ライフサイエンスコーパス: intercellular

1 Pectin plays an important role in intercellular adhesion and controlling the porosity of t

2 bute to mucosal homeostasis by strengthening intercellular adhesion between cells.

3 ntial adhesion model in which differences in intercellular adhesion mediate cell sorting.

4 cular cell adhesion molecule (VCAM), but not intercellular adhesion molecule (ICAM), suggesting they

5 E-selectin and intercellular adhesion molecule (ICAM)-1 are biomarkers

6 al region includes selected residues from an intercellular adhesion molecule (ICAM)-like motif shared

7 Surprisingly, while intercellular adhesion molecule 1 (ICAM-1) was significa

8 Surprisingly, the genetic deficiency of intercellular adhesion molecule 1 (ICAM-1), an establish

9 y TM-thrombin complex and in upregulation of intercellular adhesion molecule 1 (ICAM-1).

10 t of BMI on inflammatory biomarkers [soluble intercellular adhesion molecule 1 (sICAM-1), high sensit

11 han antibodies to transferrin receptor-1 and intercellular adhesion molecule 1 (TfR-1 and ICAM-1).

12 egulation of the cellular adhesion molecules Intercellular Adhesion Molecule 1 and Vascular Cell Adhe

13 trast to most other rhinoviruses, which bind intercellular adhesion molecule 1 receptors via a capsid

14 ession for ACE2 and TMPRSS2, and for ICAM-1 (intercellular adhesion molecule 1) (rhinovirus receptor

15 chemistry of eNOS, endothelin-1, P-selectin, intercellular adhesion molecule 1, and vascular cell adh

16 or necrosis factor alpha, caspase-1 (CASP1), intercellular adhesion molecule 1, IL-10, heme oxygenase

17 ndent decrease in cell surface levels of the intercellular adhesion molecule PECAM-1 (CD31) when exam

18 ICAM (intercellular adhesion molecule)-1 and PFKFB3 were also

19 endothelial cells had higher levels of ICAM (intercellular adhesion molecule)-1 and TF expression fol

20 h factor, von Willebrand factor, E-selectin, intercellular adhesion molecule, vascular cell adhesion

21 e kinase, von Willebrand factor, E-selectin, intercellular adhesion molecule, vascular cell adhesion

22 Intercellular adhesion molecule-1 (ICAM-1) expressing ne

23 Blocking intercellular adhesion molecule-1 (ICAM-1) inhibited the

24 Intercellular adhesion molecule-1 (ICAM-1) is up-regulat

25 called 3DNA coupled with antibodies against intercellular adhesion molecule-1 (ICAM-1), a glycoprote

26 This study investigated intercellular adhesion molecule-1 (ICAM-1), a membrane p

27 NAME also blocked blast-induced increases in intercellular adhesion molecule-1 (ICAM-1), a molecule t

28 using polymer nanocarriers (NCs) targeted to intercellular adhesion molecule-1 (ICAM-1), an endotheli

29 scular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1), endothelial

30 Soluble intercellular adhesion molecule-1 (sICAM1) was measured

31 e vascular cell adhesion molecule-1, soluble intercellular adhesion molecule-1) and immune (soluble t

32 th changes in von Willebrand factor, soluble intercellular adhesion molecule-1, soluble E-Selectin, P

33 levels of C-reactive protein, interleukin-6, intercellular adhesion molecule-1, soluble tumor necrosi

34 , angiopoietin-1 and angiopoietin-2, soluble intercellular adhesion molecule-1, soluble vascular cell

35 geal fibroblasts after LIGHT stimulation via intercellular adhesion molecule-1.

36 M [vascular cell adhesion molecule-1], ICAM [intercellular adhesion molecule-1], and MCP1 [monocyte c

37 Intercellular adhesion of keratinocytes depends critical

38 Cadherins are intercellular adhesion proteins that assemble into clust

39 The physiological demands of intercellular adhesion require that the AJ be responsive

40 -mesenchymal transition as marked by loss of intercellular adhesion, and differentiate into VICs.

41 proper distribution of pectin, a mediator of intercellular adhesion, whereas the pectin esterificatio

42 nt of cell-cell junctions required to couple intercellular adhesions and cortical cues to spindle ori

43 antly regulated and responded differently to intercellular aggregation and surface attachment.

