ライフサイエンスコーパス: basolateral surface

1 uptake from the apical surface than from the basolateral surface.

2 eate a more efficient budding process at the basolateral surface.

3 arized targeting of membrane proteins to the basolateral surface.

4 y epithelia first released adenovirus to the basolateral surface.

5 cycling of transferrin from endosomes to the basolateral surface.

6 culovirus entry may require contact with the basolateral surface.

7 y cells, CAR is expressed exclusively on the basolateral surface.

8 er penetration of the epithelium through the basolateral surface.

9 e polarized distribution of receptors on the basolateral surface.

10 re not involved in receptor retention on the basolateral surface.

11 IFN, facilitates antigen processing from the basolateral surface.

12 ved in transporting membrane proteins to the basolateral surface.

13 via class II molecules was restricted to the basolateral surface.

14 t vesicles destined for either the apical or basolateral surface.

15 sorting of a broader range of cargoes to the basolateral surface.

16 egraded are selectively recycled back to the basolateral surface.

17 with BCC virus either through the apical or basolateral surface.

18 ese cells, and the protein is present at the basolateral surface.

19 surface was approximately twice that of the basolateral surface.

20 27-kDa heat shock protein exclusively to the basolateral surface.

21 ect delivery to both the apical (60-75%) and basolateral surface.

22 f receptors are selectively delivered to the basolateral surface.

23 that of MUC1 were delivered primarily to the basolateral surface.

24 A to the apical surface and recycling to the basolateral surface.

25 sion of exc-5 causes defects at the tubule's basolateral surface.

26 s, and its expression is concentrated on the basolateral surface.

27 icrotubule-associated, as it migrates to the basolateral surface.

28 dye FM4-64 when the dye is presented to the basolateral surface.

29 g interaction of selected mediators with the basolateral surface.

30 causes apical proteins to relocalize to the basolateral surface.

31 dIns(3,4,5)P3 regulates the formation of the basolateral surface.

32 infection at the apical surface than at the basolateral surface.

33 his chimera was exclusively localized to the basolateral surface.

34 surface to exhibit increased delivery to the basolateral surface.

35 The highly related syntaxin 4 is at the basolateral surface.

36 were infected when virus was applied to the basolateral surface.

37 of cell polarity or increased access to the basolateral surface.

38 onolayers of polarized cells with apical and basolateral surfaces.

39 PAR-1 and PAR-2, redistribute to the inner, basolateral surfaces.

40 mically and functionally separate apical and basolateral surfaces.

41 anchor are expressed on both the apical and basolateral surfaces.

42 utant, it was reduced on both the apical and basolateral surfaces.

43 endocytosis and is present on the apical and basolateral surfaces.

44 and that they are active on both apical and basolateral surfaces.

45 used for independent perfusion of apical and basolateral surfaces.

46 e trans-Golgi network to both the apical and basolateral surfaces.

47 extensive trafficking between the apical and basolateral surfaces.

48 ytosis of cell-free virus from the apical to basolateral surfaces.

49 also requires downward contraction along the basolateral surfaces.

50 was optimal if cells were infected at their basolateral surface, a phenomenon associated with the di

51 himurium can infect epithelial cells via the basolateral surface after breaching the intestinal epith

52 llular Ca(2+) at the apical surface, but not basolateral surface, also prevented tight junction disru

53 apical surface and endocytosis of IgA at the basolateral surface, although an antibody against the in

54 meras are then rapidly internalized from the basolateral surface and a significant fraction ( approxi

55 ally applied adenovirus gained access to the basolateral surface and enhanced gene transfer.

56 ta1 subunit was localized exclusively to the basolateral surface and resulted in partial redistributi

57 ds on dIgA binding to the pIgR solely at the basolateral surface and the ability of pIgR to dimerize.

58 Particles are released from the apical and basolateral surfaces and are indistinguishable, indicati

59 s including the induction of lamellipodia at basolateral surfaces and formation of an increased numbe

60 xpressed in rabbit CE on both the apical and basolateral surfaces and function to transport lactate-H

61 onic epithelial cells, Jak3 redistributed to basolateral surfaces and interacted with adherens juncti

62 ial cells, EGFR is restricted largely to the basolateral surface, and apical or basolateral ligand de

63 xpression was more on the apical than on the basolateral surface, and this effect was more pronounced

64 staining was polarized and restricted to the basolateral surfaces, and in contrast to the epithelial

65 aces, extend lamellipodia-like structures at basolateral surfaces, and show disorganization of cell-c

66 to possess Na,K-ATPase exclusively at their basolateral surfaces; apical labeling was not detected.

