ライフサイエンスコーパス: intercellular

1 midis, independently from the polysaccharide intercellular adhesin PIA.

2 p requires proteolytic cleavage to act as an intercellular adhesin.

3 ward from the bacterial cell wall, promoting intercellular adhesion between cells in the biofilm.

4 We propose that defective intercellular adhesion contributes to uncontrolled cSCC

5 Low-affinity intercellular adhesion may play a role in favoring biofi

6 We find that intercellular adhesion molecule 1 (ICAM-1) and ICAM-2 on

7 ezrin/radixin/moesin (ERM) phosphorylation, intercellular adhesion molecule 1 (ICAM-1) clustering, a

8 ascular cell adhesion molecule (VCAM-1), and intercellular adhesion molecule 1 (ICAM-1) on endothelia

9 shown to bind to several receptors, of which intercellular adhesion molecule 1 (ICAM-1) upregulation

10 ow a group of PfEMP1 proteins interacts with intercellular adhesion molecule 1 (ICAM-1), allowing us

11 gnificant in only 1 replication set included intercellular adhesion molecule 1 (ICAM-1), anti-LG3, am

12 cell morphology alterations, and crawling on intercellular adhesion molecule 1 (ICAM-1)-expressing ce

13 in T cells increased expression of IFNG and intercellular adhesion molecule 1 (ICAM1) and induced T-

14 s, hepatic decompensation, and soluble serum intercellular adhesion molecule 1 (sICAM-1) MFI.

15 Soluble intercellular adhesion molecule 1 and soluble vascular c

16 D showed increased endothelial inflammation (intercellular adhesion molecule 1 expression) and increa

17 atter correlated with diastolic function and intercellular adhesion molecule 1 expression.

18 the lymphocyte function-associated antigen 1-intercellular adhesion molecule 1 interaction, reduced T

19 e function-associated antigen 1) for ICAM-1 (intercellular adhesion molecule 1) but significantly low

20 phaIIbbeta3 with endothelial alphavbeta3 and intercellular adhesion molecule 1, and (3) a stimulatory

21 active protein, adiponectin, leptin, soluble intercellular adhesion molecule 1, and E-selectin all fe

22 s showed increased interleukin (IL)-6, IL-8, intercellular adhesion molecule 1, and platelet endothel

23 th factor beta1 and beta2; thrombospondin 2; intercellular adhesion molecule 1; interleukin 6 [IL-6];

24 riven by an endothelial-specific promoter of intercellular adhesion molecule 2.

25 and 2, dectin 1, and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin i

26 Soluble endothelial selectin and soluble intercellular adhesion molecule concentrations decreased

27 NFAT-independent adhesion of T cells to the intercellular adhesion molecule ICAM-1, with little effe

28 ve activities involved CD40, CD80, CD86, and intercellular adhesion molecule interactions and require

29 r alpha receptor II (B = 0.07, p < .01), and intercellular adhesion molecule-1 (B = 0.04, p < .05) le

30 NOS), nuclear factor-kappa B (NF-kappaB) and intercellular adhesion molecule-1 (ICAM) (P < 0.001, res

31 f these cells, concomitant with reduction of intercellular adhesion molecule-1 (ICAM-1) and diminishi

32 otential of these cells through reduction of intercellular adhesion molecule-1 (ICAM-1) and vascular

33 udy was to identify mechanisms through which intercellular adhesion molecule-1 (ICAM-1) augments the

34 We have previously shown that intercellular adhesion molecule-1 (ICAM-1) expressed by

35 Intercellular adhesion molecule-1 (ICAM-1) mediates the

36 PfEMP1 and human endothelial proteins CD36, intercellular adhesion molecule-1 (ICAM-1), and endothel

37 of the endothelial mechanosensitive receptor intercellular adhesion molecule-1 (ICAM-1).

