ライフサイエンスコーパス: monocyte-derived macrophage

1 of cells that comprises conventional DCs and monocyte-derived macrophages.

2 49 human alveolar epithelial cells and THP-1 monocyte-derived macrophages.

3 hough the cells can be complemented by adult monocyte-derived macrophages.

4 c-derived Kupffer cells and peripheral blood monocyte-derived macrophages.

5 in both THP-1-derived macrophages and human monocyte-derived macrophages.

6 noted in postefferocytotic peripheral blood monocyte-derived macrophages.

7 an dermal CD14(+) cells are CD11b(+) CD64(+) monocyte-derived macrophages.

8 acrophages of embryonic origin distinct from monocyte-derived macrophages.

9 l functions, but were less inflammatory than monocyte-derived macrophages.

10 eased phagocytosis of the AECs by autologous monocyte-derived macrophages.

11 rior Ab-dependent cellular phagocytosis with monocyte-derived macrophages.

12 promoters in immature dendritic cells and in monocyte-derived macrophages.

13 ace of naive monocytes, as well as in GM-CSF-monocyte-derived macrophages.

14 to study apoptotic cell uptake by autologous monocyte-derived macrophages.

15 flammatory cytokine profile similar to blood monocyte-derived macrophages.

16 to accumulation of extranuclear DNA in human monocyte-derived macrophages.

17 in both monocyte-derived dendritic cells and monocyte-derived macrophages.

18 ytoplasmic and nuclear HIV-1 DNA in infected monocyte-derived macrophages.

19 CR4 (CD11c/CD18) mediated infection of human monocyte-derived macrophages.

20 totic lymphocytes or neuronal cells by human monocyte-derived macrophages.

21 prevention of phagosome maturation in human monocyte-derived macrophages.

22 sident alveolar macrophages, neutrophils and monocyte-derived macrophages.

23 d release in human blood monocytes and human monocyte-derived macrophages.

24 (monocyte/macrophage) cell line and in human monocyte-derived macrophages.

25 hial epithelial cell model and primary human monocyte-derived macrophages.

26 modified lipoproteins by human monocytes and monocyte-derived macrophages.

27 hat sRAGE directly bound human monocytes and monocyte-derived macrophages.

28 lipids up-regulated CXCL16 in primary human monocyte-derived macrophages.

29 excellent producers of IL-6 as compared with monocyte-derived macrophages.

30 man CD4(+) T lymphocytes but much less so in monocyte-derived macrophages.

31 ession by lactate was also observed in human monocyte-derived macrophages.

32 ble CD4, or in their replication capacity in monocyte-derived macrophages.

33 replicated in CF airway epithelial cells and monocyte-derived macrophages.

34 8, miRNA-150, miRNA-223, and miRNA-382) than monocyte-derived macrophages.

35 everse transcriptase activity in human blood monocyte-derived macrophages.

36 suppressed HIV-1 replication in T cells and monocyte-derived macrophages.

37 ered by phenotypic overlap of microglia with monocyte-derived macrophages.

38 (PXR), in M. tuberculosis infection in human monocyte-derived macrophages.

39 roinflammatory cytokines from mice and human monocyte-derived macrophages.

40 endent maturation of IL-1beta in human THP-1 monocyte-derived macrophages.

41 complexin monocytic THP-1 cells and primary monocyte-derived macrophages.

42 of BBI on HIV infection of peripheral blood monocyte-derived macrophages.

43 n of IFN-beta in human primary monocytes and monocyte-derived macrophages.

44 er cells control the initial accumulation of monocyte-derived macrophages.

45 vation is inhibited by PGE2 in human primary monocyte-derived macrophages.

46 receptor for bacterial RNA in primary human monocyte-derived macrophages.

47 H. ducreyi-infected monocytes and monocyte-derived macrophages activated NK cells in a con

48 Infiltrating monocyte-derived macrophages aggravate APAP hepatotoxici

49 In this article, we show the diversity of monocyte-derived macrophages along the course of experim

50 Additionally, monocyte-derived macrophages also interacted with HBsAg,

51 hIL-10, and we identify CD14(+)monocytes and monocyte-derived macrophages and DCs as major sources of

52 Primary human monocyte-derived macrophages and dendritic cells (DCs) w

53 In contrast, monocyte-derived macrophages and dendritic cells are per

54 Infection of X4 viruses in monocyte-derived macrophages and dendritic cells is enha

55 that different types of myeloid cells, i.e., monocyte-derived macrophages and dendritic cells, transf

56 nd interferon (IFN) gene expression in human monocyte-derived macrophages and dendritic cells.

57 sites of inflammation and differentiate into monocyte-derived macrophages and dendritic cells.

58 ite for enhancement of phagocytosis by human monocyte-derived macrophages and downregulation of IL-8

59 oregulatory cells, including IL-10-producing monocyte-derived macrophages and Foxp3(+) regulatory T c

60 d proinflammatory cytokine in vitro by human monocyte-derived macrophages and in vivo by resident mur

61 sis factor and interleukin-6 are released by monocyte-derived macrophages and lymphocytes in the lung

62 S accumulation of classically activated (M1) monocyte-derived macrophages and microglial expression o

63 by fluid-phase pinocytosis in cultured human monocyte-derived macrophages and mouse bone marrow-deriv

64 e defective for replication in primary human monocyte-derived macrophages and murine J774 cells yet e

65 secretion, were conducted with primary human monocyte-derived macrophages and neutrophils and freshly

66 nd survives inside these cells as well as in monocyte-derived macrophages and neutrophils for at leas

67 e ex vivo virus production was detected from monocyte-derived macrophages and nonadherent peripheral

68 In regenerative tissues, a central role of monocyte-derived macrophages and paracrine factors secre

69 eplicate in their respective cell targets of monocyte-derived macrophages and peripheral blood mononu

70 investigated the apoptotic effect of Vpr on monocyte-derived macrophages and phorbol 12-myristate 13

71 gate P2 receptor expression in primary human monocyte-derived macrophages and receptors that mediate

72 on CD11b, MerTK, and CD103 were reduced, and monocyte-derived macrophages and resident macrophages ex

73 impaired the critical conditioning of these monocyte-derived macrophages and resulted in spontaneous

74 HBsAg-induced cytokine production by KCs and monocyte-derived macrophages and subsequent NK cell acti

75 nuated the expression of M1 markers in human monocyte-derived macrophages and SVF cells isolated from

76 had an independent effect on recruitment of monocyte-derived macrophages and T cells into the brain

77 lia is differentially regulated from that in monocyte-derived macrophages and the ramified microglia

78 ociated virulence was studied in guinea pig, monocyte-derived macrophage, and lysozyme resistance ass

79 is highly expressed in CD4(+) T lymphocytes, monocyte-derived macrophages, and dendritic cells.

80 ype 1 (HIV-1) infectivity in CD4(+) T cells, monocyte-derived macrophages, and dendritic cells.

81 nterfering RNA (siRNA) transfection of human monocyte-derived macrophages, and enzymatic activity con

82 Steady-state cardiac macrophages, monocyte-derived macrophages, and locally sourced macrop

83 studies on human alveolar macrophages, human monocyte-derived macrophages, and murine bone marrow-der

84 umin in macrophage cell lines, primary human monocyte-derived macrophages, and murine bone marrow-der

85 Indeed, monocytes, monocyte-derived macrophages, and peripheral blood monon

86 nt cells (MGCs), a property not exhibited by monocyte-derived macrophages, and we detected MGCs of my

87 We show in this article that human monocyte-derived macrophages are able to engulf NETs in

88 Microglia and infiltrating monocyte-derived macrophages are now known to be functio

89 inflammation induced by obesity, bone marrow monocyte-derived macrophages are recruited to inflamed t

90 itis (HIVE) mice, where human virus-infected monocyte-derived macrophages are stereotactically inject

91 otic GECs to THP-1 cells or peripheral blood monocyte-derived macrophages as assayed by confocal micr

