Leishmania mexicana pifanoi: in vivo and in vitro interactions between amastigotes and macrophages

Macrophages of the cell line J774 were used in a comparative study of virulence involving amastigote stages of Leishmania mexicana pifanoi isolated from macrophages (AMA-M) of the aforementioned cell line, amastigote forms grown in the UM-54-cell-free medium (AMA-C), and promastigote stages. The macrophage cultures were inoculated with AMA-M and AMA-C at the culture cell to parasite ratios of 1:3, 1:5, and 1:10. The macrophages were exposed to either kind of amastigotes for 24, 48, and 72 h. At the end of each of these periods, and for each dilution, the percentages of macrophages harboring the parasites within their cytoplasm and the mean numbers of intracellular parasite/macrophage were estimated on the basis of examination of 200 phagocytes. When either AMA-M or AMA-C were employed, after 24 h, the percentages of infected macrophages were, respectively, 84.5%, 89.0%, and 94.5% for the three aforementioned dilutions, the majority of the phagocytes containing 1-5 parasites. After 48- and 72-h exposures, the macrophages harbored 6-11 and 11-20 amastigotes/cell, respectively. Evidently intracellular multiplication of the amastigotes has taken place. In contrast to the results obtained with amastigote forms, after inoculations of the macrophages cultures with promastigotes at the dilutions previously used for amastigotes, only 48-78 phagocytes were found to contain intracellular stages within their cytoplasm. Many macrophages were parasite-free, especially when exposed to fewer promastigotes. Experiments in which 5 X10(6) promastigotes, AMA-M, or AMA-C were inoculated into the footpads of hamsters yielded the following results with regard to terminal footpad volumes: 1.57, 3.31, and 3.32 cm3, respectively. Evidently both kinds of amastigotes had equal virulence for hamsters; however, the promastigote stages were much les virulent for these experimental hosts.     

向日葵未受精胚珠培养时胚状体发生的显微观察

由开花前1—4天的向日葵子房中取出胚珠,在液体培养基上进行漂浮培养,诱导了未受精的卵细胞发育为单倍体的胚状体.亦诱导了珠被绒毡层产生胚状体。对两种胚状体的发生和发育过程及其形态发生特点作了显微观察与描述。     

Are Chaoborus larvae more abundant in acidified than in non-acidified lakes in Central Canada?

Eriksson et al (1980) hypothesized that the abundance of certain macroinvertebrate predators, such as larvae of the phantom midge Chaoborus , should increase in acidified lakes because of the elimination of fish. To examine the influence of pH and presence of fish on Chaoborus abundance, we surveyed Chaoborus populations in 33 lakes in Ontario, Canada which ranged in pH from 4.5 to 7.4. Chaoborus larvae were not more abundant in the acidified lakes that were devoid of fish than in the remaining lakes. Therefore, we concluded that pH and presence of fish are not prime determinants of total Chaoborus abundance in Canadian Shield lakes. We hypothesized that significant increases in Chaoborus abundance should only be anticipated when fish populations are eliminated by acidification of relatively nutrient rich lakes.     

足籽骨的放射片研究

本文对山东枣庄市916人足放射片进行了足籽骨的观察与测量。发现每足有1-7个籽骨,其中二个者占77.8％,三个者占16.9％;籽骨位于跖骨头下方者占94.5％,位于趾间关节下方者占5.5％;各跖骨头籽骨出现率:Ⅰ占99.9％、Ⅱ占 2.2％、Ⅲ占0.3％、Ⅳ占0.5％、Ⅴ占6.4％;(足母)趾趾间关节籽骨占12.6％;二分及三分籽骨出现率占3.9％,明显低于欧美人。此外,本文认为籽骨是在先天籽骨原基基础上,加以后天运动的影响而形成。     

中国某些野生和栽培茶的核型研究

研究了茶的4个变种和广东野生毛叶茶等共12个材料的核型。所有材料的染色体数目均是2n=30,为二倍体。所有中国大叶变种(越南大叶除外)(Cametlia sinensis var. macrophylla)和阿萨姆大叶变种(C. sinensis var. assamica)均具比较对称或原始的“2A”核型;中国小叶变种(C.sinensis var.bohea)(“铁观音”品种除外),掸部变种(C.sinensis var. shan form)和广东野生毛叶茶(C. ptilophylla)均具较不对称或较进化的“2B”核型。根据核型特征,植物习性和地理分布,作者认为中国四川和云南可能是茶的起源中心,向东或北迁移,演变为中国小叶变种;向南移则演变为阿萨姆变种和掸部变种。     

琼脂糖平板制备聚焦电泳法进一步提纯胸腺素组分五

用琼脂糖平板等电聚焦电泳法,由胸腺素组分五中分离出三种在聚焦电泳谱上是单一谱线的多肽成份——CP1、CP2和CP3,等电点分别为4.3、4.9和5.6。测定了这些多肽对脐带血中淋巴细胞形成羊红细胞玫瑰花的影响。与对照相比,CP1(2微克/0.6毫升),和CP3(0.2-2微克/毫升)分别在统计学上呈显著和非常显著差异。在相同测定条件下,这三种多肽成份的活性均高于化学合成的胸腺多肽——胸腺素α_1。     

大鼠非致瘤四倍体细胞系的建立及细胞遗传学和酶学特征

从大鼠自然诱发的肉瘤细胞中,我们建立了一个四倍体细胞系(4n=84),命名为RC(ratcell)。它具有典型的成纤维细胞外形,能在玻璃表面贴壁生长,但不能生长在琼脂半固体培养基中。该细胞在含15％小牛血清的RPMI 1640培养基中生长良好,至今已连续繁殖112世代,细胞群体倍增时间约为15小时。染色体G-带分析表明,RC为整四倍体细胞,它的1条X染色体在第32至34区为均染区。RC细胞核仁组织者(NORs)活性显然比大鼠二倍体细胞NORs活性的加倍还高(P<0.001)。这个具有非常高NORs活性的RC细胞系对于研究细胞18S+28S rRNA基因转录活性的调控、基因表达与基因剂量关系有一定的意义。RC细胞还有异常高的磷酸酯酶活性,而且它的同工酶谱也与大鼠肌肉细胞明显不同。体内接种实验和扫描电镜的观察表明,RC是非致瘤细胞。RC细胞各号染色体的C-带图样与大鼠二倍体细胞无明显的差异。