ライフサイエンスコーパス: endocytic vesicle

1 can be taken up in a matter of seconds in an endocytic vesicle.

2 scission and producing a receptor-containing endocytic vesicle.

3 ion and the subsequent internalization of an endocytic vesicle.

4 ncurrently with the "touch" of a neighboring endocytic vesicle.

5 t mechanism and through contact with another endocytic vesicle.

6 sphosphate (PtdIns(4,5)P(2)) associated with endocytic vesicles.

7 the protein coats of certain post-Golgi and endocytic vesicles.

8 me when AIP4 co-localizes with arrestin-2 on endocytic vesicles.

9 cumulation of endoglin and beta-arrestin2 in endocytic vesicles.

10 ed CCV size due to impaired fusion with late endocytic vesicles.

11 sential for motility and processing of early endocytic vesicles.

12 protein directly involved in the assembly of endocytic vesicles.

13 mal hydrolases obtained via fusion with late endocytic vesicles.

14 d-bound RF receptor and its association into endocytic vesicles.

15 implicated in the formation and movement of endocytic vesicles.

16 , in which it spontaneously recycles through endocytic vesicles.

17 se upon HS degradation, and (4) leakage from endocytic vesicles.

18 may regulate the transition of early to late endocytic vesicles.

19 oated vesicles and in large, smooth-surfaced endocytic vesicles.

20 antibodies colocalized with virus-containing endocytic vesicles.

21 tail (M6tail) alone targeted to the nascent endocytic vesicles.

22 ponding to endoplasmic reticulum, Golgi, and endocytic vesicles.

23 he transport of polyplexes through important endocytic vesicles.

24 st-translationally modified and localized to endocytic vesicles.

25 tivated beta1 integrins and L1 into distinct endocytic vesicles.

26 major cargo protein of clathrin-independent endocytic vesicles.

27 als that specify incorporation of cargo into endocytic vesicles.

28 ere subsequently taken up and accumulated in endocytic vesicles.

29 h other GPCRs and internalize with them into endocytic vesicles.

30 ses uptake of CpG (but not control) DNA into endocytic vesicles.

31 ion, hTLR9 and CpG DNA are found in the same endocytic vesicles.

32 d in vesicles suggest the caveolar origin of endocytic vesicles.

33 y, rtoA cells have a defect in the fusion of endocytic vesicles.

34 after activation of gp41 by the acidic pH of endocytic vesicles.

35 L,) a compartment thought to represent GLUT4 endocytic vesicles.

36 eplicative organelle that avoids fusion with endocytic vesicles.

37 viruses that penetrate cells by fusion with endocytic vesicles.

38 that acts to prevent clustering of Env into endocytic vesicles.

39 receptors specifically to different primary endocytic vesicles.

40 e was transient, but Raf-1 remained bound to endocytic vesicles.

41 secretin and AT(1A) receptors colocalize in endocytic vesicles.

42 rane turnover than of active clustering into endocytic vesicles.

43 megalin is able to internalize insulin into endocytic vesicles.

44 d to be involved in downstream processing of endocytic vesicles.

45 esponse results in the accumulation of large endocytic vesicles.

46 rther illustrates the unique nature of these endocytic vesicles.

47 receptors from the plasma membrane and into endocytic vesicles.

48 t is believed to facilitate the formation of endocytic vesicles.

49 mechanoactive helices cleaving the necks of endocytic vesicles.

50 ocess and likely triggers an activity within endocytic vesicles.

51 rect fusion with the plasma membrane and via endocytic vesicles.

52 flg22-dependent internalization of FLS2 into endocytic vesicles.

53 ndocytosis or loading of TfR into individual endocytic vesicles.

54 ributed by the VAMP7-dependent exocytosis of endocytic vesicles.

55 in vesicles/inclusion bodies, suggestive of endocytic vesicles.

56 bservable on the plasma membrane and also in endocytic vesicles.

57 tein PrP is confined to the cell membrane or endocytic vesicles.

58 resulting in the redistribution of SAP97 to endocytic vesicles.

59 2 capsid proteins following acidification of endocytic vesicles.

60 thus serve as markers for discrete types of endocytic vesicles.

61 ation and was subsequently internalized into endocytic vesicles.

62 p85alpha knockdown enlarged SARA-containing endocytic vesicles.

63 the acidification and/or fusion with various endocytic vesicles.

