Developing LRP1 Agonists into a Therapeutic Strategy in Acute Myocardial Infarction

被引:23
|
作者
Potere, Nicola [1 ,2 ]
Del Buono, Marco Giuseppe [1 ,3 ]
Niccoli, Giampaolo [3 ]
Crea, Filippo [3 ]
Toldo, Stefano [1 ]
Abbate, Antonio [1 ]
机构
[1] Virginia Commonwealth Univ, VCU Pauley Heart Ctr, Med Coll Virginia Campus, Richmond, VA 23298 USA
[2] Campus Biomed Univ Rome, Dept Med, Unit Cardiovasc Sci, I-00128 Rome, Italy
[3] Univ Cattolica Sacro Cuore, Fdn Policlin Univ A Gemelli, IRCCS, Dept Cardiovasc & Thorac Sci, I-00168 Rome, Italy
关键词
cardioprotection; ischemia-reperfusion injury; RISK pathway; LRP1; RECEPTOR-RELATED PROTEIN-1; ISCHEMIA-REPERFUSION INJURY; INTRAVENOUS IMMUNOGLOBULIN IVIG; PLASMINOGEN-ACTIVATOR; CELL-SURVIVAL; INFLAMMATORY INJURY; NLRP3; INFLAMMASOME; SCHWANN-CELLS; KINASE; AKT;
D O I
10.3390/ijms20030544
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cardioprotection refers to a strategy aimed at enhancing survival pathways in the injured yet salvageable myocardium following ischemia-reperfusion. Low-density lipoprotein receptor-related protein 1 (LRP1) is a multifunctional receptor that can be targeted following reperfusion, to induce a cardioprotective signaling through the activation of the reperfusion injury salvage kinase (RISK) pathway. The data from preclinical studies with non-selective and selective LRP1 agonists are promising, showing a large therapeutic window for intervention to reduce infarct size after ischemia-reperfusion. A pilot clinical trial with plasma derived 1-antitrypsin (AAT), a naturally occurring LRP1 agonist, supports the translational value of LRP1 as a novel therapeutic target for cardioprotection. A phase I study with a selective LRP1 agonist has been completed showing no toxicity. These findings may open the way to early phase clinical studies with pharmacologic LRP1 activation in patients with acute myocardial infarction (AMI).
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页数:18
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