPE are not fully understood, althou

174 ssion, and augmented mAb-mediated tumor cell phagocytosis in vitro However, only STINGa reversed the

175 ve engorge-and-accumulate processes in vivo, phagocytosis in vitro inhibited macrophage migration thr

176 Abeta1-42 phagocytosis increased in both ApoE groups (P = 0.03 in

177 ses of signaling-networks for chemotaxis and phagocytosis indicate that chemoattractant receptor-sign

178 s many LPS responses, including endocytosis, phagocytosis, inflammation, and pyroptosis.

179 RNA-like ER kinase (PERK) expression, Abeta phagocytosis, intermediate M1-M2 Mvarphi type, and a Min

180 gingivalis (Pg) capsule enables evasion from phagocytosis, invasion of keratinocytes, and bacterial s

181 Thus, phagocytosis is a source of macrophage heterogeneity tha

182 breakdown, indicating that astroglial myelin phagocytosis is an early and prominent feature.

183 Phagocytosis is an essential process for the proliferati

184 Antibody-mediated phagocytosis is an important immune effector mechanism a

185 ical model, we postulate that if the rate of phagocytosis is great enough, for acute, normally self-l

186 Cell phagocytosis is impaired in type 2 diabetes and requires

187 /Syk/ROS/NLRP3 pathway during L. amazonensis phagocytosis is important for macrophage restriction of

188 s sense apoptotic cell death and discuss how phagocytosis is integrated with environmental cues to dr

189 Phagocytosis is normally inhibited by binding of cell su

190 in classical autophagy, while LC3-associated phagocytosis is ULK1 independent.

191 ytic receptor(s) responsible for tumour cell phagocytosis is(are) largely unknown.

192 It has been shown to hinder phagocytosis, is retained in tumors, and aids in cellula

193 how that Sertoli cells employ LC3-associated phagocytosis (LAP) by recruiting autophagy member protei

194 LC3-associated phagocytosis (LAP) is a novel form of non-canonical auto

195 e of apoptotic germ cells via LC3-associated phagocytosis (LAP).

196 phagy called "Light-chain 3 (LC3)-associated phagocytosis" (LAP), lacked such defects.

197 l-trafficking pathway called "LC3-associated phagocytosis" (LAP).

198 ella from polymyxins, mediates resistance to phagocytosis, limits the activation of inflammatory resp

199 ese DE genes showed enrichment for ribosome, phagocytosis, lysosome, proteasome, oxidative phosphoryl

200 phagocytosing Exserohilum Despite a lack of phagocytosis, macrophage production of tumor necrosis fa

201 Astrocytic phagocytosis, mainly of presynaptic components of large

202 al. show that the inflammatory response and phagocytosis mediated by the interaction between protect

203 tracellular signaling pathways that increase phagocytosis-mediated bacterial clearance, survival, and

204 One of these functions, phagocytosis, mediates the natural disposal of billions

205 es, chemokines, inflammatory regulators, and phagocytosis mediators, are involved in prion pathogenes

206 g array of genes, including genes related to phagocytosis, metabolism, and retinal disease in humans.

207 mbrane protrusions, were first implicated in phagocytosis more than 100 years ago, but little is stil

208 In contrast, inhibition of phagocytosis nearly completely blocks NET release to bot

209 viously described function of CD47 in normal phagocytosis of aging red blood cells and results report

210 nflammatory genes and consistently depressed phagocytosis of amyloid-beta1-42 (Abeta) by monocytes an

211 Ns) have previously been reported to mediate phagocytosis of anti-CD20-opsonized B cells from patient

212 PMNs mediate mostly trogocytosis rather than phagocytosis of anti-CD20-opsonized CLL B cells, and we

213 eptor antagonist polyinosinic acid inhibited phagocytosis of apoptotic cells by CD138(+) MPhi.

214 Phagocytosis of apoptotic cells is thus coupled to speci

215 icient dendritic cells displayed hyperactive phagocytosis of apoptotic cells, which stimulated excess

216 y reprogramming of macrophages following the phagocytosis of apoptotic cells.

