Ganglioglial Differentiation in Medulloblastoma

A case of cerebellar medulloblastoma with clusters of mature ganglion cells and glial cells is described. The patient, a 15 -year -old girl, underwent three operations followed each time by radiation and chemotherapy during the four-year clinical course. Histologically, the ganglion cells were clearly identifiable by their abundant eosino-philic cytoplasm, round nuclei with prominent nucleoli, tigroid granules, and argyrophilic fibrils and axons. Im-munohistochemically, the cells were NSE- and NF positive, and ultrastructurally they contained abundant tubules and filaments, neurosecretory granules and well developed rough endoplasmic reticulum. There were many cells transitional in appearance between primitive cells and mature ganglion cells. The tumor also had many mature yet atypical astrocytes and oligodendrocytes. The exact mechanism of the extensive neuronal and glial maturation of medulloblastoma cells is unclear, but the repetitive surgical interventions, radiation and chemotherapy might have had certain cytostatic effects on rapidly dividing medulloblastoma cells, giving them a chance to mature into postmitotic cells with potential for neuronal and glial differentiation. Acta Pathol Jpn 40: 50–56, 1990.     

晶状体膜蛋白MIP基因C末端一个新的错义突变导致双眼多形性先天性白内障

目的 定位一个双眼多形性先天性白内障家系的致病位点,寻找疾病家系的致病基因.方法 应用ABI-MD10试剂盒中的常染色体382个微卫星位点,对一个常染色体显性、双眼具有不同白内障形态的先天性白内障家系进行全基因组扫描.MLINK软件进行两点连锁分析.直接测序候选基因外显子.结果 在D12S83处获得最大LOD值Zmax=5.44(θ=0),该家系致病位点被定位到12p11.2-q15之间的区域上,在该区域的白内障候选基因晶状体膜蛋白基因(major intrinsic protein,MIP)的第4外显子中发现单个碱基错义突变,702ntG→A,导致p.R233K.结论 该先天性白内障由MIP基因702ntG→A突变所致,导致MIP蛋白质的C-末端中p.R233K,从而可能减少了氢键的形成,影响了该蛋白C-末端的稳定性,推测影响了MIP对水的调节及由该蛋白质形成的细胞之间的连接.这一新突变为目前世界上首次报道.     

糖尿病肾病患者治疗前后AT-Ⅱ,VEGF,ET和ANP水平变化

目的 :检测糖尿病肾病 (DN)患者治疗前后血管紧张素Ⅱ (AT -Ⅱ )、血管内皮生长因子(VEGF)、内皮素 (ET)和心钠素 (ANP)含量变化 ,以比较不同药物的治疗效果。方法 :对象为DN患者分为 2组 :中药治疗观察组 35例 ;对照组 35例 ;正常对照组 35例。用放免法和ELISA法分别测定治疗前后血浆AT -Ⅱ、VEGF、ET和ANP水平。结果 :2组DN患者治疗前AT -Ⅱ、VEGF、ET和ANP含量均明显高于正常对照组 (p <0 0 5～ 0 0 1) ,治疗后较治疗前明显降低 (p<0 0 5～ 0 0 1)。观察组治疗后各含量下降较对照组明显。糖尿病肾病患者AT -Ⅱ含量与VEGF呈正相关 (r=0 4 6 5 ,p<0 0 5 ) ,血浆ET含量与ANP呈正相关 (r=0 6 1,p <0 0 5 ) ,观察组疗效稍好于对照组。结论 :AT -Ⅱ、VEGF、ET和ANP与DN的发生发展和病情的严重程度有关 ,它们之间可相互作用共同参与DN病变过程。以它们的指标作为疗效观察 ,中西药结合治疗糖尿病肾病患者效果较好。     

纤维蛋白原与吸附白蛋白、肝素的新型血管支架材料氧化钛的血液相容性

探索纤维蛋白原(Fibrinogen,FIG)与吸附白蛋白、肝素的新型血管支架材料氧化钛(Titanium Oxide,Ti-O)的血液相容性。(1)研制Ti-O,切割成薄膜;(2)Ti-O薄膜涂层白蛋白和肝素;(3)血小板(platelet,PL)吸附试验;(4)酶联免疫试验测FIG吸附量;(5)动物犬股动脉内植入涂层的Ti-O薄膜与对照试片Ti-O和不锈钢(Stainless steel,SS)薄膜。结果发现:Ti-O完全具有固定白蛋白和肝素的结构与性能,比未涂层的Ti-O能更一步减少PL和FIG的吸附,实验动物体内薄膜6个月后取出扫描电镜观察黏附的PL少,形态无改变,血管内无血栓,优于未涂层的Ti-O,更明显优于SS。Ti-O为N型半导体,不易接受FIG的电荷,并且与血细胞有相似的界面张力,决定生物材料Ti-O有较好的血液相容性。Ti-O对白蛋白、肝素有极好的亲和力是因以化学键相结合,在血中进一步减少FIG和PL被涂层的Ti-O吸附。实验证明涂层的Ti-O有持久和稳定的抗凝血性能。     