64 dynamin 2, a protein involved in scission of endocytic vesicles.

65 t postendosomal trafficking, are sorted into endocytic vesicles.

66 ng proteins that recruit cargo proteins into endocytic vesicles.

67 ontributing to neck formation in presynaptic endocytic vesicles.

68 resulting in accumulation of the material in endocytic vesicles.

69 envelope is induced by the acidic pH of the endocytic vesicle [1].

70 s thought to accompany the 'pinching off' of endocytic vesicles [1] [4].

71 entirely localised to the cytosolic face of endocytic vesicles [3] [4].

72 mediate association with clathrin-containing endocytic vesicles: a putative dileucine motif at positi

73 pid trafficking defect, Tangier disease late endocytic vesicles accumulated both cholesterol and sphi

74 with the BCR on the cell surface and TLR9 in endocytic vesicles, achieving synergy must involve uniqu

75 ng with activated beta2AR, D1AR, and ETAR in endocytic vesicles, activation of AT1AR and NTR triggers

76 Agents that block the acidification of endocytic vesicles also arrest vesicular trafficking.

77 tween progression of clathrin-coated pits to endocytic vesicles and an activation-deactivation cycle

78 ation has reported roles in the formation of endocytic vesicles and autophagosomes and in the inactiv

79 Macropinosomes are distinct from endocytic vesicles and autophagosomes in that they are s

80 ing images of nucleoporins, TORC1 complexes, endocytic vesicles and Bax pores.

81 to redistribution of beta-arrestin2-GFP into endocytic vesicles and classical receptor desensitizatio

82 hat enzyme activity in fractions enriched in endocytic vesicles and cytosol was preferentially inhibi

83 presence of monensin, which raises the pH of endocytic vesicles and has been shown to inhibit FMDV re

84 g that myo6 has a transient association with endocytic vesicles and is released upon early endosome f

85 sis is elevated, which translocates Eiger to endocytic vesicles and leads to activation of apoptotic

86 rom mitochondria but colocalize in part with endocytic vesicles and lysosomes.

87 diate common to a subset of clathrin derived endocytic vesicles and macropinosomes.

88 or driving force for retrograde transport of endocytic vesicles and membranous organelles.

89 of early endocytic antigen 1 (EEA1)-positive endocytic vesicles and of vesicles containing internaliz

90 cterial and viral pathogens, and motility of endocytic vesicles and other membrane-bound organelles.

91 TbCLH is present on both endocytic vesicles and post-Golgi elements, suggesting a

92 showed further that TTP is localized to late endocytic vesicles and that it facilitates the intracell

93 owed that these vesicles were newly uncoated endocytic vesicles and that myo6 was recruited to these

94 rect fusion with the plasma membrane and via endocytic vesicles and that this is not dependent on the

95 lipoprotein acceptors, traffics between late endocytic vesicles and the cell surface.

96 results in the depletion of alpha5 from both endocytic vesicles and the recycling compartment, provid

97 ong-standing question in cell biology is how endocytic vesicles and tubules detach from the plasma me

98 -enhanced green fluorescent protein-positive endocytic vesicles and tubulovesicular structures underg

99 nt capsid accumulated in caveolin-1-mediated endocytic vesicles and was then translocated to the endo

100 up to five times during the formation of an endocytic vesicle, and suggest revising quantitative mod

101 teins may be partially excluded from nascent endocytic vesicles, and are likely to have implications

102 g G protein coupling, targeting receptors to endocytic vesicles, and initiating G protein-independent

103 asma membrane proteins to define all primary endocytic vesicles, and labelling of specific proteins w

104 its internalization and localization to the endocytic vesicles, and pretreatment of cardiomyocytes w

105 e cells, repair neurons, promote scission of endocytic vesicles, and seal phagosomes.

106 transiently interact with one another, late endocytic vesicles, and the cell surface.

107 re not rapidly replenished from recycling of endocytic vesicles; and (iv) exocytosis of vesicles in r

108 /3 complex activation to assemble F-actin as endocytic vesicles are being formed.

109 that at least 95% of the earliest detectable endocytic vesicles arise from clathrin-coated pits.

