ライフサイエンスコーパス: macrophage-derived

1 This confirmed that macrophage-derived 15-PGDH was responsible for catalyzin

2 y, stress markedly increased the contents of macrophage-derived [(3)H]cholesterol in the intestinal l

3 n of vascular and cardiac CB(1) receptors by macrophage-derived and platelet-derived endocannabinoids

4 responsible for the increased expression of macrophage-derived angiogenic activity.

5 To determine the role of macrophage-derived angiotensin in the development of ath

6 Macrophage-derived AnxA1 plays a functional role in modu

7 ata provide in vivo evidence suggesting that macrophage-derived apoE delays development of atheroscle

8 Macrophage-derived apoE in the vessel wall has important

9 we evaluated whether the effect produced by macrophage-derived apoE3 is related to its ability to bi

10 Macrophage-derived apolipoprotein E (apoE) in the vessel

11 Thus, macrophage-derived Arg I protects hosts against excessiv

12 The monocyte- and macrophage-derived beta-chemokines were sufficient to bl

13 HA challenge resulted in cleavage of macrophage-derived caspase1 and IL-1beta, suggesting a r

14 d by Ly6C(high)CCR2(+) inflammatory monocyte/macrophage-derived CCL11.

15 s in the liver and highlight a rationale for macrophage derived cell therapy in regenerative medicine

16 LAL and chLAL distributed to macrophages and macrophage-derived cells of various organs.

17 localize to the actin-rich phagocytic cup of macrophage-derived cells, suggesting the complex may reg

18 ts: nitrosoperoxycarbonate (ONOOCO(2)(-)), a macrophage-derived chemical mediator of inflammation, an

19 sion of macrophage inflammatory proteins and macrophage-derived chemokine (CCL22) in the synovial tis

20 p-regulation of CCR4 and one of its ligands, macrophage-derived chemokine (CCL22), and that tolerance

21 s toxin, neutralization of the CC chemokine, macrophage-derived chemokine (CCL22), or by desensitizat

22 One anti-CXCR4 factor is macrophage-derived chemokine (chemokine ligand 22, CCL22

23 Macrophage-derived chemokine (MDC) is a potent chemoattr

24 Interestingly, neutralization of macrophage-derived chemokine (MDC) with Ab caused a sign

25 nd activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC)), CD (10 proteins), a

26 We analyzed the functional role of macrophage-derived chemokine (MDC), a potent mononuclear

27 (IL)-12, tumor necrosis factor (TNF)-alpha, macrophage-derived chemokine (MDC), and C10, known to en

28 crophage colony-stimulating factor (GM-CSF), macrophage-derived chemokine (MDC), and macrophage infla

29 induce the release of CC chemokines, RANTES, macrophage-derived chemokine (MDC), macrophage inflammat

30 It is now reported that the macrophage-derived chemokine (MDC), thymus activation-re

31 arily as a mixture of three beta chemokines [macrophage-derived chemokine (MDC), thymus and activatio

32 and I-309 were induced by LPS; in addition, macrophage-derived chemokine (MDC), thymus and activatio

33 nd activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC).

34 induced protein of 10-kDa (IP-10)/CXCL10 and macrophage-derived chemokine (MDC)/CCL22 production were

35 activation-regulated chemokine (TARC)/CCL17, macrophage-derived chemokine (MDC)/CCL22, I-309/CCL1) an

36 rombin, or others like epinephrine (EPI) and macrophage-derived chemokine (MDC, CCL22).

37 te chemoattractant protein-3 (MCP-3/CCL7) or macrophage-derived chemokine (MDC/CCL22), elicited anti-

38 kine/CC chemokine ligand 17 (TARC/CCL17) and macrophage-derived chemokine (MDC/CCL22), which preferen

39 on regulated chemokine (TARC; or CCL17), and macrophage-derived chemokine (MDC; or CCL22).

