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

1 genes but not for the activation of MAPKs in bone marrow-derived macrophage.

2 in either mouse primary cortical neurons or bone marrow derived macrophages.

3 liensis infection of BALB/c (wild-type [WT]) bone marrow derived macrophages.

4 wever expression is increased over 2-fold in bone marrow derived macrophages.

5 Typhimurium, in a comparable manner to mouse bone marrow derived macrophages.

6 cytokines, which is attenuated in Mrp14(-/-) bone marrow-derived macrophages.

7 ec kinases and LPS in primary peritoneal and bone marrow-derived macrophages.

8 10, and GM-CSF, was also markedly reduced in bone marrow-derived macrophages.

9 viral infection on inflammasome responses in bone marrow-derived macrophages.

10 in murine RAW 264.7 macrophages and primary bone marrow-derived macrophages.

11 rease of RANKL-induced osteoclastogenesis in bone marrow-derived macrophages.

12 n monocytes, murine RAW 264.7, and wild-type bone marrow-derived macrophages.

13 emphasis on proteolytic efficiency in murine bone marrow-derived macrophages.

14 ulus for interleukin (IL)-1beta secretion by bone marrow-derived macrophages.

15 ed in MHV-infected Ifit2(-/-) relative to wt bone marrow-derived macrophages.

16 also activating ERK MAPK pathways in murine bone marrow-derived macrophages.

17 D88-NF-kappaB-dependent mode of induction in bone marrow-derived macrophages.

18 ory cytokines nor inflammasome activation in bone marrow-derived macrophages.

19 as aeruginosa are known to activate NLRC4 in bone marrow-derived macrophages.

20 ugh the alteration of potassium transport in bone marrow-derived macrophages.

21 r expression in RAW-264.7 cells and in mouse bone marrow-derived macrophages.

22 in cultured murine macrophages (B6-MCL) and bone marrow-derived macrophages.

23 2-like inflammatory response from ABCA1(+/+) bone marrow-derived macrophages.

24 lia virus infection of murine cell lines and bone marrow-derived macrophages.

25 rapidly down-regulated upon LPS exposure in bone marrow-derived macrophages.

26 B7-2, but not B7-1, on the surface of mouse bone marrow-derived macrophages.

27 nflammatory cytokine production by Cyld(-/-) bone marrow-derived macrophages.

28 human monocytic cell line (THP-1) and mouse bone marrow-derived macrophages.

29 r lipopolysaccharide-induced cytotoxicity in bone marrow-derived macrophages.

30 ts intracellular cycle within primary murine bone marrow-derived macrophages.

31 were recapitulated by hyperglycemia in mouse bone marrow-derived macrophages.

32 high-power field) of TAMs were GFP-positive, bone marrow-derived macrophages.

33 inflammasome is attenuated in Nrf2-deficient bone marrow-derived macrophages.

34 poorly and induced rapid cell death in mouse bone marrow-derived macrophages.

35 phage cell line RAW264.7, but not in primary bone marrow-derived macrophages.

36 abolished in Toll-like receptor (TLR2)(-/-) bone marrow-derived macrophages.

37 uced mRNA and protein expression of IL-18 in bone marrow-derived macrophages.

38 ta and interleukin 6 messenger RNAs in mouse bone marrow-derived macrophages.

39 potently inhibited Leishmania replication in bone marrow-derived macrophages.

40 uced IL-1beta secretion and NO production in bone marrow-derived macrophages.

41 phage phenotype was absent in peritoneal and bone marrow-derived macrophages.

42 re supported by experiments with Ifitm3(-/-) bone marrow-derived macrophages.

43 optotic cells and are better phagocytes than bone marrow-derived macrophages.

44 man monocyte-derived macrophages, and murine bone marrow-derived macrophages.

45 duced chemokine secretion by neutrophils and bone marrow-derived macrophages.

46 s, but GM-CSF has also been used to generate bone marrow-derived macrophages.

47 39 significantly regulated 105 probe sets in bone marrow-derived macrophages.

48 on of IL-1beta by murine dendritic cells and bone-marrow derived macrophages.

