Hydrogen Sulfide Promotes Platelet Autophagy via PDGFR-α/PI3K/Akt Signaling in Cirrhotic Thrombocytopenia.

Background and Aims: The role of platelet autophagy in cirrhotic thrombocytopenia (CTP) remains unclear. This study aimed to investigate the impact of platelet autophagy in CTP and elucidate the regulatory mechanism of hydrogen sulfide (H2S) on platelet autophagy. Methods: Platelets from 56 cirrhotic patients and 56 healthy individuals were isolated for in vitro analyses. Autophagy markers (ATG7, BECN1, LC3, and SQSTM1) were quantified using enzyme-linked immunosorbent assay, while autophagosomes were visualized through electron microscopy. Western blotting was used to assess the autophagy-related proteins and the PDGFR/PI3K/Akt/mTOR pathway following treatment with NaHS (an H2S donor), hydroxocobalamin (an H2S scavenger), or AG 1295 (a selective PDGFR-α inhibitor). A carbon tetrachloride-induced cirrhotic BALB/c mouse model was established. Cirrhotic mice with thrombocytopenia were randomly treated with normal saline, NaHS, or hydroxocobalamin for 15 days. Changes in platelet count and aggregation rate were observed every three days. Results: Cirrhotic patients with thrombocytopenia exhibited significantly decreased platelet autophagy markers and endogenous H2S levels, alongside increased platelet aggregation, compared to healthy controls. In vitro, NaHS treatment of platelets from severe CTP patients elevated LC3-II levels, reduced SQSTM1 levels, and decreased platelet aggregation in a dose-dependent manner. H2S treatment inhibited PDGFR, PI3K, Akt, and mTOR phosphorylation. In vivo, NaHS significantly increased LC3-II and decreased SQSTM1 expressions in platelets of cirrhotic mice, reducing platelet aggregation without affecting the platelet count. Conclusions: Diminished platelet autophagy potentially contributes to thrombocytopenia in cirrhotic patients. H2S modulates platelet autophagy and functions possibly via the PDGFR-α/PI3K/Akt/mTOR signaling pathway.

A BODIPY-carbazole hybrid as a fluorescent probe: the design, synthesis, and discrimination of surfactants and the determination of the CMC values.

Surfactants play important roles in chemical industries and have become well-known environmental pollutants owing to their extensive use in different fields. In this work, we reported a fluorescent probe, namely, BDP-Zn2+ for the discrimination of four kinds of surfactants and the determination of CMC values. BDP-Zn2+ was composed of covalently linked BODIPY, carbazole, N,N-bis(2-pyridylmethyl)ethylenediamine (BPEA) and zinc ions to fabricate a novel push-pull molecular structure. Upon the addition of surfactants, the probe exhibited a turn-on fluorescence response and the emission was enhanced on increasing the surfactant concentrations. This indicated that the fluorescence intensity and the ratios of the emission at 607 nm to that at 514 nm as fingerprints could be used to identify the CMC values of the surfactants. Our current work provides an alternative method to efficiently discriminate different surfactants for the further studies of their physical and chemical functions.

Synthesis and biological evaluation of vanadium complexes as novel anti-tumor agents.

A class of vanadium complexes were prepared and investigated for their antiproliferative effects by MTT assay. The structure-activity relationship was extensively studied through the ligand variation. The results showed that the synthetic vanadium complexes demonstrated moderate to good antiproliferative activities against the four cancer cell lines including MGC803, EC109, MCF7 and HepG2, respectively. Of note was that most of the complexes showed preferential growth inhibitory activity to some degree toward gastric cancer line MGC803. Among them, complex 19 exhibited the most and broad-spectrum proliferative inhibition against the tested cell lines. In addition, mechanism studies illustrated that complex 19 could prevent the colony formation, migration and EMT process, as well as induce apoptosis of MGC803 cells. Furthermore, Western blot experiments revealed that the expression of apoptosis-related proteins changed, including up-regulation of Bax, PARP and caspase-3/9, as well as down-regulation of Bcl-2.

[Simulation of Inorganic Nitrogen Fluxes at the Sediment-water Interface in a Typical Intertidal Zone, Eastern China].

Taking 12 typical intertidal zones along the eastern coast of China as the research object, indoor tide simulation experiments were conducted to measure exchange fluxes of nitrate nitrogen (NO3--N) and ammonia nitrogen (NH4+-N) between overlying water and sediments, to investigate their spatial distribution, and to clarify controlling factors such as salinity, temperature, and organic matter. Results showed that the total NO3--N flux was -2.91-3.34 mmol·(m2·h)-1, while the total flux of NH4+-N was -4.36-2.34 mmol·(m2·h)-1. The average flux, at 12℃ and 35℃, was -0.04 mmol·(m2·h)-1, indicating that typical intertidal zone sediment is an effective sink for ammonia nitrogen and nitrate nitrogen. There was a significant difference in the spatial distribution of nitrate and ammonia nitrogen fluxes. At 12℃, the higher the latitude, the greater the ammonia nitrogen flux; results for the 25°-35°N intertidal nitrate flux were as follows:<15°-25°N < 35°-45°N at 25℃ and 35℃, while the flux of ammonia nitrogen was 25°N-35°N > 15°-25°N > 35°-45°N. The fluxes of the three intertidal zones decreased with increase in temperature, which controls the coupled nitrification-denitrification taking place in the upper layer of sediment and at the bottom of overlying water. NO3--N fluxes first increased and then decreased with temperature at 15°-25°N and 35°-45°N, while NO3--N fluxes at 25°-35°N always decreased with temperature. At each latitude, the higher the temperature, the lower the NH4+-N flux. There was no single significant effect of environmental factors on fluxes. Salinity, sediment organic carbon (OC), sediment total nitrogen (TN), concentrations of ammonia nitrogen and nitrate nitrogen in pore water, and bulk density synergistically affected the spatial differentiation of exchanged NO3--N and NH4+-N fluxes.