40 CP-4, IL-8, interferon-inducible protein-10, macrophage-derived chemokine [MDC], and platelet factor-

41 TSLP-activated human pDCs secrete macrophage-derived chemokine CCL-22 and thymus- and acti

42 ed CD169(+)marginal zone macrophages and the macrophage-derived chemokine CCL22 to increase splenic C

43 Alcohol increased IL-10 and decreased macrophage-derived chemokine concentrations, whereas the

44 d other inflammatory diseases by suppressing macrophage-derived chemokine production via the EP4 rece

45 ial paracrine effect of endogenous PGE(2) on macrophage-derived chemokine production, we co-cultured

46 Macrophage-derived chemokine was present in all samples.

47 (thymus and activation-regulated chemokine, macrophage-derived chemokine) correlated with airway eos

48 d activation-regulated chemokine) and CCL22 (macrophage-derived chemokine).

49 ated chemokines CCL11 (eotaxin-1) and CCL22 (macrophage-derived chemokine).

50 Enhanced secretion of IL-8, macrophage-derived chemokine, and MIP-1alpha was also ob

51 L-6, IL-8, CD38, and CD69 and down-regulated macrophage-derived chemokine, human leukocyte antigen DR

52 38, and CD69 were reduced, whereas levels of macrophage-derived chemokine, human leukocyte antigen DR

53 ymus- and activation-regulated chemokine and macrophage-derived chemokine, ligands for CCR4, were mea

54 ruiting chemotactic factors, including IL-8, macrophage-derived chemokine, macrophage inflammatory pr

55 platelet aggregation induced by SDF-1alpha, macrophage-derived chemokine, or thymus and activation-r

56 A-specific IgE responses, but have defective macrophage-derived chemokine-mediated CD4+ T cell migrat

57 a) but lower levels of the anti-inflammatory macrophage-derived chemokine.

58 and activation-regulated chemokine/CCL17 and macrophage-derived chemokine/CCL22 in the lung after all

59 L, the production of the Th2-chemokines MDC (macrophage-derived chemokine/CCL22) and TARC (thymus and

60 ted chemokine; also known as CCL17) and MDC (macrophage-derived chemokine; CCL22).

61 ion regulated chemokine; TARC) and CCL22 (or macrophage-derived chemokine; MDC), in Th2-type cytokine

62 ct the entire lung and induce high levels of macrophage-derived chemokines and cytokines, which resul

63 A)R expression was increased in macrophages, macrophage-derived chemokines were reduced in response t

64 mus-expressed chemokine, eotaxin, eotaxin 2, macrophage-derived chemokines, and C10 were also induced

65 m, i.e., the inhibition of the production of macrophage-derived chemokines.

66 LA-apoA-I-/- mice had significantly reduced macrophage-derived cholesterol esterification and revers

67 ch led to a significant increase in LDL- and macrophage-derived cholesterol fecal excretion (both P <

68 absorption, which in turn promotes LDL- and macrophage-derived cholesterol fecal excretion.

69 These data identify Cat-S as a monocyte/macrophage-derived circulating PAR2 agonist and mediator

70 Taken together, our results indicate that macrophage-derived CO permits efficient and coordinated

71 VIP and PACAP inhibit the expression of the macrophage-derived CXC chemokines macrophage inflammator

72 esity is associated with accumulation of the macrophage-derived cytokine osteopontin (OPN) in adipose

73 However, macrophage-derived cytokine production is diminished by

74 anied by changes in plasma concentrations of macrophage-derived cytokine, eotaxin, IL10, TIMP1, VEGF,

75 -1beta, and TNF-alpha) and chemokine (MCP-1, macrophage-derived cytokine, monokine-induced IFN-gamma,

76 oinflammatory and anti-inflammatory monocyte/macrophage derived cytokines in serum/plasma), reduced T

77 Proinflammatory macrophage-derived cytokines may sustain and/or enhance

78 conditioning of tissue microenvironments by macrophage-derived cytokines may therefore lead to defec

79 mouse colons identified the neutrophil- and macrophage-derived damage products 3-chlorotyrosine (Cl-

80 We now show that tumor ascites macrophage-derived dendritic cells induced tumor-associa

81 Furthermore, exposure of macrophage-derived dendritic cells to apoptotic non-T ce

82 urther cytokine stimulation, and, similar to macrophages derived during EAU recovery, behave operatio

83 ion of IL-12 and IFN-gamma, and induction of macrophage-derived effector molecules like NO.