38 active protein (CRP), serum amyloid A (SAA), intercellular adhesion molecule-1 (sICAM-1) and vascular

39 Clinical risk factors, soluble intercellular adhesion molecule-1 and endocan (both form

40 [sRAGE]) and endothelial biomarkers (soluble intercellular adhesion molecule-1 and endocan [full-leng

41 n, including the metastasis-related proteins intercellular adhesion molecule-1 and urokinase-type pla

42 alpha receptor II) and endothelial function (intercellular adhesion molecule-1 and vascular cell adhe

43 ges have been assumed to mediate adhesion to intercellular adhesion molecule-1 for T-cell conjugation

44 uced pulmonary adhesion molecule expression (intercellular adhesion molecule-1) and tissue infiltrati

45 MC releasate elevated ICAM-1 (intercellular adhesion molecule-1) expression on HUVEC (

46 expression of NF-kappaB target genes VCAM-1, intercellular adhesion molecule-1, E-selectin, and tissu

47 sitivity C-reactive protein, fibrinogen, and intercellular adhesion molecule-1, suggested that GlycA

48 ecreted levels of the proangiogenic proteins intercellular adhesion molecule-1, vascular cell adhesio

49 ls of plasma endothelial biomarkers (soluble intercellular adhesion molecule-1: OR, 1.58; 95% CI, 1.2

50 RBCs to endothelial cells is mediated by the intercellular adhesion molecule-4 (ICAM-4), which appear

51 epidermis YAP/WBP2 activity is controlled by intercellular adhesion rather than canonical Hippo signa

52 Intercellular adhesion within the biofilm is mediated by

53 sm that couples cell division orientation to intercellular adhesion.

54 y promoting filopodia formation and reducing intercellular adhesion.

55 lium (RPE) cells that may have a key role in intercellular adhesion.

56 ness that is required by the matrix to break intercellular adhesions and initiate cell invasion.

57 rams via which epithelial cells reduce their intercellular adhesions and proliferative capacity while

58 ccelerated by propagation of tension through intercellular adhesions.

59 The formation of intercellular adhesive junctions is initiated by trans b

60 Desmosomes are intercellular adhesive junctions that impart strength to

61 eighbors, and this involves various types of intercellular adhesive structures such as tight junction

62 ly programmed stages: substratum attachment, intercellular aggregation and architecture maturation.

63 Here it is shown that Lsr2 participates in intercellular aggregation, but substratum attachment of

64 The mesophyll surface area exposed to intercellular air space per leaf area (Sm ) is closely a

65 (gm ) describes the movement of CO2 from the intercellular air spaces below the stomata to the site o

66 s CO2 concentration drawdown capacity in the intercellular airspace and chloroplast stroma.

67 Intercellular amino acid transport is essential for the

68 posttranslational modification that induces intercellular and extracellular responses by regulating

69 cleus must continually resist and respond to intercellular and intracellular mechanical forces to tra

70 cellular functions including cell motility, intercellular and intracellular signaling, gene expressi

71 fic labelling of target proteins in confined intercellular and organotypic tissues, with reduced ster

72 ering via cis interactions further increases intercellular binding.

73 M-3, a known binding partner [9], to promote intercellular bridge stability and limit localization of

74 Given this inconsistency, the mechanism of intercellular bridge stabilization is unclear.

75 ytokinetic rings are enriched on stably open intercellular bridges [1, 3, 4].

76 Intercellular bridges are proposed to arise from stabili

77 lts, negative regulators of NMM-II stabilize intercellular bridges in the Drosophila egg chamber [10,

78 conserved mechanism for the stabilization of intercellular bridges that can occur by diverse molecula

79 Germ cells in most animals are connected by intercellular bridges, actin-based rings that form stabl

80 anillin and non-muscle myosin II (NMM-II) to intercellular bridges.

81 identifying molecular mechanisms regulating intercellular bridges.

82 The Ca(2+) response depends on the prestress intercellular Ca(2+) activity and not on the magnitude o

83 entials even in the absence of ATP-dependent intercellular Ca(2+) signaling in the nonsensory cells.

84 Thus, intercellular Ca(2+) waves in developing epithelia may b

85 ential conditions for generating organ-scale intercellular Ca(2+) waves in Drosophila wing discs that

86 Mechanically induced intercellular Ca(2+) waves rely on IP3R-mediated Ca(2+)-

87 We discovered that mechanically induced intercellular Ca(2+) waves require fly extract growth se

88 s sufficient, but not necessary, to initiate intercellular Ca(2+) waves.

