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AIM: To investigate the protective effect of "DuZhong-DangGui" (DZ-DG) on the knee tissue of rats with osteoarthritis (OA) and its regulation role on NLPR3 inflammasome. METHODS: Twenty-four SPF male SD rats, eighteen rats were randomly selected to establish OA model by anteri- or cruciate ligament amputation (ACLT) method, and rats were divided into control group, OA model group, DZ-DG group and positive drug group, 6 in each group, treatment for 8 weeks. The peripheral blood were collected, ELISA was used to detect the levels of IL-1β, IL-6, IL-18, and TNF-α; cartilage tissue of knee joint were collected, HE staining was used to observe pathology changes, OARSI staining was used to observe cartilage calcification and preform quantitative OARSI scoring; immunohistochemistry and TUNEL staining were used to detect the contents of Caspase1 and Collagen II and the number of apoptosis in the tissue, respectively, and western blot was used to detect the protein expressions of matrix metalloproteinase-13 (MMP-13), tissue inhibitor of metalloproteinase-1 (TIMP-1), p53, p21, NLPR3, apoptosis-associated speck-like protein containing a CARD (ASC) and Pro-Caspase-1. RESULTS: Compared to control group, OA model group rats serum levels of IL-1β, IL-6, IL-18, and TNF - α significantly increased (P<0.01), OARSI scores significantly increased (P<0.01), chondrocyte apoptosis was increased (P<0.01), Caspase-1 content and MMP-13, p53, p21, NLPR3, ASC, Pro-Caspase-1 protein expressions significantly increased (P <0.01), while Collagen II content and TIMP-1 protein expression significantly decreased (P<0.01). Compared with the OA model group, DZ-DG group and positive drug group rats serum levels of IL-1β, IL-6, IL -18 and TNF - α significantly decreased (P< 0.05), chondrocyte apoptosis were significantly decreased (P<0.01), Caspase1 content, MMP-13, p53, NLPR3, Pro-Caspase-1 significantly decreased (P< 0.05), Collagen Ⅱ content and TIMP- 1 protein expression (P<0.01); DZ-DG group rats protein expression of p21 and ASC were decreased (P<0.01). CONCLUSION: The DZ-DG have protection role on cartilage of OA rats, its effect may related to mediation of NLPR3/ASC/Pro-Caspase-1 pathway, to decrease of IL-1β, and inhibition of cell apoptosis.
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Particulate matter (PM) can damage respiratory system, cardiovascular system, nervous system and immune system, but there are few researches on reproductive damage of particulate matter. The objectives of this study were to investigate the effect of short-term particulate matter 2.5 (PM
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Pyroptosis is the process of inflammatory cell death. The primary function of pyroptosis is to induce strong inflammatory responses that defend the host against microbe infection. Excessive pyroptosis, however, leads to several inflammatory diseases, including sepsis and autoimmune disorders. Pyroptosis can be canonical or noncanonical. Upon microbe infection, the canonical pathway responds to pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs), while the noncanonical pathway responds to intracellular lipopolysaccharides (LPS) of Gram-negative bacteria. The last step of pyroptosis requires the cleavage of gasdermin D (GsdmD) at D275 (numbering after human GSDMD) into N- and C-termini by caspase 1 in the canonical pathway and caspase 4/5/11 (caspase 4/5 in humans, caspase 11 in mice) in the noncanonical pathway. Upon cleavage, the N-terminus of GsdmD (GsdmD-N) forms a transmembrane pore that releases cytokines such as IL-1
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The aim of this paper was to study the effect and mechanism of alcohol extract from Polygonum cuspidatum(PCE) on acute gouty arthritis in C57 BL/6 mice through NLRP3/ASC/caspase-1 axis. The model mice which injected with ankle joint injection of sodium urate crystals(MSU) were orally administrated with three different concentration of PCE, with colchicine as positive control. HE staining was used for observing the morphological changes of synovial tissue; concentration of IL-1β, IL-6 and TNF-α secreted by synovial tissue of the ankle joint were detected by ELISA; mRNA and protein expression of NLRP3, ASC and caspase-1 in synovial tissue were detected by RT-PCR and Western blot respectively. The results showed that the swelling degree of ankle joint in model mice were significantly elevated; expression of IL-1β, IL-6 and TNF-α were significantly increased; mRNA and protein expression of NLRP3, ASC and caspase-1 also significant increase, compared with normal control group. The swelling degree of ankle joint significantly relief; expression of IL-1β, IL-6 and TNF-α in joint synovium significantly decrease; mRNA and protein expression of NLRP3, ASC and caspase-1 were significantly decrease in PCE treatment group compared with model group. Our research implied that alcohol extract from P. cuspidatum had positive effect on acute gouty arthritis in mice, and the regulation of NLRP3/ASC/caspase-1 axis may be its mechanism.
