ライフサイエンスコーパス: scavenger receptor

1 DC-ASGPR), a lectinlike receptor, is a known scavenger receptor.

2 es with canonical GPCRs in its function as a scavenger receptor.

3 ds, with some receptors being categorized as scavenger receptors.

4 ribed in this report only refer to mammalian scavenger receptors.

5 CD16 can cross-block MDALDL binding to other scavenger receptors.

6 n damage via overactivation of innate immune scavenger receptors.

7 ing endocytotic uptake, membrane-fusion, and scavenger receptors.

8 issue macrophages expressing CD163 and CD204 scavenger receptors.

9 equence, they express a unique repertoire of scavenger receptors.

10 nd higher plasma levels of the soluble CD163 scavenger receptor (0.84 vs .59 ug/mL, P = .003) than co

11 collagenous structure (MARCO) and macrophage scavenger receptor 1 (MSR1).

12 ugh K63 polyubiquitylation of the macrophage scavenger receptor 1 (MSR1).

13 express, together with Vgamma4 and CCR6, the scavenger receptor 2 and are mainly restricted to innate

14 r levels of Toll-like receptor 2 (TLR-2) and scavenger receptor A (SR-A) than those on CD16(+) and BD

15 ges express the pattern recognition receptor scavenger receptor A (SR-A).

16 age proliferation through the involvement of scavenger receptor A (SR-A).

17 of the major macrophage scavenger receptor, scavenger receptor A (SRA), in the immune response again

18 Because the receptors scavenger receptor A (SRA), macrophage receptor with col

19 We show here that scavenger receptor A (SRA/CD204), a pattern recognition

20 gnificantly increased the expression of SRA (scavenger receptor A), modified low-density lipoprotein

21 Overall, the levels of CD68, macrophage scavenger receptor A, CD64, CD32 and the number of macro

22 ptor Iba-1, lysosome marker CD68, macrophage scavenger receptor A, Fcgamma receptors I (CD64) and II

23 a42 load correlated directly with macrophage scavenger receptor A-positive clusters and inversely wit

24 r A, CD64, CD32 and the number of macrophage scavenger receptor A-positive plaque-related clusters we

25 ells, required the uptake of alphaGalCer via scavenger receptor A.

26 Class A scavenger receptors, scavenger receptor-A (SR-A) and macrophage receptor with

27 f mannose receptor, and absent expression of scavenger receptor-A (SR-A).

28 We show that serum levels of soluble scavenger receptor-A (sSR-A) are increased in patients w

29 Studies with scavenger receptor-A1 null mice reveal reduced IL-13 gen

30 Scavenger receptor A5 (SCARA5) is a member of the class

31 Collectively, our findings suggest scavenger receptor activity of CD16 may, in part, contri

32 This led to a hypothesis that CD16 may have scavenger receptor activity.

33 Allosamidin decreased scavenger receptor AI, CD36, ABCA1, and ABCG1 expression

34 te that expression of C-type lectin receptor scavenger receptor-AI (SR-AI) is crucial for promoting M

35 Recent studies showed loss of CD36 or scavenger receptor-AI/II (SR-A) does not ameliorate athe

36 Macrophages from scavenger receptor-AI/II (SR-A)-deficient mice cleared C

37 ched a consensus regarding the definition of scavenger receptors and a proposed scavenger receptor no

38 Health to help develop a clear definition of scavenger receptors and a standardized nomenclature base

39 e, which supports their targeting of class A scavenger receptors and endocytosis via a lipid-raft-dep

40 these results establish a novel link between scavenger receptors and MyD88 that together function as

41 r peripheral blood cells takes place through scavenger receptors and over time causes disruption in c

42 ipocyte glucose uptake and expression of AGE scavenger receptors and Rho signaling mediators, includi

43 rsomes, which are internalized by binding to scavenger receptors and subsequently escape the early en

44 19)Apoe(-/-) mice expressed higher levels of scavenger receptors and took up more modified lipoprotei

45 anti-Marco-neutralizing Abs and the class A scavenger receptor antagonist polyinosinic acid inhibite

46 Macrophage scavenger receptors appear to play a major role in the c

47 hereas silencing ATP-binding cassette G-1 or scavenger receptor B-1 abrogated the effect of HDL but n

48 cassette A-1, ATP-binding cassette G-1, and scavenger receptor B-1.

