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

5 Macrophage-derived AnxA1 plays a functional role in modu

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

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

8 ive immune response in mice was initiated by macrophage-derived, caspase 1-processed cytokines and re

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 ry and activation-regulated chemokine, CCL22/macrophage-derived chemokine, and CCL26/eotaxin-3), T(H)

37 axin-3, interferon gamma-induced protein 10, macrophage-derived chemokine, and macrophage inflammator

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

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

40 38, and CD69 were reduced, whereas levels of macrophage-derived chemokine, human leukocyte antigen DR

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 However, macrophage-derived cytokine production is diminished by

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

59 -1beta, and TNF-alpha) and chemokine (MCP-1, macrophage-derived cytokine, monokine-induced IFN-gamma,

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

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

62 temic type 2 immune response was mediated by macrophage-derived cytokines of the IL1 family.

63 arrival of neutrophils and their exposure to macrophage-derived cytokines.

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

65 and its efferocytic/pro-resolving action to macrophage-derived DEL-1.

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

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

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

69 Macrophage-derived endocannabinoids have been implicated

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

71 Macrophage-derived EVs accumulate in Er1(F/-) animal ser

72 communication function of inflammasomes via macrophage-derived EVs.

73 More importantly, by purifying microglia/macrophage derived exosomes in the CSF of Parkinson's di

74 ances in drug delivery using M1 macrophages, macrophage-derived exosomes, and macrophage-membrane-coa

75 Macrophage-derived extracellular vesicles (EVs) were tes

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

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

78 However, little is known about the macrophage-derived factors that promote tumor progressio

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

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

81 eloid lineage allowing the identification of macrophage-derived fibroblasts.

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

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

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

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

86 Macrophage-derived foam cells promote selective migratio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 Herein, we used bone marrow macrophages derived from adult male CCR3-proficient and

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

103 Peritoneal macrophages derived from all three genotypes overexpress

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

105 Macrophages derived from animals lacking SLAT show an el

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

107 Macrophages derived from bone marrow of MyD88-deficient

108 Macrophages derived from bone marrow produced sufficient

109 spleens, and sera were collected, along with macrophages derived from bone marrow.

110 The adult heart contains macrophages derived from both embryonic and adult bone m

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

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

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

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

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

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

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

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

119 We found that macrophages derived from donor hematopoietic precursors

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

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

122 Macrophages derived from female donors were less suscept

123 Our data show that CD11b(HI) macrophages derived from fetal liver are the major pro-i

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

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

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

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

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

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

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

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

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

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

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

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

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

137 ntrol or high-fat diet, we demonstrated that macrophages derived from male mice are intrinsically mor

138 A) receptor, GPR120, are upregulated only in macrophages derived from male mice when cultured in the

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

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

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

142 Moreover, Dgkzeta levels are increased in macrophages derived from mice with CSS or exposed to pla

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

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

145 depresses steady-state expression of LynA in macrophages derived from mice.

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

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

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

149 Dendritic cells and macrophages derived from murine bone marrow and human pe

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

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

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

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

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

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

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

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

158 Human macrophages derived from peripheral blood monocytes expr

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

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

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

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

163 2(-) and chemokine (C-C motif) receptor 2(+) macrophages derived from primitive yolk sac, recombinati

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

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

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

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

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

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

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

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

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

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

174 ges (CIMs) retain characteristics of primary macrophages derived from the bone marrow yet allow for e

175 e tested the innate immune response of mouse macrophages derived from the embryonic yolk sac and from

176 eta et al. (2019) elegantly demonstrate that macrophages derived from the heart tube contribute to lo

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

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

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

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

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

182 Macrophages derived from these recruited monocytes parti

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

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

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

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

187 Macrophages derived from volunteers homozygous for the r

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

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

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

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

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

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

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

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

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

197 compare gene expression in activated primary macrophages derived from WT and Lrrk2 knockout mice.

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

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

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

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

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

203 Using a 3-D co-culture system, we show that macrophage-derived Gas6 activates its receptor Axl and d

204 s6 in premalignant lesions in vivo, and that macrophage-derived Gas6 induces a tumor-like phenotype e

205 These studies suggest that macrophage-derived Gas6 is a critical regulator of the t

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

207 2+))-binding protein oncomodulin as a potent macrophage-derived growth factor for RGCs and other neur

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

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

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

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

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

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

214 Our data support a role for macrophage-derived IGF-1 as a key neurotrophic and sensi

215 Mechanistically, we demonstrate that macrophage-derived IGF-1 promotes sprouting neurogenesis

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

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

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

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

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

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

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

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

224 We found that interstitial macrophage-derived IL-1beta primes a subset of AT2 cells

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

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

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

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

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

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

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

232 levels of circulating Ly6C(+) monocytes and macrophage-derived inflammatory cytokines.

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

234 Macrophage-derived insulin-like growth factor-1 is a key

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

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

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

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

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

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

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

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

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

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

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

246 Macrophage-derived MMP-12 regulates elastin degradation

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

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

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

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

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

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

253 Alveolar macrophage-derived MVs were fully internalized by alveol

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 er hand, the aggressive phenotype involved a macrophage-derived Sema4D signaling engagement, which in

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

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

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

277 celerates tumor progression by stimulating a macrophage-derived "surge" of proinflammatory cytokines

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

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

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

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

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

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

284 PD-L1, caspase-8 and GSDMC are required for macrophage-derived TNFalpha-induced tumour necrosis in v

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

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

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

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

289 ic LDLr plays a critical role in the flow of macrophage-derived UC to feces, while the plasma increas

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

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

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

293 ervation in both sexes, specifically whether macrophage-derived vascular endothelial growth factor-A

294 We conclude that macrophage-derived Vegf is a key component of NMJ recove

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

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

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

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

299 to cellular reconstitution and characterizes macrophage-derived WNT signals required for this compens

300 e and core liver function genes dependent on macrophage-derived WNT/beta-catenin signaling.