ライフサイエンスコーパス: alpha5beta1 integrin

1 iRNAs directed against both collagenases and alpha5beta1 integrin.

2 nct roles in regulating alphaIIbbeta3 versus alpha5beta1 integrin.

3 domain III (residues 240-248) binds purified alpha5beta1 integrin.

4 cells frequently up-regulate the FN receptor alpha5beta1 integrin.

5 VEGF-induced association of VEGFR-2 with the alpha5beta1 integrin.

6 y inhibited the association of RhoA with the alpha5beta1 integrin.

7 ntibodies, suggesting the involvement of the alpha5beta1 integrin.

8 tion mediated by the alpha4beta1 but not the alpha5beta1 integrin.

9 n forces, which are transduced to Fn through alpha5beta1 integrin.

10 hich mesodermal cells migrate using the same alpha5beta1 integrin.

11 microm2 in cells attached to fibronectin via alpha5beta1 integrin.

12 ally identified as a binding partner for the alpha5beta1 integrin.

13 ress fibers and the consequent clustering of alpha5beta1 integrin.

14 h affinity VEGF receptor 1 and antibodies to alpha5beta1 integrin.

15 sitive to the normal outside-in signals from alpha5beta1 integrin.

16 SRN sequence, which induced invasion through alpha5beta1 integrin.

17 as reduced in the presence of mAbs to FN and alpha5beta1 integrin.

18 rn typical of that seen with fibronectin and alpha5beta1 integrin.

19 binding site (LIBS) on the beta1 subunit of alpha5beta1 integrin.

20 a tempering the bacterium's interaction with alpha5beta1 integrin.

21 is an absolute requirement for initiation by alpha5beta1 integrin.

22 f beads bound per cell nor the clustering of alpha5beta1 integrin.

23 o effect on the extracellular aggregation of alpha5beta1 integrin.

24 nds to an integrin receptor, most likely the alpha5beta1 integrin.

25 ckdown of either fibronectin or its receptor alpha5beta1 integrin.

26 did not bind to alternative ANGPT2 receptor alpha5beta1 integrin.

27 oupling protein (RCP)-dependent recycling of alpha5beta1 integrin.

28 d to decreased expression of fibronectin and alpha5beta1 integrin.

29 ress both functional p53 and a high level of alpha5beta1 integrin.

30 ls and restores the association of uPAR with alpha5beta1 integrin.

31 A binding to uPAR and fibronectin binding to alpha5beta1-integrin.

32 nriched in plasma membrane-localized, active alpha5beta1-integrin.

33 in Rab25-knockdown cells reversed losses of alpha5beta1-integrin.

34 omaterials have focused on ligands that bind alpha5beta1 integrins.

35 d migration mediated by both alpha4beta1 and alpha5beta1 integrins.

36 and to a lesser extent with alphaVbeta5 and alpha5beta1 integrins.

37 0-kDa RGD-containing fragment that activates alpha5beta1 integrins.

38 ectin required alpha2beta1, alpha4beta1, and alpha5beta1 integrins.

39 lanoma cells was mediated by alpha4beta1 and alpha5beta1 integrins.

40 sters of PINCH that are colocalized with the alpha5beta1 integrins.

41 st cell receptors, including alpha-5 beta-1 (alpha5beta1) integrin.

42 ization and direct association of Rab25 with alpha5beta1-integrins.

43 ing a selective, small-molecule inhibitor of alpha5beta1 integrin, 2-aroylamino-3-{4-[(pyridin-2-ylam

44 ena forms an adhesion-regulated complex with alpha5beta1 integrin, a fibronectin receptor involved in

45 We show here that the alpha5beta1 integrin, a fibronectin receptor, is an effi

46 complex comprised of the cytoplasmic tail of alpha5beta1 integrin, actin, and the signaling molecules

47 mechanoreceptors have been identified, with alpha5beta1 integrin acting as a predominant mechanorece

48 egrins, alpha4beta1 and an RGD-directed, non-alpha5beta1 integrin, activate ERK2 in response to mecha

49 alize, with their internalization regulating alpha5beta1 integrin activation and signalling.