84 cates macrophage metalloelastase (MMP-12), a macrophage-derived elastinolytic protease in inflammatio

85 Macrophage-derived endocannabinoids have been implicated

86 and contained remarkably few macrophages and macrophage-derived epithelioid cells and giant cells.

87 Therefore macrophage-derived EV-packaged WNTs are essential for re

88 s, would impact on ERalpha and we found that macrophage-derived factors caused loss of ERalpha expres

89 Importantly, a combined blocking M2 macrophage-derived factors TGF-beta, VEGF and SDF-1 abol

90 If stimulated by macrophage-derived factors, however, RGCs can regenerate

91 macrophage infiltration but also exploiting macrophage-derived fibroblast growth factors (FGFs).

92 the exact relationship between ER stress and macrophage-derived foam cell formation and whether ER st

93 here they differentiate into macrophages and macrophage-derived foam cells and cause atherosclerotic

94 Macrophage-derived foam cells are thought to play a majo

95 Macrophage-derived foam cells in atherosclerotic lesions

96 Macrophage-derived foam cells in developing atherosclero

97 These data indicate that macrophage-derived foam cells in the lesion derive mainl

98 Co-culture of large SMCs with macrophage-derived foam cells induced a transition to th

99 Macrophage-derived foam cells promote selective migratio

100 consistent with multiple roles for Prx I in macrophage-derived foam cells that include functionality

101 plaque tissues of the diseased portion, only macrophage-derived foam cells were retrieved.

102 hanism of action, we treated macrophages and macrophage-derived foam cells with exogenous TIMP-2 in v

103 and diseased portions after co-culture with macrophage-derived foam cells).

104 rnatively activated alveolar macrophages and macrophage-derived foam cells, both cell types relevant

105 f ritonavir on cholesterol efflux from human macrophage-derived foam cells, which is a critical facto

106 rosclerotic lesions through the formation of macrophage-derived foam cells.

107 ic properties and biological activity to the macrophage-derived FOG(7).

108 ucive to increase in motility and control of macrophage-derived free radicals provides survival and p

109 o anti-inflammatory effects on LPS-activated macrophages (derived from THP-1 cell line) and using the

110 LPS-stimulated elicited peritoneal macrophages derived from 12/15-LO-deficient (Alox15) mic

111 extended to other TLR ligands and to primary macrophages derived from a healthy donor.

112 B6) restricts L. pneumophila growth, whereas macrophages derived from A/J mice allow >10(3)-fold bact

113 whereas the capacity for bone marrow-derived macrophages derived from A7(-/-) mice to take up oligome

114 Adoptive transfer of alveolar macrophages derived from Abx-treated mice was sufficient

115 ys than their conventional counterparts, and macrophages derived from aged germ-free mice maintain an

116 Peritoneal macrophages derived from all three genotypes overexpress

117 cal hypotheses, we performed WGBS of primary macrophages derived from an experimental rat system of g

118 Macrophages derived from animals lacking SLAT show an el

119 Complement C5-deficient (C5(-/-)) macrophages derived from B.10 congenic mice were found t

120 Macrophages derived from bone marrow of MyD88-deficient

121 Macrophages derived from bone marrow produced sufficient

122 l-like receptor 4, as each was diminished in macrophages derived from C3H/HeJ mice.

