Item Type: | Article |
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Title: | Endothelial cell O-glycan deficiency causes blood/lymphatic misconnections and consequent fatty liver disease in mice |
Creators Name: | Fu, J., Gerhardt, H., McDaniel, J.M., Xia, B., Liu, X., Ivanciu, L., Ny, A., Hermans, K., Silasi-Mansat, R., McGee, S., Nye, E., Ju, T., Ramirez, M.I., Carmeliet, P., Cummings, R.D., Lupu, F. and Xia, L. |
Abstract: | Mucin-type O-glycans (O-glycans) are highly expressed in vascular ECs. However, it is not known whether they are important for vascular development. To investigate the roles of EC O-glycans, we generated mice lacking T-synthase, a glycosyltransferase encoded by the gene C1galt1 that is critical for the biosynthesis of core 1-derived O-glycans, in ECs and hematopoietic cells (termed here EHC T-syn(-/-) mice). EHC T-syn(-/-) mice exhibited embryonic and neonatal lethality associated with disorganized and blood-filled lymphatic vessels. Bone marrow transplantation and EC C1galt1 transgene rescue demonstrated that lymphangiogenesis specifically requires EC O-glycans, and intestinal lymphatic microvessels in EHC T-syn(-/-) mice expressed a mosaic of blood and lymphatic EC markers. The level of O-glycoprotein podoplanin was significantly reduced in EHC T-syn(-/-) lymphatics, and podoplanin-deficient mice developed blood-filled lymphatics resembling EHC T-syn(-/-) defects. In addition, postnatal inactivation of C1galt1 caused blood/lymphatic vessel misconnections that were similar to the vascular defects in the EHC T-syn(-/-) mice. One consequence of eliminating T-synthase in ECs and hematopoietic cells was that the EHC T-syn(-/-) pups developed fatty liver disease, because of direct chylomicron deposition via misconnected portal vein and intestinal lymphatic systems. Our studies therefore demonstrate that EC O-glycans control the separation of blood and lymphatic vessels during embryonic and postnatal development, in part by regulating podoplanin expression. |
Keywords: | Cultured Cells, Endothelial Cells, Fatty Liver, Galactosyltransferases, Lymphatic Vessels, Microvessels, Transgenes, Transgenic Mice, Animals, Mice |
Source: | Journal of Clinical Investigation |
ISSN: | 0021-9738 |
Publisher: | American Society for Clinical Investigation |
Volume: | 118 |
Number: | 11 |
Page Range: | 3725-3737 |
Date: | November 2008 |
Official Publication: | https://doi.org/10.1172/JCI36077 |
PubMed: | View item in PubMed |
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