89 itiated at lower hormone concentrations, and intercellular calcium wave propagation rates were faster

90 by which T cell-derived microvesicles act as intercellular carriers of functional miR-4443, which mig

91 aLbeta2 binding with soluble and immobilized intercellular cell adhesion molecule 1.

92 Here, we show that intercellular Celsr1 complexes that connect dividing cel

93 Gap junctions (GJs), intercellular channels composed of subunit connexins, ca

94 electrical activity of neurons and forms an intercellular chemical communication channel.

95 uggesting that future therapies could target intercellular cleft separation as a compliment or altern

96 ating extracellular electric field coupling, intercellular cleft sodium nanodomains, and LQT3-associa

97 cute interstitial edema was used to increase intercellular cleft width in isolated guinea pig heart e

98 Models predict that significantly decreasing intercellular cleft widths slows conduction because of r

99 nt channels, myocytes produced EADs for wide intercellular clefts, whereas for narrow clefts, EADs we

100 rin promoted epithelial cell apoptosis while intercellular Clusterin modulated the expression of the

101 cadherin (Ecadherin) is responsible for the intercellular cohesion of epithelial tissues.

102 Extracellular vesicles (EVs) are involved in intercellular communication and affect processes includi

103 They mediate several forms of intercellular communication and are upregulated in diver

104 d by reports indicating their unique role in intercellular communication and potential connection to

105 Tumor-released RNA may mediate intercellular communication and serve as biomarkers.

106 e important roles of KSHV-associated VLVs in intercellular communication and the viral life cycle.

107 Consequently, we identify an innate intercellular communication arming resident MCs with key

108 sues, they now emerge as novel regulators of intercellular communication between adjacent and remote

109 Vesicles mediate intercellular communication between both neighboring and

110 t many cancer behaviors critically depend on intercellular communication between cancer cells themsel

111 for miR-19a carried through the exosomes in intercellular communication between HCV-infected hepatoc

112 There is reciprocal intercellular communication between local muscle cell co

113 nctional proteins and small RNAs, facilitate intercellular communication between neighbouring cells,

114 lar vesicles (EVs) are critical mediators of intercellular communication between tumor cells and stro

115 angement of connexins is thought to regulate intercellular communication by establishing an ordered s

116 ld facilitate the transition of the study of intercellular communication by membrane nanotubes from c

117 defensins and receptor-like kinases mediate intercellular communication during both the immune respo

118 and functional data suggest that the altered intercellular communication governed by mutated Cx50 pro

119 Intercellular communication has not been described previ

120 ws that exosomes are involved in fine-tuning intercellular communication in asthma.

121 s are small signaling molecules that mediate intercellular communication in microbial populations and

122 teractions on fertility and the evolution of intercellular communication in pollination.

123 icated a novel mechanism of exosome-mediated intercellular communication in the activation of HSC for

124 ers and quorum sensing signals indicative of intercellular communication in the aqueous environment w

125 is study contributes to the understanding of intercellular communication in the pathogenesis of liver

126 Intercellular communication is a vital yet underdevelope

127 Exosome-dependent intercellular communication is an emerging signaling mec

128 In biological systems, intercellular communication is mediated by membrane prot

129 A striking example of this intercellular communication is the vascularization of th

130 In addition, intercellular communication mediated by the delivery of

131 dynamics have demonstrated that substantial intercellular communication occurs between cells of the

132 d cells form multiple nanotubes that mediate intercellular communication of Ca(2+) signals and active

133 Here, we describe a new mechanism of intercellular communication originating from large oncos

134 Exocytosis is a highly regulated intercellular communication process involving various me

135 Intercellular communication sets the pace for transforme

136 bclass of extracellular vesicles involved in intercellular communication that are released by all cel

137 Exosomes are important vehicles of intercellular communication that shape host responses to

138 iological signature that MSCs may employ for intercellular communication to facilitate tissue repair.

139 Intercellular communication via chemical signaling proce

140 xosomes are extracellular vesicles conveying intercellular communication with possible diagnostic and

141 temporal expression of SCN neuronal state or intercellular communication within the SCN network.

