1.Research progress in relationship between vitamin D and inflammatory bowel disease
Chinese Journal of Clinical Nutrition 2016;24(4):251-256
Inflammatory bowel disease (IBD) is a group of chronic inflammatory diseases of the intestine mediated by abnormal immunological mechanism caused by multiple etiological factors.The main treatment at present is anti-inflammation and immunosuppression,but with severe side effects and poor efficacy.Vitamin D3 has immunoregulatory,anti-inflammatory,and antineoplastic functions.Vitamin D,as a novel immunoregulator,may provide a new treatment option for patients with IBD.This article will review the research progress on the following four aspects:the relationship of vitamin D with innate immunity,adaptive immunity,and pathogenesis of IBD,and vitamin D supplement in IBD patients.
2.Correlation between the peripapillary retinal nerve fiber layer thickness,structure changes in non - proliferative diabetic retinopathy and the changes of visual function
International Eye Science 2014;(7):1209-1211
AlM: To study the correlation between and the peripapillary retinal nerve fiber layer ( RNFL ) thickness, structure changes in non-proliferative diabetic retinopathy ( NPDR) and the the changes of visual function
METHODS:Eighty cases ( 80 eyes ) of patients with NPDR who were in our hospital from January 2011 to December 2013 as group NPDR, 60 cases of patients ( 60 eyes) without retinopathy who were in the hospital were selected as non-diabetic retinopathy group ( NRD) group, meanwhile, 50 healthy people who had health examination in our hospital as control group. The RNFL thickness and visual electrophysiological testing were performed on the study objects in the three groups, and the results were compared among groups.
RESULTS: Group NPDR's above, below, nasal, temporal and average RNFL thickness were 91. 52 ± 18. 52, 88.63±21. 65, 63. 62±11. 72, 60. 42±9. 13, 69. 36±12. 52μm, those of group NPDR were 111. 32 ± 21. 90, 113. 57 ± 22. 67, 74.31±11. 74, 67. 64±12. 34, and 97. 31±11. 43μm,those of group control were 121. 65±21. 42, 129. 32±23. 31, 82. 42±9. 28, 80. 32±8. 51, 102. 54±21. 82μm. To compare of average thickness of RNFL of three groups, groups NPDR and NPD were thinner than that of control group;To compare each quadrant phase, above, below, nasal, the RNFL thickness among three groups had statistical significance (P<0.05), while nasal sides had no obviously changes (P>0. 05);At the same time, 60′P100 latency (MS), 60′P100 amplitude ( V ) , 15′ P100 latency ( MS ) and 15′ P100 amplitude ( V) of three groups had statistical significance (P<0. 05).
CONCLUSlON: The changes of RNFL thickness have occurred in the early time of NPDR, and mainly the above, below and temporal , and it has a significant relevance with the changes of visual function.
3.Management of orbit fracture and correction of enophthalmos.
Chinese Journal of Stomatology 2008;43(11):658-661
Enophthalmos
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surgery
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Humans
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Orbital Fractures
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diagnosis
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surgery
6. Progress in research on tumor-associated lymphatic endothelial cells
Tumor 2011;31(3):280-284
Tumor lymphatic endothelial cells play an important role in tumor metastasis and affect the treatment outcomes and the long-term survival. Studying the characteristics of tumor lymphatic endothelial cells such as morphology, cell biology and molecular biology, will provide a good platform for the deep research on the mechanism of tumor metastasis, which can prevent the spread of tumor cells and provide effective evidence for the clinical prevention and treatment of cancer. Recently, the research on tumor lymphatic endothelial cells has improved rapidly. This paper reviews the current research on tumor lymphatic endothelial cells, and hopes to provide the references for the study of tumorigenesis and metastasis. Copyright© 2011 by the Editorial Board of Tumor.
