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http://purl.uniprot.org/citations/31581792http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31581792http://www.w3.org/2000/01/rdf-schema#comment"

Background

Cardiac kinases play a critical role in the development of heart failure, and represent potential tractable therapeutic targets. However, only a very small fraction of the cardiac kinome has been investigated. To identify novel cardiac kinases involved in heart failure, we used an integrated transcriptomics and bioinformatics analysis and identified Homeodomain-Interacting Protein Kinase 2 (HIPK2) as a novel candidate kinase. The role of HIPK2 in cardiac biology is unknown.

Methods

We used the Expression2Kinase algorithm for the screening of kinase targets. To determine the role of HIPK2 in the heart, we generated cardiomyocyte (CM)-specific HIPK2 knockout and heterozygous mice. Heart function was examined by echocardiography, and related cellular and molecular mechanisms were examined. Adeno-associated virus serotype 9 carrying cardiac-specific constitutively active MEK1 (TnT-MEK1-CA) was administrated to rescue cardiac dysfunction in CM-HIPK2 knockout mice.

Results

To our knowledge, this is the first study to define the role of HIPK2 in cardiac biology. Using multiple HIPK2 loss-of-function mouse models, we demonstrated that reduction of HIPK2 in CMs leads to cardiac dysfunction, suggesting a causal role in heart failure. It is important to note that cardiac dysfunction in HIPK2 knockout mice developed with advancing age, but not during development. In addition, CM-HIPK2 knockout mice and CM-HIPK2 heterozygous mice exhibited a gene dose-response relationship of CM-HIPK2 on heart function. HIPK2 expression in the heart was significantly reduced in human end-stage ischemic cardiomyopathy in comparison to nonfailing myocardium, suggesting a clinical relevance of HIPK2 in cardiac biology. In vitro studies with neonatal rat ventricular CMscorroborated the in vivo findings. Specifically, adenovirus-mediated overexpression of HIPK2 suppressed the expression of heart failure markers, NPPA and NPPB, at basal condition and abolished phenylephrine-induced pathological gene expression. An array of mechanistic studies revealed impaired extracellular signal-regulated kinase 1/2 signaling in HIPK2-deficient hearts. An in vivo rescue experiment with adeno-associated virus serotype 9 TnT-MEK1-CA nearly abolished the detrimental phenotype of knockout mice, suggesting that impaired extracellular signal-regulated kinase signaling mediated apoptosis as the key factor driving the detrimental phenotype in CM-HIPK2 knockout mice hearts.

Conclusions

Taken together, these findings suggest that CM-HIPK2 is required to maintain normal cardiac function via extracellular signal-regulated kinase signaling."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.org/dc/terms/identifier"doi:10.1161/circulationaha.119.040740"xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Guo Y."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Kim K."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Zhang Z."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Barnett J.V."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Willette R.N."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Nam Y.J."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Knollmann B.C."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Force T."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Lal H."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Qu X.A."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/author"Sui J.Y."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/name"Circulation"xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/pages"1820-1833"xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/title"Cardiomyocyte Homeodomain-Interacting Protein Kinase 2 Maintains Basal Cardiac Function via Extracellular Signal-Regulated Kinase Signaling."xsd:string
http://purl.uniprot.org/citations/31581792http://purl.uniprot.org/core/volume"140"xsd:string
http://purl.uniprot.org/citations/31581792http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31581792
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