Given recent progress in regenerative medicine, we need a means to expand chondrocytes in quantity without losing their regenerative capability. Although many reports have shown that growth factor supplementation can have beneficial effects, the use of growth factor–supplemented basal media has widespread effect on the characteristics of chondrocytes. Chondrocytes were in vitro cultured in the 2 most widely used chondrocyte growth media, conventional chondrocyte culture medium and mesenchymal stem cell (MSC) culture medium, both with and without fibroblast growth factor-2 (FGF2) supplementation. Their expansion rates, expressions of extracellular matrix–related factors, senescence, and differentiation potentials were examined in vitro and in vivo. Our results revealed that chondrocytes quickly dedifferentiated during expansion in all tested media, as assessed by the loss of type II collagen expression. The 2 basal media (chondrocyte culture medium vs. MSC culture medium) were associated with distinct differences in cell senescence. Consistent with the literature, FGF2 was associated with accelerated dedifferentiation during expansion culture and superior redifferentiation upon induction. However, chondrocytes expanded in FGF2-containing conventional chondrocyte culture medium showed MSC-like features, as indicated by their ability to direct ectopic bone formation and cartilage formation. In contrast, chondrocytes cultured in FGF2-supplemented MSC culture medium showed potent chondrogenesis and almost no bone formation. The present findings show that the chosen basal medium can exert profound effects on the characteristics and activity of in vitro–expanded chondrocytes and indicate that right growth factor/medium combination can help chondrocytes retain a high-level chondrogenic potential without undergoing hypertrophic transition.

Human brain mapping of low-frequency electrical conductivity tensors can realize patient-specific volume conductor models for neuroimaging and electrical stimulation. We report experimental validation and in vivo human experiments of a new electrodeless conductivity tensor imaging (CTI) method. From CTI imaging of a giant vesicle suspension using a 9.4 T MRI scanner, the relative error in the reconstructed conductivity tensor image was found to be less than 1.7% compared with the measured value using an impedance analyzer. In vivo human brain imaging experiments of five subjects were followed using a 3 T clinical MRI scanner. With the spatial resolution of 1.87 mm, the white matter conductivity showed considerably more position dependency compared with the gray matter and cerebrospinal fluid (CSF). The anisotropy ratio of the white matter was in the range of 1.96 to 3.25 with mean value of 2.43, whereas that of the gray matter was in the range of 1.12 and 1.19 with mean value of 1.16. The three diagonal components of the reconstructed conductivity tensors were from 0.08 to 0.27 S/m for the white matter, from 0.20 to 0.30 S/m for the gray matter, and from 1.55 to 1.82 S/m for the CSF. The reconstructed conductivity tensor images exhibited significant inter-subject variabilities in terms of frequency and position dependencies. The high-frequency and low-frequency conductivity values can quantify the total and extracellular water contents, respectively, at every pixel. Their difference can quantify the intracellular water content at every pixel. The CTI method can separately quantify the contributions of ion concentrations and mobility to the conductivity tensor.