| Literature DB >> 20664912 |
Noam Shomron1, Nobuko Hamasaki-Katagiri, Ryan Hunt, Klilah Hershko, Elie Pommier, S Geetha, Adam Blaisdell, Alexandra Dobkin, Andrew Marple, Isabella Roma, Jordan Newell, Courtni Allen, Scott Friedman, Chava Kimchi-Sarfaty.
Abstract
Although ADAMTS13, the von Willebrand factor (VWF)-cleaving protease, is expressed in a range of tissues, the physiological significance of tissue-specific ADAMTS13 alternative splicing isoforms have yet to be clarified. Screening a panel of human tissues and cell lines revealed a spliced ADAMTS13 transcript in hepatic stellate cells and a hepatoma cell line that retains the 25th intron. A nonsense codon within the intron truncates the protease, which gains 64 novel amino acids in lieu of both CUB domains. This isoform, while retaining VWF-cleaving capability, accumulates intracellularly and its biological inaccessibility may prevent its participation in regulating haemostasis and other physiologic functions.Entities:
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Year: 2010 PMID: 20664912 PMCID: PMC2982681 DOI: 10.1160/TH09-12-0860
Source DB: PubMed Journal: Thromb Haemost ISSN: 0340-6245 Impact factor: 5.249