50 The effects of alpha5beta1 integrin activation on both whole-cell and s

51 Our results show that alpha5beta1 integrin activation potentiates BK channel a

52 ovel EGF-dependent mechanism controlling the alpha5beta1 integrin activation state.

53 Thus, BK channel activity is enhanced by alpha5beta1 integrin activation, likely through an intra

54 Following alpha5beta1 integrin activation, native CaL channels in

55 its (mSlo) are acutely potentiated following alpha5beta1 integrin activation.

56 l isoforms are acutely potentiated following alpha5beta1 integrin activation.

57 myosin II contractility and is necessary for alpha5beta1-integrin activation and leading edge adhesio

58 -4 (VLA-4; alpha4beta1 integrins) and VLA-5 (alpha5beta1 integrins) activation.

59 integrin and uPAR drive the translocation of alpha5beta1 integrin-acylated Fyn signaling complexes in

60 s forming a complex, while expression of the alpha5beta1 integrin also increases the Nischarin/PAK1 a

61 Activation of alpha5beta1 integrin also markedly potentiates the recru

62 ction which involves FN-f stimulation of the alpha5beta1 integrin and activation of the nonreceptor t

63 on EP4 was inhibited by an antibody against alpha5beta1 integrin and by inhibitors of phosphoinositi

64 n by controlling the population of activated alpha5beta1 integrin and cytoskeleton strength during ce

65 In a reciprocal manner, TGF-beta1 activates alpha5beta1 integrin and downstream signalling to focal

66 sociation of Rab-coupling protein (RCP) with alpha5beta1 integrin and drove RCP-dependent recycling o

67 alpha5beta1 integrin and endoglin form a complex on the

68 and used to measure binding strength between alpha5beta1 integrin and fibronectin by quantifying the

69 maturation by regulating surface density of alpha5beta1 integrin and fibronectin.

70 ve regarding the consistent up-regulation of alpha5beta1 integrin and FN in many tumors and their cor

71 at two additional focal adhesion components, alpha5beta1 integrin and focal adhesion kinase (FAK), ar

72 cell-matrix interactions and survival (e.g., alpha5beta1 integrin and its ligand, fibronectin).

73 this framework, PPFIA1 interacts with active alpha5beta1 integrin and localizes close to EC adhesions

74 gs indicate that negative cross-talk between alpha5beta1 integrin and p53 supports glioma resistance

75 al type I repeats of fibronectin bind to the alpha5beta1 integrin and support cell adhesion.

76 cellular matrix molecule fibronectin-induced alpha5beta1 integrin and supports a critical role for th

77 l, Thy-1 is capable of independently binding alpha5beta1 integrin and syndecan-4 (Syn4) receptors.

78 Functionally, endoglin-mediated fibronectin/alpha5beta1 integrin and TGF-beta pathway crosstalk alte

79 R with the amino-terminal fragment recruited alpha5beta1 integrin and the acylated form of the Src fa

80 zed using the PR_b peptide that binds to the alpha5beta1 integrin and the AG86 peptide that binds to

81 ngly dependent on ligation of fibronectin by alpha5beta1 integrin and the capacity of Rab25 to intera

82 gradients requires intact signaling between alpha5beta1 integrin and the epidermal growth factor rec

83 depletion suggests that the interactions of alpha5beta1 integrin and uPAR drive the translocation of

84 f tensin and actin with N-cadherin, released alpha5beta1 integrins and tensin from cell-cell contacts

85 in matrix assembly has been shown to recruit alpha5beta1 integrins and tensin into fibrillar adhesion

86 part through an interaction between beta1 or alpha5beta1 integrins and the EBV BMRF-2 protein; and (i

87 ar adhesions (FBs) containing high levels of alpha5beta1 integrins and the tensin3 adaptor protein ar

88 D and PHSRN sequences of fibronectin to bind alpha5beta1 integrins and triggers signalling for cell a

89 receptor (uPAR) expression, which activated alpha5beta1-integrin and epidermal growth factor recepto

90 ubiquitin-mediated proteasome degradation of alpha5beta1-integrin and facilitating effective beta1-in

91 ase influences tensin production to regulate alpha5beta1-integrin and fibrillar adhesion assembly and

92 the cell surface and total protein levels of alpha5beta1-integrin and increased its degradation.

