A case of slipped capital femoral epiphysis results from hypophosphatemic rickets： treatment and midterm follow-up

In this case, a male patient presented with a clinically and radiographieally unstable slipped capital femoral epiphysis （SCFE） as well as slipped calcaneal epiphysis years. Subsequent thorough at the age of 23 work-up revealed that he had some features of rickets and labo- ratory test demonstrated he had hypophos- phatemia （2.3mg/dl）, normocalcemia, normal vi- tamin D metabolite levels, and secondary hy- perparathyroidism.     

间充质干细胞的来源

目的:间充质干细胞具有强大的增殖能力和多向分化潜能,文章对其主要的来源途径予以综述。资料来源:应用计算机检索Medline1991-01/2006-01期间的相关文章,检索词为“mesenchyma stem cells,origin,research progress”,并限定文章语言种类为English。同时计算机检索中国期刊全文数据库1998-01/2006-10期间的相关文章,检索词为“间充质干细胞,来源,研究进展”,并限定文章语言种类为中文。资料选择:对资料进行初审,并查看每篇文献后的引文。纳入标准:①间充质干细胞的起源。②间充质干细胞研究进展、干细胞的分离及鉴定。排除标准:重复研究、个案报告或Meta分析类文章。资料提炼:共收集到96篇相关文献,40篇文献符合纳入标准,排除的56篇文献为内容陈旧或重复。符合纳入标准的40篇文献中,分别涉及骨髓、肌肉、脐血、胎盘、外周血、脂肪组织、血管及其他来源的间充质干细胞。资料综合:间充质干细胞是属于中胚层的一类多能干细胞,具有强大的增殖能力和多向分化潜能,动物模型试验和临床应用研究也取得了一定的效果。间充质干细胞来源广泛,易于获得,临床上为神经损伤及其他系统的损伤修复提供了更为广泛的途径。结论:间充质干细胞主要来源于骨髓、肌肉、脐血、外周血、胎盘等组织,具有广阔的应用前景。     

颈动脉血管重构特征在自发性高血压大鼠体内的表现

目的:血管重构是高血压的重要病理变化,是高血压导致器官损害的结构基础。实验观察自发性高血压大鼠颈动脉中层组织学的相关变化,以验证血管重构的特点。方法:实验于2006-06/2007-03在福建医科大学附属协和医院心血管内科实验室完成。①实验材料及分组:12周龄雄性自发性高血压大鼠10只,同性别周龄的WKY大鼠10只为对照,喂养18周后终止实验。②实验过程及评估:开始及每2周测鼠尾收缩压。实验结束后,麻醉后取颈动脉,行苏木精-伊红、苦味酸-天狼星红、弹力纤维和胶原纤维的双重染色(P/VB法),利用计算机辅助成像系统测算颈动脉中膜厚度、腔径、血管中膜厚/腔径、中膜横截面积、中膜细胞平均核面积及中膜的胶原面积百分比、弹性纤维面积百分比、弹性纤维面积与胶原面积的比值。SP免疫组织化学染色检测α-平滑肌肌动蛋白、增殖细胞核抗原、纤维粘连蛋白、层粘连蛋白等抗原在颈动脉壁的表达,并计算颈动脉中膜细胞增殖指数;以原位末端标记法标记血管壁的凋亡细胞,计算颈动脉中膜细胞凋亡指数。结果:20只大鼠全部进入结果分析。①自发性高血压大鼠实验开始和结束前的收缩压均>150mmHg,高于WKY大鼠(P<0.01)。②自发性高血压大鼠颈动脉中膜厚度、腔径、中膜厚度/腔径、中膜横截面积、中膜胶原面积百分比均高于WKY大鼠(P<0.01),而中膜弹性纤维面积百分比、弹性纤维面积与胶原面积比值均低于WKY大鼠(P<0.01)。③α-平滑肌肌动蛋白在两组大鼠颈动脉中膜均可表达,提示中膜细胞为血管平滑肌细胞。④自发性高血压大鼠中膜血管平滑肌细胞平均核面积大于WKY大鼠(P<0.01),中膜细胞增殖指数与WKY大鼠差异无显著性(P>0.05),中膜细胞凋亡指数显著低于WKY大鼠(P<0.01)。⑤自发性高血压大鼠颈动脉中膜纤维粘连蛋白、层粘连蛋白的光密度值(IA值)及染色阳性面积百分比高于WKY大鼠(P<0.01)。⑥颈动脉中膜血管平滑肌细胞凋亡指数与中膜横截面积呈显著负相关(r=-0.872,P<0.01);纤维连接蛋白表达的吸光度值与中膜横截面积呈显著正相关(r=0.954,P<0.01)。结论:自发性高血压大鼠颈动脉存在明显的重构,其特点为中膜肥厚、平滑肌细胞肥大、凋亡减少及胶原、纤维粘连蛋白、层粘连蛋白的过度沉积。     

New insights into the genetics of glioblastoma multiforme by familial exome sequencing

Glioblastoma multiforme (GBM) is the most aggressive and malignant subtype of human brain tumors. While a family clustering of GBM has long been acknowledged, relevant hereditary factors still remained elusive. Exome sequencing of families offers the option to discover respective genetic factors.We sequenced blood samples of one of the rare affected families: while both parents were healthy, both children were diagnosed with GBM. We report 85 homozygous non-synonymous single nucleotide variations (SNVs) in both siblings that were heterozygous in the parents. Beyond known key players for GBM such as ERBB2, PMS2, or CHI3L1, we identified over 50 genes that have not been associated to GBM so far. We also discovered three accumulative effects potentially adding to the tumorigenesis in the siblings: a clustering of multiple variants in single genes (e.g. PTPRB, CROCC), the aggregation of affected genes on specific molecular pathways (e.g. Focal adhesion or ECM receptor interaction) and genomic proximity (e.g. chr22.q12.2, chr1.p36.33). We found a striking accumulation of SNVs in specific genes for the daughter, who developed not only a GBM at the age of 12 years but was subsequently diagnosed with a pilocytic astrocytoma, a common acute lymphatic leukemia and a diffuse pontine glioma.The reported variants underline the relevance of genetic predisposition and cancer development in this family and demonstrate that GBM has a complex and heterogeneous genetic background. Sequencing of other affected families will help to further narrow down the driving genetic causes for this disease.     

A prophylactic and therapeutic AIDS vaccine containing as a component the innocuous Tat Toxoid

Extracellular Tat can act as a viral toxin on uninfected cells of different tissues, including the CNS and the immune system, thus in order to immunize humans against Tat we have prepared a biologically inactivated but immunogenic Tat (Tat Toxoid). Tat Toxoid is not toxic in mice even at high doses. It triggers high levels of specific Tat Abs in the mouse and rabbit. Furthermore, in humans Tat Toxoid immunization was safe and induced in seronegatives persistent high levels of Tat Abs and in immunodeficient patients a significant rise of these specific Abs. Facing acute HIV-1 infection, the presence of high level of circulating Tat Abs promoted by Tat Toxoid vaccine should prevent Tatinduced immunosuppression and allow anti-HIV-1 cellular response to develop. As a consequence, early release of β-chemokines could enhance host resistance towards HIV-1, and, in infected people, inhibit viral replication and evolution towards AIDS.