Key result
Conditional inactivation of Lats1/2 caused severe sinus node dysfunction, dysregulated calcium handling, and increased fibrosis in the sinoatrial node, which was rescued by genetic deletion of Yap and Taz.
Why the study?
Although Hippo pathway abnormalities are linked to cardiac arrhythmias in humans, the role of this pathway in the sinoatrial node is unknown.
Does conditional inactivation of Lats1 and Lats2 cause sinus node dysfunction in mice?
Does conditional inactivation of Lats1 and Lats2 cause sinus node dysfunction in mice?
The canonical Hippo-Yap pathway plays a pivotal role in maintaining sinoatrial node homeostasis, offering potential new targets for understanding and treating sinus node dysfunction.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“Our physical findings in the mouse heart were consistent with our observations made at the molecular level, all pointing to the canonical Hippo-Yap signaling pathway playing a vital role in sinoatrial node homeostasis. Because the Hippo pathway is highly conserved between mice and humans, these insights are likely to be applicable for developing new therapeutic targets in the treatment of patients with heart conduction disorders.”
Does not alter sinus node dysfunction management; leaves open whether Hippo-Yap modulation offers therapeutic targets.
Background: The sinoatrial node (SAN) functions as the pacemaker of the heart, initiating rhythmic heartbeats. Despite its importance, the SAN is one of the most poorly understood cardiac entities because of its small size and complex composition and function. The Hippo signaling pathway is a molecular signaling pathway fundamental to heart development and regeneration. Although abnormalities of the Hippo pathway are associated with cardiac arrhythmias in human patients, the role of this pathway in the SAN is unknown. Methods: We investigated key regulators of the Hippo pathway in SAN pacemaker cells by conditionally inactivating the Hippo signaling kinases Lats1 and Lats2 using the tamoxifen-inducible, cardiac conduction system–specific Cre driver Hcn4 CreERT2 with Lats1 and Lats2 conditional knockout alleles. In addition, the Hippo-signaling effectors Yap and Taz were conditionally inactivated in the SAN. To determine the function of Hippo signaling in the SAN and other cardiac conduction system components, we conducted a series of physiological and molecular experiments, including telemetry ECG recording, echocardiography, Masson Trichrome staining, calcium imaging, immunostaining, RNAscope, cleavage under targets and tagmentation sequencing using antibodies against Yap1 or H3K4me3, quantitative real-time polymerase chain reaction, and Western blotting. We also performed comprehensive bioinformatics analyses of various datasets. Results: We found that Lats1/2 inactivation caused severe sinus node dysfunction. Compared with the controls, Lats1/2 conditional knockout mutants exhibited dysregulated calcium handling and increased fibrosis in the SAN, indicating that Lats1/2 function through both cell-autonomous and non–cell-autonomous mechanisms. It is notable that the Lats1/2 conditional knockout phenotype was rescued by genetic deletion of Yap and Taz in the cardiac conduction system. These rescued mice had normal sinus rhythm and reduced fibrosis of the SAN, indicating that Lats1/2 function through Yap and Taz. Cleavage Under Targets and Tagmentation sequencing data showed that Yap potentially regulates genes critical for calcium homeostasis such as Ryr2 and genes encoding paracrine factors important in intercellular communication and fibrosis induction such as Tgfb1 and Tgfb3 . Consistent with this, Lats1/2 conditional knockout mutants had decreased Ryr2 expression and increased Tgfb1 and Tgfb3 expression compared with control mice. Conclusions: We reveal, for the first time to our knowledge, that the canonical Hippo-Yap pathway plays a pivotal role in maintaining SAN homeostasis.
No takes yet. Share an insight, caveat, or question.
Zheng et al. (2022) studied Sinus node dysfunction. Conditional inactivation of Lats1 and Lats2 vs. Control mice was evaluated on Sinus node dysfunction (heart rate, RR intervals, fibrosis, calcium handling). Conditional inactivation of Lats1/2 caused severe sinus node dysfunction, dysregulated calcium handling, and increased fibrosis in the sinoatrial node, which was rescued by genetic deletion of Yap and Taz.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: