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1.
China Pharmacy ; (12): 321-324, 2020.
Article in Chinese | WPRIM | ID: wpr-817337

ABSTRACT

OBJECTIVE:To study the ecological suitability zoning of Astragalus membranaceus var. mongholicus in Dingxi city. METHODS :Taking 1 001 batches of A. membranaceus var. mongholicus in Dingxi city as the investigation samples (each natural village with A. membranaceus var. mongholicus cultivation as the collection unit ),the longitude and latitude information of them were obtained from Dingxi economic crop technology promotion station ,and 55 environmental ecological factors (including climate,terrain,soil,etc.)were obtained from the Grid Database of Spatial Information of TCM Resources . Combined with the information of longitude ,latitude and environmental ecological factors ,the maximum entropy model (MaxEnt model ) was established with 75% samples as the training set ,and the main ecological factors were screened out ,and 25% samples were set as the validation set for model validation. Then the suitable growing areas of A. membranaceus var. mongholicus were divided by using ArcGIS. RESULTS :Established MaxEnt model had good prediction (the area under the working characteristic curve of subjects in training set and verification set was 0.970 and 0.968). Eight main ecological factors ,such as altitude ,precipitation and temperature , were selected (the total contribution rate was 98.90%). The comprehensive analysis found that the altitude was 1 800 to 2 650 m, the average precipitation in April was 25 to 50 mm,the lowest temperature of the coldest month was -16 to -8 ℃,the wettest monthly precipitation was 95 to 110 mm,and the seasonal variation of temperature was 70 to 80,the average temperature in December was -6 to -3 ℃ ,the average precipitation in October was 30 to 50 mm,and the average precipitation in December was 0 to 10 mm,which was the suitable environmental parameter for the growth of A. membranaceus var. mongholicus in Dingxi city. Based the results of ArcGIS analysis ,in Dingxi city ,A. membranaceus var. mongholicus was generally suitable for growth ;in the northwest of Lintao county ,the north of Anding district ,the south of Tongwei county ,a small area in the south of Longxi county and the south of Minxian county ,the border between Weiyuan county ,Zhangxian county and Minxian county ,A membranaceus var. mongholicus was not suitable for growth. CONCLUSIONS: Ther results of established model is in E-mail:961308817@qq.com line with the actual investigation , can provide reference for the planting regional planning of A. membranaceus var. mongholicus in Dingxi city.

2.
Chinese Journal of Medical Genetics ; (6): 353-357, 2015.
Article in Chinese | WPRIM | ID: wpr-239471

ABSTRACT

<p><b>OBJECTIVE</b>To explore the subcellular localization of ataxin-3 and the effect of polyglutamine (polyQ) expansion mutation on the morphology of mitochondrion, golgi apparatus and endoplasmic reticulum.</p><p><b>METHODS</b>Transient transfection was employed to build cell models expressing wild-type or mutant ataxin-3 proteins. Indirect immunofluorescence was applied to identify markers of organelle membrane. The results were observed under a laser scanning confocal microscope.</p><p><b>RESULTS</b>No co-localization was observed for ataxin-3 protein and mitochondrial marker TOM20, but the percentage of cells with mitochondrial fragmentation has increased in cells expressing mutant ataxin-3 (P<0.05). No co-localization was observed for ataxin-3 protein and golgi marker GM130, and mutant ataxin-3 did not cause golgi fragmentation. Wide type and polyQ-expanded ataxin-3 both showed partial co-localization with ER marker calnexin. The latter showed more overlap with calnexin, and the overlapping signals were mostly located in the places where aggregates were situated.</p><p><b>CONCLUSION</b>PolyQ-expanded ataxin-3 protein may indirectly affect the integrity of mitochondria, but may cause no effect on the structure and functions of golgi apparatus. Endoplasmic reticulum may be another place where extended ataxin-3 protein can induce cytotoxicity in addition to the nucleus.</p>


Subject(s)
Humans , Ataxin-3 , Cytoplasm , Genetics , Metabolism , Endoplasmic Reticulum , Genetics , Metabolism , HeLa Cells , Machado-Joseph Disease , Genetics , Metabolism , Mitochondria , Genetics , Metabolism , Nerve Tissue Proteins , Genetics , Metabolism , Nuclear Proteins , Genetics , Metabolism , Protein Transport , Repressor Proteins , Genetics , Metabolism
3.
Chinese Journal of Tissue Engineering Research ; (53): 1532-1538, 2014.
Article in Chinese | WPRIM | ID: wpr-444044

ABSTRACT

BACKGROUND:Recent studies have found that adipose mesenchymal stem cells can inhibit immune responses of T cells, B cells and dendritic cells. But it is unclear whether adipose mesenchymal stem cells are able to regulate the immune responses of macrophages. OBJECTIVE:To observe the expression of interleukin-6 and tumor necrosis factorαin J774.1 cells co-cultured with adipose mesenchymal stem cells co-cultured. METHODS:Adipose mesenchymal stem cells at a density of 2×107 per wel were inoculated into the upper chamber of the transwel and 24-wel plates. Then, J774.1 cells were suspended with cellculture medium containing 1 mg/L lipopolysaccharide and planted into the lower chamber of the transwel and 24-wel plates containing adipose mesenchymal stem cells as co-culture group. Meanwhile, inactive J774.1 cells to lipopolysaccharide-activat J774.1 cells served as negative and positive control groups, respectively. After 48 hours, the J774.1 cells were col ected to extract the RNA samples. Then, mRNA expressions of interleukin-6 and tumor necrosis factorαwere measured by real-time quantitative PCR. RESULTS AND CONCLUSION:Compared with the positive control group, direct-contact co-culture of adipose mesenchymal stem cells and J774.1 cells significantly reduced expressions of interleukin-6 and tumor necrosis factorαin J774.1 cells, but non-contact co-culture only reduced interleukin-6 expression. These findings indicate that adipose mesenchymal stem cells can inhibit the immune response of J774.1 cells activated by lipopolysaccharide.

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