123 translocation were discerned in bone marrow macrophages derived from C57BL/6 mice, which are primary

124 The profiles classify macrophages derived from CBA/Ca mice as M1-like (pro-inf

125 LPS-stimulated cytokine responses of mature macrophages derived from CD117 and ER-MP12 bone marrow p

126 ivation of HCMV, since virus was observed in macrophages derived from CD14(+) monocytes stimulated by

127 IL-1beta release was inhibited in peritoneal macrophages derived from CD44-deficient mice, in an MH-S

128 thesis was supported by the observation that macrophages derived from chronic proliferative dermatiti

129 ed AKI, there was an early increase in renal macrophages derived from circulating inflammatory (M1) m

130 ne corresponded with an increasing number of macrophages derived from circulating monocytes (bromodeo

131 Similarly, the addition of hyaluronan to macrophages derived from cryopyrin-deficient mice increa

132 We found that macrophages derived from donor hematopoietic precursors

133 induced SOCS-1 expression in comparison with macrophages derived from Egr-1(+/+) littermate controls.

134 and inhibition of TLR4 expression is lost in macrophages derived from Enos(-/-) mice.

135 Macrophages derived from Fpr2-KO mice showed a more pote

136 tudies were performed using peripheral blood macrophages derived from healthy donors and treated with

137 cell line THP-1, and extend these results to macrophages derived from healthy individuals and HH pati

138 uring development and throughout adult life, macrophages derived from hematopoietic progenitors are s

139 Here, we describe an approach using macrophages derived from human induced pluripotent stem

140 cts of conditioned media from CCL5-activated macrophages derived from human-CCR5ki mice on PA-SMCs fr

141 VS intracellular growth by as much as 95% in macrophages derived from IFN-gamma receptor knockout (IF

142 Moreover, macrophages derived from IL-10(-/-) mice exhibit enhance

143 Bone marrow macrophages derived from IL-23p19(-/-) mice showed a slo

144 ated with iNOS inhibitor, and primary murine macrophages derived from iNOS knockout mice.

145 o 2.5 times as efficient as that observed in macrophages derived from littermate controls.

146 similar findings were observed with primary macrophages derived from lung, peritoneum, and blood but

147 ctivation of the inflammasome is enhanced in macrophages derived from lupus patients.

148 LXRbeta selectivity was confirmed using macrophages derived from LXR mutant mice.

149 r mRNAs was greatly attenuated in peritoneal macrophages derived from LXRalpha/beta null mice.

150 replication in cultures of CD4+ T cells and macrophages derived from macaques.

151 was prevented by SB 203580 and suppressed in macrophages derived from MAPKAP-K2-deficient mice.

152 utively phosphorylated on residue Thr(72) in macrophages derived from mice homozygous for the motheat

153 Using macrophages derived from mice unable to make TNF-alpha,

154 Also, in vitro studies with polarized macrophages derived from mice with macrophage-specific l

155 lysis to interrogate the transcriptome of M1 macrophages derived from mice with macrophage-specific l

156 Furthermore, we observed that macrophages derived from Mmp28(-/-) mice migrated faster

157 ually been considered to represent activated macrophages derived from monocytes entering the lesions

158 In macrophages derived from most mouse strains, the LCP is

159 The utilization of macrophages derived from MyD88-, TRIF-, Toll-like recept

160 Moreover, IL-1beta production from macrophages derived from Nlrp3(A350V) knockin mice, whic

161 Furthermore, using macrophages derived from NOS(-/-) and Phox(-/-) mice, we

162 es in EAE, an adoptive transfer of activated macrophages derived from Notch1(fl/fl) x Mx1cre(+/-) (No

163 production of proinflammatory cytokines from macrophages derived from overweight/obese subjects with

164 Ex vivo studies indicate that alveolar macrophages derived from overweight/obese subjects with

165 nd treated with TNF and using synovial fluid macrophages derived from patients with RA.

166 It is unknown to what extent macrophages derived from peripheral blood adopt the phen

167 Human macrophages derived from peripheral blood monocytes expr

168 ethods were applied to NAD biosynthesized by macrophages derived from peripheral blood monocytes.

