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81.
Misawa A Hosoi H Imoto I Iehara T Sugimoto T Inazawa J 《Journal of human genetics》2004,49(10):586-589
Malignant rhabdoid tumor (MRT) is a highly malignant pediatric cancer, which arises in various sites such as the kidney, brain, and soft tissues. Cytogenetic studies have revealed alterations of 22q11 in MRT. Recently, deletions and mutations of the SNF5/INI1 locus in 22q11.2 have been reported in MRT, suggesting that SNF5/INI1 is a tumor suppressor gene for MRT. Here we report our molecular cytogenetic study for a newly established cell line from extrarenal MRT with t(1;22)(p36;q11.2). Consequently, the reciprocal translocation was associated with the interstitial deletion of a small segment including SNF5/INI1, and another, chromosome 22, showed terminal deletion, the breakpoint of which was located 70–80 kb centromeric to SNF5/INI1, resulting in homozygous deletion of SNF5/INI1 in this cell line. 相似文献
82.
IL-13对大鼠急性肾缺血再灌注时IL-1β表达的影响 总被引:2,自引:0,他引:2
目的:观察IL-13对急性肾缺血再灌注时IL-1β表达的影响。方法:Wistar雄性大鼠57只,随机分为8组:正常组(normal);假手术组(sham);缺血组:(I)缺血再灌注组(I/R);治疗对照组-1(C-1);治疗对照组-2(C-2);治疗组-1(T-1)和治疗组-2(T-2)。阻断大鼠双侧肾脏血流45min再灌注24h建立急性肾缺血再灌注模型;治疗组分别于阻断血流前、后分别从双侧肾动脉开口注射入1.5μg/50gbw鼠重组白细胞介素13(rmIL-13);检测各组大鼠IL-1β血清水平和肾脏表达,以及肾功能和肾脏病理。结果:(1)治疗组肾脏IL-1β基因(TtoC:P<0.01)和蛋白表达(T-1toC-1:P<0.01;T-2toC-2:P<0.05)明显减少,血清IL-1β水平明显下降;(2)肾功能障碍和肾组织病理变化明显减轻,肾小管损害评分减少(C-1toT-1:45.20±8.64to21.05±8.82,P<0.01;C-2toT-2:42.25±11.15to23.25±7.31,P<0.01);(3)血清IL-1β水平与BUN、Cr成正相关(r=0.708,P<0.01;r=0.770,P<0.01)。结论:IL-13能有效地抑制大鼠急性肾缺血再灌注损伤IL-1β的表达。 相似文献
83.
84.
QIU YAN LIU TAO YONG CHEN HUA BIAO CHEN NAN LI MING HUI ZHANG PENG CHENG MA XUE TAO CAO Institute of Immunology Zhejiang University Hangzhou P.R.China Institute of Immunology Second Military Medical University Shanghai P.R.China Institute of Dermatology Chinese Academy of Medical Sciences Nanjing P.R.China 《中华微生物学和免疫学杂志(英文版)》2005,3(1):66-72
Extracts of Tripterygium wilfordii Hook F.(TWHF ) are effective in traditional Chinesemedicine for treatment of autoimmune diseasessuch as rheumatoid arthritis, systemic lupus ery thematosus, nephritis and asthma [1, 2]. Trip tolide, a diterpenoid triepoxide, is derived fromTWHF and is responsible for most of the immuno suppressive and anti inflammatory effects ofTWHF. Triptolide has been shown to be effectivein the treatment of autoimmune diseases, … 相似文献
85.
目的:通过研究细胞因子对FN表达的调节,探讨FN在围着床期子宫内膜表达的调节机理。方法:给孕早期小鼠注射不同的细胞因子,收集子宫内膜。分别用Immuno-blot法及RT-PCR法测定子宫内膜FN蛋白和nRNA的水平。结果:LIF低、高剂量组的FNmRNA和蛋白水平都比对照组高,统计分析差异有显著性(P<0.05,P<0.01),IL-1和IL-1ra各组FN水平与对照组比无显著差异。结论:LIF在转录和转录后水平上调早期子宫内膜FN的表达,LIF参与着床与调节粘附分子的表达有关。IL-1系统则不影响子宫内膜FN的合成。 相似文献
86.
