ライフサイエンスコーパス: phagocytic

1 an brain slices shows DAM with intracellular/phagocytic Abeta particles.

2 mice have functional defects, with decreased phagocytic ability and a decreased capacity to generate

3 l interfering RNA enhanced FcgammaR-mediated phagocytic ability but have little effect on cytokine pr

4 autoantigen presentation while retaining the phagocytic ability of homeostatic myeloid cells.

5 face expression of immunological markers and phagocytic ability were assessed by flow cytometry.

6 By assessing in vivo MRI of mononuclear cell phagocytic ability with (19)F nanoparticles, MRI with du

7 SIRPalpha in microglia and restricted their phagocytic ability.

8 lbicans-containing phagosomes independent of phagocytic ability.

9 ar macrophages with low pro-inflammatory and phagocytic ability.

10 or M2 phenotype, was reduced by DHA, but the phagocytic activation was not altered.

11 human macrophages with CARs to direct their phagocytic activity against tumors.

12 Macrophages from KO mice showed increased phagocytic activity and elevated expression of LDL recep

13 These include modulation of phagocytic activity and responses to injury.

14 n of TNF-alpha and interleukin-10, inhibited phagocytic activity and stimulated production of ROS.

15 ults suggested that astrocytes may engage in phagocytic activity during extended wake, but direct evi

16 ich cells remove cell debris when microglial phagocytic activity is impaired.

17 Additionally, increased phagocytic activity of differentiating microglia was obs

18 ouse orthologs of many AD risk genes and the phagocytic activity of mouse microglial cells.

19 we investigated whether increased microglial phagocytic activity that clears amyloid can also cause p

20 invariably followed by a sharp reduction in phagocytic activity that could persist for days.

21 The microglial phagocytic activity toward Abeta was restored after adip

22 hondrial superoxide dismutase), (2) enhanced phagocytic activity toward red blood cells (an in vitro

23 Immune cell numbers and phagocytic activity were evaluated by flow cytometry and

24 appears to occur as a result of an enhanced phagocytic activity within the lung and an associated al

25 as inflammatory cytokines, NOS 2, increased phagocytic activity, and a greater osteoclast differenti

26 on of a K(+) conductance, the UDP-stimulated phagocytic activity, and the ATP-dependent laser lesion-

27 etabolism under conditions of chronic myelin phagocytic activity, as TREM2 LOF causes pathogenic lipi

28 NK cells poorly and drove moderate monocyte phagocytic activity, both likely compromised because of

29 KO mice was associated with perturbations in phagocytic activity, defective transition of macrophages

30 exercise regimen displayed higher macrophage phagocytic activity, enhanced RvD1 levels, and earlier n

31 duction, phagocytic receptor expression, and phagocytic activity, enhancing parasite clearance by mac

32 y evoked membrane currents, stimulated basal phagocytic activity, evoked intracellular Ca(2+) transie

33 Gene expression, phagocytic activity, production of reactive oxygen speci

34 of myocytes to stimulated endothelial cells, phagocytic activity, uptake of oxidized low-density lipo

35 tokines with LPS stimulation and showed more phagocytic activity.

36 o exhibited higher levels of active RhoA and phagocytic activity.

37 lting in killing of encapsulated bacteria by phagocytic activity.

38 the aortic wall by enhanced proteolytic and phagocytic activity; however, the cells do not transdiff

39 Here, we show that the phagocytic adaptor protein Gulp1 regulates EphB/ephrinB

40 actor (TNF), and Abeta peptides enhance both phagocytic and antifungal activity from BV-2 cells.

41 ly derived cardiac tissue macrophages play a phagocytic and antigen presenting role.

42 showed transcriptional evidence of abnormal phagocytic and cell-survival programs.Conclusions: Our f

43 mplex class II that was coupled with reduced phagocytic and chemotactic activity compared to controls

44 Altogether, both the phagocytic and immunomodulatory functions of Mer regulat

45 This assay can also be used with other phagocytic and non-phagocytic cells to study the individ

46 he recruitment and differentiation of highly phagocytic and stimulatory macrophages within tumours.

47 r TIM4(lo) and TIM4(-) cells, which were not phagocytic and were more abundant than Kupffer cells.