92 We found that primary human monocyte-derived macrophages as well as THP-1 macrophage

93 ed with the CCL5 gene and intragraft CD14(+) monocyte-derived macrophages at graft reperfusion and ea

94 ed inflammatory cytokine production by human monocyte-derived macrophages; autocrine IL-1 production

95 pectively, cannot replicate in primary human monocyte-derived macrophages because they trigger innate

96 Mechanistically, poly(I:C) given to human monocyte-derived macrophages before or after Schu 4 or L

97 anti-FcgammaR F(ab')2 fragments on uptake by monocyte-derived macrophages (both M1 and M2 macrophages

98 er in CNS-derived microglia than observed in monocyte-derived macrophages, both basally and under all

99 es readily completed its life cycle in human monocyte-derived macrophages but not in CD4(-) cells.

100 sDNA) genome in human cell lines and primary monocyte-derived macrophages but not in mouse macrophage

101 IV-1 and other primate lentiviruses in human monocyte-derived macrophages by impairing reverse transc

102 Stimulation of primary monocyte-derived macrophages by muramyl dipeptide (MDP),

103 on and intracellular killing of GBS by human monocyte-derived macrophages, by approximately 50%, but

104 the power of this approach by imaging human monocyte-derived macrophage cells that have been exposed

105 ion is primarily based on the study of blood monocyte-derived macrophages, cells that have never been

106 L are shown to bind and enhance the monocyte/monocyte-derived macrophage clearance of modified forms

107 criptional and functional data revealed that monocyte-derived macrophages coordinate cardiac inflamma

108 tudies using primary cultures of bone marrow monocyte-derived macrophages, demonstrated that glatiram

109 its MDP-induced cytokine production in human monocyte-derived macrophages, demonstrating a key role f

110 asing IL-10 secretion in donor-matched human monocyte-derived macrophages differentiated by GM-CSF or

111 Thus, monocyte-derived macrophages display distinct phenotypes

112 7A induced a unique transcriptome pattern in monocyte-derived macrophages distinct from known macroph

113 cell line, differentiated with vitamin D, or monocyte-derived macrophages enhanced CXCL8 release.

114 ith age and are progressively substituted by monocyte-derived macrophages, even in the absence of inf

115 extracellular trap (MET) formation by bovine monocyte-derived macrophages exposed to M. haemolytica o

116 We demonstrate that monocyte-derived macrophages express gp340 and that HIV-

117 rrelia burgdorferi sensu lato, we stimulated monocyte-derived macrophages from healthy human donors w

118 Although monocytes and monocyte-derived macrophages from humans and chimpanzees

119 ther supported by the skewed polarization of monocyte-derived macrophages from multicentric carpotars

120 PPBP expression by monocyte-derived macrophages from patients with ABPA or

121 Monocyte-derived macrophages from subjects with the Fcga

122 e upon exposure to pathogenic stimuli, human monocyte-derived macrophages generated in the presence o

123 ne bone marrow-derived macrophages and human monocyte-derived macrophages generated mROS in response

124 Human monocyte-derived macrophages have been used to character

125 We show that monocyte-derived macrophages have elevated expression of

126 Although monocyte-derived macrophages have high dUTP levels, thes

127 observations, including those obtained from monocyte-derived macrophages, have argued that ribonucle

128 rnatants harvested from HIV-1-infected human monocyte-derived macrophages (HIV/MDM), we found that Ca

129 In human monocytic THP-1 cells and primary monocyte-derived macrophages, HIV gp120-stimulated produ

130 Here, we employed infection of primary human monocyte-derived macrophages (HMDMs) and THP-1 cells as

131 eumophila to be defective in growth in human monocyte-derived macrophages (hMDMs) but not in Acantham

132 1q bound to immobilized C1q (imC1q) on human monocyte-derived macrophages (HMDMs) obtained from healt

133 regulating apoE secretion from primary human monocyte-derived macrophages (HMDMs) remain unclear.