49 l production of NPY was observed in cultured bone marrow derived macrophage and dendritic cells (DCs)

50 as LVS clpB grew similarly to LVS in primary bone marrow-derived macrophages and a variety of cell li

51 strongly impairs many effector functions of bone marrow-derived macrophages and bone marrow-derived

52 Whereas TLR9-induced TNF-alpha secretion of bone marrow-derived macrophages and conventional dendrit

53 ts lytic replication of gammaHV68 in primary bone marrow-derived macrophages and decreases transcript

54 also observed by in vitro experiments, using bone marrow-derived macrophages and dendritic cells as r

55 TARM1 expression was also upregulated by bone marrow-derived macrophages and dendritic cells foll

56 osis and internalization of CpG-ODN by mouse bone marrow-derived macrophages and directly interacts w

57 A-induced macrophage cell death with primary bone marrow-derived macrophages and high-fat diet-induce

58 Murine bone marrow-derived macrophages and human monocyte-deriv

59 wild-type and T2S mutant bacteria in murine bone marrow-derived macrophages and human U937 cells.

60 ion, infection experiments were performed in bone marrow-derived macrophages and in mice using threon

61 These strains were highly attenuated both in bone marrow-derived macrophages and in vivo compared wit

62 s isolated from Anxa2-deficient (Anxa2(-/-)) bone marrow-derived macrophages and lung parenchyma disp

63 Using both mouse bone marrow-derived macrophages and mouse embryo fibrobl

64 In murine bone marrow-derived macrophages and murine embryonic fib

65 Using STAT3-deficient bone marrow-derived macrophages and pharmacologic inhibi

66 transendothelial migration (TEM) activity of bone marrow-derived macrophages and Raw264.7 cells accor

67 In vitro, both the WT bone marrow-derived macrophages and renal mesangial cell

68 TEM activity was decreased in Ninjurin1 KO bone marrow-derived macrophages and siNinj1 Raw264.7 cel

69 ted peritoneal macrophages) as compared with bone marrow-derived macrophages and the RAW264 cell line

70 In primary bone-marrow-derived macrophages and mouse embryonic fibr

71 function of anti-inflammatory intestinal and bone-marrow-derived macrophages and their ability to sec

72 tates its survival and replication in murine bone marrow-derived macrophages, and E. tarda infection

73 ity in vivo by tracking fluorescence-labeled bone marrow-derived macrophages, and found that tPA-defi

74 ly active, rescue replication of MHV(Mut) in bone marrow-derived macrophages, and inhibit RNase L-med

75 Murine macrophage-like cell line RAW264.7, bone marrow-derived macrophages, and primary peritoneal

76 more, after phagocytosis of myelin in vitro, bone marrow-derived macrophages are much more susceptibl

77 y lipoprotein (LDL)-mediated signaling using bone marrow-derived macrophage as well as an in vivo mod

78 uced increased migration of THP-1 and murine bone marrow-derived macrophages as well as activated mon

79 ymosan-induced peritonitis, M1- and M2a-like bone marrow derived macrophages, as well as by mesotheli

80 pro-inflammatory cytokines were increased in bone marrow derived macrophage (BMDM) from PLTP-/-, whil

81 ignificantly higher IL-6 secretion by murine bone marrow derived macrophages (BMDM) compared to cultu

82 heir synthases in the primary cultured mouse bone marrow derived macrophages (BMDM).

83 d that treatment of RANKL-stimulated primary bone marrow-derived macrophage (BMDM) cultures with smal

84 d TBK1 activity was significantly reduced in bone marrow-derived macrophage (BMDM) from OPTN(D477N/D4

85 rom 129 mice is sufficient to enhance the B6 bone marrow-derived macrophage (BMDM) inflammasome respo

86 ulture of atrophied myotubes with or without bone marrow-derived macrophages (BMDM) and/or M-CSF reve

87 lations of wild-type mice with Nrp1-depleted bone marrow-derived macrophages (BMDM) confers resistanc

