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 ribed in this report only refer to mammalian scavenger receptors.

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

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

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

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

7 issue macrophages expressing CD163 and CD204 scavenger receptors.

8 (APOJ), lipoprotein lipase (LPL), macrophage scavenger receptor 1 (MSR1), and tumor necrosis factor r

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

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

11 We previously identified scavenger receptor A (SR-A) as an early target in alteri

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

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

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

15 acrophages from mice deficient in macrophage scavenger receptor A (SR-A; CD204) had absent IgM bindin

16 tor (MR) to the complement receptor CR3, the scavenger receptor A (SRA), and the Fcgamma receptor (Fc

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 previously reported that scavenger receptor A (SRA/CD204), a binding structure on

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

21 we report a previously unrecognized role of scavenger receptor A (SRA; also known as CD204) as a sig

22 activation that requires the activity of the scavenger receptor A and the Ca(2+)-activated potassium

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

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

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

26 onectin in mouse macrophages using the human scavenger receptor A-I gene enhancer/promoter.

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

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

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

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

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

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

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

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

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

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

37 m MARCO-deficient mice, but not wild-type or scavenger receptor AI/II-deficient mice, showed impaired

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

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

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

41 was bound by the LDL receptor but not by the scavenger receptor and had increased binding affinity fo

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

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

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

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

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

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

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

49 stimulated both the uptake (by up-regulating scavenger receptors) and efflux of cholesterol (by activ

50 Bacterial uptake, mediated mainly by class A scavenger receptors, and activation of mitogen-activated

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

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

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

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

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

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

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

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

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

60 81, while HEPC98 primarily blocks binding to scavenger receptor B1 and heparan sulfate.

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

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

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

64 One of these molecules is the scavenger receptor BI (SR-BI), a receptor for high densi

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

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

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

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

69 Using scavenger receptor BI mice as the first relative adrenal

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

71 Scavenger receptor BI null and adrenal-specific scavenge

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

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

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

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

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

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

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

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

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

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

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

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

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

85 The scavenger receptor CD36 is a critical factor initiating

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

87 The scavenger receptor CD36 is injurious in acute experiment

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

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

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

91 nesis and are involved in pathways common to scavenger receptor CD36 signaling, their role in CD36-de

92 We report that the scavenger receptor CD36, a membrane glycoprotein that bi

93 to functionally link Parkin and the class B scavenger receptor CD36, suggesting a novel and complex

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

95 (15-LO), a lipid-peroxidating enzyme and the scavenger receptor CD36.

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

97 idative enzyme 15-lipoxygenase (15-LO) and a scavenger receptor CD36.

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

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

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

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

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

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

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

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

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

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

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

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

110 ter A1, ATP-binding cassette transporter G1, scavenger receptor class B type 1) have been evaluated.

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

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

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

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

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

116 the murine high density lipoprotein receptor scavenger receptor class B type I (SR-BI) in hepatocytes

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

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

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

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

121 Wild-type (WT) C57BL/6 mice and scavenger receptor class B type I (SR-BI) knockout mice

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

123 ng cassette subfamily A member 1 (ABCA1) and scavenger receptor class B type I (SR-BI), but not ATP-b

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

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

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

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

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

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

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

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

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

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

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

135 .31 for rs4765623, which maps to SCARB1, the scavenger receptor class B, member 1 gene (P = 2.6 x 10)

136 phosphate-binding cassette G5/G8 [ABCG5/G8], scavenger receptor class B, member 1) and bile acid (ABC

137 05.12 +/- 1.13 nm) conjugated to recombinant scavenger receptor class B, member 2 (SCARB2) protein wi

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

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

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

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

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

143 Scavenger receptor class B, type I (SR-BI), a CD36 super

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

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

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

147 rol efflux that causes signal initiation via scavenger receptor class B, type I, and plasma membrane

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

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

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

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

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

153 The HDL receptor, scavenger receptor, class B, type I (SR-BI), is a homool

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

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

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

157 Scavenger receptors constitute a large family of protein

158 m cells." Recently, we reported that CD36, a scavenger receptor, contributes to activation of Vav-fam

159 163 has previously been shown to involve the scavenger receptor cysteine-rich (SRCR) domain 3.

