Branched-Chain Amino Acid Negatively Regulates KLF15 Expression via PI3K-AKT Pathway.

Recent studies have linked branched-chain amino acid (BCAA) with numerous metabolic diseases. However, the molecular basis of BCAA's roles in metabolic regulation remains to be established. KLF15 (Krüppel-like factor 15) is a transcription factor and master regulator of glycemic, lipid, and amino acids metabolism. In the present study, we found high concentrations of BCAA suppressed KLF15 expression while BCAA starvation induced KLF15 expression, suggesting KLF15 expression is negatively controlled by BCAA.Interestingly, BCAA starvation induced PI3K-AKT signaling. KLF15 induction by BCAA starvation was blocked by PI3K and AKT inhibitors, indicating the activation of PI3K-AKT signaling pathway mediated the KLF15 induction. BCAA regulated KLF15 expression at transcriptional level but not post-transcriptional level. However, BCAA starvation failed to increase the KLF15-promoter-driven luciferase expression, suggesting KLF15 promoter activity was not directly controlled by BCAA. Finally, fasting reduced BCAA abundance in mice and KLF15 expression was dramatically induced in muscle and white adipose tissue, but not in liver. Together, these data demonstrated BCAA negatively regulated KLF15 expression, suggesting a novel molecular mechanism underlying BCAA's multiple functions in metabolic regulation

Geochronology and geochemistry of the Shanagen hydrothermal vein-type Mo deposit in Derbugan metallogenic belt of the NE China and their geological significance

The Shanagen hydrothermal vein-type Mo deposit belongs to the Derbugan metallogenic belt, which is located in the Ergun block, NE China. The Mo mineralization is mainly developed in sericitized quartz siltstone around alkali-feldspar granite. In this paper, we present Molybdenite Re–Os dating, zircon U–Pb dating and geochemical data with the aim of determining metallogenic epoch and tectonic setting. Molybdenite Re–Os and zircon U–Pb dating of the alkali-feldspar granite indicate that the ore-formation and alkali-feldspar granite emplacement occurred at 143.1 ± 3.8 Ma, and 144.7 ± 0.7 Ma. Both were formed in the early Cretaceous. Chemically, the alkali-feldspar granites are enriched in L rare earth element and LILEs, depleted in H rare earth element and HFSEs, and pronounced negative Eu anomalies, are metaluminous and belong to the high-K calc-alkaline series and highly differentiated I-type granite. Geochemical features and concave upwards rare earth element pattern imply that alkali-feldspar granites were formed from magma generated by partial melting of lower crust. Combining the geochemistry, chronology, and the regional tectonic evolution, we infer that Shanagen hydrothermal vein-type Mo deposit was formed the extensional environment after the closure of the Mongol-Okhotsk Ocean

Tetra­ethyl­ammonium 4-hy­droxy­benzoate monohydrate

In the title compound, C8H20N+·C7H5O3 −·H2O, the carboxyl­ate group is slightly out of the plane of the parent benzene ring, the C—C—C—O torsion angles being 2.3 (2) and 2.0 (2)°. The carboxyl­ate group and the hy­droxy group form O—H⋯O hydrogen bonds, generating a head-to-tail chain along the b axis. Neighbouring hydrogen-bonded chains are linked by the water mol­ecule, generating two independent O—H⋯O donor hydrogen bonds. The carboxyl­ate group thus constructs a hydrogen-bonded host layer parallel to (10). The tetra­ethyl­ammonium cation is contained between these layers, forming a sandwich-like structure with an approximate inter­layer distance of 10.03 Å

Cryopreservation of human failed-matured oocytes followed by in vitro maturation: vitrification is superior to the slow freezing method

<p>Abstract</p> <p>Background</p> <p>Oocyte cryopreservation is an important method used in a number of human fertility circumstances. Here, we compared the survival, <it>in vitro </it>maturation, fertilization, and early embryonic development rates of frozen-thawed human immature oocytes using two different cryopreservation methods.</p> <p>Methods</p> <p>A total of 454 failed-matured oocytes [germinal vesicle (GV) and metaphase I (MI) stages] were collected from 135 patients (mean age 33.84 +/- 5.0 y) who underwent intracytoplasmic sperm injection (ICSI) cycles between February 2009 and December 2009 and randomly divided into a slow freezing group [1.5 mol/L-1, 2-propanediol (PROH) + 0.2 mol/l sucrose] and vitrification group [20% PROH + 20% ethylene glycol (EG) + 0.5 mol/l sucrose].</p> <p>Results</p> <p>The vitrification protocol yielded a better survival rate than the slow freezing protocol at each maturation stage assessed. Regardless of the maturation stage (GV + MI), the slow freezing protocol had a significantly lower survival rate than the vitrification protocol (p < 0.001). In addition, a significant difference was found in the survival rates between GV and MI oocytes regardless of the protocol used (90.1 vs. 64.7%, respectively; p < 0.01). We also found that the maturation rates of GV and MI oocytes from the slow freezing and vitrification groups were 16.7 vs. 24.4% and 50.8 vs. 55.4%, respectively. Regardless of the protocol used, the GV oocytes had significantly lower viability than MI oocytes after 36 h of <it>in vitro </it>maturation (21.2 vs. 54.0%, respectively; p < 0.01). In addition, the GV and MI oocytes from the slow freezing group had a markedly lower maturation rate than those from the vitrification group (33.6 vs. 43.1%, respectively), but no statistical difference was found between the two groups (P > 0.05). For the GV-matured oocytes, no fertilized eggs were obtained in the slow-freezing group, while a 19.0% (4/21) fertilization rate was observed in the vitrification group. For the MI-matured oocytes, fertilization rates for the slow freezing and vitrified groups were 36% and 61.1%, respectively, but no significant difference was found between the two groups (PIn the Methods section in the MS, all procedures were compliant with ethical guidelines, i.e. approved by the Ethical Committee of our university and Informed Consent signed by each patient. > 0.05). In the GV vitrification group, no embryo formed; however, in the MI slow freezing group, 12 oocytes were fertilized, but only two achieved cleavage and were subsequently blocked at the 2-cell stage. In the MI vitrification group, a total of 22 embryos were obtained, five of which developed to the blastocyst stage.</p> <p>Conclusions</p> <p>Vitrification is superior to the slow freezing method in terms of the survival and developmental rates for the cryopreservation of human failed-matured oocytes. In addition, GV oocytes appeared to be more resistant than MI oocytes to the low temperature and cryoprotectant used during cryopreservation.</p