110 bedded ErbB-2, through endocytosis using the endocytic vesicle as a vehicle, importin beta1 as a driv

111 ast endocytosis can retrieve a single, large endocytic vesicle as fast as 50-100 ms after synaptic ve

112 ab5 interacting protein that may function on endocytic vesicles as a receptor for rab5-GDP and partic

113 e plasma membrane, prior to the formation of endocytic vesicles, as it is insensitive to dansylcadave

114 hosphomimetic mu2 mutant increases levels of endocytic vesicle-associated AP2.

115 e detailed proteomic analysis and mapping of endocytic vesicle-associated proteins.

116 segregates scarce macropinosomes from other endocytic vesicles at a high purity and in a low-cost an

117 sibly inhibited, permitting the isolation of endocytic vesicles at defined stages of maturation.

118 ur data indicate that TWIST1 is expressed in endocytic vesicles at the apical surface and interacts w

119 er surface proteins), perhaps by focusing of endocytic vesicles at the Golgi complex.

120 s most important for the initial movement of endocytic vesicles away from the plasma membrane, which

121 s been implicated in the docking of incoming endocytic vesicles before fusion with early endosomes.

122 These studies suggested that endocytic vesicles bind to and travel along microtubules

123 gulated by the endolysosomal system, wherein endocytic vesicles bud from the plasma membrane into the

124 Thus, NO regulates endocytic vesicle budding by S-nitrosylation of dynamin.

125 The GTPase dynamin regulates endocytic vesicle budding from the plasma membrane, but

126 ons may have implications for the process of endocytic vesicle budding in general.

127 living synapse has implicated endophilin in endocytic vesicle budding.

128 RIDalpha localizes to endocytic vesicles but is not homologous to Rab7 and is

129 revealed that they block virion escape from endocytic vesicles but not virion binding or internaliza

130 trafficking of CD89 to lamp1-containing late endocytic vesicles, but not class II-containing vesicles

131 are believed to infect target cells through endocytic vesicles, but the details of this pathway are

132 ate from the cytoplasm and bind to incoming, endocytic vesicles carrying TrkA concentrated at the tip

133 l replication begins due to acidification of endocytic vesicles, causing the breakdown of the viral c

134 as a helical polymer at the neck of budding endocytic vesicles, constricting the underlying membrane

135 pe assay to observe the interaction of early endocytic vesicles containing fluorescent ASOR with fluo

136 xes, evidently by inhibiting pinching off of endocytic vesicles containing the clustered IgE receptor

137 n added to cells, both peptides are found in endocytic vesicles containing the transferrin receptor a

138 Endocytic vesicles containing these complexes are acidif

139 The formation of endocytic vesicles containing transferrin at plasma memb

140 Endocytic vesicles corral a central exocytic zone, tight

141 mune receptors that couple ligand binding to endocytic vesicle damage to permit MHC class I antigen p

142 ]Galbeta1-4Glcbeta1-1'-ceramide (G(M2)) into endocytic vesicles depends on the presence of NPC1 prote

143 titution of receptor-ligand sorting in early endocytic vesicles derived from rat liver.

144 On the other hand, normal processing of the endocytic vesicles does appear to require the elevation

145 Studies of receptor recycling from endocytic vesicles employing fluorescently and HRP-tagge

146 , one can detect the formation of individual endocytic vesicles (EVs) with an unmatched temporal reso

147 ions, with acidic pH similar to that seen in endocytic vesicles favoring the beta-oligomer and neutra

148 min 2, a Vav-interacting protein involved in endocytic vesicle fission, significantly blocked oxLDL u

149 us lysosomes via tethering and clustering of endocytic vesicles followed by exchange of their content

150 Because TLR9 is observed in endocytic vesicles following exposure to CpG ODN, our da

151 eruloplasmin and sequesters excess copper to endocytic vesicles for further export out of the cell.

152 t it is packed after its action into visible endocytic vesicles for its disposal.

153 or complex is often rapidly internalized via endocytic vesicles for trafficking into various intracel

154 Thus, endocytic vesicle formation and capture of the newly rel

155 nstrate that exogenous C(6)-ceramide induces endocytic vesicle formation and causes enlarged late end

156 dynamin isoforms have redundant functions in endocytic vesicle formation, but can be targeted to and

157 During endocytic vesicle formation, distinct subdomains along t

158 ed in hyaluronic capsule production and host endocytic vesicle formation, GAS GTPases and host fibrin

159 ng live cell imaging techniques to visualize endocytic vesicle formation, we find that the N-terminal

160 nover is required for multiple stages during endocytic vesicle formation.