67 w that APP-TR chimeras internalized from the basolateral surface are found in tubulo-vesicular endoso

68 In epithelia, distinct apical and basolateral surfaces are maintained by tight junctions t

69 The alpha2CAR also is enriched on the basolateral surface at steady-state and, like the alpha2

70 These results were further confirmed by basolateral surface biotinylation.

71 In contrast, all basolateral surface-bound Cbl was internalized and retai

72 EGF added to the basolateral surface but not apical surface of Caco-2/NHE

73 -length proteins were first delivered to the basolateral surface but then concentrated in the apical

74 or (SPI-I) was not required to enter via the basolateral surface but to promote another virulence-ass

75 -TR chimeras are selectively targeted to the basolateral surface by a tyrosine-dependent sorting sign

76 selective and regulated flux from apical to basolateral surfaces by transcellular passage through ce

77 Ectopic PtdIns(4,5)P2 at the basolateral surface causes apical proteins to relocalize

78 that preferential ectodomain cleavage at the basolateral surface contributes to apical domain localiz

79 l cells, sorting of membrane proteins to the basolateral surface depends on the presence of a basolat

80 reatment with EGTA to increase access to the basolateral surface did not increase transduction of api

81 TLR9 activation through apical and basolateral surface domains have distinct transcriptiona

82 at least two vectorial routes to apical and basolateral surface domains.

83 plasma membrane (PM) proteins to apical and basolateral surface domains.

84 to ensure delivery of the transporter to the basolateral surface, especially at high levels of protei

85 ertion of the alpha2BAR into both apical and basolateral surfaces followed by selective retention on

86 contrast, when the virus was applied to the basolateral surface, gene transfer was much more efficie

87 targeting membrane proteins to the apical or basolateral surfaces have remained elusive.

88 ially transduces human airway cells from the basolateral surface; however, virus release remains in a

89 elivery of newly synthesized proteins to the basolateral surface in polarized epithelial cells.

90 ependent biosynthetic sorting pathway to the basolateral surface in polarized epithelial cells.

91 d not reduce the expression on the apical or basolateral surface in polarized Madin-Darby canine kidn

92 helial cells occurred predominantly from the basolateral surface in polarized monolayers of Caco-2 ce

93 ha2ARs) are localized to and function on the basolateral surface in polarized renal epithelial cells

94 egulates early steps in endocytosis from the basolateral surface in polarized WIF-B cells.

95 high E-/P-cadherin cells, Na/K ATPase was on basolateral surfaces in addition to microvilli.

96 bacteria were added to either the apical or basolateral surfaces, indicating that the RTX toxin rece

97 cells and OVA(323-339) peptide placed on the basolateral surface (inverted) was 2- to 3-fold greater

98 /2 the apical surface is 15-30 min; t1/2 the basolateral surface is 8-10 h).

99 ons, the majority (>65%) of recycling to the basolateral surface is likely to occur from early endoso

100 t localized preferentially (over 99%) to the basolateral surface, like constitutive caveolae of MDCK

101 which was consistent with the apical and not basolateral surface localization of two essential viral

102 epithelial cells revealed a similar punctate basolateral surface localization.

103 binding and post-trans-Golgi trafficking to basolateral surface membranes but not for its turnover a

104 tion through inducing internalization of the basolateral surface NKCC1.

105 tracellularly from the apical surface to the basolateral surface occurred over time, and bacterial re

106 on of viral receptors and coreceptors to the basolateral surface of airway epithelial cells has been

107 hanger AE1 that is normally expressed at the basolateral surface of alpha-intercalated cells in the d

108 eveloped a method of applied pressure to the basolateral surface of alveolar epithelia.

109 s regulated by Na+/K+-ATPase activity on the basolateral surface of alveolar epithelial cells.

110 ing that it is vectorially secreted from the basolateral surface of ARPE-19 cells.

111 of the Let-23 growth factor receptor to the basolateral surface of body epithelia.