134 em using primary human lymphocytes and human monocyte-derived macrophages (HMDMs) to characterize the

135 sed including donor matched human monocytes, monocyte-derived macrophages (HMDMs), and dendritic cell

136 t upon attachment of L. pneumophila to human monocyte-derived macrophages (hMDMs), the host farnesyla

137 ct in intracellular replication within human monocyte-derived macrophages (hMDMs), U937 macrophages a

138 pression of ABCA1 in comparison with intimal monocyte-derived macrophages, however, are unknown.

139 Monocyte-derived macrophages, however, encounter a gradu

140 red to stimulate production of CCL2 by human monocyte-derived macrophages (huMDM).

141 ith their cardiac derivatives, monocytes and monocyte-derived macrophages in conventional cell cultur

142 also indicate that many cells identified as monocyte-derived macrophages in human atherosclerosis ar

143 5(+)CD14(+) monocytes and intragraft CD14(+) monocyte-derived macrophages in immunohistochemistry of

144 nfiltration of monocytes and accumulation of monocyte-derived macrophages in inflammation.

145 ility complex class II on both monocytes and monocyte-derived macrophages in joints.

146 the individual role(s) of Kupffer cells and monocyte-derived macrophages in the induction of LPC pro

147 The demonstration of monocyte-derived macrophages in the steady state in huma

148 In contrast, tissue macrophages and monocyte-derived macrophages in vitro are highly suscept

149 crophages in vivo and that it is produced by monocyte-derived macrophages in vitro, after Helicobacte

150 wing viral infection or envelope exposure in monocyte-derived macrophages in vitro.

151 n N-terminal kinase in Nod2-stimulated human monocyte-derived macrophages, in the absence of autocrin

152 es multiple protein kinases in primary human monocyte-derived macrophages, including the Src family k

153 pattern recognition receptors (PRR) in human monocyte-derived macrophages induces interleukin (IL)-1,

154 The temporal response of primary human monocyte-derived macrophages infected with highly pathog

155 l replication or eliminate CD4(+) T cells or monocyte-derived macrophages infected with SIV variants

156 n cell death and apoptosis pathways in human monocyte-derived macrophages ingesting modified LDL; thi

157 Proinflammatory activation of monocyte-derived macrophages is associated with a concom

158 marginal differences in LPS responses, human monocyte-derived macrophages killed Escherichia coli and

159 Finally, human monocyte-derived macrophages knocked down for MR express

160 ng intracellular infection of peritoneal and monocyte-derived macrophages, known to secrete lysozyme,

161 In injured liver, infiltrating monocyte-derived macrophages largely augment the hepatic

162 Ingestion of apoptotic cells by monocyte-derived macrophages led to up-regulation of col

163 Monocyte-derived macrophages, located in atherosclerotic

164 Infiltrating monocyte-derived macrophages (M-MPhi) influence stroke-i

165 lease of infectious HIV-1 from primary human monocyte-derived macrophages (MDM) acutely infected with

166 Monocyte-derived macrophages (MDM) also expressed a mixe

167 o explain the presence of inflammatory CD14+ monocyte-derived macrophages (MDM) and immunoglobulin G+

168 dation of Abeta using primary cultured human monocyte-derived macrophages (MDM) and microglia using p

169 px, the accessory protein can be provided to monocyte-derived macrophages (MDM) and monocyte-derived

170 Monocyte-derived macrophages (MDM) can polarize into dif

171 Studies with monocyte-derived macrophages (MDM) demonstrated various

172 ary cell-based coculture model, we show that monocyte-derived macrophages (MDM) efficiently transmit

173 esh human blood monocytes were compared with monocyte-derived macrophages (MDM) for their IL-1beta re

174 erefore, ATM were isolated and compared with monocyte-derived macrophages (MDM) from the same obese p

175 -meso-diaminopimelic acid (GM-triDAP), human monocyte-derived macrophages (MDM) produced an order of

176 ytes and that the bacteriostatic activity of monocyte-derived macrophages (MDM) requires NOX2 and gam

177 In vitro, HIV replication in monocyte-derived macrophages (MDM) selectively reduces H

178 te in human macrophages, we infected primary monocyte-derived macrophages (MDM) that had been differe

179 er a respiratory burst in blood monocytes or monocyte-derived macrophages (MDM), and phagosomes conta

180 le annexin A2 tetramer (A2t) activates human monocyte-derived macrophages (MDM), resulting in secreti

181 role of PKCalpha in CRIg expression in human monocyte-derived macrophages (MDM).

