Key result
Modulation of the cGMP/cGKI pathway in cardiac myocytes offers potential targets for predictive biomarkers and optimized therapeutic strategies in various heart diseases.
Why the study?
Although numerous targets of cGMP/cGKI in the heart have been identified, neither their exact pathophysiological functions nor their cell-type specific roles are clear.
Understanding the specific actions of cGMP and cGKI in cardiomyocytes may guide future studies for predictive biomarkers and therapeutic strategies in heart disease.
cGMP/cGKI signaling may inform cardiac biomarker and therapy development; leaves open validation of myocyte targets in prospective studies.
The 3',5'-cyclic guanosine monophosphate (cGMP)-dependent protein kinase type I (cGKI aka PKGI) is a major cardiac effector acting downstream of nitric oxide (NO)-sensitive soluble guanylyl cyclase and natriuretic peptides (NPs), which signal through transmembrane guanylyl cyclases. Consistent with the wide distribution of the cGMP-generating guanylyl cyclases, cGKI, which usually elicits its cellular effects by direct phosphorylation of its targets, is present in multiple cardiac cell types including cardiomyocytes (CMs). Although numerous targets of cGMP/cGKI in heart were identified in the past, neither their exact patho-/physiological functions nor cell-type specific roles are clear. Herein, we inform about the current knowledge on the signal transduction downstream of CM cGKI. We believe that better insights into the specific actions of cGMP and cGKI in these cells will help to guide future studies in the search for predictive biomarkers for the response to pharmacological cGMP pathway modulation. In addition, targets downstream of cGMP/cGKI may be exploited for refined and optimized diagnostic and therapeutic strategies in different types of heart disease and their causes. Importantly, key functions of these proteins and particularly sites of regulatory phosphorylation by cGKI should, at least in principle, remain intact, although upstream signaling through the second messenger cGMP is impaired or dysregulated in a stressed or diseased heart state.
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Adler et al. (2020) conducted a review in Heart disease. cGMP/cGKI pathway was evaluated. Modulation of the cGMP/cGKI pathway in cardiac myocytes offers potential targets for predictive biomarkers and optimized therapeutic strategies in various heart diseases.
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