44 m production in M. bovis BCG, to distinguish intercellular aggregation from attachment to a surface.

45 onic cells despite its downregulation at the intercellular aggregation step.

46 as shown elsewhere that lsr2 participates in intercellular aggregation, while groEL1 was required for

47 eases in cell size, succulence and decreased intercellular air space.

48 tance (g(m) ) is the diffusion of CO(2) from intercellular air spaces (IAS) to the first site of carb

49 We found that evolutionarily-conserved intercellular and intracellular signaling mechanisms cri

50 invasively monitor time-dependent changes in intercellular and intracellular signaling, which can be

51 quire B cells to respond to a dynamic set of intercellular and microenvironmental signals that instru

52 cally encoded Ca(2+) indicators has revealed intercellular and subcellular heterogeneity of mitochond

53 The intercellular and systemic trafficking of small interfer

54 tory pathway and increased the expression of intercellular and vascular cell adhesion molecules in EC

55 hanistic understanding of how the cell-cell (intercellular) and cell-ECM (extracellular) traction for

56 Collectively, we show that intercellular antigen transfer of DBY is tightly regulat

57 Intercellular antigen transfer was shown to be independe

58 Further mechanism study indicates that the intercellular assemblies interact with multiple ECM comp

59 covered that microtubules promote actomyosin intercellular attachments in epithelia during Drosophila

60 Such intercellular bands extended into a large-scale network

61 al integrity of the barrier by degrading the intercellular barrier proteins at tight and adherens jun

62 cleated cells by stabilizing the cytokinetic intercellular bridge (ICB).

63 The midbody is an organelle assembled at the intercellular bridge between the two daughter cells at t

64 chinery that promotes the degradation of the intercellular bridge, a transient protein structure conn

65 , a transient structure in the middle of the intercellular bridge, where they recruit CUL4 and MDM2 u

66 abscission leading to the formation of long intercellular bridges and multinucleated cells, which mi

67 cellular communication facilitated by stable intercellular bridges connecting developing germ cells.

68 with each other during gametogenesis through intercellular bridges, often called ring canals (RCs), t

69 that germ cells die as clones independent of intercellular bridges, suggesting that shared intrinsic

70 f L-type Ca(2+) channels, action potentials, intercellular Ca(2+) waves and contractions in LSMC.

71 An Ano1 channel antagonist inhibited intercellular Ca(2+) waves and LM contractions.

72 Rhythmic action potentials and intercellular Ca(2+) waves are generated in smooth muscl

73 variety of spatiotemporal characteristics of intercellular Ca(2+) waves in hESC colonies induced by s

74 Intercellular calcein transfer from myofibroblasts to ca

75 in, which undergo kinetic turnover, transmit intercellular calcium transients and mediate directional

76 produce paracrine signals that manifested as intercellular calcium waves (ICWs), observed in cell lin

77 chronous calcium responses into co-ordinated intercellular calcium waves that spread throughout the l

78 ng tissues: CXE in xylem and cells bordering intercellular canals and MXE in sclerenchyma.

79 ibble away parts of neighboring cells, is an intercellular cannibalism process conserved from protozo

80 .17 mmol/L; CB: 1.30 mmol/L; P = 0.021), and intercellular cell adhesion molecule-1 (WA: 153.9 ng/mL;

81 known to affect the structure, stability and intercellular channel activity of gap junctions; however

82 Regulation of molecular transport via intercellular channels called plasmodesmata (PDs) is imp

83 Gap junctions are arrays of intercellular channels formed by the docking of two hemi

84 incorporate native connexin-46/50 (Cx46/50) intercellular channels into a dual lipid nanodisc system

85 Gap junctions contain intercellular channels that enable intercellular communi

86 that nonheritable noise predominantly drives intercellular circadian period variation in clonal cell

87 tiple extracellular spaces, specifically the intercellular cleft and bulk interstitial space, in a no

88 tating formation of Na(+) nanodomains in the intercellular cleft between cells.