Interleukin-1 beta gene polymorphism related with allergic pathogenesis in Iris constitution 总被引:1,自引:0,他引:1
Um JY Do KR Hwang WJ Shin TY Hwang CY Kim CH Kim YK Hong SH Kim HM 《Immunopharmacology and immunotoxicology》2004,26(4):653-661
Iridological constitution has a strong familial aggregation and is implicated in heredity. The aetiology of inflammatory bowel disease is still unknown. However, from genetic epidemiological studies there is considerable evidence that genetic factors are associated with both Crohn's disease and ulcerative colitis. We investigated the relationships between Iridological constitution and interleukin 1 beta (IL-1β) gene polymorphism. IL-1β is a major proinflammatiry cytokine, and the polymorphisms of this gene have been shown to be of importance in a number of diseases. Especially, IL-1 has been suspected of involvement in allergic pathogenesis. Also, IL-1β genotype is one of the genetic markers of gastric cancer. Therefore, we classified 166 individuals according to Iris constitution, and determined IL-1β genotype. The frequencies of Iris constitutions as follows: neurogenic type, 41 (24.7%); abdominal connective tissue weakness type, 53 (31.9%); cardio-renal connective tissue weakness type, 50 (30.1%); the others type, 22 (13.3%). Especially, the frequency of abdominal connective tissue weakness type was higher in C/T genotype than in the remaining constitutions although the statistical power was very weak. Furthermore, we first attempted to explore possible involvement of the IL-1β polymorphism and the Iris constitution. 相似文献
87.
Human multiple myeloma cells express peroxisome proliferator-activated receptor gamma and undergo apoptosis upon exposure to PPARgamma ligands 总被引:8,自引:0,他引:8
Multiple myeloma is essentially an incurable malignancy and it is therefore of great interest to develop new therapeutic approaches. We previously reported that human B cell-lymphomas express the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARgamma) and are killed by PPARgamma ligands. Herein, we investigate the therapeutic potential of PPARgamma ligands for multiple myeloma. The human multiple myeloma cell lines ANBL6 and 8226 express PPARgamma mRNA and protein. The PPARgamma ligands, 15-deoxy-Delta12,14-prostaglandin J2 (15d-PGJ2) and ciglitazone, induced multiple myeloma cell apoptosis as determined by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) assay, loss of mitochondrial membrane potential, and caspase activation. Importantly, the ability of PPARgamma ligands to kill both multiple myeloma cell lines was not abrogated by Interleukin-6 (IL-6), a multiple myeloma growth survival factor. Finally, the RXR ligand 9-cis retinoic acid (9-cis RA) in combination with PPARgamma ligands greatly enhanced multiple myeloma cell killing. These new findings support that PPARgamma ligands may represent a novel therapy for multiple myeloma. 相似文献
88.
目的 研究两种不同的IL-15真核表达质粒对乙肝蛋白疫苗诱导的免疫应答的影响。方法:构建IL-15真核表达质粒(简称pIL-15)和含有IL-12信号肽的IL-15真核表达质粒(简称pIL-2s-15),CTLL-2细胞增殖实验验证两种质粒真核表达产物的生物学活性。将这两种质粒分别与HBsAg共免疫BALB/C小鼠,用ELISA法检测小鼠血清抗-HBs IgG及IgGl、IgG2a亚类的效价。结果:与HBsAg蛋白疫苗共免疫时,pIL-15可使HBsAg诱导的抗-HBsIgG效价升高,显著高于载体pcDNA3.1与HB—sAg共免疫对照组,pIL-2s-15对HBsAg诱导抗-HBsIgC效价没有明显影响。与HBsAg pcDNA3.1组相比,HBsAg pIL-2s-15组和HBsAg pIL-15组诱生的抗HBsIgG2a亚类均升高,但前者IgG2a/IgG1比值最高,与HBsAg pcDNA3.1组相比差别有显著性;HBsAg pIL-15组IgG2a/IgG1比值与HBsAg pcDNA3.1组相比差别无显著性。结论 pIL-15真核表达质粒可增强蛋白疫苗诱导的体液免疫应答,pIL-2s-15真核表达质粒则主要使免疫应答趋向Th1型。 相似文献
89.
90.
Hiroki Kurahashi Kenzo Akagi Ikuo Yana Thomas Melot Olivier Delattre Gilles Thomas Shintaro Okada Shin-ichiro Takai Isamu Nishisho 《Journal of human genetics》1994,39(2):243-248
Summary Eight cosmid clones were regionally assigned to small subregions of chromosome 22 by hybridization with a total of 22 somatic cell hybrids. One cosmid was localized to the proximal part of 22q which contained the region commonly deleted in the DiGeorge syndrome. Seven cosmids showing restriction fragment length polymorphisms were localized to the telomeric region distal to the MB locus, which was reported to be frequently deleted in sporadic meningioma. These cosmids, when finely mapped and ordered, are considered useful for the identification of genetic alterations on this chromosome arm. 相似文献