7.Modified procedure for primary culture of retinal Müller cell in newborn rat
Chinese Journal of Experimental Ophthalmology 2012;30(4):336-339
BackgroundMüller cells has been recognized as being vital in both healthy and diseased retina.Recently,these cells even have been identified to be the source of retinal progenitor cells.In order to study the possible function of the retinal Müller cells,it is important to establish a practical procedure to obtain the purified cells. ObjectiveThis study was to simplify the procedure of primary culture and purification of retinal Müller cells in vitro. MethodsEyeballs of SPF newborn SD rats were enucleated and retinas were dissected free after soaking the eyeballs overnight in DMEM/F12 medium in room temperature.Then the retinas were mechanically dissociated into micro aggregates and cultured in DMEM/F12 medium containing 10% FBS for 8-10 days.The floating retinal aggregates and debris were removed and the medium was changed in 2-3 days interval to get more purified flat cell population.Cultured cells were passaged after confluent.Immunofluorescence staining was used to detect the response to glutamine synthetase (GS) and Vimentin for the identification of the cultured Müller cells,and flow cytometry (FCM) was used to estimate the purity of the cells. Results Cultured Müller cells had large cellular body and richer cytoplasm.More than 95% of the cells showed the positive response for GS with the brown staining in cytoplasm and cellular nuclei,and the positive stainiug also was seen for Vimentin in cytoplasm.FCM showed that 99.7% of the cells were GS positive after 3 passages.Conclusions Modified procedure in this experiment is a simple and practical method for culturing retinal Müller cells.
8.Progress in retinal stem cells research
Chinese Journal of Experimental Ophthalmology 2011;29(9):852-856
Retina is subjected to many acquired and inherited neuronal degenerative diseases such as agerelated macular degeneration (AMD), diabetic retinopathy (DR) and retinitis pigmentosa (RP). All of these diseases are associated with the progressive damage and loss of photoreceptors, which is causing visual impairment and irreversible blindness. Stem-cell therapy is being widely considered as a promising treatment of these incurable retina diseases. However, in mammals including humans, there seems to be little or no recovery of lost cells. By contrast, nonmammalian vertebrates, such as amphibians and fish, have robust regenerative responses to injury, which can lead to the near complete restoration of the neurons lost through injury. Nevertheless ,over the past several years, studies have investigated that stem cells do exist in the adult mammalian eyes, and at least some types of neurons can be regenerated in the mammalian retina by stimulating with growth factors or transcription factors. These recent results suggest that some part of the regenerative program occurring in lower vertebrates remains in the mammalian retina.Here, the origin of various of adult retinal stem cells for the self-renewal and proliferation. and the relevant influencing factors were summarized.
9.The Structural Parameters-functional Activity Relationship of Alpha-helical Antimicrobial Peptides
Tian-Tang DONG ; Zi-Gang TIAN ; Jian-Hua WANG ;
China Biotechnology 2006;0(09):-
In response to problems from the development of multi-drug-resistant pathogenic bacteria,it is urgent to find new antimicrobials.Antimicrobial peptides(AMPs) are a kind of ideal new antimicrobials with the advantages including their potential for broad-spectrum activity,rapid bactericidal activity and low propensity for resistance development,and have a bright future.Alpha-helical antimicrobial peptides are a main kind of AMPs.The following features was reviewed and elucidated including the structure and activity relationship(SAR) from different aspects including the degree of helicity,hydrophobic moment,hydrophobicity,net positive charges and so on,and the application of SAR on the molecular design and improvement of AMPs.
10. A new method for primary culture of mouse dorsal root ganglion neurons
Journal of Xi'an Jiaotong University(Medical Sciences) 2019;40(2):302-304
Objective: To establish a simple method for primary culture of mouse dorsal root ganglion neurons of high purity. Methods: The dorsal root ganglions from healthy C57BL/6 mice of 6-8 weeks were taken to obtain dorsal root ganglion neurons by using type collagenase and trypsin digestion. Identification and purification were evaluated by neuron specific enolase (NSE) monoclonal antibody immunocytochemistry staining. Results: The cultured primary neurons grew well and the purity could reach about 90%. The survival time was 60 days when cultured with the DMEM medium containing nerve growth factor (NGF). Conclusion: The culture program is simple and stable, and can cultivate a large number of high-purity neurons, which provides a reliable model for in-depth study of neurons.