49 oprotein lipase and hepatic uptake of HDL by scavenger receptor B-I are the driving forces of HDL-cho

50 overview of SLU mediated by the HDL receptor scavenger receptor B-type I (SR-BI), and highlights seve

51 s due to a splice donor site mutation in the scavenger receptor B1 (SCARB1; also known as SR-B1) gene

52 We identify scavenger receptor B1 (SR-B1) as an EsxA receptor on air

53 ee HCV and cell receptors that include CD81, scavenger receptor B1 (SR-B1), claudin-1 (CLDN1), and oc

54 Hepatitis C virus (HCV) entry involves scavenger receptor B1 (SRB1).

55 81, while HEPC98 primarily blocks binding to scavenger receptor B1 and heparan sulfate.

56 les from several classes of genes coding for scavenger receptors, beta-carotene oxygenases, and ketol

57 Recent studies revealed that scavenger receptor BI (SR-BI or Scarb1) plays a critical

58 Scavenger receptor BI (SR-BI) is the major receptor for

59 ells and live or dead Listeria monocytogenes scavenger receptor BI (SR-BI), an anti-atherogenic lipid

60 nct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR-BI), respectively, to infect h

61 CV entry by lipid transfer receptors such as scavenger receptor BI (SR-BI).

62 ation between neutralization sensitivity and scavenger receptor BI dependency during viral entry.

63 This regulation appears tightly linked with scavenger receptor BI dependency, suggesting a role of t

64 igation and puncture; using adrenal-specific scavenger receptor BI mice as an inducible corticosteroi

65 Using scavenger receptor BI mice as the first relative adrenal

66 vival in cecal ligation and puncture-treated scavenger receptor BI mice but causes more septic death

67 Scavenger receptor BI null and adrenal-specific scavenge

68 venger receptor BI null and adrenal-specific scavenger receptor BI null mice.

69 ry monocyte subtype and partially via SR-BI (scavenger receptor BI).

70 y antibodies against the entry factors CD81, scavenger receptor BI, and claudin-1; by interferon; and

71 , through direct targeting and repression of scavenger receptor BI, and to inhibit cholesterol biosyn

72 The class B scavenger receptors BI (SR-BI) and BII (SR-BII) are high

73 PIP2 on HDL is taken up by target cells in a scavenger receptor-BI-dependent manner.

74 here it can be taken up via the HDL receptor scavenger receptor-BI.

75 reactive protein, soluble CD163, and soluble scavenger receptor CD14 were significantly higher during

76 lication of the gene encoding the hemoglobin scavenger receptor CD163 in late evolution.

77 Scavenger receptor CD163 is exclusively expressed on mon

78 nism of detoxification of Hb by the monocyte scavenger receptor CD163, independent of the well-known

79 sed on reciprocal expression of CD14 and the scavenger receptor CD163.

80 as a high binding affinity to the macrophage scavenger receptor CD36 and participates in CD36-mediate

81 to increased foam cell formation by inducing scavenger receptor CD36 and SR-A1 expression.

82 and elevated transcript levels for the lipid scavenger receptor CD36 and the nuclear receptor PPARgam

83 uptake of triacylglycerol substrates via the scavenger receptor CD36 and their subsequent lipolysis b

84 Scavenger receptor CD36 contributes significantly to lip

85 ocytosis was mediated by the upregulation of scavenger receptor CD36 expression.