88 LRP1-deficient bone marrow-derived macrophages (BMDM) expressed higher

89 Here we show that bone marrow-derived macrophages (BMDM) from high fat-fed

90 Using bone marrow-derived macrophages (BMDM) from wild-type an

91 Compared to Sn-expressing bone marrow-derived macrophages (BMDM) from wild-type mi

92 Mouse bone marrow-derived macrophages (BMDM) grown in M-CSF (C

93 this study, we confirm that tolerized mouse bone marrow-derived macrophages (BMDM) selectively incre

94 of the eicosanoid metabolic network in mouse bone marrow-derived macrophages (BMDM) upon stimulation

95 Primary bone marrow-derived macrophages (BMDM) was isolated from

96 e treated rat neonatal cardiomyocytes, mouse bone marrow-derived macrophages (BMDM), or mouse neutrop

97 d rectifier potassium channels (Kir) in mice bone marrow-derived macrophages (BMDM).

98 uction in response to LPS treatment in mouse bone marrow-derived macrophages (BMDM).

99 eficient RAW cells and primary PHD2 knockout bone marrow-derived macrophages (BMDM).

100 n vivo and by isolated resident alveolar and bone marrow-derived macrophages (BMDM).

101 In addition, infection of bone marrow-derived macrophages (BMDMs) and mice (C57BL/

102 3 or Pyrin inflammasome activation in murine bone marrow-derived macrophages (BMDMs) as an indicator

103 Using bone marrow-derived macrophages (BMDMs) derived from wil

104 In vitro, LPS-treated LysM PTP1B bone marrow-derived macrophages (BMDMs) displayed increa

105 d NLRP3 was revealed when Nlrc4(S533A/S533A) bone marrow-derived macrophages (BMDMs) expressing phosp

106 Infected Chil1-deficient mice and bone marrow-derived macrophages (BMDMs) from Chil1-defic

107 aB pathway (IKKalpha/beta, NF-kappaB p65) in bone marrow-derived macrophages (BMDMs) from knockout mi

108 n of IFN regulatory factor 3 (IRF3), whereas bone marrow-derived macrophages (BMDMs) from mice carryi

109 Cytokine production was measured in bone marrow-derived macrophages (BMDMs) from wild-type (

110 human monocytic leukemia cell line THP-1 and bone marrow-derived macrophages (BMDMs) from wild-type a

111 Elavl1Mo KO), we show that HuR expression in bone marrow-derived macrophages (BMDMs) is needed to mai

112 Both lung macrophages and bone marrow-derived macrophages (BMDMs) isolated from p4

113 Injection of wild-type bone marrow-derived macrophages (BMDMs) or M2-differenti

114 Interestingly, IL-4 treatment of bone marrow-derived macrophages (BMDMs) significantly do

115 Following exposure of murine bone marrow-derived macrophages (BMDMs) to inactivated F

116 and adoptive transfer studies revealed that bone marrow-derived macrophages (BMDMs) traffic to the l

117 S induced secretion of IL-6 and TNF-alpha by bone marrow-derived macrophages (BMDMs) was significantl

118 esser extent at Il1a) reaches high levels in bone marrow-derived macrophages (BMDMs), and the enhance

119 In LPS/ATP-stimulated bone marrow-derived macrophages (BMDMs), CLIC1 or CLIC4

120 and is proteolytically processed in resting bone marrow-derived macrophages (BMDMs), dendritic cells

121 was transiently induced in LPS-activated WT bone marrow-derived macrophages (BMDMs), expression pers

122 In bone marrow-derived macrophages (BMDMs), the IRAK2-TRAF6

123 In bone marrow-derived macrophages (BMDMs), we also observe

124 fy H. capsulatum genes required for lysis of bone marrow-derived macrophages (BMDMs), we identified a

125 nstituted mouse bone marrow neutrophils, and bone marrow-derived macrophages (BMDMs), we showed that

126 rous chemokines and cytokines that activated bone marrow-derived macrophages (BMDMs).

127 ived LPS enhanced the level of miR-15a/16 in bone marrow-derived macrophages (BMDMs).

128 of CD40 on the surface of T. gondii-infected bone marrow-derived macrophages (BMdMs).

129 of inflammatory factors in BV2 microglia and bone marrow-derived macrophages (BMDMs).

