Mentors And The Butterfly Effect: Triggers For Discovering Signalling by Proteinases via Proteinase-Activated Receptors (PARs) And More

被引:0
|
作者
Hollenberg, Morley D. [1 ,2 ]
机构
[1] Univ Calgary, Fac Med, Dept Physiol & Pharmacol, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Fac Med, Dept Med, Calgary, AB T2N 4N1, Canada
来源
CLINICAL AND INVESTIGATIVE MEDICINE | 2012年 / 35卷 / 06期
基金
加拿大健康研究院;
关键词
GASTRIC SMOOTH-MUSCLE; THROMBIN RECEPTOR; MOLECULAR-CLONING; (PAR(2))-ACTIVATING PEPTIDES; STRUCTURAL REQUIREMENTS; INDUCE INFLAMMATION; HORMONE-BINDING; CELL-DIVISION; CATHEPSIN-G; TRYPSIN-IV;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The essential role of proteinases as regulatory digestive enzymes, recognized since the late 1800s, has been underscored by the discovery that more than 2% of the genome codes for proteinases and their inhibitors. Further, by the early 1970s it was appreciated that in addition to their digestive actions, proteinases can affect cell function: (1) by the generation or degradation of peptide hormones and (2) by the direct regulation of signalling by receptors like the one for insulin. It was the discovery in the 1990s of the novel G-protein-coupled 'proteinase-activated receptor' (PAR) family that has caused a paradigm shift in the understanding of the way that proteinases can regulate cell signalling. This overview provides a perspective for the discovery of the PARs and my laboratory's role in (1) understanding the molecular pharmacology of these fascinating receptors and (2) identifying the potential pathophysiological roles that the PAR family can play in inflammatory disease. In this context, the overview also portrays the essential impact that seemingly minor comments/insights provided by my lifelong mentors have had on kindling my intense interest in proteinase-mediated signalling. The 'butterfly effect' of those comments has led to an unexpectedly large impact on my own research directions. Hopefully my own 'butterfly comments' will also be heard by my trainees and other colleagues with whom I am currently working and will promote future discoveries that will be directly relevant to the treatment of inflammatory disease.
引用
收藏
页码:E378 / E391
页数:14
相关论文
共 5 条
  • [1] Biased signalling and proteinase-activated receptors (PARs): targeting inflammatory disease
    Hollenberg, M. D.
    Mihara, K.
    Polley, D.
    Suen, J. Y.
    Han, A.
    Fairlie, D. P.
    Ramachandran, R.
    BRITISH JOURNAL OF PHARMACOLOGY, 2014, 171 (05) : 1180 - 1194
  • [2] Molecular mechanisms regulating Proteinase-Activated Receptors (PARs)
    Chandrabalan, Arundhasa
    Ramachandran, Rithwik
    FEBS JOURNAL, 2021, 288 (08) : 2697 - 2726
  • [3] Proteinase-activated receptors (PARs) as targets for antiplatelet therapy
    Cunningham, Margaret
    McIntosh, Kathryn
    Bushell, Trevor
    Sloan, Graeme
    Plevin, Robin
    BIOCHEMICAL SOCIETY TRANSACTIONS, 2016, 44 : 606 - 612
  • [4] Proteinase-Activated Receptors (PARs) and Calcium Signaling in Cancer
    Kaufmann, Roland
    Hollenberg, Morley D.
    CALCIUM SIGNALING, 2012, 740 : 979 - 1000
  • [5] N-Linked Glycosylation Regulates Human Proteinase-activated Receptor-1 Cell Surface Expression and Disarming via Neutrophil Proteinases and Thermolysin
    Xiao, Yu Pei
    Morice, Alyn H.
    Compton, Steven J.
    Sadofsky, Laura
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (26) : 22991 - 23002