89 ly predicted that narrowing the width of the intercellular cleft can suppress APD prolongation and EA

90 Na(+) channel mutations because of increased intercellular cleft Na(+) ion depletion.

91 Thus, we predict that intercellular cleft Na(+) nanodomain formation and colla

92 ions are consistent with the conclusion that intercellular cleft narrowing or expansion regulates APD

93 s of chemical synaptic-like contacts: narrow intercellular cleft, keratinocyte synaptic vesicles expr

94 nd spatially uniform increases in leaf-level intercellular CO(2) and intrinsic water use efficiency t

95 hloroplastic CO(2) concentration (c(c) ) and intercellular CO(2) concentration (c(i) ) modified by sa

96 sponse to rapid changes in ambient light and intercellular CO(2) concentration.

97 mitigation (TRIM), is reported, to minimize intercellular cohesion loss for accurate antibacterial t

98 eatures plays a critical role in maintaining intercellular cohesion of the epidermis during photother

99 GJ intercellular communication (GJIC) can be mediated by mu

100 ic to Cx43, we show that Cx43-gap junctional intercellular communication (GJIC) influences Cx43-depen

101 Gap junctional intercellular communication (GJIC) is widely known for i

102 GJ intercellular communication (GJIC) plays a critical role

103 rotein and small RNA cargo and have roles in intercellular communication among parasites and influenc

104 y being recognized as important vehicles for intercellular communication and as promising sources for

105 unknown cellular and molecular mechanisms in intercellular communication and in organ homeostasis and

106 nctional vehicles capable of contributing to intercellular communication and metastasis.

107 e and possess an extraordinary repertoire of intercellular communication and social behaviors, includ

108 ique role of extracellular RNAs in mediating intercellular communication and their potential role as

109 aques and highlights cellular plasticity and intercellular communication at the site of disease.

110 Tunneling nanotubes (TNTs) mediate intercellular communication between animal cells in heal

111 ated microRNAs may have a functional role in intercellular communication between immune cells respond

112 ingly, we found that the amebic EVs impacted intercellular communication between parasites and altere

113 EVs mediate intercellular communication by shuttling functional sign

114 cellular vesicles (EVs) are a unique mode of intercellular communication capable of incredible specif

115 ave helped reveal how cells communicate, how intercellular communication controls development, how si

116 Gametogenesis is dependent on intercellular communication facilitated by stable interc

117 s an effector to manipulate PD-mediated host intercellular communication for maximizing the spread of

118 , ligand-receptor pairs can be used to infer intercellular communication from the coordinated express

119 ecade has shed significant light on how this intercellular communication functions.

120 Extracellular vesicle-directed intercellular communication has been found to be an impo

121 ing realization of microRNA's implication in intercellular communication have led to a proliferation

122 by cell surface receptors are essential for intercellular communication in multicellular organisms.

123 sicles (sEVs), playing a crucial role in the intercellular communication in physiological as well as

124 ovesicles, represent an understudied form of intercellular communication in polarized cells.

125 therapeutic strategies aiming at preserving intercellular communication in the heart.

126 icles (EVs) represent an important method of intercellular communication in the human host.

127 es are a previously undescribed mechanism of intercellular communication in the inner ear that can me

128 Here, we review the different means of intercellular communication including soluble factors in

129 Intercellular communication is critical for organismal h

130 The orchestration of intercellular communication is essential for multicellul

131 In plants, intercellular communication is largely dependent on plas

132 The best characterized means of intercellular communication is the release of soluble fa

133 Intercellular communication is vital to tumor progressio

134 tively, our study provides insights into the intercellular communication mechanisms that operate duri

135 nificance of extracellular vesicles (EVs) as intercellular communication mediators has been increasin

136 ion of rare cell types, new cell states, and intercellular communication networks that may be masked

137 Mapping intercellular communication networks within the heart, w

138 nges towards a deeper understanding of these intercellular communication networks.

139 s contain intercellular channels that enable intercellular communication of small molecules while als

140 he neighboring parenchyma via a gap junction intercellular communication pathway.

141 n semen, and because they play a key role in intercellular communication pathways and immune regulati

142 This type of intercellular communication permits the coordination of

143 Therefore, intercellular communication players have emerged as attr

144 minal vesicles (ILVs), have emerged as a new intercellular communication process.