130 ro was assessed in parental and congenic rat bone marrow-derived macrophages (BMDMs).

131 or NF-kappaB activation in HEK 293 cells and bone marrow-derived macrophages (BMDMs).

132 7BL/6, and CD1 mice models and C57BL/6 mouse bone-marrow-derived macrophages (BMDMs) were used as inf

133 uction in lipopolysaccharide (LPS)-activated bone marrow derived-macrophages (BMM) was detected in 6-

134 gated Nur77 in macrophage polarization using bone marrow-derived macrophages (BMM) from wild-type and

135 ation of ns2 mutant viruses is attenuated in bone marrow-derived macrophages (BMM) generated from wil

136 Treatment of activated bone marrow-derived macrophages (BMM) with WP1130 signif

137 Interestingly, in nfkappab1(-/-) bone marrow-derived macrophages (BMM), the formation of

138 RNase L activation and replicates poorly in bone marrow-derived macrophages (BMM), while ns2(H126R)

139 ly upregulated in human monocytes and murine bone marrow-derived macrophages (BMM).

140 CD200R-deficient bone marrow derived macrophages (BMMPhi) were used to de

141 ession of CTMP is also observed increased in bone marrow-derived macrophages (BMMPhi) from DIO mice a

142 ining 3 (NLRP3) inflammasome in primed mouse bone marrow-derived macrophages (BMMPhi), inducing a rob

143 the effect of Fh12 on the function of mouse bone marrow-derived macrophages (bmMPhis).

144 ATG5-knockout bone marrow-derived macrophages (BMMs) also had decrease

145 irus replication was attenuated in wild-type bone marrow-derived macrophages (BMMs) and partially res

146 in LPS (1 ng/ml)-stimulated wild-type murine bone marrow-derived macrophages (BMMs) but failed to do

147 tion of miR-155 expression in primary murine bone marrow-derived macrophages (BMMs) during H. pylori

148 Here, we used fibroblasts and bone marrow-derived macrophages (BMMs) from knockin mice

149 lysis, the bacterial modulation of miRNAs in bone marrow-derived macrophages (BMMs) in which activity

150 r ligation were severely reduced in Hck(-/-) bone marrow-derived macrophages (BMMs) or in RAW/LR5 mac

151 Subsequently, rat bone marrow-derived macrophages (BMMs) were cultured in

152 Bone marrow-derived macrophages (BMMs) were stimulated w

153 Stimulation of bone marrow-derived macrophages (BMMs) with endotoxin re

154 ligand (RANKL)-induced osteoclastogenesis in bone marrow-derived macrophages (BMMs).

155 in the RAW 264.7 macrophage line and primary bone marrow-derived macrophages but did not affect LXR-d

156 n rates and mROS expression in mock-infected bone marrow-derived macrophages but reduced caspase-depe

157 deficiency adversely affected the ability of bone marrow-derived macrophages, but not dendritic cells

158 L-1beta secretion was impaired in Pgam5(-/-) bone marrow-derived macrophages, but not in Ripk3(-/-) b

159 se activation in TRIF-deficient immortalized bone-marrow-derived macrophage, but was fully inhibitory

160 RP3-dependent interleukin-1beta secretion by bone marrow-derived macrophages by activating nuclear fa

161 her, overexpression of NAIP1 in immortalized bone marrow-derived macrophages by retroviral transducti

162 significantly higher by wild-type (C57BL/6) bone marrow-derived macrophages compared with TLR2-defic

163 Bone marrow-derived, macrophage-CSF-induced cells with a

164 hemozoin was purified and added to in vitro bone marrow-derived macrophage cultures concurrently exp

165 Moreover, incubation of LPS-stimulated bone marrow-derived macrophage cultures with MaR1 reduce

166 Coculture of VSMC with bone marrow-derived macrophages demonstrated that the Ru

167 kout of ASC in lipopolysaccharide-stimulated bone marrow-derived macrophages depressed HMGB1 activity

168 d J20/A7(-/-) mice, whereas the capacity for bone marrow-derived macrophages derived from A7(-/-) mic

169 In bone marrow-derived macrophages derived from these mice

170 ed the regulation of AC7 with that of AC2 in bone marrow-derived macrophages devoid of AC7.