182 drug particles readily accumulated in human monocyte-derived macrophages (MDM).

183 in experimentally infected human skin and in monocyte-derived macrophages (MDM).

184 cytic killing by primary human monocytes and monocyte-derived macrophages (MDM).

185 FOXO3a translocation to the nucleus in human monocyte-derived macrophages (MDM).

186 n a potent block to HIV-1 infection in human monocyte-derived macrophages (MDM).

187 pes to induce cytokine secretion from mature monocyte-derived macrophages (MDMphis) from either patie

188 Studies with monocyte-derived macrophages (MDMs) and animal models ha

189 nerated primary myeloid cells, specifically, monocyte-derived macrophages (MDMs) and dendritic cells

190 Comparison of the migR and fevR mutants in monocyte-derived macrophages (MDMs) and epithelial cell

191 aive and lipopolysaccharide (LPS) stimulated monocyte-derived macrophages (MDMs) and IPSDMs using RNA

192 NF-kappaB transcriptional activity in human monocyte-derived macrophages (MDMs) and the murine macro

193 Neutrophils and monocyte-derived macrophages (MDMs) are the main source

194 X3CR1 signaling in intraspinal microglia and monocyte-derived macrophages (MDMs) attenuates their abi

195 ts the first in vivo comparative analysis of monocyte-derived macrophages (MDMs) between rhesus macaq

196 5) virus that, using CCR5 only, could infect monocyte-derived macrophages (MDMs) but not CD4(+) T cel

197 We report that a major subpopulation of monocyte-derived macrophages (MDMs) contains high levels

198 Here, we sought to determine whether monocyte-derived macrophages (MDMs) contribute to recove

199 d poorly to IFN-gamma, whereas monocytes and monocyte-derived macrophages (MDMs) did not.

200 (EBOV); knockdown of TIM-3 in differentiated monocyte-derived macrophages (MDMs) enhances HIV-1 produ

201 Monocyte-derived macrophages (MDMs) exhibit a high degre

202 ug levels reached 6 mug/10(6) cells in human monocyte-derived macrophages (MDMs) for nanoparticle tre

203 this article, we analyze CF and non-CF human monocyte-derived macrophages (MDMs) for ROS production,

204 ertook an in vitro comparative assessment of monocyte-derived macrophages (MDMs) from both nonhuman p

205 We found that human monocyte-derived macrophages (MDMs) from rs917997 AA ris

206 y over the past few years has involvement of monocyte-derived macrophages (MDMs) in CNS repair receiv

207 tor T cells to suppress viral replication in monocyte-derived macrophages (MDMs) in ESs and CPs.

208 rts demonstrating the presence of CD14+CD16+ monocyte-derived macrophages (MDMs) in the gingival tiss

209 ripheral blood mononuclear cells (PBMCs) and monocyte-derived macrophages (MDMs) in vitro and induces

210 vary continuously in their ability to enter monocyte-derived macrophages (MDMs) in vitro, and MDMs v

211 miRNA expression profiles were determined in monocyte-derived macrophages (MDMs) incubated in conditi

212 to T-tropic viruses, M-tropic viruses infect monocyte-derived macrophages (MDMs) on average 28-fold m

213 Here we report that human monocyte-derived macrophages (MDMs) rapidly spread HIV-1

214 igen presentation in MERS-CoV-infected human monocyte-derived macrophages (MDMs) versus SARS-CoV-infe

215 ripheral blood mononuclear cells (PBMCs) and monocyte-derived macrophages (MDMs) were isolated from p

