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. 2017 Aug 10;40(8):550–557. doi: 10.14348/molcells.2017.0019

Fig. 1.

Fig. 1

FGF-2 treatment induces and maintains the fibroblastic feature in hPDLSCs.

(A, B) Cellular phenotypes of hPDLSCs treated with various concentration of FGF-2 in low density of cell culture (A) and in confluent culture (B). (a), no treatment; (b), 3 ng/ml; (c), 5 ng/ml; (d), 10 ng/ml; (e), 50 ng/ml; (f), 100 ng/ml; (g), 200 ng/ml; (h), 500 ng/ml. (C) Evaluation of mRNA expression of PDLs17 by qRT-PCR. Significant differences from statistical analysis were indicated as *P < 0.01 versus 0 ng/ml. (D) Evaluation of vimentin expression by western analysis. Endogenous vimentin was detected as multiple bands on SDS-PAGE of 43–57 kDa (α-vim). Used protein amount was indicated in lower panel (total protein).