Generation and decay of Higgs mode in a strongly interacting Fermi gas.

We investigate the life cycle of the large amplitude Higgs mode in strongly interacting superfluid Fermi gas. Through numerical simulations with time-dependent density functional theory and the technique of the interaction quench, we verify the previous theoretical predictions on the mode's frequency. Next, we demonstrate that the mode is dynamically unstable against external perturbation and qualitatively examine the emerging state after the mode decays.

Dissipative Dynamics of Quantum Vortices in Fermionic Superfluid.

In a recent article, Kwon et al. [Nature (London) 600, 64 (2021)NATUAS0028-083610.1038/s41586-021-04047-4] revealed nonuniversal dissipative dynamics of quantum vortices in a fermionic superfluid.

Mitochondrial dysfunction reactivates α-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models.

Signaling circuits crucial to systemic physiology are widespread, yet uncovering their molecular underpinnings remains a barrier to understanding the etiology of many metabolic disorders. Here, we identified a copper-linked signaling circuit activated by disruption of mitochondrial function in the murine liver or heart that resulted in atrophy of the spleen and thymus and caused a peripheral white blood cell deficiency. We demonstrated that the leukopenia was caused by α-fetoprotein, which required copper and the cell surface receptor CCR5 to promote white blood cell death.

Homoharringtonine demonstrates a cytotoxic effect against triple-negative breast cancer cell lines and acts synergistically with paclitaxel.

The lack of targeted therapies for triple-negative breast cancer (TNBC) contributes to their high mortality rates and high risk of relapse compared to other subtypes of breast cancer. Most TNBCs (75%) have downregulated the expression of CREB3L1 (cAMP-responsive element binding protein 3 like 1), a transcription factor and metastasis suppressor that represses genes that promote cancer progression and metastasis. In this report, we screened an FDA-approved drug library and identified four drugs that were highly cytotoxic towards HCC1806 CREB3L1-deficient TNBC cells.

Homeostatic control of nuclear-encoded mitochondrial gene expression by the histone variant H2A.Z is essential for neuronal survival.

Histone variants are crucial regulators of chromatin structure and gene transcription, yet their functions within the brain remain largely unexplored. Here, we show that the H2A histone variant H2A.Z is essential for neuronal survival.