216 Human monocyte-derived macrophages (MDMs) were studied in nonc

217 We hypothesize that infection of human monocyte-derived macrophages (MDMs) with Salmonella ente

218 epithelial cell monolayer, (ii) attached to monocyte-derived macrophages (MDMs), (iii) bound monocyt

219 Using lung epithelial cells, primary human monocyte-derived macrophages (MDMs), and neutrophils fro

220 We found that monocyte-derived macrophages (MDMs), including granulocy

221 onstrate that HIV infection in primary human monocyte-derived macrophages (MDMs), THP-1 macrophages,

222 d a subset of interferon-stimulated genes in monocyte-derived macrophages (MDMs), which differed from

223 everal microRNAs (miRNAs) in polarized human monocyte-derived macrophages (MDMs).

224 rowth of Mycobacterium tuberculosis in human monocyte-derived macrophages (MDMs).

225 lood mononuclear cells and differentiated to monocyte-derived macrophages (MDMs).

226 IV-1 infections of IFN-alpha-treated primary monocyte-derived macrophages (MDMs).

227 to EBOV and RESTV infection in primary human monocyte-derived macrophages (MDMs).

228 is in Vpx+ virus-like particle (VLP)-treated monocyte-derived macrophages (MDMs).

229 rphine may modulate HIV-1 infection of human monocyte-derived macrophages (MDMs).

230 K293 cells (HEK293-ABCC10), CD4(+) cells and monocyte-derived macrophages (MDMs).

231 uberculosis H37Rv in subpopulations of human monocyte-derived macrophages (MDMs).

232 -1, 293T, or Jurkat T cells or primary human monocyte-derived macrophages (MDMs).

233 ectivity in cultures of Vero cells and human monocyte-derived macrophages (MDMs).

234 5-tropic) HIV-1 to induce BAFF production by monocyte-derived macrophages (MDMs).

235 How monocyte fate is directed toward monocyte-derived macrophages (mo-Macs) or monocyte-deriv

236 cluding activated microglia and infiltrating monocyte-derived macrophages (mo-MPhi).

237 Monocyte-derived macrophages (mo-MPhis) and T cells have

238 Upon experimental APAP overdose in mice, monocyte-derived macrophages (MoMFs) massively accumulat

239 To generate monocyte-derived macrophages, monocytes were cultured fo

240 Comparative analysis of human monocyte-derived macrophages (Mph) demonstrated greater

241 n (myeloid-derived suppressor cells [MDSCs], monocyte-derived macrophages [Mphis], and dendritic cell

242 phages, Kupffer cells (KCs), but not hepatic monocyte-derived macrophages or dendritic cells (DCs), a

243 lls (PBMC) and a CD4 T-cell line compared to monocyte-derived macrophages, or dendritic cells (DC).

244 Monocyte-derived macrophages play a key role in atheroge

245 In conclusion, HCVc inhibits monocyte-derived macrophage polarization via TLR2 signal

246 tion, local arterial inflammation, driven by monocyte-derived macrophages, predicts future cardiovasc

247 virus maintained the ability to replicate in monocyte-derived macrophages, primary CD4(+) T cells, an

248 Monocyte-derived macrophages prime acute cellular reject

249 Monocytes and monocyte-derived macrophages promote atherosclerosis thr

250 Finally, a model including monocyte-derived macrophage recruitment by neutrophils s

251 storation of HO-1 expression in HIV-infected monocyte-derived macrophages reduces neurotoxin release

252 ediated neurotoxicity, in which HIV-infected monocyte-derived macrophages release excitatory neurotox

253 cytoid dendritic cells, and in vitro derived monocyte-derived macrophages, responded normally to both

254 to determine the effect of CD40L absence on monocyte-derived macrophage responses.

255 ccessful efferocytosis of apoptotic cells by monocyte-derived macrophages resulted in the suppression

256 ses carrying monocyte-derived envelopes: (1) monocyte-derived, macrophage-specific R5 (MDMS-R5) virus

257 In monocyte-derived macrophages, SSRI treatment decreased e

258 al of two divergent lineage-determined human monocyte-derived macrophage subpopulations.