112 Imaging and analysis of the basolateral surface of cells expressing some 50 molecule

113 CXCL12 is expressed at the basolateral surface of CNS endothelial cells in normal s

114 When applied to the basolateral surface of colonocytes, PAR2 agonists and ma

115 us-mediated gene transfer from the apical or basolateral surface of confluent AEC monolayers (R(t) >

116 apical surface and aerobic conditions at the basolateral surface of cultured IECs, producing an in vi

117 Mammalian Ferroportin1 is expressed at the basolateral surface of duodenal enterocytes and could ex

118 at intestinal ZnT-1 was most abundant at the basolateral surface of enterocytes lining the villi of t

119 In the duodenum, FPN1 localizes to the basolateral surface of enterocytes where it appears to e

120 aps by mediating cholesterol efflux from the basolateral surface of enterocytes, it remains unclear w

121 ily infected lymphatic cells carry MV to the basolateral surface of epithelial cells, supporting MV s

122 t of many membrane proteins destined for the basolateral surface of epithelial cells.

123 of the Let-23 growth factor receptor to the basolateral surface of epithelial cells.

124 jejuni invasion occurs preferentially at the basolateral surface of eukaryotic cells.

125 ntrast, infected MDMs and DCs applied to the basolateral surface of HAE grown on large-pore (3.0-mum)

126 ikewise, infected MDMs or DCs applied to the basolateral surface of HAE grown on small-pore (0.4-mum)

127 d nectin-4 to efficiently deliver MeV to the basolateral surface of HAE.

128 ed that the NTCP protein is expressed on the basolateral surface of hepatocytes.

129 nd functional IL-17R signaling occurs on the basolateral surface of human bronchial epithelial (HBE)

130 or reduced expression of the protein on the basolateral surface of injured cells permits spontaneous

131 ed that TLR5 is expressed exclusively on the basolateral surface of intestinal epithelia, thus provid

132 ss of heparan sulfate proteoglycans from the basolateral surface of intestinal epithelial cells durin

133 ecific loss of heparan sulfate (HS) from the basolateral surface of intestinal epithelial cells only

134 ptor shown to be abundantly expressed on the basolateral surface of intestinal epithelium.

135 6 +/- 12.8 nM (n = 6) when positioned at the basolateral surface of isolated perfused MD cells and [N

136 istribution of many membrane proteins to the basolateral surface of LLC-PK1 kidney cells.

137 urrent study we found that DCs docked to the basolateral surface of lymphatic vessels and transited t

138 ry from the trans-Golgi network (TGN) to the basolateral surface of Madin-Darby canine kidney (MDCK)

139 ha and that TGF-alpha is not detected at the basolateral surface of Madin-Darby canine kidney (MDCK)

140 When Y8 was applied to the basolateral surface of Madin-Darby canine kidney cells e

141 3i loop tethering of the alpha(2A)-AR to the basolateral surface of Madin-Darby canine kidney cells.

142 HA+8 was also sorted efficiently to the basolateral surface of Madin-Darby canine kidney cells.

143 Addition of PtdIns(3,4,5)P3 to the basolateral surface of MDCK cells grown as cysts caused

144 sis than dyn1(K44A) in HeLa cells and at the basolateral surface of MDCK cells.

145 hich was secreted predominantly (80%) to the basolateral surface of MDCK cells.

146 that stabilization of the alpha2A-AR on the basolateral surface of MDCKII cells involves multiple me

147 hree alpha 2-AR subtypes, is enriched at the basolateral surface of MDCKII cells.

148 nic composition of the fluid surrounding the basolateral surface of outer hair cells.

149 vo, laminin is primarily concentrated at the basolateral surface of pneumocytes where they rest on th

150 abundantly expressed on the apical than the basolateral surface of polarized airway epithelia.

151 opose that translocation of ExoU through the basolateral surface of polarized airway epithelial cells

152 ng signal that directs Env expression to the basolateral surface of polarized cells.

153 These data demonstrate that the basolateral surface of polarized epithelia is more susce

154 alpha) and amphiregulin are delivered to the basolateral surface of polarized epithelial cells where

155 rtain virus receptors are sequestered on the basolateral surface of polarized epithelial cells.

156 gradation, thus ensuring its delivery to the basolateral surface of polarized epithelial cells.

157 taining vesicles to a distinct region at the basolateral surface of polarized epithelial cells.

158 ical for retention of these receptors at the basolateral surface of polarized Madin-Darby canine kidn

159 alpha2A AR) is critical for retention at the basolateral surface of polarized Madin-Darby canine kidn

160 lly, EREG is preferentially delivered to the basolateral surface of polarized Madin-Darby canine kidn

161 etaine transporter (BGT) is expressed on the basolateral surface of polarized Madin-Darby canine kidn

162 ly tether cargo vesicles directed toward the basolateral surface of polarized Madin-Darby canine kidn

163 and that spinophilin is enriched beneath the basolateral surface of polarized MDCK cells prompted us

164 een fluorescent protein--specifically to the basolateral surface of polarized MDCK cells.

