ライフサイエンスコーパス: conditioned media

1 in 1 (Ucp1), in adipocytes cultured with the conditioned media.

2 ibodies blunted the proapoptic effects of M2-conditioned media.

3 but not transforming growth factor-beta1 in conditioned media.

4 oward an odontoblast phenotype by culture in conditioned media.

5 BMP4 abrogated the proviral activity of LSEC-conditioned media.

6 he chemoattracting properties of the myotube-conditioned media.

7 r forms of secreted hCG were measured in the conditioned media.

8 tment with superior effects using cocultured conditioned media.

9 ed the migration of these progenitors toward conditioned media.

10 response to AEBP1(TG) macrophages and their conditioned media.

11 DMs when incubated with apoptotic lymphocyte conditioned media.

12 Etanercept production was verified from the conditioned media.

13 l of breast cancer cells as well as in their conditioned media.

14 ric and intestinal mucosa to generate stroma-conditioned media.

15 creased in the reactive astrocytes and their conditioned media.

16 epithelium-derived factor (PEDF) levels from conditioned media.

17 o increased the level of active MMP-2 in the conditioned media.

18 f endothelial cells induced by neuroblastoma-conditioned media.

19 cells and endothelial cells cultured in EPC-conditioned media.

20 IL-31 were also observed in MPD CD3(+) cell-conditioned media.

21 duced this selective recruitment toward both conditioned media.

22 dy-depleted VEGF and FGF2 from breast cancer-conditioned media.

23 eted these growth factors from breast cancer-conditioned media.

24 mes and exosome-depleted media (EDM)) of the conditioned media.

25 e nucleus and cytoplasm, and was detected in conditioned media.

26 A did not alter VEGFA bioavailability in the conditioned media.

27 our necrosis factor alpha (TNFalpha) and MAC-conditioned media.

28 ndent of soluble factors present in PDL cell-conditioned media.

29 y activin A IgG blocked the effect of EC-ASC conditioned media.

30 Adipocyte-conditioned media (ACM) treatment of macrophages for 48

31 howed that recombinant Tat or Tat-containing conditioned media activated Hes1 transcription and prote

32 Notably, cells exposed to conditioned media also elicit a genome-destabilizing eff

33 This conditioned media also enhanced oligodendrocyte precurso

34 Conditioned media and cells were collected from UMs cult

35 Conditioned media and cells were harvested to measure TF

36 Exosomes were isolated from the culture-conditioned media and delivered to athymic rats after is

37 s then used to measure PSA concentrations in conditioned media and human plasma samples.

38 entiation was enhanced in vitro with M2 cell conditioned media and impaired in vivo following intra-l

39 -treatment of melanoma cell lines with WNT3A-conditioned media and recombinant TRAIL significantly en

40 M-CSF was identified in tumor-conditioned media and shown to be capable of differentia

41 n human mesenchymal stem cell and fibroblast conditioned media, and identified 11 enriched in the mes

42 cell Erk1/2 phosphorylation conferred by EC conditioned media, and preincubation with CypA augmented

43 forms of MMP-1, MMP-2, MMP-3, and MMP-14 in conditioned media, and the low-molecular-weight fragment

44 antially higher release of IL-1beta into the conditioned media, and when exposed to dexamethasone, fa

45 macrophages that are cultured in tumour cell-conditioned media as well as an iNOS activity-dependent

46 from typical contaminants including CHO cell conditioned media, ascites fluid, DNA, and other antibod

47 tures and reduces the activity of macrophage-conditioned media, but inhibition of tumor necrosis fact

48 Recombinant Wnt3a and ISO-603B-conditioned media, but not ISO alone, protected isolated

49 Secretion of S100A4 was measured in conditioned media by immunoblotting, and MMP-13 was meas

50 sion at the protein level in lysates and MSC-conditioned media by Western blot analysis and ELISA.