Thymocyte-thymocyte interaction for efficient positive selection and maturation of CD4 T cells

Despite numerous reports on MHC class II expression by T cells from a wide spectrum of mammalian species including humans, the biological relevance of this phenomenon has never been tested with appropriately designed animal models. To address this issue, we developed mouse models in which immature thymocytes are the only positively selecting antigen-presenting cells in the thymus. In these mice, CD4+ T cells were generated with the appropriate maturation phenotype and showed a diverse repertoire of TCR Vbetas. The CD4+ T cells were functionally competent, mediating effective allogeneic responses that involved polyclonal TCR Vbetas. These results suggest that the thymocyte-thymocyte (T-T) interaction operates as an independent pathway for CD4+ T cell selection in the thymi of species with MHC II-positive thymocytes. This T-T interaction appears to be the basis for the generation of donor MHC-restricted CD4+ T cells in xenogeneic hosts.     

抗CD3单克隆抗体重、轻链可变区基因的克隆及序列分析

目的：抗CD3单克隆抗体（WuT3)可变区基因克隆及序列分析。方法；采用RT-PCR技术，从WuT3杂交瘤细胞总RNA中扩增VH，VL片段，经酶切后通过链接反应构建重组克隆载体，测序鉴定。结果：通过国际联机检索发现VH，VL基因与Ig同源，分别符合小鼠IgVH,Vк基因特征。VH基因属于鼠重链VH第ⅡB亚类，全长363bp，可编码121个氨基酸；VL基因属于鼠к轻链第Ⅲ亚类，全长330bp，可编码110个氨基酸，结论：成功获得WuT3单抗的重，轻链可变区基因。     

镁对在体兔缺血—再灌心脏的电生理效应

本实验通过结扎兔冠状动脉左室支复制动脉缺血－再灌注模型，应用心外膜接触电极记录单相动作电位，观察后除极电位在再灌注性心律失常中及镁离子的拮抗作用。结果表明，再灌性心律失常的５２．６％与早期后去极化有关。硫酸镁可终止及预防ＲＡ，对再灌中出现触发活动有抑制作用。     

120例青壮年轻型颅脑损伤脑电图分析

对120例青壮年轻型颅脑损伤患者进行脑电图(EEG)分析,结果显示颅脑损伤组EEG异常率异著高于正常对照组(P<0.01),表明早期EEG检查,对颅脑损伤程度分析有帮助。     

宫颈细胞学ASCUS/LSIL的临床意义及处理

目的探讨宫颈不典型鳞状上皮，低度鳞状上皮内病变（ASCUS／LSIL）的临床意义及处理方法。方法对中国医学科学院肿瘤医院2004～2006年妇科门诊用TCT（宫颈液基细胞学）的方法检出的254例ASCUS／LSIL以病理结果为金标准进行回顾性分析，其中136例进行了阴道镜检查。结果在140例ASCUS中，宫颈上皮内瘤变（CIN）病变占51．5％，其中高度病变占22．9％，114例LSIL中CIN病变占59．6％，其中高度病变占30．7％，两组资料比较差异无统计学意义，P〉0．05。其中136例中阴道镜诊断炎症47例，低度宫颈上皮内病变53例，高度宫颈上皮内病变36例及病理检查结果炎症55例，低度宫颈上皮内病变41例，高度宫颈上皮内病变40例，阴道镜与病理对照进行了～致性检验，Kappa=0．314，U=0．064，P〈0．05，一致性好。病理证实人乳头状瘤病毒（HPV）阳性的妇女中CIN发生率79％（67／84），而HPV阴性者中CIN发生率43．5％％（74／170），结果显示两组资料比较差异有统计学意义，X^2=29．88，P〈0．05。本组资料中年龄在35～55岁的妇女占83．5％与HPV阳性的妇女年龄高峰一致。结论对ASCUS的患者应与LSIL同样重视，立即进行阴道镜检查以避免22．9％的高度病变的患者漏诊或失访，对35～55岁的HPV感染的妇女应更加重视。     

PBX1基因对系统性红斑狼疮易感基因IFI16表达的影响

探讨PBX1基因转染人单核细胞系THP1后,对IFI16基因表达的影响。以携带人PBX1基因表达序列的复制缺陷型5型腺病毒载体(pDC315-PBX1-EGFP)转染THP1细胞后,采用实时定量PCR(RT-PCR)和Western blot技术分别在mRNA水平和蛋白水平检测PBX1和IFI16表达的变化。结果,pDC315-PBX1-EGFP转染THP1细胞后,PBX1基因的表达水平都增高,同时发现IFI16基因的表达水平降低。PBX1作为一种转录因子,能调节干扰素诱导蛋白IFI16的表达。