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. 2013 Jan 3;8(1):e52997. doi: 10.1371/journal.pone.0052997

Table 3. Proteins differentially expressed in the intra-cellular proteomes of controls MSCs and MSCs labeled with M-SPIO particles.

UniProt accession No. Protein Name MSCs labeled with M-SPIO particles:MSCs
Experiment 1 Experiment 2 Experiment 3
Significant Up-Regulated Proteins
P30530 Tyrosine-protein kinase receptor UFO 1.45 (1.40)
P04114 Apolipoprotein B-100 (1.34) 1.45
P35625 Metalloproteinase inhibitor 3 1.38 (1.26)
P05067 Amyloid beta A4 protein 1.28 (1.15)
Q76M96 Coiled-coil domain-containing protein 80 (0.84) 1.23 1.26
Q13501 Sequestosome-1 (1.06) 1.26 (1.13)
Q14566 DNA replication licensing factor MCM6 (1.15) (1.06) 1.25
P02765 Alpha-2-HS-glycoprotein 1.24 (1.15) (0.96)
P05121 Plasminogen activator inhibitor 1 (1.01) (1.09) 1.23
P33993 DNA replication licensing factor MCM7 (1.07) 1.22
P33991 DNA replication licensing factor MCM4 (1.05) 1.22
Significant Down-Regulated Proteins
P17813 Endoglin 0.79 (0.93) (0.86)
Q14498 RNA-binding protein 39 (0.85) (0.83) 0.77
P16403 Histone H1.2 0.75 (0.71)
P84103 Splicing factor, arginine/serine-rich 3 (0.47) (0.71) 0.73
P16401 Histone H1.5 (0.76) 0.66 0.61
P53999 Activated RNA polymerase II transcriptional coactivator p15 0.52 0.65 0.60

Control MSCs or MSCs labeled with M-SPIO particles were held in culture for 72 hours in Standard Media. The MSCs were subsequently collected, processed and the tryptic peptides were labeled with an isobaric tag for iTRAQ analysis using a Q-Star Elite. The experiment was repeated in triplicate. A total of 3059 proteins were identified. The fold-change values of the proteins which changed by >1.2 and <0.8 and had a p-value<0.05 in one or more experiments have been included. The fold-change values that did not meet these criteria in each experiment are depicted in brackets. A blank space indicates that a relative fold-change was not obtained for the specified protein in that replicate. For each of these proteins, the UniProt identification number, protein name, percentage of protein coverage (and number of unique peptides contributing to the sequence coverage), and fold change between the proteins in the MSCs labeled with M-SPIO particles versus control MSCs, for all replicates, are included.