161 a2p positively regulates Sla2p for efficient endocytic vesicle formation.

162 concentration of Sjl2 during late stages of endocytic vesicle formation.

163 on and downstream signaling only occur after endocytic vesicle formation.

164 The GTPase dynamin is required for endocytic vesicle formation.

165 ors are differentially sorted at the time of endocytic vesicle formation.

166 Here we show that nascent endocytic vesicles formed in mutant cells displaying rap

167 ynamin, a GTPase required for the fission of endocytic vesicles from plasma membrane.

168 for the efficient transportation of nascent endocytic vesicles from the actin-rich peripheries of ep

169 Here, we find that scission of endocytic vesicles from the plasma membrane (PM) provide

170 100 kDa GTPases involved in the scission of endocytic vesicles from the plasma membrane [1].

171 Defects in the trafficking of endocytic vesicles from the plasma membrane to the Golgi

172 Endophilins A1 and A2 promote the budding of endocytic vesicles from the plasma membrane, whereas end

173 pool that functions in the separation of the endocytic vesicles from the plasma membrane.

174 n family of GTPases mediates the scission of endocytic vesicles from the plasma membrane.

175 In mammalian cells, fusion between early endocytic vesicles has been shown to require the ubiquit

176 least one population of class II- containing endocytic vesicles (i.e., CIIV) has been identified and

177 nally, the mutant receptors are localized in endocytic vesicles, identical to wild-type receptors sti

178 ment in gene expression: (i) pH buffering in endocytic vesicles, (ii) displacement of polycations fro

179 he rates of mass transfer into and among the endocytic vesicles in a model cell line, 3T3 fibroblasts

180 orescein-labeled transferrin co-localized in endocytic vesicles in Fq/11 cells, indicating that endoc

181 s are direct precursors of indented pits and endocytic vesicles in intact cells.

182 We find that alpha5 and beta1 are in endocytic vesicles in PMNs and that alpha5 colocalizes w

183 he EGFR are internalized and co-localized in endocytic vesicles in response to EGF.

184 tion of large vacuoles originating from late endocytic vesicles in sensitive mammalian cells.

185 Actin assembles around late endocytic vesicles in the growth cone of the cell, reach

186 We show that Delta is retained in endocytic vesicles in the mesoderm but expressed on the

187 that the formation, movement, and fusion of endocytic vesicles in the region between the extruding n

188 Stat3 co-localizes with endocytic vesicles in transit from the cell membrane to

189 d on lipid tubules, akin to necks of budding endocytic vesicles, in a guanosine diphosphate (GDP)-bou

190 d did not reside in the cell surface derived endocytic vesicles, in PC-3 cells, suggesting impaired t

191 and the localization of the hook protein to endocytic vesicles indicate that the hook gene encodes a

192 le for maintaining a pH above 6 within early endocytic vesicles, inhibited the growth of C. trachomat

193 enhanced by Ca2+ ions, whereas transfer from endocytic vesicles into the cytosol requires endosomal a

194 rovilli, transporting intact gold-containing endocytic vesicles into the extrusions along with mitoch

195 acted by the cross-linker fimbrin before the endocytic vesicle is released from the plasma membrane.

196 the protein coats of certain post-golgi and endocytic vesicles is clathrin, which appears as a three

197 However, the fate of the large endocytic vesicles is not known.

198 Early endocytic vesicles loaded with Texas Red asialoorosomuco

199 ich increases progressively as secretory and endocytic vesicles mature.

200 Endocytic vesicle-mediated internalization of pre-formed

201 In those epithelial cells, endocytic vesicle-mediated internalization was observed

202 via the action of FAK, thereby affecting the endocytic vesicle-mediated protein trafficking events th

203 nt manner such that the pool of myosin VI in endocytic vesicles, membrane ruffles, and cytosol migrat

204 itochondria and mTOR pathways might regulate endocytic vesicle-mitochondria interactions and dynamics

205 ng and/or depolymerization are important for endocytic vesicle morphogenesis.

206 Additionally, endocytic vesicles move toward early endosomes on actin

207 nd that 74% of rOATP1A4-containing rat liver endocytic vesicles (n = 12,044) also contained rOATP1A1.