93 ement in coordinating polarized transport of alpha5beta1-integrin and likely of other specialized end

94 This contrasts with the behavior of the alpha5beta1-integrin and paxillin, which do not co-flux.

95 correlates with expression of CD36 receptor, alpha5beta1 integrin, and alphavbeta3 integrin on prolif

96 a mechanism involving brain endothelial cell alpha5beta1 integrin, and the subsequent neuroprotective

97 The inhibitor of PI3-K, Wortmannin, and anti-alpha5beta1 integrin antibodies abrogated the effect of

98 bloodstream, we intravenously injected anti-alpha5beta1 integrin antibody and 10 minutes to 24 hours

99 Intense vascular labeling by anti-alpha5beta1 integrin antibody co-localized with the unif

100 oreover, a specific blocking monoclonal anti-alpha5beta1 integrin antibody, PB-1, blocks insulin-stim

101 RK becomes activated, uPAR is overexpressed, alpha5beta1-integrins are activated, and dormancy is int

102 eta receptor (TbetaRII) and the FN receptor (alpha5beta1 integrin) are required.

103 We identify alpha5beta1 integrin as a major RhoJ cargo and show that

104 Using RGD-based peptides for the alpha5beta1 integrin as a model system, we have demonstr

105 Our data identify the alpha5beta1 integrin as a potential therapeutic target t

106 H. pylori and its cag-T4SS exploit alpha5beta1 integrin as a receptor for CagA translocatio

107 As IGFBP-1 binds both the alpha5beta1 integrin as well as IGF-I in vitro, we asked

108 n and its interaction with and activation of alpha5beta1-integrin as determinants of the in vivo grow

109 er preclinical validation of fibronectin and alpha5beta1-integrin as targets for breast cancer therap

110 In this new matrix assembly mechanism, alpha5beta1 integrin-based focal adhesions slide activel

111 ell attachment but over time are switched to alpha5beta1 integrin-based sliding focal adhesions to as

112 This effect is mediated through the alpha5beta1 integrin because blockade of fibronectin-alp

113 that L1 binding to L1, TAG-1, or F3, and L1-alpha5beta1 integrin binding are not essential for norma

114 ence of three distinct activation states for alpha5beta1 integrin binding to adsorbed fibronectin for

115 neering hydrogel materials to promote alpha3/alpha5beta1 integrin binding, we can promote the formati

116 1 homophilic binding was lost, along with L1-alpha5beta1 integrin binding.

117 process is known to involve both the central alpha5beta1 integrin-binding and the C-terminal heparin-

118 Fn fragments containing both the alpha5beta1 integrin-binding domain (III 9 to 10) and th

119 y click-chemistry (CuAAC) trimerization of a alpha5beta1 integrin-binding pseudopeptide on the triaza

120 Additionally, alpha5beta1-integrin blockade reversed the membrane retr

121 d cell surface expression of alphaVbeta3 and alpha5beta1 integrins, both FN receptors.

122 ferentiation was controlled by the levels of alpha5beta1 integrin bound to Fn, and differentiation wa

123 Activation of alpha5beta1 integrin by an appropriate, insoluble alpha5

124 e cooperative binding of heparan sulfate and alpha5beta1 integrin by the AAV2 capsids.

125 Activation of alpha5beta1-integrin by uPAR generates persistently high

126 alpha5beta1 integrin can occupy several distinct conform

127 We demonstrate that syntaxin 6 and alpha5beta1 integrin colocalize in EEA1-containing early

128 ediated adhesion is only facilitated through alpha5beta1 integrin complex and is not a function of ei

129 The alpha5beta1 integrin complex is important for anchoring

130 L-8 and ROS production and activation of the alpha5beta1 integrin complex on HAECs.

131 C surface, suggesting that both activate the alpha5beta1 integrin complex on the endothelial surface.

132 udy showed that PA binds to alpha4beta1- and alpha5beta1-integrin complexes, leading to their conjoin

133 Cell binding to fibronectin through either alpha5beta1 integrins (constitutively expressed) or alph

134 The impact of this site on alpha5beta1 integrin-dependent cell functions was examin

135 oblasts and soluble fibronectin that promote alpha5beta1 integrin-dependent fibronectin fibril assemb