259 eover, these results were confirmed in human monocyte-derived macrophages, suggesting that global imm

260 e primary macrophages as well as human THP-1 monocyte-derived macrophages, suggesting that Grp170 rel

261 Cultured monocyte-derived macrophages take up large amounts of na

262 an give rise to heterogeneous populations of monocyte-derived macrophages that are characterized by d

263 , after injury, these cells were replaced by monocyte-derived macrophages that are proinflammatory an

264 ency virus type 1 (HIV-1) infection of blood monocyte-derived macrophages that expressed IFN-lambda r

265 lesterol accumulation in monocytes and human monocyte-derived macrophages that ingested oxidized LDL,

266 on in the retina, and in the infiltration of monocyte-derived macrophages that were absent from contr

267 ) modulates innate immunity in human primary monocyte-derived macrophages through toll-like receptor

268 se cells were preferentially phagocytosed by monocyte-derived macrophages, thus linking proteasome ac

269 clear cells, purified monocytes, T cells and monocyte-derived macrophages to examine functional immun

270 migratory response of human peripheral blood monocyte-derived macrophages to oxLDL.

271 T-Regs decrease the ability of alveolar and monocyte-derived macrophages to restrict the growth of M

272 nhibit astroglial CCL2-driven trafficking of monocyte-derived macrophages to the CNS during acute MS

273 ) on the pro-inflammatory responses of human monocyte-derived macrophages to the saturated fatty acid

274 at in an ex vivo model, M-CSF-differentiated monocyte-derived macrophages uniformly infected with rep

275 In monocyte-derived macrophages, URMC-099 induction of auto

276 Expression of DHRS9 within a panel of monocyte-derived macrophages was investigated by quantit

277 ycobacterial growth in infected alveolar and monocyte-derived macrophages was significantly diminishe

278 gulfment of EMPs or cMPs by peripheral blood monocytes-derived macrophages was associated with signif

279 rophage-mediated cancer cell activity, human monocyte derived-macrophages were subjected, for a week,

280 Monocyte-derived macrophages were also infected with NTH

281 Monocyte-derived macrophages were chosen as natural targ

282 H37Rv-infected alveolar and monocyte-derived macrophages were cocultured with autolo

283 st this hypothesis fresh human monocytes and monocyte-derived macrophages were compared for MAIL expr

284 Pulmonary and monocyte-derived macrophages were cultured in vitro with

285 es isolated from peripheral blood, and human monocyte-derived macrophages were either coincubated wit

286 eboid migration mode of HIV-1-infected human monocyte-derived macrophages were inhibited, whereas the

287 perfusate-derived KCs and in vitro-generated monocyte-derived macrophages were investigated for funct

288 nt model was used where HIV-1-infected human monocyte-derived macrophages were stereotactically injec

289 d enteroid monolayers co-cultured with human monocyte-derived macrophages were used to evaluate barri

290 icroglia, an endogenous cell population, and monocyte-derived macrophages, which infiltrate from the

291 the peripheral nervous system, infiltrating monocyte-derived macrophages, which use the chemokine re

292 M-CSF drives the generation of human monocyte-derived macrophages with a potent anti-inflamma

293 +) cells are a tissue-resident population of monocyte-derived macrophages with a short half-life of <

294 macrophage differentiation, we next treated monocyte-derived macrophages with conditioned media from

295 ave previously shown that treatment of human monocyte-derived macrophages with EBV-encoded dUTPase in

296 We sought to compare pair-matched monocyte-derived macrophages with m isolated from chroni

297 In addition, treatment of human monocyte-derived macrophages with the anti-EBV-encoded d

298 Incubation of human monocyte-derived macrophages with the isolated extracell

299 Infection of primary human monocyte-derived macrophages with virulent F. tularensis

300 imics induced a proinflammatory phenotype in monocyte-derived macrophages, with enhanced expression a