86 ion of unesterified fatty acid (FA) with the scavenger receptor CD36 has been actively researched, wi

87 The scavenger receptor CD36 is a critical factor initiating

88 Here, we tested the hypothesis that scavenger receptor CD36 is an effector of EP2-regulated

89 The scavenger receptor CD36 is injurious in acute experiment

90 We show that preformed scavenger receptor CD36 is redistributed to the cell mem

91 pidemic conditions is enhanced when platelet scavenger receptor CD36 recognizes oxidized lipids in ox

92 Antibody to the scavenger receptor CD36 reduced the internalization of S

93 TAMs expressed elevated levels of the scavenger receptor CD36, accumulated lipids, and used fa

94 Fyn kinase, in conjunction with the class B scavenger receptor CD36, regulates the microglial uptake

95 d to preexisting compartments containing the scavenger receptor CD36, which then become VCCs.

96 (15-LO), a lipid-peroxidating enzyme and the scavenger receptor CD36.

97 ch as the tetraspanins CD63 and CD81 and the scavenger receptor CD36.

98 iated ROS production is due to activation of scavenger receptor CD36.

99 n vitro was dependent on the presence of the scavenger receptors CD36 and MSR1.

100 phages exhibited increased expression of the scavenger receptors CD36 and SCARA1 (encoded by MSR1), w

101 The uptake of Pyr-OVA was reduced in scavenger receptor class A (SR-A)-deficient BMDCs, but n

102 n of surface scavenger receptors (i.e. CD36, scavenger receptor class A member 1, triggering receptor

103 marker Ki-67 and the reactive oxygen species scavenger receptor class A member 3.

104 Recently, we have identified scavenger receptor class A member I (SR-AI) as a recepto

105 O system transferase, coagulation factor XI, scavenger receptor class A5 (SCARA5), and tumor necrosis

106 inding cassette A1, ATP-binding cassette G1, scavenger receptor class B family member (CD36), scaveng

107 t genes for its biliary excretion, including scavenger receptor class B member 1 (Scarb1) and ABC sub

108 arsenic exposure, the hepatic expression of scavenger receptor class B member 1 (Scarb1), which is i

109 LDL receptor (LDLR), the very LDLR, and the scavenger receptor class B member 1 in hepatocytes; knoc

110 as SDC1, as well as LDLR, very LDLR, and the scavenger receptor class B member 1, which promote HCV e

111 Scavenger receptor class B member 2 (SCARB2) is the majo

112 Tetraspanin CD81, scavenger receptor class B member I, and the tight-junct

113 Scavenger receptor class B type 1 (SCARB1) plays an impo

114 By binding with scavenger receptor class B type 1 (SCARB1), reconstitute

115 herapeutic effect of eHNP-A1-CD15-LDE225 via scavenger receptor class B type 1 (SR-B1) and CD15 on br

116 Here we show in mice that scavenger receptor class B type 1 (SR-B1) in endothelial

117 serum adiponectin; ii) marked inhibition of scavenger receptor class B type 1 glycosylation, its pla

118 Because scavenger receptor class B type 1 is the cholesterol upt

119 l modification, trafficking, and function of scavenger receptor class B type 1 may account for alcoho

120 major HDL-dependent m-RCT pathway via SR-BI (scavenger receptor class B type 1) to the liver, a CETP-

121 SR-B1 (scavenger receptor class B type 1), encoded by the gene

122 t four cellular factors, including CD81, the scavenger receptor class B type I (SCARB-1), occludin (O

123 s to the host cell through interactions with scavenger receptor class B type I (SR-BI) and CD81, and

124 transcriptionally regulate the expression of scavenger receptor class B type I (SR-BI) and SR-BI-link

125 l nine variants showed reduced dependence on scavenger receptor class B type I (SR-BI) for infection.

126 tween wild-type mice and mice overexpressing scavenger receptor class B type I (SR-BI) in the intesti

127 Lentiviral short hairpin RNA knockdown of scavenger receptor class B type I (SR-BI) in vitro and S

128 antibodies (mAbs) against the HCV coreceptor scavenger receptor class B type I (SR-BI) inhibit HCV in

129 Scavenger receptor class B type I (SR-BI) is a high-dens

130 te subfamily G member 5 and 8 (ABCG5/G8) and scavenger receptor class B type I (SR-BI) to sterol meta

131 These factors include scavenger receptor class B type I (SR-BI), CD81, claudin

132 enerated a human monoclonal antibody against scavenger receptor class B type I (SR-BI), monoclonal an

133 Scavenger receptor class B type I (SR-BI)-deficient mice

134 achment factors and the coreceptors CD81 and scavenger receptor class B type I (SR-BI).