145 Intercellular communication refers to the different ways

146 Tunneling nanotubes (TNTs) are novel intercellular communication structures transporting diff

147 s are extracellular vesicles involved in the intercellular communication system that can exert an imm

148 Intercellular communication through the secretion of sol

149 ssion of genes encoding proteins involved in intercellular communication was more likely to have dive

150 omes for degradation, but they also modulate intercellular communication when secreted as exosomes.

151 junction function by Ad5 leading to loss of intercellular communication which would contribute to da

152 or FAK signaling in CAFs that regulate their intercellular communication with tumor cells to promote

153 Extracellular RNAs participate in intercellular communication, and are being studied as pr

154 networks for tight junction, gap junctional intercellular communication, and transmembrane transport

155 the cell-environment interface, and modulate intercellular communication, from development to pathoge

156 tify that Cx43 hemichannel function, but not intercellular communication, induces leader cell activit

157 ed with profound changes in key processes of intercellular communication, involving gap junctions, ex

158 from hypoxic mammary tumor cells facilitate intercellular communication, leading to alterations in m

159 damage have been identified-such as altered intercellular communication, loss of proteostasis and er

160 Intercellular communication, specifically via connexin (

161 EVs are best known as mediators of intercellular communication.

162 Exosomes are emerging as new regulators of intercellular communication.

163 al basis for understanding their function in intercellular communication.

164 small cell-derived vesicles that function in intercellular communication.

165 e, failure to produce biofilms, and impaired intercellular communication.

166 brane-bound compartments that participate in intercellular communication.

167 have been described as a novel mechanism for intercellular communication.

168 ical signaling, information propagation, and intercellular communication.

169 cell types, revealing TSK cells as a hub for intercellular communication.

170 rstandings of the tumor microenvironment and intercellular communications in CCA and their role in tu

171 epigen and concentrate it within nanolumina-intercellular compartments sealed by cell-cell junctions

172 zations at apical junctions, where they form intercellular complexes that link neighboring cells [1-3

173 We observed a loss of intercellular connections, and condensation of chromatin

174 Our results reveal heterogeneous intercellular connectivity and a variety of spatiotempor

175 Tissue morphogenesis requires dynamic intercellular contacts that are subsequently stabilized

176 Myocardial scar cell types and intercellular contacts were analyzed using a three-dimen

177 Moreover, our model shows that intercellular coupling alone does not regulate force dev

178 propagation and force development depend on intercellular coupling and cellular excitability is not

179 Remodelling increases intercellular coupling and cellular excitability, which

180 ctrical propagation and force development on intercellular coupling and cellular excitability.

181 This model reveals that intercellular coupling determines the conduction velocit

182 rnalization of Cx43, preserving gap junction-intercellular coupling in cardiomyocytes.

183 Connexin-43 (Cx43) gap junctions provide intercellular coupling, which ensures rapid action poten

184 rophage cellular/exosome-HuR, alterations in intercellular cross talk with fibroblasts, and its impac

185 Nevertheless, studying intercellular crosstalk in vivo remains a relevant chall

186 t cells via microfusions that form temporary intercellular cytoplasmic continuities.

187 s a potentially novel mechanism in mammalian intercellular cytoplasmic transfer and communication.

188 The elucidation of the critical intercellular dependencies that constitute the LGG neuro

189 cterial lipopolysaccharide (LPS) were due to intercellular desynchronization of the molecular clock,

190 Here, we quantified intercellular differences in DeltaPsim in unsynchronized

191 live imaging for continuous visualization of intercellular dye transfer and Ca(2+) diffusion in hESC

192 ntact area suggesting a role in establishing intercellular electrical connections in scar tissue.

193 on, and independent of canonical LPS-induced intercellular feedback in the tumor necrosis factor (TNF

194 c-dependent assembly into twisted, rope-like intercellular filaments in the biofilm.

195 42 governs the formation and distribution of intercellular filopodia and stress fibers in follicle ce

196 de of follicle cells, emerges from polarized intercellular filopodia that radiate from basal stress f

197 esults indicate that the neuron-to-microglia intercellular FKN/CX3CR1 signaling plays a role in gp120

198 ctin and microtubule cytoskeletal systems in intercellular force transmission during tissue morphogen

199 bution, contractile moment of the cell pair, intercellular force, and number of focal adhesions.