136 and cyclin D1 and decreases p21 and PTEN via alpha5beta1 integrin-dependent signals that include PI3-

137 We found that alphavbeta6- and alpha5beta1-integrin-dependent activation of Rac1 was me

138 itro, alpha-defensins specifically inhibited alpha5beta1-integrin-dependent migration of bovine retin

139 We further determine that alpha5beta1-integrin depends on an AnkB/RabGAP1L complex

140 Recycling of alpha5beta1 integrin did not affect its regulation or ab

141 ocalization and levels of active SMAD2/3 and alpha5beta1-integrin distinguish patient-protective from

142 grounds studied here, loss of fibronectin or alpha5beta1 integrin does not contribute to tumorigenesi

143 Due to its unique ability to bind to alpha5beta1 integrin, EETI 2.5F showed superior in vivo

144 Adhesion to fibronectin through the alpha5beta1 integrin enables endothelial cells to prolif

145 protein (RCP)-driven endocytic recycling of alpha5beta1 integrin enhances invasive migration of canc

146 ted cohesivity, we used a series of chimeric alpha5beta1-integrin-expressing cells cultured as multil

147 Clinically, alpha5beta1 integrin expression was associated with a mo

148 amined by conventional immunohistochemistry, alpha5beta1 integrin expression was strong on most blood

149 Targeted CEU imaging of alpha(v)- and alpha5beta1-integrin expression was performed with micro

150 sed expression of alphaSMA, fibronectin, and alpha5beta1 integrin (fibronectin receptor components) i

151 he catalytic monomer, in causing loss of the alpha5beta1 integrin (fibronectin receptor) from HGF.

152 en bonds in a particular allosteric state of alpha5beta1 integrin-fibronectin complex, a conformation

153 mechanism requires localized myosin-IIA- and alpha5beta1 integrin/fibronectin-mediated migration and

154 noprecipitation suggests that uPAR, EGFR and alpha5beta1 integrin formed a ternary complex.

155 mbining FN secretion and recycling of active alpha5beta1 integrin from the trans-Golgi network (TGN)

156 ased adhesions and that the translocation of alpha5beta1 integrins from cell-cell contacts into fibri

157 ed with immunoprecipitates of alpha4beta1 or alpha5beta1 integrins from lysates of FN-adherent NK cel

158 s Alix on the substratum and have defects in alpha5beta1-integrin functions.

159 Increased FN and alpha5beta1 integrin gene expression was observed in pho

160 et and inhibit alphavbeta3, alphavbeta5, and alpha5beta1 integrins have generated great interest beca

161 The alpha5beta1 integrin heterodimer regulates many processe

162 Blocking alpha5beta1 integrin highly inhibited ShlA-dependent aut

163 ts with the alpha7beta1 integrin but not the alpha5beta1 integrin in C2C12 myoblasts, suggesting an i

164 ates the intracellular trafficking of active alpha5beta1 integrin in endothelial cells to repress fib

165 ntiated migration toward fibronectin through alpha5beta1 integrin in human embryonic kidney 293 cells

166 lasts was attributed to higher expression of alpha5beta1 integrin in myoblasts.

167 such as FN and the corresponding integrins, alpha5beta1 integrin in particular.

168 at these defects probably arise from loss of alpha5beta1 integrin in subsets of specialised Prox1(+)P

169 are able to spread on fibronectin using the alpha5beta1 integrin in the absence of activin-A inducti

170 Here, we mapped the distribution of alpha5beta1 integrin in three murine tumor models and id

171 ct is not seen with expression of a chimeric alpha5beta1 integrin in which the cytoplasmic portion of

172 and oligomerization state of alphavbeta3 and alpha5beta1 integrins in bilayers, which contain coexist

173 This contrasts with the role played by alpha5beta1 integrins in promoting close apposition betw

174 circuitry underlying polarized recycling of alpha5beta1-integrin in mouse embryonic fibroblasts, whi

175 Fibronectin and alpha5beta1 integrin increase Smad1/5/8 signalling by pr

176 HL-525 cells (which have a high level of the alpha5beta1 integrin) incubated on FN differentiated int

177 okinase receptor (uPAR) which, by activating alpha5beta1 integrin, initiates an intracellular signal

178 termined the signaling mechanisms induced by alpha5beta1 integrin interaction with its high-affinity

179 f this binding site, and of the lateral uPAR-alpha5beta1 integrin interaction, to ERK pathway activat

180 -cadherin ligation recruited both tensin and alpha5beta1 integrins into nascent cell-cell adhesions.

