Ectopic Over-expression of Oncogene Pim-2 Induce Malignant Transformation of Nontumorous Human Liver Cell Line L02

Ke Ren,Wentao Duan,Yujun Shi,Bo Li,Zuojin Liu,Jiangping Gong 대한의학회 2010 Journal of Korean medical science Vol.25 No.7

In order to prove that ectopic over-expression of Pim-2 could induce malignant transformation of human liver cell line L02, three groups of cells were set up including human liver cell line L02 (L02), L02 cells transfected with Pim-2 gene (L02/Pim-2) and L02cells transfected with empty-vector (L02/Vector). Pim-2 expression levels were detected. The morphology, proliferation level, apoptosis rate and migration ability of the cells were detected respectively. Then the cells were subcutaneously inoculated into athymic mice and the microstructures of the neoplasm were observed. Compared with the controls, Pim-2expression levels were significantly higher in L02/Pim-2 cells (P<0.05), and their morphology had obvious malignant changes. They also showed a significantly increased proliferation rate (P<0.05) and migration capacity (P<0.05), as well as a significantly decreased apoptosis rate (P<0.05). Only the athymic mice inoculated with L02/Pim-2 cells could generate neoplasm, and the morphology of the neoplasm coincided with that of the hepatoma. The results manifest that ectopic Pim-2 gene could be stably expressed in L02/Pim-2 cells. Both the morphological and biological changes of L02/Pim-2 cells demonstrate the trend of malignant transformation. L02/Pim-2 cells could generate hepatoma in athymic mice. In conclusion, Pim-2 could induce malignant transformation of human liver cell line L02.

Novel spherical TiO2 supported PdNi alloy catalyst for methanol electroxidation

Jianfeng Ju,Donghui Wu,Xi Chen,Yujun Shi,Ping Hua 한국공업화학회 2014 Journal of Industrial and Engineering Chemistry Vol.20 No.4

A novel PdNi/TiO2 electrocatalyst for methanol oxidation is fabricated using spherical TiO2 nanoparticles as support. The structural and electrochemical properties of the PdNi/TiO2 catalyst are characterized by XRD, TEM and electrochemical analysis. The cyclic voltammograms of PdNi/TiO2 catalyst show that there is a large methanol oxidation peak in about 0.882 V that is much bigger than that of the commercial PtRu/C catalyst in 0.7 V. The composite TiO2 material has high catalytic activity without UV light illumination. The electrocatalytic activity and anti-poisoning capability of the PdNi/TiO2 catalyst are promising, which may become a potential candidate for direct methanol fuel cell.

Genipin-Crosslinked, Immunogen-Reduced Decellularized Porcine Liver Scaffold for Bioengineered Hepatic Tissue

Xiujuan Wu,Yujia Wang,Qiong Wu,Yi Li,Li Li,Jing Tang,Yujun Shi,Hong Bu,Ji Bao,Mingjun Xie 한국조직공학과 재생의학회 2015 조직공학과 재생의학 Vol.12 No.6

Liver disease affects millions of patients each year worldwide. Decellularized biologic matrices are plausible biomedical materials for bioengineered replacement hepatic tissue. However, one of the concerns for its safe medical application is the lack of objective assessment of the immunogen within the materials and in vivo immune responses to the matrices. The purpose of this study was to produce immunogen- reduced and biocompatible matrices from porcine liver. Whole porcine livers were perfusion decellularized and cross-linked with glutaraldehyde (GA) or genipin (GP). Proteins were extracted, and the migratory response of human leukocytes toward protein extracts was examined using an in vitro migration chamber. In addition, biopsy specimens of decellularized scaffolds were implanted subcutaneously into rodents to investigate scaffold immunogenicity. Histological staining confirmed cellular clearance from pig livers, with removal of nuclei and cytoskeletal components and widespread preservation of structural extracellular molecules. Polymerase chain reaction analysis showed that galactose-alpha-1,3-galactose-beta-1,4-N-acetylglucosamine (1,3 gal), swine leukocyte antigen, and porcine endogenous retrovirus were completely removed in the matrices. Decellularization significantly reduced the migration of monocytes compared with native porcine tissue. Although the proportion of transmigrating lymphocytes was much lower, repeating the cross-linking procedure reduced the migratory response. After implantation for 4 weeks, the decellularized and native samples were degraded, and the GA-treated group demonstrated a severe inflammatory reaction; however, minimal inflammatory cell infiltration was seen in the GPtreated group during the 8-week investigation period. In conclusion, our study provided evidence that GP crosslinking could significantly reduce the immunogenicity of decellularized liver biomaterials.