169 The six mutants also were tested in macrophages derived from peripheral blood mononuclear ce

170 In contrast, macrophages derived from premorbid rats do not exhibit a

171 Here we have used macrophages derived from primary explants of bone marrow

172 on using a clinical isolate of HCMV (TR) and macrophages derived from primary human monocytes.

173 monary epithelial cells (A549) as well as in macrophages derived from primary human peripheral blood

174 2(-) and chemokine (C-C motif) receptor 2(+) macrophages derived from primitive yolk sac, recombinati

175 ed from mouse bone marrow and synovial fluid macrophages derived from RA patients were also tested fo

176 y of Rac2 to Rac1 (92% amino acid identity), macrophages derived from Rac2-/- mice, which continue to

177 high-throughput sequencing of RNA in primary macrophages derived from rodents and humans, we establis

178 essing cells were MCMV-infected RPE cells or macrophages derived from RPE cells.

179 -induced events were compared in bone marrow macrophages derived from SHIP(+/+) and SHIP(-/-) mice.

180 CR3-mediated phagocytosis in macrophages derived from SHIP(-/-) mice was up to 2.5 ti

181 o this end, we used immortalized bone marrow macrophages derived from SHP-1-deficient motheaten mice

182 nduced TNF and IL-1 production are normal in macrophages derived from spin mice.

183 In addition, macrophages derived from SR-A-/- mice were substantially

184 olded protein response (UPR) is activated in macrophages derived from the bone marrow of HLA-B27 tran

185 Consistently, macrophages derived from the bone marrow of Sirt6(-/-) m

186 e lipophilic antioxidant drug, probucol, and macrophages derived from the human monocyte cell line, T

187 nd multimer formation also occurred in human macrophages derived from the monocyte cell line THP-1.

188 induce an IL-1beta response in primary human macrophages derived from the same blood donors as the mo

189 ppeared normal, but cultured fibroblasts and macrophages derived from them exhibited increased stabil

190 In bone marrow-derived macrophages derived from these mice LTbetaR-induced cros

191 itro studies with bone marrow and peritoneal macrophages derived from these mice showed that treatmen

192 Macrophages derived from these recruited monocytes parti

193 It is still not clear if macrophages derived from these two populations differ in

194 LPS-activated peritoneal macrophages derived from TIA-1-/- mice produced signific

195 In this study, we have utilized macrophages derived from TRAF6 knock-out mice and myeloi

196 IL-10 expressed by macrophages derived from transduced BMCs inhibited ather

197 Macrophages derived from volunteers homozygous for the r

198 tion by, and TNF messenger RNA expression of macrophages derived from volunteers with known TNF (-308

199 In this report, we used macrophages derived from wild type (wt) mice and from mi

200 Using macrophages derived from wild type and Cd36(-/-) mice to

201 In this study, we analyzed the responses of macrophages derived from wild-type (IFN-beta(+/+)) mice

202 Peritoneal macrophages derived from wild-type and TIA-1-/- mice wer

203 Microarray analysis with macrophages derived from wild-type and TLR4-deficient mi

204 lar processing of CpG-siRNA, we used primary macrophages derived from wild-type and Tlr9-deficient mi

205 t of B7-1 and B7-2 expression on B cells and macrophages derived from wild-type BALB/c mice after in

206 In this report, by using macrophages derived from wild-type mice (having both rec

207 dysregulated cytokine production compared to macrophages derived from wild-type mice.

208 igration in response to sFasL compared to M1 macrophages derived from young animals.

209 nt differences between the responsiveness of macrophages derived from younger donors and that from ol

210 nhanced the engulfment of necrotic debris by macrophages derived from zymosan-induced peritonitis, M1

211 espective global gene expression profiles of macrophages, derived from human monocytes by GM-CSF or M

212 ferences between the respective profiles for macrophages, derived from murine bone marrow cells by ea

213 SAP triggers a potent, complement-dependent, macrophage-derived giant cell reaction that swiftly remo

214 2+))-binding protein oncomodulin as a potent macrophage-derived growth factor for RGCs and other neur

215 ts of inflammation were shown to require the macrophage-derived growth factor Oncomodulin (Ocm).

216 monstrate that human monocytes, by releasing macrophage-derived HB-EGF, enhance DDR in neighboring ce

217 cate that strategies to reduce activation of macrophage derived HIF-1alpha may be used as a target to

218 These combined data demonstrate that macrophage-derived HL significantly contributes to early

219 with macrophages they did respond to LPS via macrophage-derived IFN-beta; (2) macrophages required ty

220 ediated by an extremely low concentration of macrophage-derived IFNbeta.

221 ugh the induction of astrocyte and microglia-macrophage-derived IGF-1.

222 eation; and 4) increasing levels of infected macrophage derived IL-10 promotes bacterial persistence

223 In response to Ad, macrophage-derived IL-1 alpha triggered IL-1RI-dependent

224 ing reinforced an autocrine feedback loop of macrophage-derived IL-10 and this synergized with inhibi

225 We previously demonstrated that macrophage-derived IL-10 could contribute to disease exa

226 We found macrophage-derived IL-10 dispensable for gut homeostasis

227 Further, following mucosal injury, macrophage-derived IL-10 resulted in epithelial cAMP res

228 ine effect of IFN-gamma on the production of macrophage-derived IL-10 with lipoprotein as a stimulant

229 h a cytokine-signaling network that involves macrophage-derived IL-1beta and fibroblast-derived CXCR2

230 both peripheral blood monocyte- and uterine macrophage-derived IL-1beta induce secretion of antimicr

231 Macrophage-derived IL-1beta production was induced by HF

232 culture experiments identified the effect of macrophage-derived IL-1beta to promote IL-22 and IL-17 p

233 in the intestine by inhibiting expression of macrophage-derived IL-23.

234 A novel role for the macrophage-derived immunoregulatory cytokine IL-27 was i

235 MMP-12 is solely macrophage derived in this model, being expressed by tum

236 adipose tissue and muscle, and it suppresses macrophage-derived inflammation.

237 However, most of the analyzed macrophage-derived inflammatory and regulatory cytokines

238 ity was elevated in recurrent GBM, driven by macrophage-derived insulin-like growth factor-1 (IGF-1)

239 Macrophage-derived insulin-like growth factor-I (IGF-I)

240 s) in a mouse hepatitis virus (MHV)-infected macrophage-derived J774.1 cell line showed activation of

241 by the abnormal clonal proliferation of the macrophage-derived Langerhans cell.

242 functioning as anti-inflammatory cells, and macrophage-derived matrix metalloproteinases regulate fi

243 Wound macrophage-derived MFG-E8 was recognized as a critical d

244 Here, we characterized macrophage-derived microvesicles and explored their role

245 F) circulates in plasma, largely on monocyte/macrophage-derived microvesicles that can bind activated

246 We found that RNA molecules contained in the macrophage-derived microvesicles were transported to tar

247 We also identified the miRNA content of the macrophage-derived microvesicles.

248 ng antimelanoma immune responses reveal that macrophage-derived MIF participates in macrophage altern

249 lymerase chain reaction array, we found that macrophage-derived miR-342-5p and miR-155 are selectivel

250 Macrophage-derived miR-342-5p promotes atherosclerosis a

251 Macrophage-derived MMP-12 regulates elastin degradation

252 These findings suggest that macrophage-derived MMP-9 and mesenchymal cell MMP-2 are

253 Although monocyte- and macrophage-derived molecules are known to promote extrac

254 mouse model of AAA, we now demonstrate that macrophage-derived MT1-MMP plays a dominant role in dise

255 network during AAA formation is dependent on macrophage-derived MT1-MMP, which unexpectedly serves as

256 d triggers the rapid clearance of amyloid by macrophage-derived multinucleated giant cells.

257 litates hydroxyapatite nucleation within the macrophage-derived MV membrane.