48 yed a TM cell-like genotypic profile, became phagocytic, and responded to dexamethasone stimulation,

49 ith primate microglia, including complement, phagocytic, and susceptibility genes to neurodegeneratio

50 to as SYNB1891, targets STING-activation to phagocytic antigen-presenting cells (APCs) in the tumor

51 Six subsets of phagocytic APC (HLA-DR(+)) were consistently observed.

52 method made it possible not only to perform phagocytic assays with functionalized droplets and beads

53 ive anticipatory responses against impending phagocytic attack and promote host colonisation.

54 interactions resulting in microbial growth, phagocytic attack and secretion of host antimicrobial fa

55 altering the actomyosin cytoskeleton affects phagocytic behavior.

56 released were temporally correlated with OS phagocytic burst after light onset.

57 P2X7L-transfected HEK 293 cells have phagocytic but not channel, pore, or membrane-blebbing f

58 Marrow-derived macrophages are highly phagocytic, but whether they can also traffic into solid

59 ages to an active M1 phenotype, and superior phagocytic capabilities as compared to individual drug t

60 Thus, the phagocytic capability of cells that present self-peptide

61 demonstrate a dramatic and lasting change in phagocytic capacity after serum exposure.

62 astrocytes are accompanied by alterations in phagocytic capacity and effects on neuronal calcium sign

63 eostatic to a functional state with enhanced phagocytic capacity but reduced motility and synapse eng

64 reased Iba1 and C1q expression with enhanced phagocytic capacity in Pten(m3m4/m3m4) microglia, indica

65 Defective phagocytic capacity in Slc2a1(M-/-) BMDMs may have contr

66 macrophage marker expression, and augmented phagocytic capacity of human MDMs stimulated with LPS or

67 n were not different between groups, and the phagocytic capacity of Kupffer cells was preserved follo

68 ains of F. nucleatum significantly increased phagocytic capacity of neutrophils.

69 globulin levels and a modest decrease in the phagocytic capacity of pulmonary macrophage populations

70 of host-pathogen interactions, for instance phagocytic capacity or phenoloxidase activation, or at t

71 targeting lung macrophages to increase their phagocytic capacity, enhance their ability to make retin

72 ntrols, both AH monocyte subsets had greater phagocytic capacity, enhanced ability to drive memory T

73 vealed impeded M2 polarization and decreased phagocytic capacity.

74 to purified SL-1 enhanced the trafficking of phagocytic cargo to lysosomes.

75 Phagocytic cargo, upon internalization, follows a define

76 We conclude that highly phagocytic, CD138(+) SPM-like cells with an anti-inflamm

77 ammatory cells to the peritoneum, or improve phagocytic cell killing of pathogens.

78 GS-9620 induced phagocytic cell maturation and improved effector-mediate

79 d raises the fundamental question of how the phagocytic cell optimizes the acidification process to p

80 Phagocytic cell reduction in nitric oxide production dur

81 s replace CCR2(+) macrophages as the primary phagocytic cell.

82 is their rapid recognition and engulfment by phagocytic cells (a process called efferocytosis).

83 However, many phagocytic cells also act as antigen-presenting cells an

84 Neutrophils are phagocytic cells and are vital components in the human i

85 d light on the interactions between NETs and phagocytic cells and provide new insights regarding the

86 plicate in professional and non-professional phagocytic cells and subvert immune responses for chroni

87 hogens encounter numerous insults, including phagocytic cells designed to degrade bacteria, while est

88 suggesting that the pathogen may not target phagocytic cells for intracellular growth during natural

89 n of LRRK2 and its substrate Rab10 occurs in phagocytic cells in the immune system.

90 Previously, we found that phagocytic cells ingest bacteria directly from the cytos

91 Microglia are phagocytic cells involved in homeostasis of the brain an

92 Clodronate-mediated depletion of phagocytic cells markedly prolonged the serum half-life

93 Phagocytic cells of the innate immune system appear to b

94 ssion analysis by RNA sequencing of F4/80(+) phagocytic cells revealed activation of the activating t

95 totic tissue is recognized for engulfment by phagocytic cells such as macrophages.

96 n also be used with other phagocytic and non-phagocytic cells to study the individual or collective r

97 d the effect of this mutation on mononuclear phagocytic cells was examined.

98 Bacterial ascent and the cell dynamics of phagocytic cells were assessed by biophotonic imaging an

99 METH interferes with phagocytic cells' phagosomal maturation, resulting in im

100 isease (CGD) is a rare inherited disorder of phagocytic cells(1,2).