Protection of chickens against infectious bronchitis virus with a multivalent DNA vaccine and boosting with an inactivated vaccine

Fang Yan,Zhong Li,Yongting Hu,Jianyang Qiu,Wenxin Lei,Wenhui Ji,Xuying Li,Qian Wu,Xiumin shi,Yujun Zhao 대한수의학회 2013 Journal of Veterinary Science Vol.14 No.1

The protective efficacy of DNA plasmids encoding avian infectious bronchitis virus (IBV) S1, N, or M protein was investigated in chickens. Chickens were inoculated monovalently (with plasmid pVAX1-16S1, pVAX1-16M, or pVAX1-16N alone) or multivalently (combination of the three different plasmids, pVAX1-16S1/M/N). A prime-boost immunization protocol against IBV was developed. Chickens were immunized with the multivalent DNA vaccine twice and then boosted with an inactivated vaccine once. Antibody titers of the chickens immunized with pVAX1-16S1/M/N were much higher than those of the monovalent groups (p < 0.01). A protective rate up to 90% was observed in the pVAX1-16S1/M/N group. The serum antibody titers in the prime-boost birds were significantly higher than those of the multivalent DNA vaccine group (p < 0.01) but not significantly different compared to the inactivated vaccine group at 49 days of age. Additionally, the prime-boost group also showed the highest level of IBV-specific cellular proliferation compared to the monovalent groups (p < 0.01)but no significant difference was found compared to the multivalent DNA vaccine group, and the prime-boost group completely protected from followed viral challenge.

On Which Microphysical Time Scales to Use in Studies of Entrainment‐Mixing Mechanisms in Clouds

Lu, Chunsong,Liu, Yangang,Zhu, Bin,Yum, Seong Soo,Krueger, Steven K.,Qiu, Yujun,Niu, Shengjie,Luo, Shi American Geophysical Union 2018 Journal of Geophysical Research: Atmospheres Vol.123 No.7

<P>The commonly used time scales in entrainment-mixing studies are examined to seek the most appropriate one, based on aircraft observations of cumulus clouds from the RACORO campaign and numerical simulations with the Explicit Mixing Parcel Model. The time scales include the following: (evap), the time for droplet complete evaporation; (phase), the time for saturation ratio deficit (S) to reach 1/e of its initial value; (satu), the time for S to reach -0.5%; and (react), the time for complete droplet evaporation or S to reach -0.5%. It is found that the proper time scale to use depends on the specific objectives of entrainment-mixing studies. First, if the focus is on the variations of liquid water content (LWC) and S, then (react) for saturation, (satu) and (phase) are almost equivalently appropriate, because they all represent the rate of dry air reaching saturation or of LWC decrease. Second, if one focuses on the variations of droplet size and number concentration, (react) for complete evaporation and (evap) are proper because they characterize how fast droplets evaporate and whether number concentration decreases. Moreover, (react) for complete evaporation and (evap) are always positively correlated with homogeneous mixing degree (); thus, the two time scales, especially (evap), are recommended for developing parameterizations. However, and the other time scales can be negatively, positively, or not correlated, depending on the dominant factors of the entrained air (i.e., relative humidity or aerosols). Third, all time scales are proportional to each other under certain microphysical and thermodynamic conditions.</P>