Subject(s)
Animals , Mice , Ankle Joint , Arthritis, Gouty , Drug Therapy , CARD Signaling Adaptor Proteins , Metabolism , Caspase 1 , Metabolism , Fallopia japonica , Chemistry , Interleukin-1beta , Metabolism , Interleukin-6 , Metabolism , Mice, Inbred C57BL , NLR Family, Pyrin Domain-Containing 3 Protein , Metabolism , Plant Extracts , Pharmacology , Tumor Necrosis Factor-alpha , Metabolism , Uric AcidABSTRACT
OBJECTIVE To observe the effects of glycogen synthase 3β (GSK-3β) in the regula-tion of NLRP3 inflammasome activation after acute myocardial infarction (MI) in Sprague Dawley(SD) rats. METHODS Ligation of the left anterior descending (LAD) in SD rats was used to establish an acute myocardial infarction model. SD rats were randomly divided into 3 groups (n=10, each group):sham group,MI group,and MI+SB group:the GSK-3β inhibitor(SB216763)was given 1 h by intrave-nous injection(0.6 mg·kg-1·d-1)before surgery.The serum and heart tissue were collected to measure lactate dehydrogenase (LDH) and IL-1β content and mRNA and protein levels of NLRP3, ASC, Cas-pase-1,IL-1β and GSK-3β after 2 days and 7 days operation,respectively.RESULTS The serum levels of LDH and IL-1β in the MI group were significantly higher than those in the sham group(P<0.01),and the MI+SB group was obviously lower than the MI group(P<0.01).In addition,mRNA and protein levels of NNLRP3, ASC, Caspase-1, IL-1β and GSK-3β expressions in MI group were clearly increased (P<0.01) compared with those in sham group.These indicators were significantly decreased in SB+MI group (P<0.01). Interestingly, the indicators were all higher at 7 days than 2 days. CONCLUSION GSK-3β inhibition induces cardioprotection via attenuating the activation of NLRP3 inflammasome after the acute myocardial infarction in rats.
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Objective To explore the influence of apoptosis-associated speck-like protein containing a caspase recruitment do-main(ASC)and Caspase-1 on the pathogenesis of primary biliary cirrhosis(PBC).Methods The real-time PCR,Western blot,py-rophosphate sequencing and ELISA were adopted to respectively detect the relative expressions of mRNA and protein of peripheral blood mononuclear cells(PBMS)Caspase-1 and ASC as well as the methylation status of ASC promoter region and plasma Caspase-1 and IL-18 expression levels in 30 cases of PBC and healthy controls.Results The mRNA and protein expressions of PBMC Caspase-1 and ASC in the PBC group were significantly higher than those in the control group(P<0.05).The methylation rate of ASC promoter Island1(ISI)was significantly lower than that of the control group(P<0.05),which of Island 2(IS2)was smaller than the background value and had no methylation occurrence.The levels of plasma Caspase-1 and IL-18 in the PBC group were sig-nificantly higher than those in the control group(P<0.05).The ASC mRNA in the PBC group was significantly correlated with the Caspase-1 mRNA expression(P<0.05);the methylation rates at loci 1,2,4,5 of ASC promoter region CpG island were nega-tively correlated with ASC mRNA expression(P< 0.05),and which at loci 3,6 had no correlation with their expressions(P>0.05);plasma Caspase-1 and IL-18 levels showed the obviously positive correlation.Conclusion ASC and Caspase-1 are involved in the immune inflammatory response in PBC.
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En nuestro país, el cáncer de cuello uterino es aún la neoplasia maligna más frecuente en mujeres. Como prueba de tamizaje se utiliza el examen de Papanicolaou o citología cérvico-vaginal, el cual es informado utilizando el Sistema de Bethesda. En dicho sistema, la categoría ASC-H (atypícal squamous cells - cannot exclude HSIL-high grade squamous epithelial lesions, por sus siglas en inglés) designa los casos con presencia de células escamosas atípicas en las cuales los cambios son sugestivos de una lesión intraepitelial escamosa de alto grado pero insuficientes para una interpretación citopatológica definitiva, por lo que es importante determinar la correlación citohistológica de esta categoría. Objetivo. Correlacionar los resultados citopatológicos informados como ASC-H con los diagnósticos histopatológicos. Diseño. Estudio de tipo descriptivo, transversal y retrospectivo. Material. Citología cérvico-vaginal e histopatología. Métodos. Se revisó los casos con estudio citopatológico realizado entre enero de 2013 y julio de 2015, y con estudio histopatológico hasta un año después. Mediante la base de datos se determinó la cantidad poblacional y los diagnósticos. Se consideró como prueba de oro el diagnóstico histopatológico. Principales medidas de resultados. Correlación cito-histológica en casos de ASC-H. Resultados. Durante el período de estudio se realizaron 53 716 estudios de citología cérvico-vaginal convencional; de estos, 119 fueron catalogados como ASC-H; finalmente, 43 casos (0,07%) cumplieron los criterios de inclusión. El rango de edad de las pacientes fue de 22 a 70 años, siendo la media 43,8 años. El 42% de casos de ASC-H tuvo el diagnóstico de NIC2 y NIC3 en el estudio histopatológico. Conclusión. Se encontró una correlación entre los resultados de ASC-H y las lesiones intraepiteliales de alto grado (NIC II y NIC III), que concuerda con la encontrada en la bibliografía.
Cervical cancer is the most prevalent neoplasm in women in our country. The Papanicolaou test is used as a screening test, and is reported using the Bethesda System. In this system, the ASC-H (atypical squamous cells - cannot exclude HSIL-high grade squamous epithelial lesions) category designates cases with atypical squamous cells, where the changes are suggestive of a high grade squamous intraepithelial lesion but insufficient for a definitive cytopathologic interpretation. It becomes important to determine the cyto-histological correlation in this group. Objective: To correlate cytopathologic results reported as ASC-H with histopathological diagnoses. Designs: Descriptive, cross sectional retrospective study. Material: Cervicovaginal cytology and histology. Method: We reviewed the cases with a cytologicalpathological study between January 2013 and July 2015 and with a histopathological study until a year later. The population and diagnoses were determined using the database. Histopathological diagnosis was considered as the gold standard. Main outcome measures: Cyto-histological correlation in ASC-H cases. Results: Out of the total of 53 716 cervical cytology studies performed during the study period, 119 were classified as ASC-H; 43 (0.07%) cases met the inclusion criteria. The age ranged between 22 and 70 years, with an average of 43.8 years; 42% of ASC-H cases were diagnosed as presenting CIN2 and CIN3 in the histopathological study. Conclusion: This study showed correlation between ASC-H results and high-grade intraepithelial lesions (CIN2 and CIN3), in line with findings in the literature.
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The nucleotide-oligomerization domain (NOD) is an important molecule involved in host defense against bacterial infection. To study the role of NODs in the host response to Mycobacterium leprae, we measured the mRNA levels of NODs and related genes in infected mouse tissues. The mRNA expression of NOD1, NOD2, caspase-1 and ASC was increased in mouse footpads. Whereas NOD2 expression in macrophages was increased at 2 and 24 h post-infection with M. leprae, there was no expression of NOD1 at these time points. An increase in caspase-1 expression was observed at 2 h and continued at 24 h. However, the expression of ASC was increased only at the early time point. The expression of caspase-1 is regulated by NOD2-dependent pathway in established HEK 293. Our results suggest NOD2, rather than NOD1, may be associated with the host response to M. leprae and that caspase-1 activation is essential for the host response.
Subject(s)
Animals , Mice , Bacterial Infections , Macrophages , Mycobacterium leprae , Mycobacterium , RNA, MessengerABSTRACT
Acid-soluble collagen (ASC) and pepsin-soluble collagen (PSC) from the spine (ASC-SP and PSC-SP) and skull (ASC-SK and PSC-SK) of the skipjack tuna, Katsuwonus pelamis, were successfully isolated and characterized. The yields of ASC-SP, PSC-SP, ASC-SK and PSC-SK were (2.47 ± 0.39)%, (5.62 ± 0.82)%, (3.57 ± 0.40)%, and (6.71 ± 0.81)%, respectively, on the basis of dry weight. The four collagens contained Gly (330.2-339.1 residues/1 000 residues) as the major amino acid, and their imino acid contents were between 168.8 and 178.2 residues/1 000 residues. Amino acid composition, SDS-PAGE, and FTIR investigations confirmed that ASC-SP and ASC-SK were mainly composed of type I collagen, and had higher contents of high-molecular weight cross-links than those of PSC-SK and PSC-SP. The FTIR investigation also certified all the collagens had triple helical structure. The denaturation temperatures of ASC-SK, PSC-SK, ASC-SP, and PSC-SP were 17.8, 16.6, 17.6, and 16.5 °C, respectively. All isolated collagens were soluble at acidic pH (1-5) and lost their solubilities when the NaCl concentration was above 2% (W/V). The isolated collagens from the spines and skulls of skipjack tuna could serve as an alternative source of collagens for further application in food, cosmetic, biomedical, and pharmaceutical industries.
Subject(s)
Animals , Acids , Chemistry , Amino Acids , Collagen , Chemistry , Collagen Type I , Chemistry , Hydrogen-Ion Concentration , Molecular Structure , Molecular Weight , Pepsin A , Chemistry , Skull , Chemistry , Sodium Chloride , Solubility , Spine , Chemistry , Temperature , TunaABSTRACT
Objective To investigate the expression of TMS1/ASC gene induced by gemcitabine(GEM) in pancreatic carcinoma cell line PANC-1.To study the relationship between cysteine aspartase(caspase-1),nuclear factor-κB(NF-κB) and the expression of TMS1/ASC.Methods The pancreatic carcinoma cell line PANC-1 was cultured in Dnlbecco's modification of Eagle's medium(DMEM).Methyl thiazolyl tetrazolium (MTT)method was used to measure the effect of GEM at different time points(24,48 h)at different concentrations(1,2,4,8,16 μg/ml) on growth of PANC-l.RT-PCR was used to detect the expression of TMS1/ASC mRNA stimulated by medium alone and by GEM(4.27μg/ml)for 24 h and 48 h.Western blot analysis was performed with inhibitory protein of NF-κB multiclonal antibody,caspase-1 multiclonal antibody and β-actin monoclonal antibody to observe the expression of β-actin,caspase-1 and IκBα in GEM group and in the control group.The activation state of caspase-1 and NF-κB was examined.Results GEM inhibited the growth of PANC-1 cells in a concentrationand-time-dependent manners and its half maximal inhibitory concentration(IC50)was 4.27 μg/ml on 24 h.The expression of TMS1/ASC was 0.3 ±0.004 and 0.63 ±0.007 respectively in GEM group while it was 0.1 ±0.001 and 0.21 ± 0.006 in the control group on 24h and 48h.The difference between the 2 groups at the same time point had statistical significance (P ＜ 0.01).Western blot showed that GEM caused the activation of caspase-1.The expression of IκBα had no obvious differencebetween the 2 groups.GEM couldn't induce the activation of NF-κB.Conclusions GEM can inhibit proliferation of PANC-1 cells and induce their apoptosis.The drug sensitivity decreased with prolongation of exposure time.GEM might induce and increase the expression of TMS1/ASC,which might influence the apoptosis of the cells later.The apoptosis of PANC-1 cells induced by GEM is dependent of caspase-1 signaling pathway and independent of NF-κB signaling pathway.