51 7-polarizing cytokines, and the keratinocyte-conditioned media caused IL-17 production by naive T cel

52 onic epithelium were exposed to concentrated conditioned media (CCM) from E. faecalis V583 and E. fae

53 when confronted with tumor cells (confronted conditioned media, CCM) contribute to inhibition of tumo

54 In particular, the analysis of conditioned media, cell surface proteins, and whole-cell

55 ASC-conditioned media (CM) collected after 1 week of iAs exp

56 Incubation of osteocytic MLO-Y4 cells with conditioned media (CM) collected after continuous FFSS i

57 Conditioned media (CM) collected from MLO-Y4 osteocyte c

58 We showed that conditioned media (CM) collected from osteocytes treated

59 aromatase expression following incubation in conditioned media (CM) collected from the obese-patient,

60 Conditioned media (CM) from A. fumigatus, A. niger, and

61 8a function in fibroblasts demonstrated that conditioned media (CM) from CAFs overexpressing miR-148a

62 d with interleukin-12 (IL-12) and IL-15, and conditioned media (CM) from these cultures evaluated for

63 mary adult rat cardiomyocytes incubated with conditioned media (CM) generated from explants of EAT bi

64 er show that both murine and human astrocyte conditioned media (CM) increase synapse density, reduce

65 However, conditioned media (CM) obtained from fibroblasts alone (

66 Conditioned media (CM) obtained from MMTV-PyMT and MMTV-

67 Neutralizing TNF in gamma-IR conditioned media (CM) of WT and p55KO BM-EPCs largely a

68 tment of monkey TM cultures, MYOC protein in conditioned media (CM) was measured by Western blot and

69 Conditioned media (CM) were collected from cultured adul

70 ed intravenously with 4 x 10(6) hADSCs (Tx), conditioned media (CM), or vehicle (unconditioned media)

71 Astrocyte-conditioned media collected from astrocytes pre-exposed

72 In these experiments, conditioned media collected from polymorphonuclear leuko

73 Soluble CD36 from macrophage-conditioned media comprises 2 species based on Western b

74 imental assays of chemotaxis towards culture conditioned media confirm this hypothesis.

75 In addition, these conditioned media could induce phase shifts in SCN PER2

76 were used to generate a diseased splenocyte conditioned media (D-SCM) containing immune cell secrete

77 ctor Machine (SVM) cluster analysis of three conditioned media derived fractions corresponding to a 1

78 Conditioned media derived from activated lymphocyte cult

79 pression of the TTBK1 gene or treatment with conditioned media derived from lipopolysaccharide-stimul

80 ugs and polyvinyl alcohol sponges containing conditioned media derived from long-term cultures of mou

81 Decreased angiogenesis was observed in conditioned media derived from long-term cultures of mou

82 t, on leukocyte migration and recruitment to conditioned media derived from long-term cultures of mou

83 and determining the therapeutic potential of conditioned media derived from MSCs.

84 Immunoblotting analysis of conditioned media derived from primary cultures of human

85 A2B5(+) oligodendrocyte progenitors grown in conditioned media derived from TIMP-1 KO primary glial c

86 irect effect on progenitor cell recruitment, conditioned media derived from vascular smooth muscle ce

87 her with recombinant human IFN-gamma or with conditioned media-derived IFN-gamma exhibited low levels

88 In mESC-CM monolayers, CF-conditioned media did not alter CM spreading or MEK-ERK

89 okine array and western blotting using tumor-conditioned media displayed modulated secretory levels o

90 Fetal CF-conditioned media distinctly enhanced CM spreading and c

91 cells from liver metastases or myeloid cell conditioned media down-regulated ANGPTL7 expression.

92 F concentrations were also lower in islet EC-conditioned media (ECCM) from IUGR, and islets incubated

93 onditioned by human adult CSps and CDCs; CDC-conditioned media exerted antiapoptotic effects on neona

94 culture that were exposed to RENCA macrobead-conditioned media exhibited cell-cycle accumulation in S

95 apeutic, prevented detrusor proliferation in conditioned media experiments as well as in a mouse mode

96 -E reduced TER in both cultures; however, in conditioned media fhRPE cells did not respond to VEGF-E

97 ese two secreted gelatinases, present in the conditioned media from 3T3-L1 cells, established that an

98 Finally, conditioned media from activated ASC-MNC cocultures inhi

99 Overexpression of AFP, or conditioned media from AFP+ cells, inhibits miR-29a expr

100 In media transfer experiments, conditioned media from AGE-treated endothelial cells wer

101 Conditioned media from Alb/AEG-1 hepatocytes induced mar

102 Conditioned media from an IGFBP-3-treated non-small cell

103 media from wild-type cells, but not dialyzed conditioned media from aprA(-) cells.

