1.Microscopic changes of freeze-dried vessels
Jieyuan XU ; Meiping ZHUANG ; Sufang CHEN ; Jing LIN ; Caihong HONG ; Mengfang LIU ; Leren TAO
Chinese Journal of Tissue Engineering Research 2015;(37):5950-5954
BACKGROUND:Mechanical properties of the blood vessels include axial and radial tension which is important to guarantee the tissue perfusion and its pressure. OBJECTIVE:To test and analyze stretching and puncture parameters that can ful y characterize the performance of blood vessels, so as to predict the health condition of the vessels transplanted into recipients. METHODS:Mechanical properties as circumferential tension, axial tension and puncture were tested on the porcine aorta, and then pathological and staining analysis was done to explore whether freeze-dried vessels can withstand the blood pressure in al directions after transplanted into the body. RESULTS AND CONCLUSION:Specific trend on the curves of freeze-dried vessels during circumferential tension, axial tension and puncture process was closer to that of fresh vessel curves, suggesting that structural components and arrangement of the freeze-dried vessels were not changed greatly. Meanwhile, the microscopic observations of slice and tensile section were taken into account so that the reason was studied and explained for the mechanical properties of the experimental data and results. The macroscopic mechanical result was analyzed based on the change of microstructure. These findings indicate that the vacuum freeze-drying is a better method to maintain the performance of blood vessels.
2.Development and application of TaqMan-MGB real-time quantitative PCR assay for detection of goat pox virus.
Zhentao CHENG ; Jun YUE ; Yongming LI ; Leren XU ; Kaigong WANG ; Bijun ZHOU ; Junyi CHEN ; Jun LI ; Nan JIANG
Chinese Journal of Biotechnology 2009;25(3):464-472
The complete gene sequences of eight capripoxvirus strains in GenBank were aligned and analyzed with DNAStar software. We selected a size of 64 bp gene fragment that was located in gp064 region of goat pox virus (GPV) genome, and designed a pair of primers and a TaqMan-MGB probe against the gene fragment with Primer Express 2.0 software. Then, the fluorescence quantitative PCR (FQ-PCR) assay was developed and the standard curve of different dilution series was described. We extracted the DNA samples from clinical skin pox, scab and GPV infected materials of artificial challenge animals. The FQ-PCR assay has been performed for all kinds of DNA samples. The results showed that the FQ-PCR assay was sensitive, specific, stable and could be used for clinical diagnosis. This method provided an important tool for rapid diagnosis of goat pox clinically, and for study GPV pathogenesis in the course of disease occurrence, development and convalescence.
Animals
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Base Sequence
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Capripoxvirus
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genetics
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isolation & purification
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Goats
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Molecular Sequence Data
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Polymerase Chain Reaction
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methods
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Poxviridae Infections
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diagnosis
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virology
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Sensitivity and Specificity