Enhanced anti-corrosion and biocompatibility of a functionalized layer formed on ZK60 Mg alloy via hydroxyl (OH-) ion implantation.

Magnesium and its alloys have piqued the interest of researchers due to their promising mechanical properties and biocompatibility. Moreover, the excessively fast corrosion rate of Mg alloys impedes their development in biomedical fields. Inspired by conventional ion implantation, a less-toxic functional group (hydroxyl) is used as the ion source to bombard the ZK60 Mg alloy surface to form a functionalized oxide layer. The surface characterization, corrosion resistance, and biocompatibility are systematically investigated before and after hydroxyl ion implantation. A smoother surface mainly constituted of hydroxide/oxide is formed for the treated samples. The formed functionalized layer significantly improves the corrosion resistance of the ZK60 Mg alloy substrate and the proliferation of MC3T3-E1 cells, as demonstrated by electrochemical, immersion, and in vitro cytocompatibility tests. In summary, less-toxic functional ion implantation can be an effective strategy for preventing corrosion of Mg alloy implants and promoting their biocompatibility.

Rab21 Protein Is Degraded by Both the Ubiquitin-Proteasome Pathway and the Autophagy-Lysosome Pathway.

Rab21 is a GTPase protein that is functional in intracellular trafficking and involved in the pathologies of many diseases, such as Alzheimer's disease (AD), glioma, cancer, etc. Our previous work has reported its interaction with the catalytic subunit of gamma-secretase, PS1, and it regulates the activity of PS1 via transferring it from the early endosome to the late endosome/lysosome. However, it is still unknown how Rab21 protein itself is regulated. This work revealed that Rab21 protein, either endogenously or exogenously, can be degraded by the ubiquitin-proteasome pathway and the autophagy-lysosome pathway. It is further observed that the ubiquitinated Rab21 is increased, but the total protein is unchanged in AD model mice. We further observed that overexpression of Rab21 leads to increased expression of a series of genes involved in the autophagy-lysosome pathway. We speculated that even though the ubiquitinated Rab21 is increased due to the impaired proteasome function in the AD model, the autophagy-lysosome pathway functions in parallel to degrade Rab21 to keep its protein level in homeostasis. In conclusion, understanding the characters of Rab21 protein itself help explore its potential as a target for therapeutic strategy in diseases.

[Annual review of capillary electrophoresis technology in 2015].

This paper reviews the capillary electrophoresis (CE) in 2015. The literatures searched from ISI Web of Science ranged in 2015. 1. 1-2015. 12. 31 are classified and introduced based on CE-MS method, methodology research, detection and enrichment, chiral separation and basic applications of CE. Six international and two national conferences are included and the important reports are introduced briefly. In the end, the standards of CE method for the analyses of monoclonal antibodies, water, wines and food approved in China and some other countries are listed.

Inhibition of nemo-like kinase increases taxol sensitivity in laryngeal cancer.

Several studies have shown that nemo-like kinase (NLK) plays a vital role in apoptosis of cancer cells. The present research concerned effects and mechanisms of Taxol on NLK knockdown human laryngeal cancerHep-2 cell lines in vitro. Using RNAi, methyl-thiazoltetrazolium (MTT) assays, real-time RT-PCR, Western blotting and flow cytometry analysis, growth and the cell cycle progression of NLK knockdown Hep-2 cells and expression of downstream molecules were observed. Cell growth was obviously suppressed in the Taxol treated group (P<0.001, 48 hours). Cell numbers of combined Taxol-based chemotherapy with lentivirus mediated RNAi treatment group (Lv-shNLK+Taxol goup) were significantly different from NLK-specific siRNA lentivirus infected group (Lv-shNLK group) (p<0.001). Flow cytometry analysis revealed that Lv-shNLK+Taxol caused the G0/G1-phase DNA content to decrease from 44.1 to 3.33% (p<0.001) and the S-phase DNA content to increase from 38.4 to 82.0% (p<0.001), in comparison with the Lv-shNLK+Taxol group. Immunoblot analysis showed that knockdown of NLK led to significant reduction in the levels of cyclin D1, PCNA and PARP, whereas cyclin B1 was elevated in. Cell growth was also obviously suppressed in the Hep-2 cell line, knockdown of NLK making them more sensitive to Taxol treatment. NLK is expected to become a target of new laryngeal cancer gene therapies.