200 tic regulation is a notable exception, where intercellular forces drive exposure of a cryptic proteas

201 for a chemorepellent confers specificity of intercellular fusion of a specific muscle progenitor wit

202 chips to resolve fine morphological detail (intercellular gaps) in experiments monitoring changes in

203 actin networks and induces the formation of intercellular gaps.

204 formation decomposition, we next compute the intercellular gene-gene information flow to estimate the

205 Our results reveal substantial intercellular heterogeneity in response to specific comp

206 Overall, our results showed that intercellular heterogeneity of DeltaPsim is mainly modul

207 Psim indicator and it is not correlated with intercellular heterogeneity of plasma membrane potential

208 ircadian period is associated with increased intercellular heterogeneity.

209 ized link between circadian oscillations and intercellular heterogeneity.

210 c plasticity, invoking previously unexplored intercellular, homeostatic signaling at a tripartite syn

211 ve developed ImmunoGlobe, a manually curated intercellular immune interaction network extracted from

212 ich in turn alter cellular function; and (2) intercellular immunometabolism-conditions in which inter

213 Intercellular interaction between Frizzled3 and Vangl2 i

214 rs DRG neuron activity indirectly through an intercellular interaction between non-neuronal cells and

215 roadly applicable technology to characterize intercellular interaction-specific pathways at high reso

216 Our results demonstrate the role of intercellular interactions and intracellular NF2-YAP sig

217 phase separation; the process is mediated by intercellular interactions and shear-induced depletion.

218 he root meristem in plants are maintained by intercellular interactions and signalling networks invol

219 Age-associated decay of intercellular interactions impairs the cells' capacity t

220 or intrinsic (genetic, epigenetic or due to intercellular interactions).

221 ubstrate, a simple laboratory setup to study intercellular interactions.

222 its extracellular matrix also play a role in intercellular interactions.

223 rates also have a new type of cadherin-based intercellular junction called the desmosome, which allow

224 tor complexes and their assembly into larger intercellular junction structures and discuss emerging p

225 y arrest and form radially symmetric, stable intercellular junctions termed immunological synapses wh

226 Similarly, loss of desmosomes (intercellular junctions) was seen in placental tissues f

227 otypic and heterotypic signaling critical to intercellular junctions, cell-matrix interactions, and c

228 e, exceptionally reinforced, E-cadherin-rich intercellular junctions.

229 lationally modify pre-existing components of intercellular junctions.

230 plaques are well addressed at the intra- and intercellular levels in short timescales, an understandi

231 Despite their role as intercellular mediators, most lack the leader peptide ty

232 ending to surprisingly long distances in the intercellular medium.

233 on of retrotransposon Gag genes and mediates intercellular messenger RNA transfer.

234 onies to further global understanding of how intercellular metabolic interactions affect the internal

235 Here we show that intercellular morphological transition of peptide assemb

236 in isogenic cultures, which we formalize as 'intercellular mosaic methylation' (IMM).

237 With live imaging, we directly observe the intercellular movement of GFP and a subset of endogenous

238 cleus, resulting in siRNA production and the intercellular movement of these siRNAs to reinforce TE s

239 to IL-17RE represents a genetically ancient intercellular network regulating local tissue homeostasi

240 e brain to the periphery, cell-intrinsic and intercellular networks converge to stimulate and propaga

241 Notch signaling is a highly conserved intercellular pathway with tightly regulated and pleiotr

242 ecules in the context of cells by discussing intercellular, peri/intracellular, and subcellular ENS f

243 in the CryoEM map, localized throughout the intercellular permeation pathway and contributing to the

244 ent by the concerted action of tissue-level, intercellular planar cell polarity (PCP) signaling and a

245 isation via plasmodesmata, which function as intercellular pores linking the cytoplasm of adjacent ce

246 We further find that intercellular propagation of death occurs following trea

247 mploying an assay that readily detects these intercellular protein-protein interactions in the less t

248 etween groups, most notably genes related to intercellular proteins.

249 tated nuclei, finding that both cellular and intercellular regions contribute to CNN accuracy.