101 ractions of live B. bacteriovorus with human phagocytic cells, determining the uptake mechanisms, per

102 icroglia (MG), a heterogeneous population of phagocytic cells, play important roles in central nervou

103 ated kinetoplastid parasites that parasitize phagocytic cells, principally macrophages, of vertebrate

104 the capacity to concentrate drug delivery to phagocytic cells, significantly reducing off-target toxi

105 the clearance of cell debris and bacteria by phagocytic cells, the role of CRP in additional immunolo

106 ar survival of S. aureus in non-professional phagocytic cells, via modulation of MazEF and Agr.

107 and molecular functions and may be deadly to phagocytic cells, which may result in increased suscepti

108 ighly immunogenic C. albicans hyphae attract phagocytic cells, which rapidly engulf adherent S. aureu

109 h apoptotic cells are cleared from tissue by phagocytic cells.

110 polarization, and activation of mononuclear phagocytic cells.

111 the ultimate fate of B. bacteriovorus inside phagocytic cells.

112 by liver-, spleen-, and bone marrow-resident phagocytic cells.

113 the interactions between A. pittii and human phagocytic cells.

114 everal cell types, including mitotic and non-phagocytic cells.

115 amentous actin and altered actin dynamics in phagocytic cells.

116 lammasome, Th17 signaling and recruitment of phagocytic cells.

117 isingly, feedback inhibition is abrogated in phagocytic cells.

118 cells evade the immune system by disrupting phagocytic clearance and the effect of phagocytosis chec

119 We sought to test the significance of phagocytic clearance by resident and recruited phagocyte

120 ction produces elongated hyphae resistant to phagocytic clearance compelling alternative neutrophil e

121 L expression in the adult brain promotes the phagocytic clearance of Abeta and ameliorates Abeta-depe

122 myloidogenesis is accelerated due to reduced phagocytic clearance of amyloid seeds despite reduced pl

123 re currently being explored to stimulate the phagocytic clearance of apoptotic cells; however, these

124 Phagocytic clearance of apoptotic germ cells by Sertoli

125 In addition, the phagocytic clearance of apoptotic tumor cells (efferocyt

126 and the discovery of cellular immunity, the phagocytic clearance of cellular debris has been conside

127 ses from glia, including glial migration and phagocytic clearance of damaged neurons.

128 During the progression of the disorder, phagocytic clearance of dead photoreceptor cell bodies h

129 interactions, which are known to mediate the phagocytic clearance of degenerating neurons.

130 ating parasite sequestration to host organs, phagocytic clearance of parasites, and regulation of imm

131 stasis in the central nervous system through phagocytic clearance of protein aggregates and cellular

132 ins to constitute a functional LC3-dependent phagocytic complex.

133 leading to the extension and closure of the phagocytic cup around the target.

134 nvolving membrane-cytoskeletal crosstalk for phagocytic cup closure.

135 se and induce actin polymerization to form a phagocytic cup for engulfment of the bead.

136 over that EhActn2 plays an important role in phagocytic cup formation and might constitute a new drug

137 Cdc42 is not critical for filopodia or phagocytic cup formation, but plays a key role in drivin

138 role in phagocytic processing lies near the phagocytic cup in a myosin-independent fashion.

139 Cdc42-deficient macrophages exhibited rapid phagocytic cup kinetics, but reduced particle clearance,

140 Focal complex-like adhesions formed in the phagocytic cup that contained beta(2) integrins, focal a

141 y, CD82 organized Dectin-1 clustering in the phagocytic cup.

142 ith RBCs EhRab35 is recruited to the site of phagocytic cups as well as to the nascent phagosomes tha

143 Microglia first extend processes that end in phagocytic cups at the motoneuron surface, then they clo

144 days after injury, characterized by frequent phagocytic cups, high phagosome content and CD68 upregul

145 with the interior of both macropinocytic and phagocytic cups.

146 Mfge8 partly rescued the phagocytic defect of Smad3 null macrophages, without aff

147 release was not dramatically regulated, yet phagocytic defects hindered MPhi function in chronic dis

148 cells, as well as rescue the cells from the phagocytic dysfunction induced by cholesterol crystals a

149 Axl and Mertk, which partially explains the phagocytic dysfunction.

150 CD22 mediates the anti-phagocytic effect of alpha2,6-linked sialic acid, and in

151 enzymatic means is shown to markedly enhance phagocytic efficiency.

