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The topological $θ$-angle is central to the understanding of a plethora of phenomena in condensed matter and high-energy physics such as the strong CP problem, dynamical quantum topological phase transitions, and the confinement--deconfinement transition. Difficulties arise when probing the effects of the topological $θ$-angle using classical methods, in particular through the appearance of a sign problem in numerical simulations. Quantum simulators offer a powerful alternate venue for realizing the $θ$-angle, which has hitherto remained an outstanding challenge due to the difficulty of introducing a dynamical electric field in the experiment. Here, we report on the experimental realization of a tunable topological $θ$-angle in a Bose--Hubbard gauge-theory quantum simulator, implemented through a tilted superlattice potential that induces an effective background electric field. We demonstrate the rich physics due to this angle by the direct observation of the confinement--deconfinement transition of $(1+1)$-dimensional quantum electrodynamics. Using an atomic-precision quantum gas microscope, we distinguish between the confined and deconfined phases by monitoring the real-time evolution of particle--antiparticle pairs, which exhibit constrained (ballistic) propagation for a finite (vanishing) deviation of the $θ$-angle from $π$. Our work provides a major step forward in the realization of topological terms on modern quantum simulators, and the exploration of rich physics they have been theorized to entail., $7+7$ pages, $4+7$ figures, $1+0$ table

Gauge theory and thermalization are both foundations of physics and nowadays are both topics of essential importance for modern quantum science and technology. Simulating lattice gauge theories (LGTs) realized recently with ultracold atoms provides a unique opportunity for carrying out a correlated study of gauge theory and thermalization in the same setting. Theoretical studies have shown that an Ising quantum phase transition exists in this implemented LGT, and quantum thermalization can also signal this phase transition. Nevertheless, it remains an experimental challenge to accurately determine the critical point and controllably explore the thermalization dynamics in the quantum critical regime due to the lack of techniques for locally manipulating and detecting matter and gauge fields. Here, we report an experimental investigation of the quantum criticality in the LGT from both equilibrium and non-equilibrium thermalization perspectives by equipping the single-site addressing and atom-number-resolved detection into our LGT simulator. We accurately determine the quantum critical point agreed with the predicted value. We prepare a $|Z_{2}\rangle$ state deterministically and study its thermalization dynamics across the critical point, leading to the observation that this $|Z_{2}\rangle$ state thermalizes only in the critical regime. This result manifests the interplay between quantum many-body scars, quantum criticality, and symmetry breaking., Comment: 6+4 pages, 4+7 figures

Atherosclerosis (AS) is a chronic inflammatory disease of the vascular wall with multiple causes. AS is the primary pathological basis of cardiovascular disease and stroke. Moreover, carotid plaque rupture and thrombus formation are the main causes of ischemic stroke. Therefore, understanding the formation of carotid plaques may help improve the prediction and prevention of cardiovascular and cerebrovascular events. Endothelial cell dysfunction results in re-endothelialization and angiogenesis in atherosclerotic plaques, thus promoting plaque destabilization. The aim of the present study was to evaluate the effect of circular RNA (circRNA) molecules in serum exosomes (serum-Exos) from patients with stable plaque atherosclerosis (SA) and unstable/vulnerable plaque atherosclerosis (UA). Specifically, the effect of circRNA on human umbilical vein endothelial cell (HUVEC) behavior and the mechanisms underlying plaque destabilization in AS were evaluated. Serum-Exos were isolated, then identified using transmission electron microscopy, nanoparticle tracking analysis and western blotting. The serum-Exo-circRNA expression profile of patients with SA or UA was investigated using a circRNA array. The relationship between circRNA-006896 in serum-Exos and biochemical parameters of patients with SA and UA were analyzed using Spearman's correlation. In addition, HUVECs were incubated with serum-Exos for in vitro functional assays. The present study demonstrated that circRNAs expression profiles in SA and UA serum-Exos were significantly different, indicating a potential role for circRNAs in carotid plaque destabilization. The expression of circRNA-0006896 was positively correlated with triglyceride, low-density lipoprotein cholesterol (LDL-C) and C-reactive protein levels, and negatively correlated with albumin levels in patients with UA. However, circRNA-0006896 expression was positively correlated with LDL-C in patients with SA. Using bioinformatic analysis, a competing endogenous RNA (ceRNA) network was selected to study the regulatory roles of circRNA-0006896 in serum-Exos. Additionally, in HUVECs treated with serum-Exos derived from patients with UA, the expression of circRNA-0006896 in HUVECs was upregulated. This was accompanied by decreased expression of microRNA-1264 and SOCS3, increased levels of DNMT1 and phosphorylated STAT3. HUVEC proliferation and migration were significantly increased in the UA group, compared with the mock and SA groups. This finding indicates that the circRNA-0006896-miR-1264-DNMT1 axis plays an important role in carotid plaque destabilization by regulating the behavior of endothelial cells. Moreover, it suggests that circRNA-0006896 may represent a therapeutic target for controlling JNK/STAT3 signaling in HUVECs. Thus, this study may provide insight on potential interventions against vulnerable plaque formation in patients with AS.