250 s tools to reveal cellular heterogeneity and intercellular relationships in flow cytometry data.

251 SPR operated stoplight system for functional intercellular RNA exchange (CROSS-FIRE) we uncover vario

252 pite recent efforts to capture cancer cells' intercellular secretion heterogeneity using microfluidic

253 cles (EVs), which, in general, are important intercellular signal transducers.

254 regulates these cell divisions, thus linking intercellular signaling and cell polarity with the contr

255 Thus, TWEAK and Fn14 represent an intercellular signaling axis through which microglia sha

256 of synapse formation is supported by complex intercellular signaling between potential presynaptic an

257 Investigation of intercellular signaling between these two tumor populati

258 The Wnt pathway is a key intercellular signaling cascade that regulates developme

259 recapitulate the tissue microenvironment and intercellular signaling in vitro.

260 lular adaptations at the level of long-range intercellular signaling networks in the unborn fetus.

261 (TME) promotes tumor development via complex intercellular signaling, aiding tumor growth and suppres

262 ntal programs, day/night organismal changes, intercellular signaling, and proliferative safeguards.

263 dination; however, mechanistic links between intercellular signaling, cell polarity, and cellular org

264 immune responses, and modified cellular and intercellular signaling.

265 for membrane structure as well as intra- and intercellular signaling.

266 cardiomyocyte trophism occurs through direct intercellular signalling at neuro-cardiac junctions.

267 echnologies have enabled routine analyses of intercellular signalling from gene expression measuremen

268 atic actions are initiated and controlled by intercellular signalling of ions, including Ca(2+) , Na(

269 modelled the impact of dose-rate effects and intercellular signalling on cell-killing.

270 us, the identification and quantification of intercellular signalling pathways has become a common an

271 ased the chloroplast surface area exposed to intercellular space (S(c) /S); conversely this induced a

272 ased, decreased mesophyll surface exposed to intercellular space and chloroplast density induced long

273 nd transduced from the cell surface into the intercellular space and will aid in facilitating the tre

274 Free and bound lipids in the 25 nm thick intercellular spaces were directly detected for the firs

275 n, basal zone hyperplasia (BZH), and dilated intercellular spaces, and the underlying processes that

276 lar vacuoles, and hyperreflective epithelial intercellular spaces.

277 ent to which that behavior generates uniform intercellular spacing across the mosaic.

278 nal magnification factor rises more than the intercellular spacing in the same animals, the spatial r

279 steria exploits host exocytosis to stimulate intercellular spread of bacteria.

280 in to promote its intracellular motility and intercellular spread.

281 mpartments, therefore facilitating the virus intercellular spread.

282 es continuous cell-cell contacts to form the intercellular tight junction barrier; a second protein,

283 the intestinal epithelial barrier, in which intercellular tight junction complexes block the uptake

284 Intercellular tight junctions are crucial for correct re

285 the intestinal permeability by modulation of intercellular tight junctions.

286 emonstrating that RCs are stable and open to intercellular traffic throughout spermatogenesis.

287 cells stimulating thicker TNT formation and intercellular trafficking from macrophages.

288 ein interactions are required for intra- and intercellular trafficking.IMPORTANCE Local transport of

289 EVs) form an endogenous transport system for intercellular transfer of biological cargo, including RN

290 TMTs do not allow intercellular transfer of cytoplasmic GFP.

291 We hypothesized that intercellular transfer of proteins is not the sole conse

292 an studies and disease models indicates that intercellular transmission and the subsequent templated

293 regulatory network, and the dynamics of SHR intercellular transport as a cell-cell coupling mechanis

294 brane-enclosed compartments that mediate the intercellular transport of proteins and small RNAs.

295 networks within the heart, we identified key intercellular trophic relationships and shifts in cellul

296 (18)O and gas exchange were used to estimate intercellular vapor pressure, e (i) In wild-type leaves,

297 h primary and cultured, typically reveals an intercellular variability in migration speeds.

298 domains, as global events, or as propagating intercellular waves and thereby represent the substrate

299 acellular waves not causing contractions and intercellular waves leading to excitation-contraction co

300 ral mechanisms have been proposed to mediate intercellular Wnt transport, including Wnt-binding prote