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

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

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

163 WC1 co-receptors belong to the scavenger receptor cysteine-rich (SRCR) superfamily and

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

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

166 structurally similar, both containing three scavenger receptor cysteine-rich domains in their extrac

167 Recognition by scavenger receptor cysteine-rich domains on membrane pro

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

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

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

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

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

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

174 2(Y689F) required the presence of the fourth scavenger receptor-cysteine-rich (SRCR) domain of LOXL2,

175 Scavenger receptor deficiency markedly impaired the recr

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

177 melanogaster, the EGF-like repeat containing scavenger receptor Eater is expressed by phagocytes and

178 e against P. gingivalis infection, while the scavenger receptors Eater and Croquemort played no roles

179 Hsp90-OVA peptide complexes bound to scavenger receptor expressed by endothelial cells (SREC-

180 Oligo G also reduces levels of cell-surface scavenger receptor expressed by endothelial cells I (SRE

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

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

183 In a human embryonic kidney macrophage scavenger receptor-expressing (HEK-EM) 293 model system,

184 The scavenger receptor FAT/CD36 contributes to the inflammat

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

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

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

188 typical chemokine receptor D6 is a decoy and scavenger receptor for most inflammatory CC chemokines a

189 We postulate that CD163-L1 functions as a scavenger receptor for one or several ligands that might

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

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

192 ntal evidence that CD36, a phagocyte class B scavenger receptor, functions as a novel SAA receptor me

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

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

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

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

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

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

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

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

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

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

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

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

205 The scavenger receptor inhibitors, dextran sulfate and fucoi

206 receptors on APCs, we propose that selective scavenger receptor interactions with HSPs may lead to hi

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

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

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

210 CD163, a monocyte- and macrophage-specific scavenger receptor, is shed during activation as soluble

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

216 promoted upregulation of multiple macrophage scavenger receptors linked to atherosclerosis, and suppl

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 receptors that trap pathogens, including the scavenger receptor macrophage receptor with a collagenou

221 The scavenger receptor macrophage receptor with collagenous

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

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

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

225 The scavenger receptor, macrophage receptor with collagenous

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

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

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

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

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

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

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

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

234 eptor-mediated uptake and promote macrophage scavenger receptor-mediated LDL uptake.

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

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

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

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

241 Given the presence of multiple HSP-binding scavenger receptors on APCs, we propose that selective s

242 oated with dextran sulfate to target them to scavenger receptors on macrophages, a biomarker of vulne

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

244 ed autocrine factors, but are independent of scavenger receptor or lipoprotein oxidation-dependent pa

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

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

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

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

249 Scavenger receptors represent an important class of patt

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

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

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

253 nic phagocytosis of Eap(+) S. aureus via the scavenger receptor scavenger receptor class A (SR-A), wh

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

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

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

257 Scavenger receptors showed lower and cholesterol efflux

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

259 e sought to assess the in vivo importance of scavenger receptor (SR)-mediated uptake of oxidized low-

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 Class B scavenger receptors (SR-Bs), such as SR-BI/II or CD36, b

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

267 The pattern recognition scavenger receptor SRA/CD204 attenuates the ability of D

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

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

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

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

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

273 These macrophages express CD163, a scavenger receptor that binds hemoglobin-haptoglobin com

274 CD36 is a scavenger receptor that exhibits pleiotropic functions,

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

276 CD36 is a Class B scavenger receptor that is constitutively expressed in t

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

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

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

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

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

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

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

284 that human decidual macrophages use class A scavenger receptors to internalize unopsonized C. sordel

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

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

287 dissect viral entry and validate the role of scavenger receptor type B class I for HCV uptake.

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

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

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

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

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

293 We found that uptake via scavenger receptors was essential for the CD1d presentat

294 Scavenger receptors were defined as cell surface recepto

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

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

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

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

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