135 was critically dependent on the presence of scavenger receptor class B type I and ATP Binding Casset

136 ot J6/JFH1(DeltaHVR1/D431G) while decreasing scavenger receptor class B type I coreceptor dependency.

137 s increased envelope breathing and decreased scavenger receptor class B type I HCV coreceptor depende

138 udy points to the involvement of the hepatic scavenger receptor class B type I in the uptake of both

139 audin-1, but not antibodies directed against scavenger receptor class B type I or occludin, could als

140 y with time kinetics parallel to anti-SR-BI (scavenger receptor class B type I), but significantly ea

141 erator-activated-gamma pathway and increased scavenger receptor class B type I- and CD36-mediated bas

142 t is resistant to an entry inhibitor against scavenger receptor class B type I.

143 but not in cells treated with inhibitors of scavenger receptor class B, galectin-3, or blocking anti

144 05.12 +/- 1.13 nm) conjugated to recombinant scavenger receptor class B, member 2 (SCARB2) protein wi

145 n (HDL) metabolism is facilitated in part by scavenger receptor class B, type 1 (SR-B1) that mediates

146 )-cholesteryl ester (CE) uptake, mediated by scavenger receptor class B, type 1 (SR-B1).

147 In enterocytes, scavenger receptor class B, type 1 (SR-B1, encoded by SC

148 phase and facilitated diffusion mediated by scavenger receptor class B, type 1 (SR-BI).

149 Scavenger receptor class B, type I (SR-BI) binds HDL and

150 erse roles of the high-affinity HDL receptor scavenger receptor class B, type I (SR-BI) in the modula

151 The high-density lipoprotein (HDL) receptor scavenger receptor class B, type I (SR-BI), binds HDL an

152 calization, and function of the HDL receptor scavenger receptor class B, type I (SR-BI), in hepatocyt

153 the high-density lipoprotein (HDL) receptor scavenger receptor class B, type I (SR-BI), which is imp

154 mozygous null mutations in the HDL receptor (scavenger receptor class B, type I, or SR-BI) and apolip

155 enger receptor class B family member (CD36), scavenger receptor class B1, and wound healing pathways

156 escribe for the first time the expression of scavenger receptor class F, member 1 (SCARF-1) on hepati

157 The scavenger receptor, class B type 1 (SR-B1), is a multili

158 The HDL receptor scavenger receptor, class B type I (SR-BI) controls the

159 es are captured from the blood stream by the scavenger receptor, class B, type I (SR-BI), the so-call

160 Scavenger receptors clear pathogens, transport lipid, an

161 idal endothelial cells (LSECs), hepatocytes, scavenger receptors, clotting factors, and immunoglobuli

162 The scavenger receptor cluster of differentiation (CD)36 pro

163 nserved endocytic machinery, composed of the scavenger receptor complex Cubilin/Amnionless and Dab2,

164 Scavenger receptors constitute a large family of protein

165 Four proteins (Scavenger receptor cysteine rich type 1 protein M130, Fa

166 163 has previously been shown to involve the scavenger receptor cysteine-rich (SRCR) domain 3.

167 Furthermore, the substitution of CD163 scavenger receptor cysteine-rich (SRCR) domain 5 with a

168 al region, which is composed of 4 repeats of scavenger receptor cysteine-rich (SRCR) domains in LOX-l

169 ple bacterial species involves its conserved Scavenger Receptor Cysteine-Rich (SRCR) domains, localiz

170 WC1 coreceptors are scavenger receptor cysteine-rich (SRCR) family members,

171 Surprisingly, Loxl3 N-terminal scavenger receptor cysteine-rich (SRCR) repeats, rather

172 ssed on gammadelta T cells and belong to the scavenger receptor cysteine-rich (SRCR) superfamily.

173 hloxl2 encodes four N-terminal scavenger receptor cysteine-rich domains and the highly

174 intestinal SALSA was more enriched with the scavenger receptor cysteine-rich domains.

175 nerating a 65-kDa form lacking the first two scavenger receptor cysteine-rich domains.

176 Gp340 is a member of the scavenger receptor cysteine-rich family of innate immune

177 CD163-L1 belongs to the group B scavenger receptor cysteine-rich family of proteins, whe

178 array containing 13 members, are part of the scavenger receptor cysteine-rich family.

179 s and is predicted to result in between 7-20 scavenger-receptor cysteine-rich (SRCR) domains within e

180 2(Y689F) required the presence of the fourth scavenger receptor-cysteine-rich (SRCR) domain of LOXL2,

181 Scavenger receptor deficiency markedly impaired the recr

182 clearance mechanism that requires the glial scavenger receptor Draper and downstream phagocytic engu

183 nsmission across synapses requires the glial scavenger receptor Draper and involves a transient visit

184 /CXCR7 range from those of a strictly silent scavenger receptor eventually modulating CXCR4 signaling

185 Stabilin-1, a scavenger receptor expressed by macrophages, has the pot

186 CD163 is a scavenger receptor expressed on innate immune cell popul

187 PAN-induced glomerular injury, reducing CD36 scavenger receptor expression and oxidative stress.

188 Fifteen experts in the scavenger receptor field attended the workshop and, afte

189 mokine receptor CXCR7 (ACKR3) functions as a scavenger receptor for chemokine CXCL12, a molecule that

190 CXCR7 thus appears to function as a scavenger receptor for CXCL12 on MZ B cells.

191 ry phenotype express high levels of CD163, a scavenger receptor for the hemoglobin-haptoglobin comple

192 y lipoprotein receptor-1 (LOX-1), one of the scavenger receptors for oxidized low-density lipoprotein

193 valuable model for investigating the role of scavenger receptor function and the immune system in the

194 rium Lactococcus lactis confers adherence to scavenger receptor gp340, human vaginal epithelium, and

195 gglutinin that is comprised primarily of the scavenger receptor gp340.

196 sociated with enhanced expression of surface scavenger receptors (i.e. CD36, scavenger receptor class

197 via pattern recognition receptors, including scavenger receptors, IgM natural antibodies and compleme

198 The deficiency of scavenger receptors impairs the formation of CNV and imm

199 Our findings suggest a potential role for scavenger receptors in contributing to CNV formation and

200 s study is to examine the role of macrophage scavenger receptors in immune cell recruitment and the f

201 ith emerging evidence for the involvement of scavenger receptors in innate immunity, this study addre

202 onic inflammatory liver disease, the role of scavenger receptors in regulating liver inflammation rem

203 results reveal an important contribution of scavenger receptors in the selection of lipids for CD1d

204 we investigated the role of CD36, a class-B scavenger receptor, in this process.

205 direct recognition of the target by multiple scavenger receptors including P2X7 on the phagocyte surf

206 This was supported by scavenger receptor-induced local increases in membrane c

207 CD36 is a scavenger receptor involved in fatty acid metabolism, in

208 eting is often compromised by recognition by scavenger receptors involved in clearance.

209 ar amyloid deposition, and suggest that this scavenger receptor is a putative therapeutic target for

210 CD163, a monocyte- and macrophage-specific scavenger receptor, is shed as soluble CD163 (sCD163) du

211 id destruction in the liver via Kupffer cell scavenger receptors, keeping them available for adaptive

212 uced CNV volumes were found in the eyes from scavenger receptor knockout mice compared with wild-type

213 ptors for S. pneumoniae in the lung, we used scavenger receptor knockout mice to study the roles of t

214 The class A scavenger receptor known as MARCO (macrophage receptor w

215 Increased activity of the multi-ligand scavenger receptor Lectin-like Oxidized LDL Receptor-1 (

216 whose ligand repertoire includes the typical scavenger receptor ligands, whole bacteria, and purified

217 ar matrix and its endocytic clearance by the scavenger receptor low density lipoprotein receptor-rela

218 blocking its interaction with the endocytic scavenger receptor, low-density lipoprotein receptor-rel

219 The scavenger receptor LOX-1 found in endothelial cells bind

220 One of the receptors expressed by MZM is scavenger receptor macrophage receptor with collagenous

221 The scavenger receptor macrophage receptor with collagenous

222 ophagy, augmented phagocytosis, and enhanced scavenger receptor (macrophage receptor with collagenous

223 The scavenger receptor, macrophage receptor with collagenous

224 Here we demonstrate that a cell surface scavenger receptor, macrophage receptor with collagenous

225 ages had increased expression of two class A scavenger receptors: macrophage receptor with collagenou

226 There are currently eight classes of scavenger receptors, many of which have multiple names,

227 by marginal zone macrophages expressing the scavenger receptor MARCO and are mediated in part by the

228 agocytosis have been reported, including the scavenger receptor MARCO and integrin alpha3beta1.

229 efines tumor-derived IL37 and the macrophage scavenger receptor MARCO as potential therapeutic target

230 eatment by injecting antibodies specific for scavenger receptor MARCO, which is expressed on a specif

231 proaches revealed selective induction of the scavenger receptor MARCO, which was required for enhance

232 ginally identified in the SRCR domain of the scavenger receptor MARCO.

233 l MPhi (SPM) that expressed CD138(+) and the scavenger receptor Marco.

234 vated receptor gamma-dependent regulation of scavenger receptor-mediated cholesterol uptake and ABCA1

235 Innate mechanisms include scavenger receptor-mediated uptake of Ag-SP by host APCs

236 te preserved absolute expression of the main scavenger receptors, MEGALIN and CUBILIN.

237 of genes involved in cholesterol metabolism, scavenger receptors, MERTK, and complement.

238 The class A macrophage scavenger receptor Msr1 (SR-A, CD204) has been reported

239 nition of scavenger receptors and a proposed scavenger receptor nomenclature.

240 r advanced glycation endproducts (RAGE) is a scavenger receptor of the Ig family that binds damage-as

241 ptor with collagenous structure (MARCO) is a scavenger receptor on the cell surface of macrophages th

242 ompetitively block oxidized lipid uptake via scavenger receptors on macrophages; second, for sustaine

243 ion via direct effects on ECM and by binding scavenger receptors on multiple cell types and signaling

244 monstrate for the first time that intestinal scavenger receptors participate in the absorption of die

245 ate 'pattern recognition receptors', such as scavenger receptors present on dendritic cells and monoc

246 athway in fibrogenesis in which a macrophage scavenger receptor protects against organ fibrosis by re

247 hanism that may be shared by SR-BI and CD36, scavenger receptor proteins highly homologous to LIMP-2.

248 Notably, inhibition of hDia1, but not scavenger receptors RAGE or CD36, attenuated AGE-ECM inh

249 eceptor that binds CXCL12 and functions as a scavenger receptor, regulating levels of CXCL12 availabl

250 Scavenger receptors represent an important class of patt

251 ty lipoprotein (ox-LDL) up-regulates CD36, a scavenger receptor responsible for macrophage uptake of

252 nsport (ABCA1, ABCG1 and 27-hydroxylase) and scavenger receptors, responsible for uptake of modified

253 increased the surface expression of the CD36 scavenger receptor, resulting in an increase in phagocyt

254 , macrophages and endothelial cells used the scavenger receptor SCARF1 to recognize and engulf apopto

255 The role of the major macrophage scavenger receptor, scavenger receptor A (SRA), in the i

256 Class A scavenger receptors, scavenger receptor-A (SR-A) and mac

257 markers (CD206 (mannose receptor) and CD163 (scavenger receptor)), secretion of IL-10, and TGFbeta an

258 complement factor C3, and instead relied on scavenger receptor SR-A6 (MARCO).