165 e receptor that achieves localization on the basolateral surface of polarized MDCK II cells indisting

166 ergic receptor (alpha2A-AR) retention at the basolateral surface of polarized MDCKII cells involves i

167 ent regulation of alpha(2B)AR density at the basolateral surface of polarized MDCKII cells requires t

168 g and maintenance of the EGF receptor on the basolateral surface of renal epithelial cells is perturb

169 NSP4 colocalizes with integrin alpha2 on the basolateral surface of rotavirus-infected polarized inte

170 l microvilli, whereas SAP97 localizes at the basolateral surface of RPE cells, probably through a dir

171 -associated protein of 97 kDa (SAP97) at the basolateral surface of RPE cells, which overlapped with

172 g receptor (pIgR), which is expressed on the basolateral surface of secretory epithelial cells.

173 ecretory response when it was applied to the basolateral surface of T84 cells but no response when it

174 indicated that C. jejuni binds to Fn on the basolateral surface of T84 human colonic cells.

175 d Crry regulate complement activation on the basolateral surface of TECs and that factor H regulates

176 ater complement activation occurred when the basolateral surface of TECs from Crry(-/-)fB(-/-) mice w

177 complement activation was observed when the basolateral surface of TECs was exposed to serum than wh

178 confirmed expression of mBSC2 protein on the basolateral surface of terminal IMCD segments and demons

179 8 was highly polarized and restricted to the basolateral surface of the cell.

180 larization were localized to hotspots on the basolateral surface of the cell.

181 tes with biotinylated FGF2 revealed that the basolateral surface of the cells remained intact, withou

182 When the basolateral surface of the cells was treated with antibo

183 tends a tubular process, or canal, along the basolateral surface of the epidermis to form the nematod

184 ntigen 2 within the hemidesmosomes along the basolateral surface of the epithelial cell and their lig

185 During this process, dIgA binding at the basolateral surface of the epithelial cell transmits a s

186 nonmotile organisms that advanced toward the basolateral surface of the epithelium while adhering to

187 s engagement with receptors expressed on the basolateral surface of the epithelium.

188 istochemistry localized both subunits to the basolateral surface of the mouse ileal enterocyte.

189 ocalizes with complement deposited along the basolateral surface of the proximal renal tubule in asso

190 It is distributed specifically along the basolateral surface of the RPE and is proposed to work i

191 ient from acidic endosomes to the pH-neutral basolateral surface of the syncytiotrophoblast.

192 hways that direct proteins to the apical and basolateral surface of these cells.

193 tein that mediates active I(-) uptake in the basolateral surface of thyrocytes and other cells.

194 emokines were expressed predominantly at the basolateral surface of tubular epithelial cells.

195 When HCoV-229E was applied to the apical or basolateral surface of well-differentiated primary cultu

196 of E-cadherin at the adherens junctions and basolateral surfaces of 129/Sv (DeltaN89 beta-catenin) i

197 Basolateral surfaces of cells were exposed by one of two

198 Immunohistochemistry localizes ZIP5 to the basolateral surfaces of enterocytes, acinar cells, and v

199 esults suggest that there are factors on the basolateral surfaces of epithelial cells that promote in

200 the protein was found on both the apical and basolateral surfaces of epithelial cells, as was gD.

201 otein E (gE) promotes cell-to-cell spread at basolateral surfaces of epithelial cells, but its activi

202 ted by immunofluorescence selectively at the basolateral surfaces of freshly excised human airway epi

203 dies have demonstrated that PMN contact with basolateral surfaces of intestinal epithelial cells in t

204 Exposure of the basolateral surfaces of MDCK cells to P. gingivalis (>10

205 trilysin co-localized with E-cadherin at the basolateral surfaces of migrating tracheal epithelium, a

206 in binding is also expressed in vivo on the basolateral surfaces of mucosal epithelium and lamina pr

207 ay preferentially occur at the apical or the basolateral surfaces of polarized cells, and differences

208 re found to be localized specifically at the basolateral surfaces of polarized Madin-Darby canine kid

209 ial adhesin, MrkD, mediates adherence to the basolateral surfaces of renal and pulmonary epithelia an

210 First, BFT applied to either the apical or basolateral surfaces of T84 monolayers diminished monola

211 creased significantly after PMN contact with basolateral surfaces of T84 monolayers or after incubati

212 is to form a barrier between the apical and basolateral surfaces of the epithelium.