142 Exosomes are produced by cells to mediate intercellular communication, and have been shown to perp

143 aeruginosa virulence is controlled partly by intercellular communication, and the transcription facto

144 ucinol (DAPG), function in intracellular and intercellular communication, both as autoinducers of the

145 In addition to their role in intercellular communication, exosomes are beginning to b

146 role in various cellular processes, such as intercellular communication, inflammation, cellular home

147 FGF signaling, an important component of intercellular communication, is required in many tissues

148 r compounds in tumors play critical roles in intercellular communication, tumor proliferation, and ca

149 nsfected GABAergic neurons suggests hampered intercellular communication.

150 which gap junction nexus stability modulates intercellular communication.

151 NA, and proteins, between cells as a form of intercellular communication.

152 nanotubes (TNTs) represent a novel route of intercellular communication.

153 ta-PIX, and RHOA GEFs that are implicated in intercellular communication.

154 EVs) are proposed to play important roles in intercellular communication.

155 cellular vesicles (EVs) are key mediators of intercellular communication.

156 llular stress responses and exosome-mediated intercellular communication.

157 eive cargo and machinery for cell growth and intercellular communication.

158 for LMC formation by CD4 T cells, affecting intercellular communication.

159 d disease, and are emerging as mediators for intercellular communication.

160 s in a regulated fashion and are involved in intercellular communication.

161 e immune system through a novel mechanism of intercellular communication.

162 Exosomes are involved in intercellular communication.

163 ration of motility forces and restriction of intercellular communication.

164 n adjacent cells to allow for gap junctional intercellular communication.

165 most cell types, as biological packages for intercellular communication.

166 Exosomes are emerging mediators of intercellular communication; whether the release of exos

167 astrocytes in the CNS and forms gap junction intercellular communications between astrocytes-astrocyt

168 Thus, intercellular competition creates an inescapable double

169 While intercellular competition weeds out nonfunctional cells,

170 Selection between somatic cells (i.e., intercellular competition) can delay aging by purging no

171 PCP proteins form intercellular complexes, linked by Celsr1-mediated homop

172 s a new probe for investigating this kind of intercellular connection, as well as for studying cell-c

173 n of photosynthetic enzymes and by increased intercellular connections.

174 A well-established function of intercellular connectivity is to transport cytoplasmic m

175 Taken together, we propose that intercellular connectivity supported by the fusome uniqu

176 ) Unexpectedly, glucose-induced increases in intercellular connectivity were enhanced after Pax6 dele

177 marize current knowledge on the formation of intercellular connectivity, and discuss its meaning by v

178 those in lonesome microwells, which prevent intercellular contact.

179 cells (SCs) reside in niches, which, through intercellular contacts and signaling, influence SC behav

180 Intercellular contacts in multicellular organisms are ma

181 to activate signals that reinforce stressed intercellular contacts.

182 opy reflected cAMP-induced reorganization of intercellular contacts.

183 del system to study regulation of intra- and intercellular copper trafficking pathways.

184 Here we demonstrate WNT-mediated intercellular coupling between the cell cycle and circad

185 s reveal Paneth cell-secreted WNT as the key intercellular coupling component linking the circadian c

186 We investigate local intercellular coupling in Ca-induced depolarization in i

187 The ontogeny of circadian cycling and intercellular coupling in the SCN remains poorly underst

188 elease from the endoplasmic reticulum, (iii) intercellular coupling, and (iv) both transient and long

189 a continuous and rapid process critical for intercellular coupling.

190 ced primary cilia, structures that transduce intercellular cues such as Hedgehog (Hh) signals.

191 ments from bulk cell samples, which obscures intercellular differences and prevents analyses of rare

192 rtmentalization facilitates the preferential intercellular diffusion of specific second messengers is

193 essed here through a survey of the published intercellular distribution of expressed regulatory genes

194 d quantified the contribution of exosomes to intercellular drug transfer and pharmacodynamics.

195 r release, and (b) exosome is a mechanism of intercellular drug transfer that contributes to pharmaco

196 uccessfully predicted effects of exosomes on intercellular drug transfer, cytotoxicity of PTX on Dono

197 tochrome protein complex required for direct intercellular electron transfer.