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Objetivo: identificar los factores asociados a displasia en mujeres que asisten al Hospital Central de la Policía Nacional o a diferentes dispensarios, cuya citología cérvicovaginal presentaba atipias de células escamosas de significado indeterminado (ASC-US).Materiales y métodos: estudio de prevalencia en el cual se identificaron los factores asociados a displasia de cuello uterino por medio de la correlación de las diferentes variables, por el servicio de Patología del Hospital Central de la Policía Nacional. Las diferentes variables fueron extraídas de las historias clínicas. Se realizó un reporte descriptivo de las prevalencias y se calcularon OR por medio de regresión logística para establecer la asociación entre las variables.Resultados: se encontraron porcentajes de distribución de displasia así: Sin displasia: 8.6%; Displasia leve: 80.2%; Displasia moderada: 8.2%; Displasia severa: 3.0%. La edad en la población tuvo una mediana de 47. 8 7 años. La población sin displasia fue de 8.6% y con displasia 91.4%. La asociación entre ciclos y displasia fue de 0.008 y entre antecedente personal de cáncer y displasia fue de 0.005. En la regresión logís-tica, la edad mostró asociación con una p<0.05.Conclusiones: la importancia de la toma de la citología cérvicovaginal cobra un papel cada vez más relevante en nuestra población, dado el aumento de la preva-lencia de displasia. Las principales recomendaciones son: adecuada toma de la citología y tener en cuenta la edad como factor importante para la asociación de displasia cérvicovaginal sobre los ASC-US, ya que en muchas ocasiones se pueden pasar por alto en la consulta diaria. Palabras clave: citología cérvicovaginal, asc-us, displasia
Objective: to identify factors associated with dysplasia in women attending the Central Hospital of the National Police or different clinics whose cervico-vaginal cyto-logy presented atypia squamous cell of undetermined significance (ASC-US).Materials and methods: prevalence study of what is intended to identify the factors associated with dysplasia of the cervix through the correlation of different variables, for the service of Pathology of the Central Hospital of the National Police. The variables were obtained through to medical records. It performs a report describing the prevalence's were calculated OR through logistic regression was used to establish the association between the variables.Results: the percentage of the distribution of dysplasia: Without dysplasia: 8.6%; Mild dysplasia: 80.2%; Moderate dysplasia: 8.2%; Severe dysplasia: 3.0%. The population has an average of 47 years. The percen-tage of people without dysplasia was 8.6% and 91.4% dysplasia. The analysis showed that divariado. The partnership between cycles and dysplasia was between 0,008 and personal history of cancer and dysplasia was 0005. For Multivariate logistic regression analysis age showed partnership with p <0.05.Conclusions: the importance of making the cervico-vaginal cytology charged an increasingly important role in our population, given the increased prevalence in dysplasia. Our main recommendation is, in addition to adequate and accurate making cytology, keep in mind that age is an important factor for the association cervico-vaginal dysplasia. And the ASC-US, as many times can be overlooked in the daily consultations. Key words: cervico-vaginal cytology, ASC-US dysplasia
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Atypical Squamous Cells of the Cervix , Uterine Cervical DysplasiaABSTRACT
Innate immune cells sense and respond to the cytoplasmic infection of bacterial pathogens through NLRP3, NLRC4 or AIM2 inflammasome depending on the unique molecular pattern of invading pathogens. The infection of flagellin- or type III secretion system (T3SS)-containing Gram-negative bacteria such as Salmonella enterica serovar Typhimurium (S. typhimurium) or Pseudomonas aeruginosa (P. aeruginosa) triggers NLRC4-dependent caspase-1 activation leading to the secretion of proinflammatory cytokines such as interleukin-1-beta (IL-1beta) and IL-18. Previous studies have shown that apoptosis-associated speck-like protein containing a CARD (ASC) is also required for Salmonella-induced caspase-1 activation, but it is still unclear how ASC contributes to the activation of NLRC4 inflammasome in response to S. typhimurium infection. In this study, we demonstrate that S. typhimurium triggers the formation of ASC oligomer in a potassium depletion-independent manner as determined by in vitro crosslinking and in situ fluorescence imaging. Remarkably, inhibition of potassium efflux failed to block Salmonella-promoted caspase-1 activation and macrophage cell death. These results collectively suggest that ASC is substantially oligomerized to facilitate the activation of caspase-1 in response to S. typhimurium infection. Contrary to NLRP3 inflammasome, intracellular potassium depletion is not critical for NLRC4 inflammasome signaling by S. typhimurium.