171 Bone marrow-derived macrophages did not release NE in re

172 e secretion of mature IL-1beta from unprimed bone marrow-derived macrophages during a productive infe

173 PTEN in lipopolysaccharide-stimulated mouse bone marrow-derived macrophages enhanced beta-catenin ac

174 As in RAW264.7 cells, primary bone marrow-derived macrophages exposed to a sublethal d

175 In this study, bone marrow-derived macrophages exposed to excretory/sec

176 man monocyte-derived macrophages, and murine bone marrow-derived macrophages following infection with

177 a lower parasite intake, parasite burden in bone marrow-derived macrophages from AnxA1(-/-) mice was

178 the sifA mutant was sensitive to killing by bone marrow-derived macrophages from BALB/c.D2 mice and

179 Bone marrow-derived macrophages from Bbaa1 congenic mice

180 per 1 cells or T-helper 2 cells, we obtained bone marrow-derived macrophages from both strains and in

181 Bone marrow-derived macrophages from Cryo(DeltaLRR Z/Del

182 In bone marrow-derived macrophages from different knockout

183 duction was recapitulated ex vivo in primary bone marrow-derived macrophages from Dusp1-deficient mic

184 LPS-challenged peritoneal and bone marrow-derived macrophages from IkappaBzeta-deficie

185 ry cytokines and pro-inflammatory enzymes in bone marrow-derived macrophages from LKB1 KO than those

186 Bone marrow-derived macrophages from mice lacking Abl an

187 d M2 macrophage activation were confirmed in bone marrow-derived macrophages from mice with the myelo

188 ng IL-31RA expression on both peritoneal and bone marrow-derived macrophages from mice.

189 Delivery of bone marrow-derived macrophages from miR106b-93-25(-/-)

190 The effects of estrogen are long-lasting; bone marrow-derived macrophages from ovariectomized mice

191 Consistent with our in vivo findings, bone marrow-derived macrophages from Pilrb(-/-) mice rel

192 In addition, bone marrow-derived macrophages from PLCgamma2-deficient

193 oviruses expressing WT or mutant PSGL-1 into bone marrow-derived macrophages from PSGL-1-deficient mi

194 Our previous studies showed that bone marrow-derived macrophages from S100A4(-/-) mice ex

195 hagic markers were constitutively induced in bone marrow-derived macrophages from Sphk dKO mice.

196 the lack of TTP expression in LPS-stimulated bone marrow-derived macrophages from the mice, whereas f

197 Bone marrow-derived macrophages from TLR1- and TLR6-defi

198 Bone marrow-derived macrophages from Tlr4-deficient mice

199 Using bone marrow-derived macrophages from various TLRs and nu

200 iments were performed in naive and polarized bone marrow-derived macrophages from wild-type (WT) and

201 Experiments with LPS-activated bone marrow-derived macrophages from wild-type and GILZ

202 but complementary approaches: 1) we compared bone marrow-derived macrophages from wild-type and TIM4(

203 acellular survival of the trpB mutant within bone marrow-derived macrophages from wild-type but not I

204 hoglucose enhanced the in vitro migration of bone marrow-derived macrophages from WT but not KO mice,

205 elin phagocytosis in vitro by LPS stimulated bone-marrow-derived macrophages from IL-10-null mice fai

206 Bone-marrow-derived macrophages from mice deficient for

207 Neutrophils, but not bone marrow-derived macrophages, from cmo mice secreted

208 n of caspase-1 inhibitors or the infusion of bone marrow-derived macrophages genetically engineered t

209 NAIP1 is poorly expressed in resting mouse bone marrow-derived macrophages; however, priming with p

210 appaB reporter system in immortalized murine bone marrow-derived macrophages (iBMDM).