213 mmunofluorescence was most intense along the basolateral surfaces of the PE cells.

214 ns in the context of the distinct apical and basolateral surfaces of the polarized epithelium that li

215 e of specific taurine carriers on apical and basolateral surfaces of the RPE.

216 The release of ATP from the apical and basolateral surfaces of the urothelium appears to be med

217 orrelated with CPE binding the apical versus basolateral surfaces of these two cell lines.

218 apical cell-cell junctions was reduced, and basolateral surfaces of those cells were separated by mu

219 naptic terminals (calyces) that envelope the basolateral surfaces of type I hair cells.

220 to integrin overexpressed on the abluminal (basolateral) surface of endothelial cells through vascul

221 ant L292P V2R escapes to the apical, but not basolateral, surface of polarized MDCK II cells, even in

222 tively released ATP from the apical, but not basolateral, surfaces of CF cells grown on permeable sup

223 polarized epithelia only when applied to the basolateral surface or when injury compromised tight jun

224 s FcRn-IgG complexes that transcytose to the basolateral surface pass through downstream Rab11-positi

225 Cl- removal from apical and basolateral surfaces produced cellular alkalinization (a

226 [57Co]cobalamin (Cbl), to the apical and the basolateral surfaces, respectively.

227 ut led to a relocalization the A1AdoR to the basolateral surface, revealed by immunocytochemical and

228 to virus through the apical rather than the basolateral surface showed high levels of viral replicat

229 Binding of dIgA to pIgR at the basolateral surface stimulates subsequent transcytosis t

230 a was more efficient after adsorption to the basolateral surface than after adsorption to the apical

231 of 185-kD proEGF is fourfold greater at the basolateral surface than at the apical surface and is se

232 bility to distinguish between the apical and basolateral surfaces that are located at intercellular t

233 When applied to the basolateral surface, the anti-SC Fv/alpha(1)-AT fusion p

234 n to selectively deliver wild-type TR to the basolateral surface; this result is consistent with the

235 ) in Calu-3 cells exposed from the apical or basolateral surface to cytotoxic and noncytotoxic strain

236 Fluorescent albumin crossed the gland from basolateral surface to lumen via cytoplasmic vesicles, b

237 s pIgR molecules that have bound dIgA at the basolateral surface to respond to the signal of stimulat

238 as been postulated to export iron across the basolateral surface to the circulation.

239 rmits exposure of the hair cell's apical and basolateral surfaces to different solutions, we examined

240 ls on porous filters that allowed apical and basolateral surfaces to form.

241 Infection from the apical but not the basolateral surface triggered focal adhesion kinase phos

242 n carcinoma cells detected hephaestin on the basolateral surface under steady-state conditions.

243 surface are selectively transcytosed to the basolateral surface underscoring the importance of basol

244 te HIV type 1 (HIV-1) from the apical to the basolateral surface via vesicular transcytosis.

245 Complement activation on the apical and basolateral surfaces was also greater when factor H, an

246 Although delivery to the basolateral surfaces was direct and independent of any d

247 , that is involved in sorting of proteins to basolateral surfaces was involved in targeting of PRV pa

248 s are able to form adherens junctions at the basolateral surface, we show that they have specific and

249 ion and is capable of directing GAT-3 to the basolateral surface when appended to the C terminus of t

250 tor subtype 7a (mGluR7a) is polarized at the basolateral surface when expressed in Madin-Darby canine

251 Vesicles migrated to the basolateral surface where they released FM 1-43, the flu

252 In Xenopus, the blastocoel-facing, basolateral surfaces where signaling interactions ostens

253 eceptor (TR) is selectively delivered to the basolateral surface, where it internalizes transferrin v

254 ion of polarized cells was restricted to the basolateral surface whereas virus was released apically,

255 syntaxin 2 was found on both the apical and basolateral surface, whereas the plasma membrane localiz

256 , ARTL27 was preferentially cleaved from the basolateral surface with 4-fold greater efficiency compa

257 osomal elements directly accessible from the basolateral surface with transferrin (Tf)-HRP, we show t

258 m subsp. paratuberculosis crosses apical and basolateral surfaces with approximately the same degree

259 MDCKII cells: random delivery to apical and basolateral surfaces with rapid (t(1/2) < or = 60 min) a