Disease-associated capillarization of LSEC in vivo and dedifferentiation of LSEC in vitro indicate the importance of the hepatic microenvironment. To identify the LSEC-specific molecular differentiation program in the rat we used a two-sided gene expression profiling approach comparing LSEC freshly isolated ex vivo with both lung microvascular click here endothelial cells (LMEC) and with LSEC cultured for 42 hours. The LSEC

signature consisted of 48 genes both down-regulated in LMEC and in LSEC upon culture (fold change >7 in at least one comparison); quantitative reverse-transcription polymerase chain reaction confirmation of these genes included numerous family members and signaling pathway-associated molecules. The LSEC differentiation program comprised Pritelivir distinct sets of growth (Wnt2, Fzd4, 5, 9, Wls, vascular endothelial growth factors [VEGFR] 1, 2, 3, Nrp2) and transcription factors (Gata4, Lmo3, Tcfec, Maf) as well as endocytosis-related (Stabilin-1/2, Lyve1, and Ehd3) and cytoskeleton-associated molecules (Rnd3/RhoE). Specific gene induction in cultured LSEC versus

freshly isolated LSEC as well as LMEC (Esm-1, Aatf) and up-regulation of gene expression to LMEC levels (CXCR4, Apelin) confirmed true transdifferentiation of LSEC in vitro. In addition, our analysis identified a novel 26-kDa single-pass transmembrane protein, liver endothelial differentiation-associated protein (Leda)-1, that was selectively expressed in all liver endothelial cells and preferentially localized to the abluminal cell surface. Upon forced overexpression in MDCK cells, Leda-1 was sorted basolaterally to E-cadherin-positive adherens junctions, suggesting functional involvement in cell adhesion and MCE公司 polarity. Conclusion: Comparative microvascular analysis in rat identified a hepatic microenvironment-dependent LSEC-specific differentiation program including the novel junctional molecule Leda-1. HEPATOLOGY 2010 Endothelial cells (ECs) display marked heterogeneity in different organs and in different segments of the vascular tree. Liver sinusoidal endothelial cells

(LSECs) are a prime example of uniquely differentiated microvascular EC that exert highly specialized functions as professional endocytes1 and participate in induction of hepatic immune tolerance.2 For endocytosis, LSEC express a broad range of different scavenger receptors including Stabilin-1 and Stabilin-2, two members of a novel scavenger receptor gene family selectively expressed in sinusoidal ECs that have been identified and thoroughly characterized by us.3 Stabilin-2 is the major hyaluronan scavenger receptor of the liver, whereas Stabilin-1 mediates endocytosis of acLDL (low density lipoprotein) and SPARC. Stabilin-1 and -2 use the constitutive clathrin-mediated endocytic pathway in LSEC (4); in addition, Stabilin-1 fulfills a second role as an intracellular cargo carrier.