181 Alpha5beta1 integrin is a cell surface receptor that med

182 The alpha5beta1 integrin is a key fibronectin (FN) receptor

183 During the initial phase of adhesion, alpha5beta1 integrin is activated in an energy-dependent

184 In later stages of adhesion maturation, alpha5beta1 integrin is activated to a higher binding st

185 Fibronectin's RGD-mediated binding to the alpha5beta1 integrin is dramatically enhanced by a syner

186 ely, invasive migration that is dependent on alpha5beta1 integrin is promoted by disrupting Rabaptin

187 uggesting that the ligand specificity of the alpha5beta1 integrin is regulated by the cytoskeleton.

188 a suggest that EGF-dependent inactivation of alpha5beta1 integrin is regulated through FLNa phosphory

189 ctivation of both the IGF-I receptor and the alpha5beta1 integrin is required for IGF-I to stimulate

190 Cell attachment to fibronectin or anti-alpha5beta1 integrin is sufficient to sustain the ERK si

191 Kif1C-mediated transport of alpha5beta1-integrins is required for the proper maturat

192 thus lacking the principal binding site for alpha5beta1 integrin, is deposited into the extracellula

193 Phagocytosis of FN utilizes the alpha5beta1 integrin, is mediated in part through tyrosi

194 activator receptor (uPAR) can interact with alpha5beta1 integrin leading to persistent ERK activatio

195 initiated by binding of soluble antibody to alpha5beta1 integrin, led to increased expression of the

196 Similarly, the endogenous alpha5beta1 integrin ligand fibronectin (FN) potentiated

197 ly, we found that fibronectin, an endogenous alpha5beta1 integrin ligand, enhances BK channel current

198 Thus, the alpha5beta1 integrin may protect against Abeta depositio

199 Thus, alpha5beta1 integrins mediate the inhibitory effect of t

200 we show that syntaxin 6 is also required for alpha5beta1 integrin-mediated adhesion of endothelial ce

201 conferred ephrin-B1-responsive activation of alpha5beta1 integrin-mediated cell attachment in human e

202 However, mechanisms coordinating alpha5beta1 integrin-mediated extracellular FN endocytos

203 ion, the Hep II domain had minimal effect on alpha5beta1 integrin-mediated spreading.

204 integrins and MMP-2 downregulation inhibited alpha5beta1 integrin-mediated Stat3 phosphorylation and

205 reviously reported that alpha4beta1 (but not alpha5beta1) integrin-mediated melanoma cell adhesion is

206 tastatic breast cancer cells greatly reduced alpha5beta1-integrin-mediated cell adhesion to fibronect

207 ulture substratum for NIH/3T3 cells promotes alpha5beta1-integrin-mediated cell adhesions and fibrone

208 Using these cells, alpha5beta1-integrin-mediated cell aggregation, compacti

209 tor 1alpha (SDF-1alpha) as well as decreased alpha5beta1-integrin-mediated chemoattractant-stimulated

210 We have demonstrated that the alpha5beta1-integrin mediates strong intercellular cohes

211 3-kinase (PI-3-kinase), suggesting that the alpha5beta1 integrin might interact with the PI-3-kinase

212 ctin and fibronectin polymerization, neither alpha5beta1 integrin nor tensin localize to fibrillar ce

213 tion or loss of fibronectin or its receptor, alpha5beta1 integrin, occurs frequently in tumors and tr

214 adhesive RGD peptide sequence to ligate the alpha5beta1 integrin of cocultured hepatocytes.

