1.Apoptosis in cardiac ailograft and its relation with acute rejection in rats
Hongxing ZHONG ; Hui HAN ; Yongshang ZHANG
Chinese Journal of Organ Transplantation 2000;21(3):153-155
Objectives To detemline whether apoptotic cell death is involved in rat cardiac allograft rejection and investigate the relevance of apoptosis with acute rejection and its implication.Methods Groups of Wistar rats underwent heterotopic heart transplantation from allogeneic SD or syngeneic Wistar rats.The cardiac grafts were harvested at 1,3,5,or 7 days after transplantation and underwent the detection of apoptotic cell death using in situ terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling(TUNEL).Histopathological rejeclion grade and apoptotic index(AI)were analyzed.Results The incidence of apoptotic cells was increased steadily over time in allografts,in contrast to syngeneic grafts.The apoptotic cells in allografts were mainly cardiac myocytes and few infiltrating lymphocytes.The AI of rejection grade 1,2,3 and 4 was significantly higher than that of rejection grade 0(P<0.01).Conclusions TUNEL can display apoptosis of single cell in situ.Apoptosis is an important mechanism of tissue injury in acute cardiac allograft rejection in rats.Myocyte apoptosis can be used as a valuable index to estimate the injury of grafts and monitor acute rejection.
3.Effect of Cyclosporin A to T Lymphocyte Subsets and Toxoplasmosis After Heart Allotransplantation in Rat
Hui HAN ; Hongxing ZHONG ; Yongshang ZHANG ;
Chinese Journal of Parasitology and Parasitic Diseases 1997;0(05):-
Objective To evaluate the effect of Toxoplasma gondii infection on immune function of the rat recipients and onset of Toxoplasmosis after heart transplantation and its correlation with the use of Cyclosporin A(CsA). Methods ELISA was used to detect recipient's specific circulating antigen (CAg) and antibodies (IgG, IgM) after the transplantation. T lymphocyte subsets in peripheral blood were examined by using immunofluorescence stain and flow cytometry (FCM) before and after heart allograft 5,10,15,20 days in rats. Results The use of CsA increased the risk of infection by T. gondii and accelerated the increase of CD8 + T lymphocyte after the transplantation. The incidence of donor acquired T.gondii infection was higher than that of reactivated silent infection in recipients before operation. The percentage of CD8 + T lymphocyte was evidently elevated due to the onset of toxoplasmosis and the ratio CD4 +/CD8 + was reduced or inverted in the meanwhile. Conclusion The immune suppression after use of CsA was the main reason leading to an activation of the silent infection of T.gondii . CD8 + was the main cytotoxic cell elevated during the infection.
4.Modulatoin of Macrophage-Mediated Cytotoxic Activity Thibitory Effect of a Mycotoxin, Fusarin C, on Macrophage Activation in Mice
Zhong-Yun DONG ; You-Hui ZHANG ;
Chinese Journal of Immunology 1985;0(06):-
The effect of Fusarin C, a new mutagen extracted from Fusarium moniliforme,on murine peritoneal M? activation by measuring M?-mediated MTC ADCC and CS,Fusarin C could inhibit M? activation by both MAF and FDP. The inhibitory effect was dose-and time-dependent and the curves of dose-and time-response were similar in all three assays. There is, however, apparent difference in Fusarin C dose and time needed to induce significant in hibition among these assays. Significant inhibition occured at 0.4?g/ml and 0.5?g/ml for MTC and CS respectively, but 1.6?g/ml for ADCC. Similarly, the minimal period of time necessary to bring about significant inhibition was 2 hr for MTC, but 3 hr for ADCC. Finally, significance of the inhibitory effect of Fusarin C on M? anti-tumor activity in relation to carcinogenesis was discussed.
5.Modulation of macrophage-mediated cytotoxic activity Ⅱ.The Inhibitory effect of fusarin C on macrophage activation is reversible
Zhong-Yun DONG ; You-Hui ZHANG ;
Chinese Journal of Immunology 1985;0(01):-
The inhibitory effect of Fusarin C,a new mutagen isolated from Fusarium moniliforme,on M? activation was investigated.The inhibitory effect of Fusarin C disappeared partially after 24 hr culture in the absence of the mycotoxin and completely after 72 hr.In addition,it could be overcome by high concentrations of M? activating factor or anti-serum to the target cells.