208 ely studied, as well as trafficking in early endocytic vesicles notably regulated by the small GTPase

209 ers were also used to measure the binding to endocytic vesicles of exogenously added Rab5 and to moni

210 r how pathogens that reside primarily within endocytic vesicles of infected macrophages, such as MTB,

211 fixed, this peptide is observed only in the endocytic vesicles of live cells.

212 ntigenic peptides is largely confined to the endocytic vesicles of specialized antigen-presenting cel

213 ct plasma membrane from other DC, generating endocytic vesicles of up to 1 microm in diameter.

214 microscopy and subcellular fractionation of endocytic vesicles on a Percoll gradient.

215 istinguish axially close-by membranes, early endocytic vesicles, or tubular membrane structures.

216 At the short necks of endocytic vesicles, other factors leading to tension may

217 and ultrastructural 3D analysis, we tracked endocytic vesicles over time, "frame by frame." The firs

218 the optimal type of HK polymer and the pH of endocytic vesicles (P = 0.0058).

219 lized to prepare highly purified fluorescent endocytic vesicles, permitting validation of microscopy-

220 t study provides evidence that ABCA1 in late endocytic vesicles plays a role in cellular lipid efflux

221 pe beta2AR and endogenous beta-arrestin 2 to endocytic vesicles prepared from CHO fibroblasts was obs

222 studies demonstrated that fluorescent early endocytic vesicles prepared from rat liver after injecti

223 Endocytic vesicles prepared from rat liver that had been

224 iding a system in which factors required for endocytic vesicle processing can be identified and chara

225 rom a pit before abortive CCP termination or endocytic vesicle production.

226 ned by parasite-directed modification of the endocytic vesicle rather than by the route of internaliz

227 with beta-arrestins, and found localized in endocytic vesicles rather than at the plasma membrane in

228 the complex responsible for formation of the endocytic vesicle reduced the aggregation.

229 nding mutants of Rvs167 exhibited defects in endocytic vesicle release.

230 lation with the characteristics of a primary endocytic vesicle responsible for the recycling of synap

231 nterestingly, chemicals that raise the pH of endocytic vesicles resulted in a 30 to 50% decrease in H

232 e excess cholesterol in Tangier disease late endocytic vesicles retained massive amounts of NPC1, whi

233 DNM2) is a GTP-binding protein that controls endocytic vesicle scission and defines a whole class of

234 m through the requirement of the pluripotent endocytic vesicle scission enzyme, dynamin 2 GTPase, in

235 These assays revealed that when endocytic vesicle scission fails, tubules are pulled int

236 alizes to endosomal subdomains and regulates endocytic vesicle scission in an Arp2/3-dependent manner

237 The self-assembling GTPase dynamin catalyzes endocytic vesicle scission via membrane insertion of its

238 on parallels that of prototypical dynamin in endocytic vesicle scission.

239 Endocytosis of these coated pits generates endocytic vesicles selectively enriched in B2ARs, which

240 sential role of kinesin-based MT motility in endocytic vesicle sorting, providing a system in which f

241 ediated endocytosis, polarized blebbing, and endocytic vesicle sorting.

242 mbrane but plays a unique role in collecting endocytic vesicles, sorting of internalised cargos and d

243 In mutants, components of exocytic and endocytic vesicles, such as Vamp2, Clathrin and Dynamin,

244 ortical F-actin accumulation and scission of endocytic vesicles, such that membrane tubules remain te

245 Lymphocytes treated with FITC-CTB reveal an endocytic vesicle that is enriched in TCR and CD59, whil

246 EGFR, arresting functionally active EGFR in endocytic vesicles that consequently led to aberrant ERK

247 that growth factors generate glucose-loaded endocytic vesicles that deliver glucose to the glycolyti

248 alpha 5-GFP also resided in endocytic vesicles that emanated from the leading edge o

249 Endocytic vesicles that fail to lose their coat nucleate

250 ution in the cytosol but no association with endocytic vesicles, the Golgi apparatus or the endoplasm

251 s following the addition of glucose, and the endocytic vesicles then pinch off from the plasma membra

252 Notch and Wg pathway components within early endocytic vesicles, thereby controlling the amount of pr

253 f CpG DNA with toll-like receptor (TLR)-9 in endocytic vesicles, thereby preventing CpG-induced activ

254 Aggregates that enter cells somehow escape endocytic vesicles to contact cytosolic protein.

255 ponent of the fusion machinery for targeting endocytic vesicles to early endosomes.