215 demonstrate that affinity modulation of the alpha5Beta1 integrin on CML progenitors and K562 cells b

216 r example, excess fibronectin stimulation of alpha5beta1 integrin on stromal cells in PDA results in

217 Mechanistically, TNC interacted with alpha5beta1 integrin on the cell surface of T cells, inh

218 rm overexpression and rapid accessibility of alpha5beta1 integrin on tumor vessels and may prove usef

219 Conversely, activating alpha5beta1 integrins on CHO-T cells by adherence onto f

220 fibronectin (FN) receptors, alpha4beta1 and alpha5beta1 integrins, on NK cells transduce transmembra

221 d fibronectin fragment (FN-f) that binds the alpha5beta1 integrin or with antibodies to specific inte

222 atrices was reversed by Abs directed against alpha5beta1 integrins or by a peptide (GRGDSP) that bind

223 Loss-of-function of Ena/VASP, alpha5beta1-integrins or talin in the somitic cells abol

224 o fibronectin induction was dependent on the alpha5beta1 integrin pair.

225 Neutralizing antibody against alpha5beta1 integrin partially (approximately 60%) block

226 We conclude that alpha5beta1-integrin plays a significant role in vessel

227 Antibodies or peptides that block alpha5beta1 integrins prevented fMLP-stimulated neutroph

228 The results support a mechanism whereby alpha5beta1 integrin priming by high-affinity ligands in

229 ion in MSCs, indicating that peptide-induced alpha5beta1 integrin priming can promote osteogenic diff

230 hemical analyses showed that peptide-induced alpha5beta1 integrin priming transiently increased PI3K/

231 ed Wnt regulatory gene expression induced by alpha5beta1 integrin priming.

232 We previously reported that alpha5beta1 integrin promotes osteogenic differentiation

233 imensional substrates, we show that FN-bound alpha5beta1 integrin promotes tension-dependent malignan

234 mbly by altering the activation state of the alpha5beta1 integrin receptor and suggest that changes i

235 he regulation of the activation state of the alpha5beta1 integrin receptor for fibronectin.

236 ted in the circumferential clustering of the alpha5beta1 integrin receptor, which was accompanied by

237 rapid loss of both fibronectin and its main alpha5beta1 integrin receptor.

238 of filamin A (FLNa) and inactivation of the alpha5beta1 integrin receptor.

239 in this matrix via concomitant engagement of alpha5beta1 integrin receptors and syndecan-4, a transme

240 and fibronectin (FN) through alpha3beta1 and alpha5beta1 integrin receptors, respectively.

241 gonists of the alphavbeta3, alphavbeta5, and alpha5beta1 integrin receptors, which play important rol

242 gh affinity to alphavbeta3, alphavbeta5, and alpha5beta1 integrin receptors.

243 cling of alphavbeta3, which in turn inhibits alpha5beta1 integrin recycling.

244 We conclude that inhibition of the alpha5beta1 integrin reduces lymphangiogenesis in inflam

245 We report that alpha5beta1 integrins regulate the different migratory b

246 providing preclinical proof-of-concept that alpha5beta1 integrin represents a therapeutic target for

247 rategies reveal that regulation of Cav1.2 by alpha5beta1 integrin requires phosphorylation of alpha1C

248 FN-RGD motif and that alphav-class, but not alpha5beta1, integrins retain FN-RGE binding.

249 Thus, the alpha5beta1 integrin seems to protect intestinal epithel

250 ise the hypothesis that insulin receptor and alpha5beta1 integrin signaling act synergistically to en

251 wo domains of fibronectin cannot bind to the alpha5beta1 integrin simultaneously.

252 wth on fibronectin appears to be mediated by alpha5beta1 integrin since a recombinant fibronectin fra

253 t was abolished by anti-alphaMbeta2 and anti-alpha5beta1 integrin-specific monoclonal antibodies (mAb

254 ent, fibronectin, and its cellular receptor, alpha5beta1 integrin, specifically increase TGF-beta1- a

255 that the involvement of GMFG in maintaining alpha5beta1-integrin stability may occur in part by prev

256 ncluding the 110-kDa fragment that binds the alpha5beta1 integrin, stimulate collagenase-3 (MMP-13) p

257 ere able to cross-compete for binding to the alpha5beta1 integrin, suggesting that these two domains

258 sma membrane following normal endocytosis of alpha5beta1-integrin, suggesting that the involvement of

259 We have previously shown that the alpha5beta1 integrin supports cell survival on fibronect

260 ved that imaA mutants bound higher levels of alpha5beta1 integrin than wild-type H. pylori, an outcom

261 the strength of adhesion, the proportion of alpha5beta1 integrin that could be chemically cross-link

262 GRASP depletion reduces the protein level of alpha5beta1 integrin, the major cell adhesion molecule a

263 face expression of the alpha5 subunit of the alpha5beta1 integrin, the major FN receptor in megakaryo

264 of orthotopic bladder cancer expressing the alpha5beta1 integrin, the photoacoustic imaging of targe

265 ty ratio, but in spite of a similar level of alpha5beta1-integrin, they do not assemble FN fibrils.