198 ct in dual capacities as channels for direct intercellular exchange of small molecules and as structu

199 an impact on brain vascular function through intercellular exosome signaling.

200 t cell proliferation prevents the buildup of intercellular forces within cell colonies, enabling thei

201 oids, which are fenestrated capillaries with intercellular gaps and a fragmented basement membrane, f

202 verage of tumour vessels and the presence of intercellular gaps.

203 (therapeutic) doses, dose-dependent loss of intercellular hepatic TJ-associated ZO-1 protein express

204 between organisms, but within infected hosts intercellular infection can be spread by additional mech

205 Consistent with the intercellular interaction, we found reduced expression o

206 ly 'sense' and follow topographic alignment, intercellular interactions within epithelial clusters te

207 tive of spatially distinct local signals and intercellular interactions.

208 influenced the expression of genes encoding intercellular junction (IJ) proteins, whereas the loss o

209 Endothelial cell intercellular junction formation was characterized by im

210 se and tensin homolog (PTEN), which impaired intercellular junction formation, prolactin receptor tra

211 se data suggest that stiff substrates change intercellular junction protein localization and degradat

212 -mediated feedback is a global effect on the intercellular junction.

213 ensive array of transporters and specialized intercellular junctional complex components.

214 s induced fibroblastic morphology, increased intercellular junctional distance, and induced paracellu

215 ial monolayers also developed focal adherens intercellular junctions and became more permeable when c

216 Adherens junctions (AJs) are the major intercellular junctions by which cells sense and exert m

217 ved from their off-centered position next to intercellular junctions toward extracellular matrix adhe

218 arrier, including keratinocyte cytoskeleton, intercellular junctions, and cell adhesion.

219 defect-driven extrusion mechanism depends on intercellular junctions, because the weakening of cell-c

220 or concentrating PECAM-1 at endothelial cell intercellular junctions, where it functions to facilitat

221 unction proteins occludin and claudin-2 from intercellular junctions.

222 ons and recruited by the cadherin complex to intercellular junctions.

223 al inoculation was overcome by disruption of intercellular junctions.

224 urrounding type I hair cells causes unstable intercellular K(+) concentrations, altering the biophysi

225 severe transepidermal water loss, decreased intercellular lipid lamellae in the stratum corneum, and

226 Nitric oxide (NO) is an intercellular messenger involved in multiple bodily func

227 e of extracellular vesicles that function as intercellular messengers by delivering signaling protein

228 cale membrane-derived vesicles that serve as intercellular messengers carrying lipids, proteins, and

229 In this study intercellular MHC transfer by thymic DC subsets was inve

230 efficiency of and distinct mechanisms drive intercellular MHC transfer by thymic DC subsets.

231 Intercellular MHC transfer was donor-cell specific; thym

232 acellular space and a loss of the desmosomal intercellular midline.

233 J is required for filament integrity, normal intercellular molecular exchange, heterocyst differentia

234 However, the role of microtubules in the intercellular movement of plant proteins is less clear.

235 f KinG function results in a decrease in the intercellular movement of SHR and an increase in the sen

236 ncoded by Turnip mosaic virus (TuMV), in the intercellular movement of the viral replication vesicles

237 e sufficient to support the PD targeting and intercellular movement of TuMV replication vesicles indu

238 When this interaction is impaired, the intercellular movement of TuMV replication vesicles is i

239 as a docking point for PD targeting and the intercellular movement of TuMV replication vesicles.

240 different viral proteins in coordinating the intercellular movement of viral replication vesicles.

241 w viral proteins act together to support the intercellular movement of viruses is poorly defined.

242 We show that intercellular mRNA transfer occurs in all coculture mode

243 Intercellular nanotube connections have been identified

244 odiestrase YmdB, shown previously to mediate intercellular nanotube formation.

245 hat influenza viruses can spread using these intercellular networks that connect epithelial cells, ev

246 NOTCH receptors and mediate a non-canonical intercellular NOTCH signaling.

247 n holds that in these organisms, inefficient intercellular nutrient exchange compels the fitness cost

248 sub-diploid chromosome profiles resulting in intercellular partitioning of the genome.

