Transcriptome profiling of hiPSC-derived LSECs with nanoCAGE

Mathieu Danoy and Stéphane Poulain and Yuta Koui and Yannick Tauran and Benedikt Scheidecker and Taketomo Kido and Atsushi Miyajima and Yasuyuki Sakai and Charles Plessy and Eric Leclerc

Liver Sinusoidal Endothelial Cells (LSECs) are an important component of the liver as they compose the microvasculature which allows the supply of oxygen, blood, and nutrients. However, maintenance of these cells in vitro remains challenging as they tend to rapidly lose some of their characteristics such as fenestration or as their immortalized counterparts present poor characteristics. In this work, human induced pluripotent stem cells (hiPSCs) have been differentiated toward an LSEC phenotype. After differentiation, the RNA quantification allowed demonstration of high expression of specific vascular markers (CD31, CD144, and STAB2). Immunostaining performed on the cells was found to be positive for both Stabilin-1 and Stabilin-2. Whole transcriptome analysis performed with the nanoCAGE method further confirmed the overall vascular commitment of the cells. The gene expression profile revealed the …

Transcriptome profiling of hiPSC-derived LSECs with nanoCAGE
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