<p>LMeC melanoma cells were either cultured alone or co-cultured with cAT-MSC-Mock or cAT-MSC-IFN-<i>β</i> for 72 h in a 1∶1 and 4∶1 (MSC/LMeC cell) ratio. LMeC cell growth was assessed with cAT-MSCs in a transwell format, which prevented LMeC-MSC cell contact. Data are expressed as the percentage of total cells compared with that of the control. Two cAT-MSCs exhibited a potent dose-dependent inhibitory effect on LMeC cell number. The P-value was obtained using one-way ANOVA with <i>post-hoc</i> Bonferroni's multiple comparison analysis. Each data point represents the mean +SD of three independent experiments. ** <i>p</i><0.01, *** <i>p</i><0.001.</p
<p>(A) Bone marrow (BM) cells from 13 MM patients and 2 human MM cell lines were grown in colony sup...
<p>A) Forty-eight hours post-treatment, cells were assayed for viability as described in Materials a...
<p>Western blot analysis of β-catenin in whole-cell lysates prepared from B16-F0 cells transfected w...
<p>LMeC melanoma cells were either cultured alone or co-cultured directly with CM-DiI-labeled cAT-MS...
<p>The cell cycle phase distribution of LMeC was analyzed after harvest by flow cytometery. (A, B) c...
<p>The migratory capacity of cAT-MSC-Mock and cAT-MSC-IFN-<i>β</i> were assessed by a modified trans...
<p>(A) Fluorescent analysis of CM-DiI labeled cAT-MSC homing to tumors in the frozen tumor sections....
<p>Interfering with the IFNγ pathway in MSCs can partially restore Vδ2+ cell proliferation (A) Compa...
<p>MSC (A) or EPC (B) were plated on 12-well plates at 15 000 cells per chamber of culture-insert. C...
Adipose tissue-derived mesenchymal stem cells (AT-MSCs) are attractive cell-therapy vehicles for the...
<p>Cells were treated with various dose of IFN-α or -β (<b>A</b>), or IFN-λ1 (<b>B</b>) for 5 days, ...
<p>(A) The presence of MSCs reduces the expansion of Vδ2+ cells. Representative flow cytometric anal...
<p>(A). HNSCC cells were treated with BME for 24 h, and MTS assay was performed. (B). Cal27 cells we...
<p>(A) Cell proliferation rate of melanoma cells treated with catalase for 24 h, relative to control...
<p>Malme-3M-luc cells were seeded (2 x10<sup>4</sup>/well) into 96-well round bottom microplate in t...
<p>(A) Bone marrow (BM) cells from 13 MM patients and 2 human MM cell lines were grown in colony sup...
<p>A) Forty-eight hours post-treatment, cells were assayed for viability as described in Materials a...
<p>Western blot analysis of β-catenin in whole-cell lysates prepared from B16-F0 cells transfected w...
<p>LMeC melanoma cells were either cultured alone or co-cultured directly with CM-DiI-labeled cAT-MS...
<p>The cell cycle phase distribution of LMeC was analyzed after harvest by flow cytometery. (A, B) c...
<p>The migratory capacity of cAT-MSC-Mock and cAT-MSC-IFN-<i>β</i> were assessed by a modified trans...
<p>(A) Fluorescent analysis of CM-DiI labeled cAT-MSC homing to tumors in the frozen tumor sections....
<p>Interfering with the IFNγ pathway in MSCs can partially restore Vδ2+ cell proliferation (A) Compa...
<p>MSC (A) or EPC (B) were plated on 12-well plates at 15 000 cells per chamber of culture-insert. C...
Adipose tissue-derived mesenchymal stem cells (AT-MSCs) are attractive cell-therapy vehicles for the...
<p>Cells were treated with various dose of IFN-α or -β (<b>A</b>), or IFN-λ1 (<b>B</b>) for 5 days, ...
<p>(A) The presence of MSCs reduces the expansion of Vδ2+ cells. Representative flow cytometric anal...
<p>(A). HNSCC cells were treated with BME for 24 h, and MTS assay was performed. (B). Cal27 cells we...
<p>(A) Cell proliferation rate of melanoma cells treated with catalase for 24 h, relative to control...
<p>Malme-3M-luc cells were seeded (2 x10<sup>4</sup>/well) into 96-well round bottom microplate in t...
<p>(A) Bone marrow (BM) cells from 13 MM patients and 2 human MM cell lines were grown in colony sup...
<p>A) Forty-eight hours post-treatment, cells were assayed for viability as described in Materials a...
<p>Western blot analysis of β-catenin in whole-cell lysates prepared from B16-F0 cells transfected w...