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Gillian J. Harper 《American anthropologist》1998,100(4):1048-1049
Old Age in Transition: The Geriatric Ward Revisited. Peter Woolfson. Westport, CT: Bergin & Garvey, 1997.133 pp. 相似文献
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Alexandra Zieritz Antonio G. Checa David C. Aldridge Elizabeth M. Harper 《Journal of Zoological Systematics and Evolutionary Research》2011,49(1):6-15
Microprojections of unionoid shells are virtually unstudied but could be important characters for resolving questions on the phylogeny and ecology of these bivalves. By investigating 26 unionoid and three species of their closest living relatives, the Trigonioida, using scanning electron microscopy, we identified three types of periostracal microprojections. (1) Microridges were present only in one species from each of the two unionoid families Mycetopodidae (Anodontites trapesialis) and Iridinidae (Chambardia bourguignati) and may represent a synapomorphy for the mycetopodid‐iridinid clade. In A. trapesialis, microridges were additionally equipped with (2)ensp;flag‐like projections (microfringes), possibly a synapomorphic character for the Mycetopodidae. Examination of partially bleached specimens indicated that both microridges and microfringes are predominantly or purely organic. In contrast, previously undescribed (3) spicule‐like spikes represent calcifications within the periostracum. These were found in 20 of the 29 species and four of the six unionoid families. Spikes were particularly large and abundant in umbonal (juvenile) shell regions and species characteristic of fast‐flowing habitats. These structures may thus serve in protecting the periostracum and shell underneath, and/or stabilizing life position by increasing shell friction. Microfringes and microridges, on the other hand, possibly aid in the orientation of the mussel within the sediment. 相似文献
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Leukotriene C4 and D4 formation by particulate enzymes 总被引:6,自引:0,他引:6
The homogenate of rat basophilic leukemia cells, when incubated with arachidonic acid, glutathione, and calcium, formed 3 isomers of 5,12-dihydroxyeicosatetraenoic acid and 2 isomers of 5,6-dihydroxyeicosatetraenoic acid, as well as leukotriene (LT) C4 and D4. The products were identified by high pressure liquid chromatography, ultraviolet spectral analysis, co-migration with standards, bioassay, and gas chromatography-mass spectrometry. The enzymes responsible for the formation of LTC4 and LTD4 from LTA4 were found in the 10,000 x g pellet and, therefore, appear to be particulate. The possibility that these enzymes are bound to the cell membrane suggest that the formation of these leukotrienes might be important in the basophil and mast cells release reaction. 相似文献
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Proteoglycan synthesis in normal and Lowe syndrome fibroblasts 总被引:1,自引:0,他引:1
G S Harper V C Hascall M Yanagishita W A Gahl 《The Journal of biological chemistry》1987,262(12):5637-5643
Lowe (oculocerebrorenal) syndrome (LS) is an X-linked disorder characterized by congenital cataracts, generalized hypotonia, mental retardation, and renal Fanconi syndrome. The basic defect remains unknown, but the possibility that fibroblasts express reduced sulfation of glycosaminoglycans has been studied in several laboratories. A mechanism involving overproduction of an enzyme (nucleotide pyrophosphatase) active against adenosine 3'-phosphate, 5'-phosphosulfate (PAPS) has been postulated. Decreased synthesis of normally sulfated glycosaminoglycans was also reported. We measured the synthesis of proteoglycans and glycosaminoglycans by incorporation of [3H]glucosamine and Na2(35)SO4 into cultured fibroblasts from four LS patients and related it directly to the synthesis in six normal fibroblast cultures. We found that the rate of synthesis varied greatly among the normal cultures (cv, 30%), but not significantly between LS and the normal. The LS fibroblasts' ability to sulfate glycosaminoglycans was assayed as the amount of 3H-glycosaminoglycan eluting at low ionic strength on anion exchange chromatography, the amount of non-sulfated disaccharide present in chondroitinase digests of labeled proteoglycans, and the ratio of 35S to 3H incorporation into proteoglycans. Each parameter suggested that the LS cells were synthesizing normally sulfated glycosaminoglycans (e.g. % delta Di-0S, 21 +/- 6 in normal; 27 +/- 6 in LS). The cells' ability to sulfate glycosaminoglycans was tested under conditions of markedly stimulated glycosaminoglycan synthesis, by treating the cultures with a beta-D-xyloside. LS and normal cells responded to the treatment by elevating the rate of synthesis of normally sulfated glycosaminoglycans (3.5-6-fold in normal, 3-7-fold in LS). Nucleotide pyrophosphatase activities were found to be elevated in each of our four LS cell strains as in the previous studies, excluding genetic heterogeneity as an explanation for our findings. We conclude that LS fibroblasts do not express defects in sulfation of glycosaminoglycans or in synthesis of proteoglycans. 相似文献
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