104 eurosphere assays showed that Tat-containing conditioned media from astrocytes or recombinant Tat pro

105 creased ( approximately 50%) when exposed to conditioned media from ATM-deficient, TGF-beta1-treated

106 Conditioned media from bacterial cultures of NU14 Deltaa

107 ing cytokines IL-6, IL-23, and TGF-beta, and conditioned media from BCL6-deficient macrophages promot

108 Moreover, we observed that conditioned media from beta-glucan-stimulated B lymphocy

109 in human bone mesenchymal cells treated with conditioned media from bone metastatic prostate cancer c

110 PLA(2) activity was found in conditioned media from both EOC cells and macrophages.

111 We found that conditioned media from both N- and C-terminal fragments

112 an aptamer (M9-5) that differentially bound conditioned media from cancerous and non-cancerous human

113 thelial cells was assessed after addition of conditioned media from CCD18Co cells incubated with prog

114 creted IGF-II in response to rhPG(1-80), and conditioned media from CCD18Co cells that had been incub

115 also reduced the growth-promoting effects of conditioned media from CCL5-activated macrophages derive

116 Conditioned media from cell lines established from these

117 Conditioned media from cell lines stably overexpressing

118 ine and chemokine genes are among these, and conditioned media from cells expressing the R30A mutant

119 Moreover, conditioned media from cells expressing the S316A-p65 mu

120 Conditioned media from cells in which AGR2 was silenced

121 Furthermore, conditioned media from cocaine-exposed microglia increas

122 Furthermore, conditioned media from colonic tissues of colitic Th17 c

123 iopathic PAH endothelial cells compared with conditioned media from control cells.

124 was observed with the use of TSLP containing conditioned media from corneal epithelial cultures expos

125 was mimicked by treating isolated NPCs with conditioned media from corticosterone-treated primary as

126 Conditioned media from CSE-treated macrophages induced M

127 Conditioned media from Ctsk-deficient osteoclasts, which

128 93-166]) and CT-proET-1 (ppET-1[169-212]) in conditioned media from cultured endothelial cells.

129 induced in mesenchymal stem cells exposed to conditioned media from cultured rat or human myofibrobla

130 Conditioned media from EC-ASC, but not from EC cultures,

131 xt treated monocyte-derived macrophages with conditioned media from explanted human fetal and adult i

132 Conditioned media from fibroblasts overexpressing CLIC4

133 levels was tested by studying the effects of conditioned media from Galpha(s) knockdown and cholera t

134 od monocytes in vitro and to examine whether conditioned media from Gd-exposed peripheral blood monoc

135 Conditioned media from glucose-treated HAECs increased a

136 Conditioned media from HA-induced LTBMC enhanced the che

137 fter 3 days exposure to CSC or nicotine, the conditioned media from HGFs was collected and the membra

138 IL-6 and CCL-2, and impaired the ability of conditioned media from high glucose-treated proximal tub

139 Furthermore, upon treatment with IFN or conditioned media from HPAIV-infected cells, p38 control

140 In addition, conditioned media from human airway epithelial cells inf

141 ated proliferative and migratory response to conditioned media from human idiopathic PAH endothelial

142 Conditioned media from IFN-stimulated HLSECs induced exp

143 Conditioned media from IL-17-activated PCs, but not ECs,

144 nced phagocytic capacity after activation by conditioned media from IL-17-treated PCs.

145 NE in response to stimulation with IL-4, and conditioned media from IL-4-stimulated macrophages faile

146 Enhanced macrophage migration induced by conditioned media from irradiated tumor cells was comple

147 Moreover, conditioned media from keratinocytes treated with RESV s

148 man monocyte cultures, whereas the adipocyte-conditioned media from lean volunteers had no effect on

149 bserved when MDSCs were treated with IND and conditioned media from LP07 tumor cells in vitro.

