Skip to main content
. 2019 Feb 14;9:2072. doi: 10.1038/s41598-018-37430-9

Figure 5.

Figure 5

LHX2 overexpression in iPS-HSCs changes the expression profile of the extracellular matrix (ECM), and induces gene expression related to the quiescence phenotype of HSCs. (a) Expression of LHX2 in Veh- or Dox-treated iLHX2-HSCs co-cultured with iPS-HPCs. (b,c) Expression of genes related to HSCs (b, ALCAM, PDGFRα, and WT1) and genes related to the quiescence phenotype of HSCs (c, NGFR, LRAT, Neurotrimin, and PPARγ) in Veh- or Dox-treated iLHX2-HSCs. (d) Expression of genes related to HSC activation (LOX, ACTA2, COL1A1, and Desmin) in Veh- or Dox-treated iLHX2-HSCs co-cultured with iPS-HPCs. (e) Expression profile of laminin and collagen based on microarray analysis. The y-axis represents the ratio of expression relative to Veh-treated iLHX2-HSCs co-cultured with iPS-HPCs. (f) Quantitative RT-PCR analysis of laminin (LAMA2, LAMA4, and LAMA5) and collagen (COL3A1, COL4A5, and COL5A1) in iLHX2-HSCs co-cultured with iPS-HPCs. Results represent the mean ± SD of three separate experiments. The y-axis in (ad) and (f) represents the ratio of expression relative to Veh-treated iLHX2-HSCs co-cultured with iPS-HPCs. *P < 0.05.