258 We tested the hypothesis that macrophage-derived MVs contribute directly to microcalci

259 Alveolar macrophage-derived MVs were fully internalized by alveol

260 neutrophil-specific CXC chemokines (alveolar macrophage-derived neutrophil chemotactic factor [AMCF]-

261 pes demonstrated that neural progenitor- and macrophage-derived NRP1 were dispensable, whereas endoth

262 We demonstrate that macrophage-derived ODC is a critical regulator of M1 mac

263 on to its role in inducing IL-22 production, macrophage-derived or CD103(-) CD11b(+) DC-derived IL-23

264 s-stimulated macrophages induced bone marrow macrophage-derived osteoclastogenesis.

265 Dihydroethidium (DHE) was used to detect macrophage-derived oxidants generated during phagocytosi

266 ctly affect IL-2 production by Thp cells via macrophage-derived PPARgamma ligands.

267 F4/80(+)CD11b(+)CD11c(dull/-) macrophage-derived proinflammatory cytokines significant

268 We recently identified a family of macrophage-derived proresolving and tissue regenerative

269 found to mediate pro-inflammatory effects of macrophage-derived prostaglandin E2 (PGE2) on Th17 cells

270 acrophages in inflammation, the functions of macrophage-derived proteinases are typically relegated t

271 We proposed that macrophage-derived proteinases may contribute to the ant

272 trix metalloproteinases (MMPs), particularly macrophage-derived proteinases, in COPD pathogenesis.

273 After gel-filtration chromatography, macrophage-derived proteins > or =30 kDa were found to b

274 ivation and increased expression of monocyte/macrophage-derived proteins fostering wound healing.

275 sent in the vitreous, acting in concert with macrophage-derived proteins, stimulates mature rat RGCs

276 cAMP-dependent and was augmented further by macrophage-derived proteins.

277 in mouse primary astrocytes, microglia, and macrophage-derived RAW264.7 cells induced by interferon-

278 fine for the first time, to our knowledge, a macrophage-derived regulator of placental growth during

279 baseline, demonstrating a regulatory role of macrophage-derived ROS in autoimmunity.

280 study points to the utility of monocyte- and macrophage-derived sCD163 as a marker of HIV activity th

281 ferritin, we hypothesize that ferritin is a macrophage-derived signal that promotes oligodendrogenes

282 Here, we showed that macrophage-derived soluble factors induce canonical Wnt

283 ssion of IgA class switching in B cells by a macrophage-derived sterol in response to TLR activation

284 nhancement of apoptotic neutrophil uptake by macrophage-derived TG2 restrains gout-like neutrophilic

285 -permissive environment by identification of macrophage-derived therapeutic molecules may therefore a

286 invasion, these results suggest that excess macrophage-derived TNF-alpha augments expression of MMP-

287 ed with NK cell-derived IFN-gamma and either macrophage-derived TNF-alpha or IL-1beta synergistically

288 iting TNF in pathologies primarily driven by macrophage-derived TNF.

289 of sepsis support the central role played by macrophage-derived TNFalpha in sepsis.

290 ls produced an angiogenic response driven by macrophage-derived TNFalpha.

291 The potential of macrophage-derived transforming growth factor beta1 to p

292 subjects with dAIH, indicating that monocyte/macrophage-derived triggers might play a central role in

293 Macrophage-derived tumor necrosis factor (TNF)-alpha has

294 We tested whether macrophage-derived uPA plays essential roles in macropha

295 ental role in macrophage chemotaxis and that macrophage-derived uPA promotes efficient muscle regener

296 al (ECs) and/or perivascular cells (PVCs) (a macrophage-derived vascular cell type) is implicated in

297 The switch of macrophage-derived VEGF-A during the early stage of tiss

298 repair phases, and the complementary role of macrophage-derived VEGF-A in coordinating effective tiss

299 Here, we analyse the role of macrophage-derived WNT in intestinal repair in mice by i

300 Previously, it was shown that macrophage-derived Wnt molecules promote vascular remode