150 Conditioned media from LPS-treated cells also induced an

151 We also show that conditioned media from LPS-treated TK-/- Kupffer cells w

152 reased levels of inflammatory mediators, and conditioned media from Lxralphabeta(-/-) cells increases

153 rating toward agarose beads impregnated with conditioned media from M. tuberculosis-infected monocyte

154 Conditioned media from macrophages caused activation of

155 On a stiff matrix, MSC cultured with conditioned media from mammary cancer cells expressed in

156 The conditioned media from MDA-PCa-118b induced a higher lev

157 Conditioned media from mesenchymal stem cells conferred

158 Notably, conditioned media from neuroendocrine-like cells affecte

159 Myeloperoxidase in conditioned media from neutrophils was decreased.

160 experiments, the neuroprotective efficacy of conditioned media from normal healthy endothelial cells

161 Conditioned media from Nox2 transgenic ECs induced great

162 Nox2 inhibition or conditioned media from Nox2-silenced cells attenuated LP

163 s demonstrated by measuring IL-6 and IL-8 in conditioned media from oral cancer cell lines and showin

164 Conditioned media from osteocyte-enriched bone explants

165 Conditioned media from P. aeruginosa infected epithelial

166 nd islets isolated from mice; the effects of conditioned media from pancreatic cancer cells were redu

167 Adrenomedullin and conditioned media from pancreatic cell lines inhibited g

168 However, conditioned media from PI3K mutant-expressing cells led

169 nd blocked growth of control SMCs induced by conditioned media from PTEN-deficient SMCs.

170 Furthermore, conditioned media from PTEN-deficient, patient-derived s

171 Here we demonstrate that conditioned media from PTH-treated osteoblastic and oste

172 Conditioned media from PTH-treated osteoblasts elevated

173 Interestingly, conditioned media from PTH-treated osteoblasts increased

174 posure of OV-susceptible tumor cell lines to conditioned media from RAW264.7 or primary macrophages a

175 Conditioned media from reactive astrocytes increase EPC

176 Conditioned media from Reg3beta-M2-polarized primary mac

177 s polyclonally stimulated in the presence of conditioned media from SAA-exposed DCs produced IL-17, a

178 Furthermore, conditioned media from SCN astrocyte cultures transientl

179 tion of bone marrow-derived macrophages with conditioned media from serum-starved mouse proximal tubu

180 ted 8-isoprostane was observed in plasma and conditioned media from SSc patients.

181 e of SMCs with ECs or treatment of SMCs with conditioned media from static EC monoculture (EC-CM) inc

182 L-6) were also lower in MS F1 mice serum and conditioned media from T-cell culture.

183 RK-49F fibroblast proliferation triggered by conditioned media from TGF-beta1-stimulated, control vec

184 recan degradation fragments were detected in conditioned media from the alginate cultures overexpress

185 The effect of conditioned media from the culture of fat with ROS or PG

186 The effects of conditioned media from the Gd compound-exposed monocytes

187 Specifically, conditioned media from the progeny of exposed cells can

188 tion of interleukin-8 and interleukin-1beta; conditioned media from these cells caused significant in

189 expression of paracrine factor genes and the conditioned media from these cells had reduced ability t

190 Conditioned media from these cells induced a profibrotic

191 thelial structures in vitro and in vivo, and conditioned media from these cells supported epithelial

192 human umbilical vein endothelial cells with conditioned media from these keratinocytes increased end

193 ited an amplified inflammatory response, and conditioned media from these microglia promoted death of

194 Conditioned media from these two cell lines after decidu

195 Analysis of serum-free conditioned media from three breast cancer cell lines (M

196 Conditioned media from TM cells were analyzed for MYOC-a

197 Healthy fibroblasts were incubated with conditioned media from TNFR-costimulated T lymphocytes,

198 way, HepG2/shPCSK9 cells were incubated with conditioned media from transfected HEK293 or HepG2/shPCS

199 In this study, we show that conditioned media from tumor cell lines induces expressi

200 In response to conditioned media from tumor-infiltrating monocytes/macr

201 Intriguingly, conditioned media from uninfected cultures of both LEW a

202 om a source of recombinant AprA and dialyzed conditioned media from wild-type cells, but not dialyzed

203 man GBM-derived cell lines (A172, U87-MG) or conditioned media generated in the presence or absence o

204 okines, specifically GRO-gamma, in human MSC-conditioned media have an effect on the differentiation

205 ing BMP4 treatment in the presence of feeder-conditioned media; however, this model has not been wide

206 t LH2 is present in the cell lysates and the conditioned media in a dimeric, active form in both comp

207 a trans-well assay, astrocytes or astrocyte conditioned media in the bottom chamber significantly in

208 cell viability, and generation of eosinophil-conditioned media in the presence of GM-CSF enhanced the

209 difference in their migration towards glioma conditioned media in vitro.

