Sentence examples for mouse MSCs even from inspiring English sources

Species-dependent differences in the expression and regulation of IDO paralogues were noted (e.g. significant levels of full IDO2 transcripts were not detectable in mouse MSCs even after IFN-γ treatment), which indicate that IDO activity may be dissimilar in human cells compared to rodent cells [6], [10].

Khayat et al. [ 23] showed that relatively low-frequency mechanical stimulation (0.01 Hz) could inhibit adipogenic differentiation of C3H10T1/2 mouse MSCs, even in a potent adipogenic differentiation medium.

However, full IDO2 transcripts were not detectable in mouse MSCs at significant levels even after IFN-γ treatment, suggesting that, unlike IDO1, IDO2 gene activity is not dependent on IFN-γ and/or might not be translated into a full, functional protein in these cells.

Compared to control mice, repeated administration of MSCs even tended to exacerbate arthritis (Fig. 3F).

Since their first warning, Djouad F et al. have also reported that the immunosuppressive effect of mouse MSCs in vivo depends on environmental parameters and that even "a low but relevant amount of MSCs may induce tumor rejection" [46].

As Boido et al. reported, significantly reduced lesion volume and improved hindlimb sensorimotor functions were observed after mouse MSCs were transplanted into the lesion cavity of compression SCI mouse model, even though the engrafted MSCs were observed to be neuronally undifferentiated and astroglial and microglial activation was not altered [ 65].

Mouse MSCs were prepared from bone marrow as previously described [29], [57].

In addition, mouse MSCs are shown to express VEGFα and EGF in cDNA microarray analysis [81].

Mouse MSCs were isolated and cultured as described previously [ 37].

Discussion: BADGE induced adipogenesis in human and mouse MSCs, as well as in mouse 3T3-L1 preadipocytes.

Compared to MSCs from healthy mice, MSCs from diabetic mice had the same proliferation and adipogenic potentials, but were less abundant, with altered immunophenotype and no osteogenic potential.