國家衛生研究院 NHRI:Item 3990099045/14073
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 907690      Online Users : 950
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/14073


    Title: Hydroxyindole O-methyltransferase in 5-methoxytryptophan synthesis and function in vascular smooth muscle cells
    Authors: Yet, SF;Chen, CH
    Contributors: Institute of Cellular and Systems Medicine
    Abstract: Background and Aims: Various metabolites of tryptophan participate in diverse physiological functions. We have shown that tryptophan metabolite 5-methoxytryptophan (5-MTP) reduces inflammatory cytokine-induced p38 MAPK activation in vascular smooth muscle cells (VSMCs) and protects against stenosis and restenosis in animal injury models. As such, it is important to understand the synthetic enzymes for 5-MTP. Hydroxyindole O-methyltransferase (HIOMT) is likely to be a key enzyme for 5-MTP production. Our goal is to investigate the role of HIOMT in 5-MTP synthesis and function in VSMCs. Methods: Human HIOMT has 3 isoforms, of 373, 345, and 298 amino acids, respectively. Mouse HIOMT has one isoform of 387 amino acids; however, there are two mutations, R78G and R242C, in C57BL/6 strain compared with that of C3H strain. To clarify functions of these isoforms, we generated expression plasmids of various isoforms, transfected into VSMCs, stimulated with inflammatory cytokines, and examined p38 MAPK phosphorylation levels. Results: Transfection experiments revealed that different inflammatory cytokines activated p38 phosphorylation in VSMCs. Interestingly, compared with vector control, hHIOMT373 but not hHIOMT298 isoform reduced p38 phosphorylation. Conditioned medium from hHIOMT373-transfected VSMCs also showed a similar effect. Intriguingly, mHIOMT-C3H but not mHIOMT-C57 repressed p38 activation to a similar degree as hHIOMT373 and 5-MTP, suggesting HIOMT might be defective in C57BL/6 strain. Double immunofluorescence staining showed colocalized staining of 5-MTP and hHIOMT in hHIOMT373-transfected VSMCs. Conclusions: Our results indicate that hHIOMT373 and mHIOMT-C3H rather than hHIOMT298 or mHIOMT-C57 are responsible for 5-MTP production and could functionally substitute 5-MTP for exerting anti-inflammatory effect and vascular protection in VSMCs.
    Date: 2020-12-01
    Relation: Atherosclerosis. 2020 Dec;315:E61.
    Link to: http://dx.doi.org/10.1016/j.atherosclerosis.2020.10.188
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0021-9150&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000748958900170
    Appears in Collections:[Shaw-Fang Yet] Conference Papers/Meeting Abstract

    Files in This Item:

    File Description SizeFormat
    ISI000748958900170.pdf139KbAdobe PDF148View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback