Autophagy plays an essential role in intracellular degradation and maintenance of cellular homeostasis in all cells, including neurons. Although a recent study reported a copy number variation of Ulk2, a gene essential for initiating autophagy, associated with a case of schizophrenia (SZ), it remains to be studied whether Ulk2 dysfunction could underlie the pathophysiology of the disease. Here we show that Ulk2 heterozygous (Ulk2+/-) mice have upregulated expression of sequestosome-1/p62, an autophagy-associated stress response protein, predominantly in pyramidal neurons of the prefrontal cortex (PFC), and exhibit behavioral deficits associated with the PFC functions, including attenuated sensorimotor gating and impaired cognition. Ulk2+/- neurons showed imbalanced excitatory-inhibitory neurotransmission, due in part to selective down-modulation of gamma-aminobutyric acid (GABA)A receptor surface expression in pyramidal neurons. Genetically reducing p62 gene dosage or suppressing p62 protein levels with an autophagy-inducing agent restored the GABAA receptor surface expression and rescued the behavioral deficits in Ulk2+/- mice. Moreover, expressing a short peptide that specifically interferes with the interaction of p62 and GABAA receptor-associated protein, a protein that regulates endocytic trafficking of GABAA receptors, also restored the GABAA receptor surface expression and rescued the behavioral deficits in Ulk2+/- mice. Thus, the current study reveals a novel mechanism linking deregulated autophagy to functional disturbances of the nervous system relevant to SZ, through regulation of GABAA receptor surface presentation in pyramidal neurons.
The first Si corrole complexes were synthesized in good yields by treatment of meso-triarylcorroles with tetrachlorosilane in 1,2-dichloroethane at 60 °C. The central silicon atom possesses a square-pyramidal coordination geometry with slightly longer Si-N bond lengths as compared with those of known triazacorrole Si complexes. The Si corrole complexes exhibit sharp and blue-shifted absorption spectra and larger fluorescence quantum yields as compared with the corresponding free-base corroles. A μ-oxo dimer of a Si corrole was synthesized upon treatment with methanesulfonyl chloride in pyridine at 100 °C. This dimer shows a face-to-face structure with a 90° twist in the solid state. Although the dimer exhibits a blue-shifted Soret band, reflecting the face-to-face geometry, it displays a largely red-shifted and broad fluorescence spectrum with a large Stokes shift, suggesting a large structural change in the S state. These intriguing optical properties have been comprehensively studied by magnetic circular dichroism (MCD) spectroscopy, femtosecond transient absorption (fs-TA) measurements, and theoretical calculations.
The
corrole derivative meso-oxoisocorrole has
been theoretically predicted to be antiaromatic, despite its formally
cross conjugated electronic system. In this study, this prediction
has been experimentally proven by the facile preparation of meso-oxoisocorrole via the oxidation of a meso free corrole with MnO2 and its comprehensive characterization
using NMR, UV/vis absorption, FT-IR, and transient-absorption spectroscopy,
cyclic voltammetry, and X-ray diffraction analysis. Furthermore, the
free base meso-oxoisocorrole was metalated by treatment
with Ni(acac)2, PdCl2(PhCN)2, and
Zn(OAc)2 to give the corresponding metal complexes. These
complexes are more strongly antiaromatic, and their degree of paratropicity
depends on their planarity. Thus, fine tuning of their antiaromaticity
was achieved with concomitant modulation of their HOMO–LUMO
gaps. In the presence of tris(pentafluorophenyl)borane, their antiaromaticity
is significantly enhanced due to the elongation of the CO
bond, which promotes the polarized C+–O– resonance state. Furthermore, a distinct frequency shift of the
CO vibrational mode in the triplet state was observed in the
time-resolved IR spectra in accordance with the Baird rule, which
indicates aromaticity reversal in the excited state.
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