152 ealing subcellular force patterns throughout phagocytic engulfment and force dynamics in the cytotoxi

153 om the recognition of dying cells through to phagocytic engulfment and homeostatic resolution, and hi

154 d a prorepair phenotype, and increase of the phagocytic engulfment of neutrophils by macrophages.

155 ithin the gels is used to measure successful phagocytic engulfment.

156 s are associated with a decreased success of phagocytic engulfment.

157 targets are embedded, impact the success of phagocytic engulfment.

158 orne cholera disease, uses the T6SS to evade phagocytic eukaryotes, cause intestinal inflammation, an

159 Cytochrome c oxidase dysfunction enhances phagocytic function and osteoclast formation in macropha

160 Herein, we describe a new phagocytic function for the nucleoside diphosphate kinas

161 proinflammatory cytokine production, reduced phagocytic function of alveolar macrophages, and consequ

162 rt that high dose atorvastatin increased the phagocytic function of ARPE-19 cells, as well as rescue

163 lease from hepatocytes and/or modulating the phagocytic function of macrophages represents a promisin

164 Taken together, the phagocytic function of Muller glia is responsible for re

165 ower levels of serum cytokines, and improved phagocytic function relative to wild-type (WT) mice.

166 r macrophages with more pro-inflammatory and phagocytic function respectively, and large alveolar mac

167 more, that defective MCI macrophages recover phagocytic function via omega-3.

168 O dysfunction affects inflammatory pathways, phagocytic function, and osteoclastogenesis.

169 e, an increase in cell motility, and gain of phagocytic function.

170 -associated genes, but also showed decreased phagocytic gene expression and increased epithelial-asso

171 d that IDOL inhibition upregulated lysosomal/phagocytic genes in microglia.

172 isit to the glial cytoplasm, indicating that phagocytic glia act as obligatory intermediates in aggre

173 These findings expand our understanding of phagocytic glia as double-edged players in neurodegenera

174 rophils constitute the largest population of phagocytic granulocytes in the blood of mammals.

175 acrophages quickly differentiated toward non-phagocytic, high-SIRPalpha TAMs.

176 thogenesis, including its survival inside of phagocytic host cells.

177 This process involves corralling, wherein phagocytic immune cells become confined to the necrotic

178 ole for Fmr1 in regulating the activation of phagocytic immune cells both in the body and the brain.

179 riments, we also define specific subtypes of phagocytic immune cells in An. gambiae, providing insigh

180 use of a chemical-based treatment to deplete phagocytic immune cells in Anopheles gambiae, demonstrat

181 Phagocytic immune cells such as microglia can engulf and

182 order of magnitude larger than neutrophils, phagocytic immune cells that densely surround aggregates

183 s catabolize chitin released from hemocytes (phagocytic immune cells) that traffic into the light-org

184 M nanoemulsion was intrinsically taken up by phagocytic immune cells, particularly macrophages, with

185 , cell death, estrogen receptor pathways and phagocytic immune responses.

186 tly regulate actin assembly to ensure proper phagocytic internalization, and translocate phagosomes o

187 ion, slower adhesion turnover, and deficient phagocytic internalization.

188 In particular, whether microglia become phagocytic is controversial.

189 easing complement-mediated attack, improving phagocytic killing activity of neutrophils, and preventi

190 activity of AB307.30 but failed to increase phagocytic killing of capsule-positive strains.

191 We demonstrated decreased resistance to phagocytic killing of GAS lacking EndoS in vitro and dec

192 nutritional immunity, protects them against phagocytic killing, and activates immune evasion strateg

193 eumococcal nasopharyngeal carriage, reducing phagocytic killing, and resulting in increased inflammat

194 AMP, reduce antibiotic efficacy and enhance phagocytic killing.

195 Thanks to phagocytic leucocytes and other host defenses, the vast

196 ecting the function of neutrophils and other phagocytic leukocytes are notable for an increased susce

197 surrounded by the PV membrane, suggesting a phagocytic-like process for vesicle engulfment.

198 Additional components of the phagocytic machinery are needed, but phagocytosis of pLL

199 ate that the majority of adult hemocytes are phagocytic macrophages (plasmatocytes) from the embryoni

200 d-derived immune cell populations, including phagocytic macrophages and microglia.

201 holestasis, which stalled the recruitment of phagocytic macrophages and the removal of cellular corps

202 Phagocytic macrophages expressed CD206, displayed blunte

203 ulatory secondary necrosis by binding to the phagocytic marker phosphatidylserine on dying tumour cel

204 lia in the embryonic retina are enriched for phagocytic markers and observe engulfment of nonapoptoti

205 ate synapse elimination through a novel, non-phagocytic mechanism in the retinogeniculate pathway dur

206 ed after spinal cord injury (SCI), but their phagocytic mechanisms and link to neuroprotection remain

207 Phagocytic microglia engulf more viable newborn cells in

208 Finally, we discovered that the secretome of phagocytic microglia limits the production of new neuron

209 ed the extent of amyloid plaques, oligomers, phagocytic microglia, and infiltrated T cells by 23.7%,

210 ed predominantly of a novel subset of highly phagocytic MPhi resembling small peritoneal MPhi (SPM) t

211 onses via TNF-alpha, which are essential for phagocytic myelin debris clearance and for oligodendroge

212 show a pathway for direct activation of the phagocytic NOX2 in hepatocytes by p52Shc binding and act

213 examining human peptides and the unicellular phagocytic organism Dictyostelium discoideum reveal that

214 sphoinositide signaling is critical both for phagocytic particle engulfment and subsequent phagosomal

215 k identifies a conserved crucial step in the phagocytic pathway of immune cells and provides a potent

216 Contravening the canonical phagocytic pathway, tPCs mature by fusing with endosomes

217 t macrophages, by mediating acquisition of a phagocytic phenotype and by contributing to anti-inflamm

218 They develop a phagocytic phenotype as early as 3 days after injury, ch

219 satory nerve terminal sprouts and to adopt a phagocytic phenotype on denervated NMJs in SOD1(G37R) mi

220 RhoA inhibition restored the phagocytic phenotype to that seen in control macrophages

221 molecular patterns that are engulfed during phagocytic process and danger-associated molecular patte

222 For the biggest particles, the phagocytic process involves a massive reorganization of

223 is depleted during septal thinning through a phagocytic process provides a mechanism for the clearanc

224 terized by inflammatory processes, including phagocytic processes as well as complement cascade activ

225 further highlight that Vamp7 also regulates phagocytic processing and locomotion but uses pathways d

226 ml is needed for both hemocyte migration and phagocytic processing at distinct subcellular localizati

227 tility at the cell rear, whereas its role in phagocytic processing lies near the phagocytic cup in a

228 may have emerged during evolution to couple phagocytic processing to cell migration and facilitate s

229 nohistochemistry to analyze their repair and phagocytic properties.

230 elimited cell surface domains may enable the phagocytic pruning of these 'locally dead' domains by ma

231 adenine dinucleotide phosphate/NADPH levels, phagocytic reactive oxygen species production, neutrophi

232 tion technique to directly probe the role of phagocytic receptor "colocalization" in innate immune re

233 iously identified Jedi-1 (PEAR1/MEGF12) as a phagocytic receptor expressed by satellite glia in the D

234 regulated B1 cell expansion, IgM production, phagocytic receptor expression, and phagocytic activity,

235 ssed, or excess neurons and synapses via the phagocytic receptor Mer tyrosine kinase (MerTK).

236 of cardiac macrophages or deficiency in the phagocytic receptor Mertk resulted in defective eliminat

237 that selectively inhibited efferocytosis by phagocytic receptor MerTK.

238 ody antagonist of CD47 (CD47nb)(12), an anti-phagocytic receptor that is commonly overexpressed in se

239 However, the pro-phagocytic receptor(s) responsible for tumour cell phago

240 Thus, in addition to phagocytic receptor-mediated phagocytosis, neutrophils a

241 ant GPCR/Gi signaling works independently of phagocytic receptor/tyrosine kinase signaling to promote

242 rasite clearance mediated by upregulation of phagocytic receptors and increased IgM production, and d

243 tionship between the spatial organization of phagocytic receptors and innate immune responses.

244 s and neutrophils expressed higher levels of phagocytic receptors and showed enhanced phagocytosis of

245 ns forming adducts with SecoA identified the phagocytic receptors CD206 and CD64.

246 ase bacteria through chemotaxis and then use phagocytic receptors coupled with tyrosine kinases to de

247 ic receptors, which were the main astrocytic phagocytic receptors for cell debris in the above experi

248 Blocking phagocytosis or specific phagocytic receptors may alleviate synapse loss and axon

249 components on the macrophage surface shrouds phagocytic receptors, curtailing their ability to engage

250 ic cells relies on homeostatic engagement of phagocytic receptors, in particular, receptors of the ty

251 ever, the contribution of precursor monocyte phagocytic receptors, which are the first to interact wi

252 ven in a healthy CNS, astrocytes express TAM phagocytic receptors, which were the main astrocytic pha

253 due to the inaccessibility of intracellular phagocytic receptors.

