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Li-Fei Wang

Publications and source records attributed to Li-Fei Wang.

2 recordsLinked to original sources

[An experimental study on dissolving and detaching vitreoretinal interface with enzymes].

OBJECTIVE: To investigate the safety dosage of intravitreal injection of Plasmin, Hyaluronidase and their combination and to evaluate their efficacy in the formation of posterior vitreous detachment (PVD) through animal experiments. METHODS: Eight rabbits each were randomly assigned to one of six groups and one eye of each rabbit were experimental eye, the other is control eye. The position of drug injection was in posterior 1/3 of vitreous before papillary. The drug-injection groups were assigned as following: the first group-Hyaluronidase 20 IU (0.1 ml BSS), the second group-Hyaluronidase 30 IU (0.1 ml BSS), the third group-Plasmin 1 IU (0.1 ml BSS), the forth group-Plasmin 2 IU (0.1 ml BSS), the fifth group-Plasmin 3 IU (0.1 ml BSS), the sixth group- Hyaluronidase 20 IU (0.05 ml BSS) combined with Plasmin 1 IU (0.05 ml BSS); the control eyes were injected with BSS (0.1 ml) at the same position. The experimental rabbits were followed for 2 weeks, and in this period all eyes were examined with slit-lamp biomicroscopy, +90 D preset lens, indirect ophthalmoscope, electroretinography, B-scan, and optical coherence tomography. After two weeks, the animals were killed and the eyes enucleated. Scan electron and light microscopy were performed. RESULTS: Hyaluronidase concentration of 20 IU, Plasmin concentration of 1 IU and their combination didn't produce inflammatory response and retinal toxicity in the experimental eyes. 30 IU Hyaluronidase and 2 IU Plasmin both caused mild inflammatory response in the vitreous without retinal histological changes, while the latter caused a reversible decrease in the ERG b-wave. 3 IU of Plasmin caused severe inflammatory response with retinal histological and electroretinographic changes. In safety dosage neither Hyaluronidase nor Plasmin alone were successful in producing completely posterior vitreous detachment (PVD), but the latter can produce partial PVD. The combination of Plasmin (1 IU) and Hyaluronidase (20 IU) was effective on producing completely PVD without retinal toxicity. CONCLUSION: 20 IU of Hyaluronidase and 1 IU of Plasmin are safe to retina and others structures in the eyes without any toxicity. Posterior vitreous injection of Hyaluronidase (20 IU) combined with Plasmin (1 IU) can produce complete posterior vitreous detachment.

Animals↗

[Effect of growth, temperature and media on the expression of secE promoter of Streptomyces lividans TK24].

Streptomyces are Gram-positive, filamentous soil bacteria, which produce a wide variety of metabolites that are currently being exploited in both medicine and agriculture. Moreover, Streptomyces lividans is used as a host strain to effectively express and secrete heterologous proteins to culture media. Genes encoding Sec proteins responsible for the translocation of preproteins have been identified in S. lividans. SecYEG, a complex of integral membrane proteins SecY, SecE, and SecG in the cytoplasmic membrane, constitutes a pathway for polypeptide movement. SecA plays a central role in translocation as it is the site of preprotein entry into the translocase and it is the only ATPase essential for preprotein translocation. The role of SecD and SecF is to regulate the movement of the translocating protein. A better understanding of their regulatory mechanism could help to develop S. lividans strains with hyper-secretory capacity. In this study, a reporter system was used to investigate the regulatory mechanism of secE promoter. Upstream sequence (496 bp) of secE of S. lividans TK24 was cloned and characterized in a promoter probe vector pIJ4083 upstream of promoterless xylE. Sequencing analysis revealed that secE upstream sequence of S. lividans shares 99.8% homology with the secE promoter of S. coelicolor. The transcriptive activity of this fragment approximates vsi promoter in CMI medium, a strong promoter from S. venezuelae. The activity of secE promoter was observed in different growth phase, culture temperature and culture media. The expression level of secE was higher during the log phase, but decreased at the beginning of the stationary phase. At growth temperature of 28 degrees C, the expression level was much higher than that at 37 degrees C. When the bacteria were incubated in NB, Phage, and CM medium respectively, the expression level of secE promoter was different at a certain fermentation time, but all reached the highest level at log phase. Further analysis revealed that glucose may repress secE promoter expression.

Bacterial Proteins↗