211 as used to examine gene regulation in murine bone marrow-derived macrophages in response to 90-mum-di

212 ammatory gene programs by Gsk3 inhibition in bone marrow-derived macrophages in response to TLR4 stim

213 by nephritic glomeruli ex vivo and cultured bone marrow-derived macrophages in vitro, suggesting add

214 y, we identify a signaling pathway in murine bone marrow-derived macrophages in which activation of T

215 osome damage was observed in infected murine bone marrow-derived macrophages, increased with time, an

216 Bone marrow-derived macrophages incubated with or withou

217 MDP treatment of bone marrow-derived macrophages incubated with P. gingiv

218 LLO was able to infect and replicate within bone marrow-derived macrophages indistinguishably from t

219 Coculture of PyMT cells with bone marrow-derived macrophages induced a TAM-like macro

220 Concordantly, LTbetaR activation on bone marrow-derived macrophages induced cross-tolerance

221 d AIM2 inflammasome activation and following bone marrow-derived macrophage infection with herpes sim

222 In primary cultures of mouse bone marrow-derived macrophages, inhibition of miR-29a,

223 Infusion of Ifngamma-stimulated, bone marrow-derived macrophages into macrophage-depleted

224 ased cathepsin activity determined in StB KO bone marrow-derived macrophages is not essential for inf

225 The function of IL-37 in transfected bone marrow-derived macrophages is nucleotide-binding ol

226 e very low levels of endogenous Cav-1 and in bone marrow-derived macrophages isolated from Cav-1(-/-)

227 s are confirmed by comparing Kir currents in bone marrow-derived macrophages isolated from Cav-1(-/-)

228 Specifically, bone marrow-derived macrophages isolated from CERK knock

229 d pro-inflammatory enzymes were monitored in bone marrow-derived macrophages isolated from myeloid ce

230 itro; the latter responses were abolished in bone marrow-derived macrophages isolated from Nlrp3(-/-)

231 Bone marrow-derived macrophages lacking GPSM3 expression

232 uced by dsDNA and other microbial ligands in bone marrow-derived macrophages lacking p205 revealed th

233 LPS-primed bone marrow-derived macrophages lacking pannexin-1 activ

234 rtin messenger RNA and protein expression in bone marrow-derived macrophages, liver, and spleen of mi

235 on of human blood monocyte-derived or murine bone marrow-derived macrophages (Mos) increases their AC

236 In SIRT3 knock-out bone marrow-derived macrophages, NLRP3 activation promot

237 s disrupted in macrophages using siRNA or in bone marrow-derived macrophages obtained from C57BL/6J-A

238 is mRNA stabilization response was absent in bone marrow-derived macrophages obtained from conditiona

239 In addition, bone marrow-derived macrophages obtained from NOD2/RIP2(

240 or stable inhibition of HMGB1 expression in bone marrow-derived macrophages or fibroblasts resulted

241 Inhibition of Syk in bone marrow-derived macrophages or reduction of Syk expr

242 to measure the mRNA and miRNA expression in bone marrow-derived macrophages over a time-series of 8

243 TLR2-induced TNF-alpha production by murine bone marrow-derived macrophages (p < 0.001).

244 We have found that in murine bone marrow-derived macrophages, PGE2 via the cAMP/prote

245 An expansion of bone marrow-derived macrophages preceded a second phase,

246 CD44(+/+) murine bone marrow-derived macrophages produced higher TNF-alph

247 Ex vivo, TLR9(-/-) bone marrow-derived macrophages produced more A20 than W

248 In bone marrow-derived macrophages, protective TLR ligands

249 otif) ligands 1, 10, and 12, which stimulate bone marrow-derived macrophage recruitment.

250 ll surface, but diminished TNF production by bone marrow-derived macrophages relative to wild type.