Subject(s)
Cell Death , Cytokines , Cytoplasm , Gram-Negative Bacteria , Interleukin-18 , Macrophages , Optical Imaging , Potassium , Pseudomonas aeruginosa , Salmonella , Salmonella entericaABSTRACT
OBJECTIVE: Human papillomavirus (HPV) has been identified more than 100 HPV subtypes. The distributions of subtypes are different according to nations and regions. We analysed subtype of infection with HPV among women who live in Pusan and surburbs of Pusan. We accessed the clinical usefulness of HPV DNA chip test as a supplementary method of Pap smear in the evaluation of cervical lesion. METHOD: This study was undertaken from January 2002 to January 2005 and the samples were collected from the patients who had abnormal Pap smear. We analysed subtypes of 143 positive cases with HPV DNA chip (Biomedlab) test and estimated pathologic reports of 115 patients except 28 patients who had not biopsy. We investigated pathologic results of 54 of 115 patients who had atypical squamous cells / low grade squamous intraepithelial lesion (ASC/LSIL) in Pap smear and examined high risk HPV in 54 pathologic results. RESULTS: The prevalence of HPV subtypes was 42 cases of HPV-16, 20 cases of HPV- 58, 16 cases of HPV-52, 10 cases of HPV-35, 9 cases of HPV-56, 7 cases of HPV-51, 6 cases of HPV-18 in descending order of incidence in high risk HPV group and 3 cases of HPV-6, 3 cases of HPV-42, 2 cases of HPV-34, 2 cases of HPV-43 in descending order of incidence in low risk HPV group. The results of HPV DNA chip test and 115 pathologic reports were estimated by comparative study. A pure infection with low risk HPV group was detected in low grade lesion. Infection with high risk HPV group was also detected in low grade lesion but was mainly detected in high grade lesion. The pathologic results of 54 patients who had ASC / LSIL in Pap smear were 13 patients had above high grade lesion include 2 cases of invasive carcinoma so false negative rate of Pap smear in the detection of high grade lesion was 24%. CONCLUSION: HPV subtypes were detected HPV 16, 58, 52, 35, 56, 51, 18 types in descending order of incidence and prevalence. Mass study and integrated data from larger population and various regions in many hospitals will be needed. And the supplementary use of HPV DNA chip test may provide clinical usefulness because it can reduce the false negative rate of Pap smear and improve the positive predictive value in the detection of high grade cervical lesion and it enables to decrease the incidence of cervical cancer.
Subject(s)
Female , Humans , Biopsy , Cervix Uteri , DNA , Human papillomavirus 16 , Human papillomavirus 18 , Human papillomavirus 6 , Incidence , Oligonucleotide Array Sequence Analysis , Prevalence , Uterine Cervical NeoplasmsABSTRACT
OBJECTIVE: This study was performed to investigate the efficacy of DNA chip method for detecting and genotyping of human papillomavirus (HPV) and screening of high-grade CIN (cervical intraepithelial neoplasia) or invasive cancer in the patients with atypical squamous cells of undetermined significance (ASC-US). METHODS: This study was based on 131 cases to be revealed ASC-US by Pap smear for the cervical cancer screening from July 2004 to Octorber 2004. They were evaluated by HPV DNA chip test, Cervical colposcopy and directed biopsy, and cone biopsy. The results of type 16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 54, 56, 58, 59, 66 and 68 in HPV DNA chip test were categorized as high risk HPV. We evaluate the detection rate of the high-grade CIN and invasive cancer by HPV DNA chip test. RESULTS: The incidence of high risk HPV DNA was 51.1% (67/131). Twelve of 131 (9.2%) were diagnosed as high-grade CIN or CIS on histology. The detection rate of high risk HPV DNA in high-grade CIN and invasive cancer was 83.3% (10/12). The detection rate of high risk HPV DNA was 36.0% (31/86) in normal or reactive, and 83.3% (10/12) in CIN II or above on histology. Higher the grade of biopsy, more the detection rate of high risk HPV DNA by HPV DNA chip test. CONCLUSION: The use of HPV DNA chip test in patients with ASC-US may be useful in detection of high-grade CIN or invasive cancer.