217 neurodegenerative microglia phenotype after phagocytosis of apoptotic neurons.

218 oreover, aging decreases alveolar macrophage phagocytosis of apoptotic neutrophils, downregulates the

219 that is required for reporter activation and phagocytosis of axonal debris.

220 ase II, and this enzymatic activity inhibits phagocytosis of B. pertussis in vitro.

221 itivity to bacterial infection and decreased phagocytosis of bacteria by systemic immune cells.

222 Ex vivo airway neutrophil phagocytosis of bacteria was reduced in patients with in

223 hat Fmr1 plays a cell-autonomous role in the phagocytosis of bacteria.

224 significantly enhanced peritoneal macrophage phagocytosis of both methicillin-resistant S. aureus and

225 molecule able to mediate the engulfment and phagocytosis of C. albicans cells by human immune cells

226 aused cell death of cancer cells followed by phagocytosis of cell debris by MPhi.

227 D47 is a cell surface molecule that inhibits phagocytosis of cells that express it by binding to its

228 /8 activation would be predicted to increase phagocytosis of circulating ICs, while disarming their i

229 nated off-target antibody-dependent monocyte phagocytosis of cynomolgus monkey platelets, and cynomol

230 Phagocytosis of daily shed photoreceptor outer segments

231 ow-derived Cd36 was essential for both early phagocytosis of dying cardiomyocytes and for smaller inf

232 photoreceptor cell layer, proliferation, and phagocytosis of dying cells.

233 leukocyte activation, without affecting host phagocytosis of E. coli RA101295 treatment reduced plasm

234 hich are involved in iron metabolism and the phagocytosis of erythrocytes and blood-borne pathogens a

235 FlnA deletion does not affect phagocytosis of Escherichia coli or Staphylococcus aureu

236 Neutrophil phagocytosis of F. nucleatum ssp. polymorphum was signif

237 Neutrophil phagocytosis of F. nucleatum strains and neutrophil apop

238 Phagocytosis of filamentous bacteria occurs through tubu

239 cell-specific receptors, we determined that phagocytosis of haematopoietic tumour cells during SIRPa

240 that macrophages are much more efficient at phagocytosis of haematopoietic tumour cells, compared wi

241 t of FcgRIIA, shifting neutrophils away from phagocytosis of ICs toward the programmed form of necros

242 ngly, productive viral replication decreased phagocytosis of IgG-opsonized bioparticles and Fc recept

243 These findings link phagocytosis of injured oligodendrocytes, a pathological

244 ide presentation to CD4(+) T cells following phagocytosis of injured, phosphatidylserine-exposing oli

245 ctivation, which was accompanied by enhanced phagocytosis of Klebsiella GPVI-depleted mice showed inc

246 data show that PTC124 was able to reinstate phagocytosis of labeled photoreceptor outer segments at

247 Mtb aggregates caused macrophage death, and phagocytosis of large aggregates was more cytotoxic than

248 RvD2-DRV2 interaction significantly enhanced phagocytosis of live Escherichia coli, an action depende

249 Myeloid receptor CD36 is required for early phagocytosis of myocardial infarcts and induction of Nr4

250 This suggested that CERKL may regulate the phagocytosis of OSs by the retinal pigment epithelium (R

251 complement system in the recognition and the phagocytosis of PapMV nanoparticles and identified an un

252 of phagocytic receptors and showed enhanced phagocytosis of parasite-infected erythrocytes than thos

253 f this finding, CD19-DE was found to enhance phagocytosis of patient-derived ALL blasts by human macr

254 ron-like) cells, and it increased microglial phagocytosis of PC12 cells or primary neurons, which was

255 LPS-induced microglial phagocytosis of PC12 was prevented by small interfering

256 , and exhibited marked functional defects in phagocytosis of photoreceptor outer segments.