251 ine and paracrine proinflammatory effects on bone marrow-derived macrophages, renal endothelial cells

252 oxide addition to CB3-infected NOD.Ncf1(m1J) bone marrow-derived macrophages rescued the inflammatory

253 se-1 and -11 activation determined in StB KO bone marrow-derived macrophages resulted in enhanced IL-

254 Mechanistic analysis of superoxide-deficient bone marrow-derived macrophages revealed a marked diminu

255 Ex vivo studies using splenocytes and bone marrow-derived macrophages revealed significantly d

256 Like bone marrow-derived macrophages, RNA editing in MG leads

257 In bone marrow derived macrophages, RSG-loaded nanoparticle

258 ABCA1(+/+) bone marrow-derived macrophages secrete more IL-10 but l

259 ss proinflammatory cytokines than ABCA1(-/-) bone marrow-derived macrophages, similar to alternativel

260 lity of these cells to condition co-cultured bone marrow-derived macrophages so that the macrophages

261 mokine gene expression was examined in mouse bone marrow-derived macrophages stimulated through vario

262 f IFN-beta expression was also identified in bone marrow-derived macrophages stimulated with B. burgd

263 ases TNF, IL-6, and IL-12 secretion in mouse bone marrow-derived macrophages stimulated with LPS.

264 ions of Rapamycin in LC3B and ATG5 deficient bone marrow derived macrophages, suggesting that non-aut

265 specific for Sn, since they are taken up by bone marrow derived macrophages that are derived from wi

266 a production and pyroptosis in primed murine bone marrow-derived macrophages that is mediated by the

267 Correspondingly, mouse bone marrow-derived macrophages that lack either thrombo

268 n both RAW264.7 macrophage cells and primary bone marrow-derived macrophages, the production of IFN-b

269 In bone-marrow derived macrophages, the mutants demonstrate

270 dulated the functional phenotype ascribed to bone marrow-derived macrophages: the B6 allele promoted

271 alpha was induced by strain Wakulla in mouse bone marrow-derived macrophages; this expression was dep

272 Exposure of bone marrow-derived macrophages to eRNA resulted in a co

273 at in vitro, CTLA4Ig synergizes with NO from bone marrow-derived macrophages to inhibit T cell prolif

274 Correspondingly, exposure of bone marrow-derived macrophages to oxPAPC but not PAPC r

275 Fc receptor-mediated functions, because WKY bone marrow-derived macrophages transduced with Fcgr3-rs

276 Adoptive transfer of FcgammaRIa(-/-) bone marrow-derived macrophages transfected with Fcgamma

277 In contrast, mice that received bone marrow-derived macrophages transfected with Fcgamma

278 Mechanistically, in vitro, bone marrow-derived macrophages treated with necrotic bo

279 licited in an analogous fashion using LPS in bone marrow-derived macrophages upon inhibition of caspa

280 ressed in immune cells and is upregulated in bone marrow-derived macrophages upon stimulation with in

281 F-1alpha, acting through CXCR4, expressed on bone marrow-derived macrophages, upregulated MMP-9 and s

282 d-PGJ(2) in RAW264.7 macrophages and primary bone marrow-derived macrophages was observed.

283 Moreover, using bone marrow-derived macrophages, we demonstrated that mi

284 In additional studies using bone marrow-derived macrophages, we found that Tec and B

285 Using bone marrow-derived macrophages, we observed that alpha-

286 Using bone marrow-derived macrophages, we then observed that c

287 Bone marrow-derived macrophage were polarized to an M2 p

288 Nlrc5(-/-) splenocytes and bone marrow-derived macrophages were able to up-regulate

289 Bone marrow-derived macrophages were also used to study

290 Consequently, murine bone marrow-derived macrophages were cocultured with tro

291 kers CD 11b, F4/80 in fetal liver cells, and bone marrow-derived macrophages were dependent on functi

292 mpared with TLR2-deficient or CD14-deficient bone marrow-derived macrophages when stimulated with cur

293 Incubation of bone marrow-derived macrophages with a DeltacyaA strain

294 In vitro, treatment of wild-type bone marrow-derived macrophages with advanced glycation

295 can be reproduced in vitro by stimulation of bone marrow-derived macrophages with conditioned media f

296 In the current study, in vitro treatment of bone marrow-derived macrophages with EDPs induced M1 mac

297 The study suggests that treating mouse bone marrow-derived macrophages with KLA and ATP produce

298 d 4E-BP phosphorylation after stimulation of bone marrow-derived macrophages with lipopolysaccharide

299 The interaction of WT bone marrow-derived macrophages with renal microvascular

300 Treatment of mouse bone-marrow-derived macrophages with lipotoxic hepatocyt