Subject(s)
Female , Humans , Biopsy , Cervix Uteri , Colposcopy , DNA , Incidence , Mass Screening , Oligonucleotide Array Sequence Analysis , Uterine Cervical NeoplasmsABSTRACT
Abstract Objective:FSM-2117 and FS-5416 are two bivalent hybrid strains of S.flexneri and S.sonnei, constructed by this laboratory-The FS-5416 expresses four invassive plasmid antigens(IpaA、IpaB、IpaC and IpaD) and has a good contact heamolysis activity(CHA+ ), butFSM-2117 hasn' t. To observe the immunogenicity of Shigelk vaccines through three different mucosal administration rout, the changes of ASCin the spleen and Peyer's patch(PP) , mesenteric lymph nodes(MLN) lymphocytes are detected.Methods:BALB/c mice were divided intothree groups, 20 mice per group. Mice were immunized respectively with the Ipa+ or Ipa- vaccines(4 x 10~7 CFU) three times with an intervalof two weeks by intranasal、intragastric or intraintestinal administration routs. The spleen , PP , MLN lymphocytes were isolated of seventh dayat random after immunization. An BA-EIISASPOT was done to account the numbers of ASC.Results:The numbers of SIgA and SIgG ASC ofspleen , PP , MLN lymphocytes of intranasal and intraintestinal group were significantly increased . Significant difference were only observed inthe number of spleen lymphocytes SIgA and SIgG ASC of intranasal group between Ipa+ and Ipa- . Conclusion:Two bivalent Shigelk vaccinescan induce spleen and GALT immunity reaction by nasal or small intestinal mucosal in a low dosage compared with intragastric rout (about 1/20). Ipa can significantly increased the number of spleen lymphocytes SIgA and SIgG ASC of intranasal group.
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The biometric analysis of the normal aged eye with photodocumented method (using EAS-lOOO Scheimpflug camera) was performed in 109 eyes. We measured anterior chamber depth, corneal thickness, corneal radius, lens thickness and biometric lens analysis according to the age. The lens thickness increased annually (O.O1mm) with age and the anterior chamber depth reversely decreased. The biometric analysis can provide normal critariae values about the effect of anticatar acto us drugs in long-term follow up study and the relationships between normal aged lens and highly risk groups in the cataract prevalence study.
Subject(s)
Anterior Chamber , Cataract , RadiusABSTRACT
Objective:To investigate the role of apoptosis-associated speck-like protein(ASC) in non-apoptotic,non-necrotic cell death of neutrophils induced by ONO-AE-248.Methods:The morphological changes of neutrophil nuclei and DNA fragmentation of the cells were examined by confocal microscopy and terminal-deoxynucleotidyl transferase mediated nick end labeling(TUNEL).Neutrophils were stimulated with medium alone,LPS,TNF-? or ONO-AE248 respectively.Then expression of ASC was detected by Western blot.Results:ONO-AE-248-induced neutrophil death was negative in TUNEL assay.Western blot showed that the expression of ASC protein was down-regulated by ONO-AE-248.Conclusion:The DNA degradation of the neutrophils when stimulated by ONO-AE-248 is probably different from that of the typical apoptosis.ASC might be a crosslink point between the ONO-AE-248-induced neutrophil death and spontaneous apoptosis of neutrophils.