256 ellular sterol transporter that localizes to endocytic vesicles to facilitate the redistribution of s

257 CARP-2 acts at the level of endocytic vesicles to limit the intensity of TNF-induced

258 ker protein (CLIP)-170, a protein that links endocytic vesicles to microtubules.

259 ter internalization, exosomes shuttle within endocytic vesicles to scan the endoplasmic reticulum bef

260 toplasmic domain may target CD155-containing endocytic vesicles to the microtubular network.

261 mbrane proteins, before and after inhibiting endocytic vesicle traffic from the cell surface, either

262 tes the biogenesis of its phagosome to evade endocytic vesicle traffic.

263 in cytoskeleton, transcriptional control and endocytic vesicle trafficking [1-3].

264 lgi apparatus, (iii) occurs independently of endocytic vesicle trafficking along microtubules, and (i

265 The interaction is relevant for endocytic vesicle trafficking because overexpression of

266 various endocytosis pathways and subsequent endocytic vesicle trafficking have been shown to strongl

267 Overall, excess Hyal1 secretion accelerates endocytic vesicle trafficking in a substrate-dependent m

268 ggested that WDR72 could be a facilitator of endocytic vesicle trafficking, which appears inconsisten

269 , which has been implicated in autophagy and endocytic vesicle trafficking.

270 ulates acto-myosin ring contraction but also endocytic vesicle transport to the cleavage furrow and i

271 In contrast, the movement of late-stage endocytic vesicles, traveling through the cytoplasm en r

272 clathrin-coated pits and to ensuing uncoated endocytic vesicles (UCV).

273 Endocytic vesicles undergo fission to sort ligand from r

274 hich NHE3 is rapidly endocytosed from BBM to endocytic vesicles upon treatment with carbachol; (2) mu

275 o monitor the ATP-dependent acidification of endocytic vesicles using the fluorescent dye acridine or

276 HR-49 through its cytosolic sequestration to endocytic vesicles via geranylgeranyl conjugation to the

277 were optimal transfection agents, the pH of endocytic vesicles was >6.0.

278 ct, enveloped HSV from the cell surface into endocytic vesicles was rapid (t(1/2) of 8 to 9 min) and

279 staining of the nucleus (nucleolus), but not endocytic vesicles, was abrogated by treating the cells

280 Some endocytic vesicles were acidified and colocalized with L

281 tudy, procedures to prepare fluorescent late endocytic vesicles were devised.

282 es appeared 4 s after stimulation, and these endocytic vesicles were located just above the active zo

283 h the linear HK was the optimal polymer, the endocytic vesicles were strongly acidic with a pH of <5.

284 to promote exit of vector/DNA complexes from endocytic vesicles were studied systematically to define

285 s compartment intersect class II proteins in endocytic vesicles where DM editing was facilitated.

286 pid-binding FYVE domain, CARP-2 localized to endocytic vesicles, where it interacted with internalize

287 nges and is known to directly associate with endocytic vesicles, which have been implicated in dsRNA

288 d steady-state levels of AP2 associated with endocytic vesicles, which is consistent with reduced unc

289 ncy provokes the accumulation of this NTF in endocytic vesicles, which leads to a B cell maturation a

290 he complex diffusive motions of newly formed endocytic vesicles, which move faster as the surrounding

291 required for recruitment of beta-arrestin to endocytic vesicles, which was dependent on co-expression

292 orescent protein conjugate internalizes into endocytic vesicles with agonist-activated neurotensin-1

293 ll-established role of Rab5 in the fusion of endocytic vesicles with endosomes, our results suggest t

294 beta2-adrenergic receptor that traffics into endocytic vesicles with receptors that lack serine/threo

295 thelial cells, allowing for timely fusion of endocytic vesicles with the early endosome.

296 ar, while generating large numbers of motile endocytic vesicles with which dynamin associates.

297 anti-gp60 antibody (Ab) were colocalized in endocytic vesicles within 5 min of gp60 activation.

298 PDZK1 associates with rOATP1A1-containing endocytic vesicles within cells, mediating recruitment o

299 arrestins and consequently, redistributed to endocytic vesicles without betaarr2-GFP, whereas interna

300 tered through endocytosis and accumulated in endocytic vesicles, without necessarily entering the cyt