Receptor tyrosine kinase profiling of ischemic heart identifies ROR1 as a potential therapeutic target

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Heliste , J , Jokilammi , A , Paatero , I , Chakroborty , D , Stark , C , Savunen , T , Laaksonen , M & Elenius , K 2018 , ' Receptor tyrosine kinase profiling of ischemic heart identifies ROR1 as a potential therapeutic target ' , BMC Cardiovascular Disorders , vol. 18 , 196 . https://doi.org/10.1186/s12872-018-0933-y

Title: Receptor tyrosine kinase profiling of ischemic heart identifies ROR1 as a potential therapeutic target
Author: Heliste, Juho; Jokilammi, Anne; Paatero, Ilkka; Chakroborty, Deepankar; Stark, Christoffer; Savunen, Timo; Laaksonen, Maria; Elenius, Klaus
Other contributor: University of Helsinki, Institute for Molecular Medicine Finland

Date: 2018-10-20
Language: eng
Number of pages: 12
Belongs to series: BMC Cardiovascular Disorders
ISSN: 1471-2261
DOI: https://doi.org/10.1186/s12872-018-0933-y
URI: http://hdl.handle.net/10138/260953
Abstract: BackgroundReceptor tyrosine kinases (RTK) are potential targets for the treatment of ischemic heart disease. The human RTK family consists of 55 members, most of which have not yet been characterized for expression or activity in the ischemic heart.MethodsRTK gene expression was analyzed from human heart samples representing healthy tissue, acute myocardial infarction or ischemic cardiomyopathy. As an experimental model, pig heart with ischemia-reperfusion injury, caused by cardiopulmonary bypass,was used, from which phosphorylation status of RTKs was assessed with a phospho-RTK array. Expression and function of one RTK, ROR1, was further validated in pig tissue samples, and in HL-1 cardiomyocytes and H9c2 cardiomyoblasts, exposed to hypoxia and reoxygenation. ROR1 protein level was analyzed by Western blotting. Cell viability after ROR1 siRNA knockdown or activation with Wnt-5a ligand was assessed by MTT assays.ResultsIn addition to previously characterized RTKs, a group of novel active and regulated RTKs was detected in the ischemic heart. ROR1 was the most significantly upregulated RTK in human ischemic cardiomyopathy. However, ROR1 phosphorylation was suppressed in the pig model of ischemia-reperfusion and ROR1 phosphorylation and expression were down-regulated in HL-1 cardiomyocytes subjected to short-term hypoxia in vitro. ROR1 expression in the pig heart was confirmed on protein and mRNA level. Functionally, ROR1 activity was associated with reduced viability of HL-1 cardiomyocytes in both normoxia and during hypoxia-reoxygenation.ConclusionsSeveral novel RTKs were found to be regulated in expression or activity in ischemic heart. ROR1 was one of the most significantly regulated RTKs. The in vitro findings suggest a role for ROR1 as a potential target for the treatment of ischemic heart injury.
Subject: Hypoxia
Ischemic cardiomyopathy
Myocardial ischemia
Myocardial infarction
Receptor tyrosine kinase
MYOCARDIAL-INFARCTION
NEUREGULIN RECEPTOR
CARDIAC DEVELOPMENT
PROLIFERATION
SURVIVAL
INJURY
EXPRESSION
INSULIN
ERBB2
MICE
3121 General medicine, internal medicine and other clinical medicine
3111 Biomedicine
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