Fig. 6.
Gpihbp1 and BMP-2/4 expression in subpopulations of pericytes. a Western blots and quantification of gpihbp1 expression in wild-type (WT) and laminin γ1flox/flox:Pdgfrβ-Cre+(PKO) type I pericytes in the presence of saline (Sal) or laminin-111 (Ln). Actin was used as a loading control. n = 4. b Western blots and quantification of gpihbp1 expression in WT and PKO type II pericytes in the presence of Sal or Ln. Actin was used as a loading control. n = 4. c ELISA analyses of BMP-2 and BMP-4 levels in conditioned medium from type I pericytes after adipogenic differentiation for 8 days. n = 3. d ELISA analyses of BMP-2 and BMP-4 levels in cell lysates from type I pericytes after adipogenic differentiation for 8 days. n = 3. Data are shown as mean ± SD. **p < 0.01 versus WT + Sal; # p < 0.05, ## p < 0.01 versus PKO + Sal