259 erence in phagocytosis was due to an altered scavenger receptor (SR) profile.

260 For transgenic mice generation, the human scavenger receptor (SR-A) promoter/enhancer was used to

261 le EGF-like domains 10 (Megf10) is a class F scavenger receptor (SR-F3) expressed on astrocytes and m

262 Although the class A scavenger receptors (SR-As) mediate dsRNA entry, it is u

263 Class B scavenger receptors (SR-B) are lipoprotein receptors tha

264 in A-I mimetics are known to bind to class B scavenger receptors (SR-Bs), SR-BI, SR-BII, and CD36, re

265 ocked uptake of viruses via the Kupffer cell scavenger receptor SRA-II.

266 ATP transporters, ABCA1, and ABCG1, and the scavenger receptor, SRB1.

267 Scavenger receptors (SRs) are a large family of cell-sur

268 Recently, we demonstrated that deletion of scavenger receptors (SRs) CD36 and SR-A in hematopoietic

269 rium tuberculosis (Mtb) through two types of scavenger receptors (SRs; MARCO and SR-B1), as blockade

270 iver fibrosis to show that deficiency of the scavenger receptor, stabilin-1, exacerbates fibrosis and

271 to the effects of MyD88 on phagocytosis via scavenger receptors, such as MARCO, which are not affect

272 erved yet poorly characterized member of the scavenger receptor superfamily-as a receptor for VEEV.

273 CD36 is a scavenger receptor that exhibits pleiotropic functions,

274 CD36 (cluster of differentiation 36) is a scavenger receptor that functions in high-affinity tissu

275 We examined whether CD36, a scavenger receptor that recognizes pathogen and modified

276 tein receptor-related protein 1 (LRP-1) is a scavenger receptor that regulates adaptive immunity and

277 ion receptors could be viewed as a subset of scavenger receptors that are capable of eliciting anti-i

278 stered oligonucleotides can naturally engage scavenger receptors that facilitate cellular transfectio

279 Human mesenchymal stem cells (MSCs) express scavenger receptors that internalize lipids, including o

280 cells and macrophages, unlike other typical scavenger receptors that recognize phosphatidylserine on

281 he protein levels of the class A and class B scavenger receptors, the membrane lipid transporter ABCA

282 s innate immune responses via complement and scavenger receptors to drive recruitment of and efferocy

283 ptors (TLRs), TLR4 and TLR2, in concert with scavenger receptors to regulate the inflammatory microen

284 R-146a mimic oligonucleotide conjugated to a scavenger receptor/Toll-like receptor 9 agonist (C-miR14

285 transfected cells, we further identified the scavenger receptor type A member I (SR-AI) to be a macro

286 te a cellular pathway whereby membrane-bound scavenger receptor type B-1 (SR-B1) in parent cells beco

287 Scavenger receptor type B-1 (SR-B1), found in lipid raft

288 This combination of scavenger receptor type B-1 binding and relative cholest

289 Like natural HDLs, biomimetic HDL-NPs target scavenger receptor type B-1, a high-affinity HDL recepto

290 s to the receptor for cholesterol-rich HDLs, scavenger receptor type B1 (SCARB1).

291 The increase in scavenger receptors was caused by increased activity of

292 Scavenger receptors were defined as cell surface recepto

293 We hypothesized that CD36, a scavenger receptor which facilitates recognition of apop

294 s report, we show that the Stabilin class of scavenger receptors, which were not previously thought t

295 multiple receptors, including CR3, CRIg, and scavenger receptors, which work synergistically along wi

296 ed by oxLDL were inhibited by blocking LOX-1 scavenger receptor with a specific antibody (10 mug/ml).

297 CD36 is a type 2 scavenger receptor with multiple functions.

298 h ApoA-I raising agents or blocking relevant scavenger receptors with neutralizing antibodies could,

299 eptor A5 (SCARA5) is a member of the class A scavenger receptors, with most similarity to SCARA1 (SR-

300 ng and down-regulation of both MSR1 and CD36 scavenger receptors, yielding minimal accumulation of ox