266 By analyzing the functional binding of alpha5beta1 integrin to adsorbed fibronectin in intact c

267 ting of ligand-occupied, active-conformation alpha5beta1 integrin to late endosomes/lysosomes.

268 Trafficking of alpha5beta1 integrin to lysosomes and its subsequent deg

269 previously unappreciated contribution of FN-alpha5beta1 integrin to megakaryocytosis in JAK2V617F+ P

270 This regulates the surface density of alpha5beta1 integrin to modulate fibronectin matrix asse

271 the hypothesis that RGD ligands work through alpha5beta1 integrin to modulate the activity of large c

272 D-IGFBP-1) which does not associate with the alpha5beta1 integrin to selectively abrogate each of the

273 ed rate, as assessed by the translocation of alpha5beta1 integrin to the apical surface of trophoblas

274 s and metastasis, regulates the recycling of alpha5beta1 integrin to the leading edge of cell pseudop

275 n Helicobacter pylori uses the host receptor alpha5beta1 integrin to trigger inflammation in host cel

276 ctodermal cells from the blastocoel roof use alpha5beta1 integrins to assemble a fibronectin-rich ext

277 in redistribution of pFAK-independent active alpha5beta1-integrin to assorted endosomes.

278 Moreover, increased alpha5beta1 integrin transcripts in GnT-V null MEF were

279 esions containing alphaVbeta3 integrins plus alpha5beta1 integrin translocation into proximal fibrill

280 igration by enhancing endosomal recycling of alpha5beta1 integrin under control of the Rab11 effector

281 strated association of BK B(2) receptor with alpha5beta1 integrin upon BK treatment.

282 enhanced protein degradation of paxillin and alpha5beta1 integrin via proteasome and lysosome pathway

283 10-kDa FN-f or an activating antibody to the alpha5beta1 integrin was found to increase tyrosine auto

284 luence vascular tone by interacting with the alpha5beta1 integrin was studied using rat skeletal musc

285 hese conditions, we found that expression of alpha5beta1-integrin was upregulated in malignant cells

286 VLO4, peptide inhibitors to alphavbeta3 and alpha5beta1 integrins, we showed that CCN2 binding to bo

287 ts of fibronectin, the primary ECM ligand of alpha5beta1-integrin, were also strikingly upregulated i

288 gnaling, ROCK supports a strong adhesion via alpha5beta1 integrin, whereas activation of the IGF-IR k

289 be abrogated with a blocking antibody to the alpha5beta1 integrin, which diminishes the ability of th

290 The alpha5beta1 integrin, which does not associate with TM4S

291 rectly associated with TRPC5 but rather with alpha5beta1 integrin, which opened the channel through a

292 o frequent, activating interactions with the alpha5beta1-integrin, which facilitates the formation of

293 s occurs via RGD integrins, possibly via the alpha5beta1 integrin, while cells from degenerated discs

294 embly can also be restored by stimulation of alpha5beta1 integrin with activating antibody or with Mn

295 Furthermore, BK induced association of alpha5beta1 integrin with EGFR.

296 e-glycine-arginine (NGR) motif known to bind alpha5beta1 integrin with moderate affinity.

297 d process that involves both ligation of the alpha5beta1 integrin with the Arg-Gly-Asp (RGD) sequence

298 N mAb, or by cross-linking of alpha4beta1 or alpha5beta1 integrins with alpha-chain-specific Abs.

299 n-blocking antibodies to the alpha2beta1 and alpha5beta1 integrins with increased phosphorylation of

300 a peptide that disrupts the interactions of alpha5beta1-integrin with fibronectin promoted apoptosis