257 ent with lactadherin significantly increased phagocytosis of platelets by approximately 2-fold, dimin

258 Most strikingly, phagocytosis of POS by cultured RPE cells was almost com

259 LPS-induced phagocytosis of primary neurons by primary microglia was

260 ndolysosomes against damage initiated by the phagocytosis of silica beads.

261 EL-induced PTX3 promoted the association and phagocytosis of Staphylococcus aureus into macrophages.

262 GNIFICANCE STATEMENT We find that astrocytic phagocytosis of synaptic elements, mostly of presynaptic

263 icroglial activation and enhanced microglial phagocytosis of synaptic elements, without obvious signs

264 Phagocytosis of the Lyme disease-causing pathogen Borrel

265 Notably, phagocytosis of the pathogen activates the host autophag

266 of either MHC class I or LILRB1 potentiated phagocytosis of tumor cells both in vitro and in vivo, w

267 MERTK has an essential role in phagocytosis, one of the major functions of the RPE.

268 2/3 complex is not a general requirement for phagocytosis or chemotaxis but is a critical driver of i

269 of Mertk (-/-) mice it fails to enhance RPE phagocytosis or prevent photoreceptor degeneration.

270 Blocking phagocytosis or specific phagocytic receptors may allevi

271 otype, which expressed molecules involved in phagocytosis, oxidative injury, antigen presentation and

272 as well as evidence of defective macrophage phagocytosis (p = 0.029).

273 ish-derived omega-3 emulsion increased Abeta phagocytosis, PERK expression, and UPR RNA signature, an

274 ory and have impaired Pseudomonas aeruginosa phagocytosis, phenocopying CF MPhis.

275 Cd36 deficiency led to reduced expression of phagocytosis receptor Mertk and nuclear receptor Nr4a1 i

276 s and mice with AMN, upregulation of several phagocytosis-related markers, such as MFGE8 and TREM2, p

277 radation of bacteria also attenuated further phagocytosis, resulting in elevated bacterial load.

278 eless able to observe inhibition of platelet phagocytosis several days after hexameric-Fc dosing.

279 r 2 (HER2) expressed by cancer cells and pro-phagocytosis signalling mediated by calreticulin, the mB

280 tors such as IgG1, IgG2, IgM, IL-6 and PMPhi phagocytosis, stimulation of secretion of IL-10.

281 s and to mediate antibody-dependent cellular phagocytosis, suggesting a range of anti-HIV immunologic

282 A mathematical model of phagocytosis suggests that hFcgammaRI and hFcgammaRIIIA

283 IL-2 following initiation of actin-mediated phagocytosis that leads to Src and Syk kinase activation

284 These events promote a rapid form of phagocytosis that produces an "immunologically silent" c

285 EM2 may regulate microglial inflammation and phagocytosis through coupling to the adaptor protein TYR

286 he Yops, YopO (also known as YpkA) obstructs phagocytosis through disrupting actin filament regulatio

287 ophages to maintain respiratory burst during phagocytosis via enhancing mitochondrial complex-II meta

288 abling Gal-3 binding to PC12 cells and their phagocytosis via MerTK.

289 Phagocytosis was augmented by IgG opsonization, and inhi

290 Phagocytosis was circadianally regulated and mediated by

291 Phagocytosis was enhanced in the presence of BEV + RES c

292 ation of PA in macrophages during frustrated phagocytosis was examined using these PA sensors and was

293 ost SLAM receptor functions, SLAMF7-mediated phagocytosis was independent of signalling lymphocyte ac

294 In this study, we examined whether OS phagocytosis was linked to ketogenesis.

295 However, monocyte phagocytosis was normal and oxidative burst was augmente

296 rmed Golgi-derived vesicles recruited during phagocytosis were secretory vesicles as their recruitmen

297 In the latter mixed infection, Fn evaded phagocytosis, whereas in the capsulated mixed infection

298 ygen species (ROS) production, as well as by phagocytosis, which sequesters pathogens within phagosom

299 We found that shortly after phagocytosis, wild-type (WT) L. monocytogenes escaped fr

300 he processes of spreading onto surfaces, and phagocytosis within 100 s of stimulation.