7.Experimental study on preparation and targeting ability in vitro of HCC-targeted lipid microbubble containing 10-HCPT
Jie LUO ; Zhigang WANG ; Qunxia ZHANG ; Shigen ZHONG ; Hui ZHANG
Chinese Journal of Medical Imaging Technology 2010;26(3):418-420
Objective To prepare HCC-targeted lipid ultrasound microbubble containing 10-hydroxycamptothecin (10-HCPT), and to assess its targeting function in vitro. Methods After the biotinylated monoclonal antibody Hab18 was prepared, the biotinylated degree was determined. Microbubbles containing 10-HCPT were prepared by mechanical vibration. Then the biotinylated antibody was attached to the surface of the microbubbles by avidin-biotin interaction. The physical property, entrapment efficiency and the drug-loading amounts of 10-HCPT lipid microbubbles were determined. The combination of biotinylated Hab18 with microbubbles containing 10-HCPT was proved by immunofluorescent assay, and the targeting function of the targeted microbubbles containing 10-HCPT was observed with light microscope, served non-targeted microbubbles as control group. Results About 13 biotin molecules were coupled to each antibody in average. The disposition of the prepared microbubbles was steady and the mean diameter was 1.52 μm. The drug entrapment efficiency was 76.32% and the drug-loading amounts was 21.81%. Red fluorescence was observed at the edge of the microbubbles in immunofluorescent assay, and the conjugation of the targeted microbubbles containing 10-HCPT with 7721 cells was tight while control group was negative. Conclusion HCC-targeted lipid ultrasound microbubbles containing 10-HPTC can be prepared successfully, with higher entrapment efficiency and drug-loading amounts and strong targeting function in vitro.
8.Clinical features and confocal microscopic imaging characteristics of 466 cases with infectious keratitis
Hui, XIAO ; De-Yan, ZHANG ; Zhong-Yi, FAN
International Eye Science 2014;(10):1825-1827
AIM: To observe the role of confocal microscopy in infectious keratitis management.
METHODS:Totally 466 patients (467 eyes) diagnosed as infectious keratitis from January 2010 to December 2013 were retrospectively studied. the corneas were examined early by in vivo confocal microscopy. The characteristics of their images and clinical features were studied and summarized.
RESULTS:All patients were recorded, the average age was 54. 4±13. 0 years, in which 264 cases (56. 7%) were male, and 202 cases ( 43. 3%) were female. In the 466 patients, 190 (40. 8%) were fungal keratitis, 148 (31. 8%) were viral keratitis, 125 (26. 8%) were bacterial keratitis and 3 ( 0.6%) were acanthamoeba keratitis. There were fungal hyphae in the images of fungal keratitis. Amebic cysts were found in acanthamoeba keratitis.
CONCLUSION:Confocal microscope can help the early diagnose and treatment of infectious keratitis. It is a noninvasive imaging technique that provides high resolution images of ocular structures at a cellular level and infectious keratitis represents one of its most important clinical uses.
9.Dimethylformamide induced impairment of function of liver and kidney in exposed workers and its effect on lipid metabolism.
Ju-xiang XIANG ; Jian-zhong YU ; Xin-hui ZHANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2007;25(7):404-406
Adolescent
;
Adult
;
Dimethylformamide
;
adverse effects
;
Female
;
Humans
;
Kidney
;
drug effects
;
physiopathology
;
Lipid Metabolism
;
drug effects
;
Liver
;
drug effects
;
physiopathology
;
Male
;
Middle Aged
;
Occupational Exposure
;
adverse effects
;
Young Adult
10.Experience in the treatment with intractable epistaxis by endoscopic sinus bipolar coagulation on 97 cases.
Hui-ting WANG ; Jian-zhong SANG ; Guo-zheng ZHANG
Chinese Journal of Otorhinolaryngology Head and Neck Surgery 2009;44(8):694-695
Adolescent
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Adult
;
Aged
;
Electrodes
;
Epistaxis
;
surgery
;
Female
;
Hemostasis, Endoscopic
;
methods
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Humans
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Male
;
Middle Aged
;
Young Adult