254 plex signaling network initiated by distinct phagocytic receptors.

255 he formation of oxysterol-protein adducts on phagocytic receptors.

256 insights into the cellular determinants for phagocytic recognition and uptake of P. aeruginosa.

257 This prevented phagocytic removal of dead cells, prevented maturation o

258 within Mt to microglia, where it promotes a phagocytic/reparative phenotype.

259 led by efferocytosis of dying hepatocytes by phagocytic resident liver macrophages and infiltrating G

260 ated with increased antibiotic tolerance and phagocytic resistance.

261 In addition, the microglial phagocytic response and elevation of Trem2, both necessa

262 Furthermore, the phagocytic response of BV2 cells to stressed neurones wa

263 globoid cells in nerves, suggesting that the phagocytic response of healthy macrophages, rather than

264 is via a miR-124-dependent reduction in the phagocytic response of microglia.

265 primary microglia cultures, DHA reduced the phagocytic response to myelin, which was associated with

266 tivation and robust apoptotic and microglial phagocytic responses that extensively eliminate cells wi

267 c cells (stretched cells) during their brief phagocytic role in nurse-cell engulfment.

268 tain lineage-labeled particles, suggesting a phagocytic role in the clearance of AMFs.

269 verse roles, with TPCs providing a universal phagocytic signal for a wide range of particles and TRPM

270 data reveal CD24 as a highly expressed, anti-phagocytic signal in several cancers and demonstrate the

271 Our study shows that pro-inflammatory phagocytic signaling is required for myelin debris degra

272 s, YopE and YopT, inactivate RhoA to disrupt phagocytic signaling.

273 at endo-lysosomes act as platforms for a new phagocytic signalling pathway in which FcgammaR activati

274 as the levels of PA found on phagosomes and phagocytic sites as shown with the PA probe Spo20p-GFP.

275 ession of cytokines which promote microglial phagocytic states, such as IL-6 and IL-4, and increased

276 crophages through the overexpression of anti-phagocytic surface proteins called 'don't eat me' signal

277 At the phagocytic synapse, SIRPA inhibited integrin activation

278 ion, positioning SIRPA for activation at the phagocytic synapse.

279 specific cell corpse/phagocyte interactions (phagocytic synapses) that impinge on host immunity, with

280 udies using engineered microenvironments and phagocytic targets have demonstrated how altering the ac

281 Engulfment of phagocytic targets requires the activity of myosins, act

282 phagocytosis exist that utilize a variety of phagocytic targets with different combinations of recept

283 articles with spatially patterned ligands as phagocytic targets, we can decouple the receptor pair, D

284 ns that coat pathogenic as well as malignant phagocytic targets.

285 tivated in vitro by the venom, becoming more phagocytic; these results confirm that this cell is a ta

286 In liver, highly phagocytic TIM4(hi) cells shared many transcripts with m

287 microbial pathogens and dead cells and their phagocytic uptake by specialized immune cells are essent

288 ication of bacterial peptidoglycans restored phagocytic uptake in the lysosomal degradation-defective

289 cally activates the PIP(3)-pathway to induce phagocytic uptake into primary or immortalized murine ce

290 eceptor TIM4, encoded by TIMD4, mediates the phagocytic uptake of apoptotic cells.

291 Filopodia supported the phagocytic uptake of bacterial (Escherichia coli) partic

292 to investigate the influence of size on the phagocytic uptake of macrophages.

293 elled PFCs was able to outcompete the strong phagocytic uptake of PFCs by circulating monocytes.

294 ent inhibited mannosidase-II recruitment and phagocytic uptake of serum-coated or -uncoated latex bea

295 feedback inhibition in these cells requires phagocytic uptake of the bacteria, but cannot be explain

296 phage-mediated bacterial clearance relies on phagocytic uptake of the pathogen, subsequent phagolysos

297 ecruitment of mannosidase-II vesicles during phagocytic uptake required Ca(2+) from both extra- and i

298 role of Golgi-derived secretory vesicles in phagocytic uptake, the key innate defense function.

299 uce permeabilization of Escherichia coli and phagocytic uptake.

300 Eosinophils are phagocytic white blood cells with a variety of roles in