210 ntiating osteoclasts after exposure to tumor-conditioned media, in part through activation of NFkappa

211 Eosinophil responses to GBM cell line-conditioned media included increased survival, activatio

212 exposed to bevacizumab-resistant tumor cell conditioned media increased glioma cell proliferation co

213 thermore, culture of GBM cells in eosinophil-conditioned media increased tumor cell viability, and ge

214 de synthase, and of nitrates and nitrites in conditioned media, indicating increased release of the p

215 In vitro, HLMFs produced HB-EGF and their conditioned media induced EGFR activation and promoted d

216 f purified HSPCs cultured ex vivo with tumor-conditioned media induced their proliferation as well as

217 antagonist, but not Dkk1, reduced osteoclast conditioned media-induced hMS chemokinesis.

218 Stroma-conditioned media-induced reduction in DC-stimulated Th1

219 es from the injured rat spinal cord or their conditioned media inhibit OL differentiation of adult OP

220 SSc-conditioned media inhibited EC tube formation, whereas a

221 Our results indicate that Cav-1(-/-) MSF "conditioned media" is sufficient to induce an epithelial

222 racteristics as the ligands contained in the conditioned media mainly due to the differences in their

223 his end, we studied the effect of macrophage-conditioned media (MCM) on IBC.

224 issue, CD34Exo, but not the CD34Exo-depleted conditioned media, mimicked the beneficial activity of t

225 r microenvironment in a prostate cancer cell-conditioned media model.

226 tained from fibroblasts alone (nonconfronted conditioned media, NCM) did not inhibit tumor cell proli

227 Furthermore, adipocyte-conditioned media obtained from obese patients increased

228 Conditioned media obtained from OSCC cell lines increase

229 ess and glioma tropism in response to glioma conditioned media obtained from primary glioma neurosphe

230 fluid of human subjects with AD or from the conditioned media of Abeta-secreting cells into experime

231 In vitro studies confirmed that the conditioned media of BMPC inhibited miR-155 expression a

232 d from plasma of tumor-bearing mice and from conditioned media of cultured cancer cells.

233 eased matrix metalloprotease activity in the conditioned media of eGFP-expressing constructs but not

234 In addition, the conditioned media of ex vivo cultures from wild-type or

235 We also showed that cells with the conditioned media of Fam20a WT MEFs mineralized, but tho

236 m20a WT MEFs mineralized, but those with the conditioned media of KO MEFs failed to mineralize in vit

237 edulloblastoma patients with factors also in conditioned media of metastatic MYC amplified medullobla

238 Treatment of cardiac fibroblasts with the conditioned media of miR-378-depleted myocytes activated

239 Exosomes collected from the conditioned media of mobilized human CD34(+) cells had t

240 hand, extracellular FAM20C was absent in the conditioned media of mouse embryonic fibroblasts (MEFs)

241 these assays to the systematic study of the conditioned media of N2a cells, induced pluripotent stem

242 Exosomes isolated from the conditioned media of normal human bronchial epithelial c

243 le form of MerTK (sMerTK) is released in the conditioned media of RPE-J cells during phagocytosis and

244 Conditioned media of SOX11-positive MCL cell lines induc

245 The conditioned media of these cultures promoted the differe

246 nd platelets, and exosomes isolated from the conditioned media of TSE-infected cells have caused the

247 rs3825807 had reduced migratory ability, and conditioned media of VSMCs of the G/G genotype contained

248 Among various secreted cytokines in the conditioned-media of miR-378-depleted cardiomyocytes, on

249 ant MCP-1 mimicked the stimulatory effect of conditioned media on BM and MSC migration.

250 mvastatin mitigates the effects of senescent conditioned media on breast cancer cell proliferation an

251 recapitulated the effects observed with hMSC conditioned media on hECT-developed force and expression

252 racrine mechanisms, in vitro effects of VSMC conditioned media on myofibroblast activation were asses

253 CD11c(+) cell-conditioned media or coculture stimulated fibroblast pro

254 e immunodepletion of Tat from Tat-containing conditioned media or heat inactivation of recombinant Ta

255 ligation-induced cardiac infarction, either conditioned media or male murine or male human iESCs wer

256 eomycin decreased in vitro HSC activation by conditioned media or recombinant angiogenin.

