Title : Propagation of undifferentiated human embryonic stem cells with nano-liposomal ceramide.

Pub. Date : 2009 Jan-Feb

PMID : 18393629






8 Functional Relationships(s)
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Protein Name
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1 Here, we report that ceramide, a bioactive sphingolipid, selectively eliminates hES cells differentially expressing nestin and Tuj1. Ceramides ribosome binding protein 1 Homo sapiens
2 Ceramide-resistant hES cells express higher levels of the messenger RNA for ceramide-metabolizing enzymes that convert ceramide into pro-mitogenic metabolites. Ceramides ribosome binding protein 1 Homo sapiens
3 Ceramide-resistant hES cells express higher levels of the messenger RNA for ceramide-metabolizing enzymes that convert ceramide into pro-mitogenic metabolites. Ceramides ribosome binding protein 1 Homo sapiens
4 Ceramide-resistant hES cells express higher levels of the messenger RNA for ceramide-metabolizing enzymes that convert ceramide into pro-mitogenic metabolites. Ceramides ribosome binding protein 1 Homo sapiens
5 Based on these findings, we conducted long-term studies to determine whether liposomal ceramide can be used to maintain undifferentiated hES cells free of feeder cells. Ceramides ribosome binding protein 1 Homo sapiens
6 We continuously cultured hES cells on matrigel for 4 months with liposomal ceramide in a feeder cell-free system. Ceramides ribosome binding protein 1 Homo sapiens
7 Human ES cells treated with liposomal ceramide maintained their pluripotent state as determined by in vivo and in vitro differentiation studies and contained no chromosomal abnormalities. Ceramides ribosome binding protein 1 Homo sapiens
8 In conclusion, our findings suggest that exposure to ceramide provides a viable strategy to prevent premature hES cell differentiation and to maintain pluripotent stem cell populations in the absence of feeder cells. Ceramides ribosome binding protein 1 Homo sapiens