249 to an active form when driven together by an intercellular PPI, producing bright fluorescence or cont

250 plays an important role in many cellular and intercellular processes including signal transduction, s

251 common pathways appear to be used for their intercellular propagation and spreading.

252 Additionally, we showed epithelial intercellular pulling forces at tricellular junctions an

253 dhesion, consistent with the need for larger intercellular pulling forces to compact cell aggregates.

254 ther gene expression analyses uncovered that intercellular purine metabolism was significantly change

255 pressed at the intercalated disk, and narrow intercellular separation can modulate cell-to-cell coupl

256 However, it remains unclear how intercellular signaling among somatic cells results in o

257 mechanical interactions and/or unidentified intercellular signaling between constricted airways, the

258 on between HH and XCI and support a role for intercellular signaling during XCI.

259 r vesicles (EVs) that play a central role in intercellular signaling in mammals by transporting prote

260 ated partly by tissue-specific and partly by intercellular signaling initiated by phyA.

261 standing of the integrated intracellular and intercellular signaling networks that control plant grow

262 ronment, but how biomechanics contributes to intercellular signaling remains unclear.

263 S uses a previously unknown peptide-mediated intercellular signaling system to control SpeB productio

264 Intercellular signaling via extracellular vesicles (EVs)

265 and of their Sfrp inhibitors, together with intercellular signaling via PCP proteins, polarize node

266 8-11) to controlling whole populations using intercellular signalling(12-16).

267 ands is an important mechanism of regulating intercellular signalling.

268 iopsy clinically as well as for the study of intercellular signalling.

269 hrony, and ensemble period are determined by intercellular signals and are embodied in a circadian wa

270 y similar to membrane nanotubes with unknown intercellular signals triggering their formation.

271 ophagy is known to be influenced by systemic intercellular signals, the proteins that control autopha

272 nctive Ga granules were deposited within the intercellular space in roots.

273 nt, or order, of desmosomal cadherins in the intercellular space is critical for adhesive strength.

274 Plants control nutrient availability in intercellular spaces (the apoplast) via transporters, ch

275 Cx50 KO lenses exhibited increased intercellular spaces between lens fiber cells.

276 hed over a substomatal cavity and network of intercellular spaces that is initially fluid filled.

277 helia and can be described as tightly sealed intercellular spaces.

278 zone hyperplasia, desquamation, and dilated intercellular spaces; P < .0001), lamina propria eosinop

279 The intercellular spreading of protein assemblies is a major

280 -cell junctions with concomitant decrease in intercellular stress.

281 lants, and that these forces are balanced by intercellular stresses in follower rows.

282 oscillatory patterns of traction forces and intercellular stresses that tend to pull cell-matrix adh

283 Here we focus on the growth of the intercellular surface during cell division in a Caenorha

284 ustering of integrin alpha5beta1 at lateral, intercellular surfaces.

285 ension probes can be broadly used to measure intercellular tensile forces.

286 pid and local increase in cellular traction, intercellular tension and tissue compaction.

287 a growth, but increased network formation by intercellular TMs, suggesting a functional and molecular

288 of the molecular mechanisms relevant for the intercellular trafficking of protein aggregates involved

289 by conspicuously sending out TNTs, enabling intercellular transfer of alpha-SYN to healthy astrocyte

290 ocytes respond by sending out TNTs, enabling intercellular transfer of alpha-SYN to healthy astrocyte

291 xosomes could play a role in the purging and intercellular transfer of excess free RNAs, including fu

292 cells, thus supporting their involvement in intercellular transfer of haptenated proteins.

293 nensin, revealed a corresponding increase in intercellular transfer of prion infectivity.

294 Efficient intercellular transfer of RNAs, proteins, and lipids as

295 identifying GA-hMSC-derived exosomes in the intercellular transfer of specific miRNA that enhance th

296 tuning of cell adhesion, cell mechanics, and intercellular transmission of mechanical load.

297 tudy, we describe an alternative pathway for intercellular transmission of PRRSV in which the virus u

298 tractable mathematical model that depends on intercellular transport on a cell lineage tree.

299 RATIONALE: Intercellular uncoupling and Ca(2+) (Ca) mishandling can

300 Here, by using an infection-free intercellular vesicle movement assay, we investigate the