257 Treatment with MSC conditioned media or recombinant TGF-beta1 elicits a sim

258 propagated between HEK293 cell cultures via conditioned media over multiple passages, and to culture

259 sed vaspin protein levels and secretion into conditioned media (P < 0.001).

260 We serendipitously discovered that stem cell conditioned media possessed broad antimicrobial properti

261 ntractility, proteomic analysis of hECT/hMSC conditioned media predicted activation of PI3K/Akt signa

262 We also evaluated the paracrine effects of "conditioned media" prepared from Cav-1(-/-) MSFs on wild

263 Conditioned media promoted equivalent vascular networks

264 of soluble CD36 are decreased in Adam17-null conditioned media, providing evidence for involvement of

265 CSF neutralizing Abs to GBM cell cultures or conditioned media reduced eosinophil adhesion, survival,

266 genes in MSCs, whereas in vivo myeloma cell-conditioned media reduced EphB4 expression in bone.

267 significantly induced aggrecan loss into the conditioned media, relative to replicate explants expose

268 immunodepletion of LGALS3BP from MDA-MB 231 conditioned media removes the monocyte-derived fibrocyte

269 Proteomic analysis of this "conditioned media" reveals increased levels of prolifera

270 We collected conditioned media samples before and after a 6-h in vitr

271 el plugs mixed with MMP1-stimulated, OVCAR-4-conditioned media showed a dramatic 33-fold increase in

272 analysis of HS in SC-conditioned and rat OEC-conditioned media showed that SCs secrete more highly su

273 at neutrophils treated with endothelial-cell-conditioned media showed up-regulation of the surface ad

274 VSMC conditioned media significantly inhibited collagen contr

275 Tumor-associated fibroblast-conditioned media similarly enhanced both IFN-gamma and

276 protective effect of cell-free ECFC-derived conditioned media suggest a paracrine effect.

277 h as a reporter of the nutritional status of conditioned media suggested that B. subtilis cells lacki

278 targeted cells and on naive cells exposed to conditioned media, suggesting a role for this approach i

279 creased in the presence of either tumor cell conditioned media (TCM) or tumor cells.

280 cultured in triple-negative MDA-MB-231 tumor-conditioned media (TCM) to determine the factors that ma

281 MDA-MB-231 tumor conditioned media (TCM) was employed to accelerate spont

282 re identified by analysis of RENCA macrobead-conditioned media, the properties of which offer opportu

283 fractionated mouse mesenchymal stromal cell-conditioned media to identify the biologically active co

284 FBP-4 secretion was crucial for stromal cell-conditioned media to stimulate prostate tumor cell growt

285 ic mass spectrometry, in vitro coculture and conditioned media transfer experiments show that the sol

286 Conditioned media transmission of HuWtSOD1 misfolding in

287 Cytokine arrays were performed on HGF-conditioned media treated with or without resolvin D1 an

288 We then analyzed the capacity of stroma-conditioned media-treated monocyte-derived DCs and prima

289 d NO production in astrocytes, and astrocyte conditioned media triggered neuronal death.

290 EGC-conditioned media was analyzed by high-sensitivity liqui

291 s, and functional activity of each mutant in conditioned media was assessed by EphA2 down-regulation,

292 ly, a single injection of nCPC-derived total conditioned media was significantly more effective than

293 ajority of the prosurvival functions of hUTC-conditioned media was spared after TSP knockdown, indica

294 on exposure of TAS to pancreatic cancer cell-conditioned media, we documented robust secretion of IL6

295 GFP(hi) cell conditioned media were chemotactic for fibroblasts obtai

296 t an air-liquid interface (ALI) for 3 weeks, conditioned media were sampled and RNA was extracted fro

297 ive PCR, while protein from cell lysates and conditioned media were used for immunoblot analyses and

298 cells dramatically reduced GRN levels in the conditioned media, whereas knockdown of SORT1 increased

299 EGF-E administration, but retreatment of the conditioned media with anti-PEDF antibodies allowed fhRP

300 Treatment of P. destructans-conditioned media with this antagonist blocked collagen