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981.
Summary— The clonal rat rhabdomyosarcoma cell line BA-HAN-IC is composed of proliferating mononuclear cells, some of which spontaneously fuse to terminally differentiated myotube-like giant cells. This cell line has been shown to be susceptible to differentiation induction with all-trans retinoic acid (RA). Since it is still unknown whether exclusively all-trans RA itself or also its metabolites can act as inductive compounds in our cell line, we exposed BA-HAN-1C cells to the metabolites 4-hydroxy RA, 4-oxo RA and 5,6epoxy RA. Exposure to these RA metabolites resulted in a significant inhibition of proliferation (P < 0.001) and induction of cellular differentiation, as evidenced by a significant increase in the number of myotube-like giant cells (P < 0.05) and a significant increase in creatine kinase activity (P < 0.05). However, differences in the inductive potency of these RA metabolites became apparent. Furthermore, RA metabolites exhibited a significantly weaker (P < 0.05) inductive activity when compared to all-trans RA. Summarizing our results we could demonstrate that the endogenous metabolites 4-hydroxy RA, 4-oxo RA and 5,6-epoxy RA are not merely deactivated cellular excretion products of all-trans RA, but potent inducers of differentiation and inhibitors of proliferation, possibly contributing to the complex physiological actions of retinoic acid.  相似文献   
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983.
A study was made to find a better method of analyzing the glutamate pool in seaweeds than the use of HPLC, which provides unsatisfactory results with material rich in alginates and salts. A method recommended elsewhere (Inglis A, Bartone N, Finlayson J, 1988, J. Biochem. Biophys. Methods 15: 249–254) for physiological fluids has been assayed and improved for algal samples. It consisted of the addition of lithium acetate before the phenylisothiocyanate derivatization, omission of one drying step and extraction of the derivative with heptane before chromatographic analysis. Neither salt nor alginates interfered with analysis.  相似文献   
984.
The ultrastructure of the atmophytic lime-encrusted filamentous blue-green algaScytonema julianum (Frank) Richter which grows in caves, is studied here for the first time. The cytology of this organism is compared with that of another filamentous and lime-encrusted cyanophycea,Geitleria calcarea Friedmann, which grows in the same biotope. The authors also discuss the nomenclature of this quite rare species.
Ultrastructure d'une cyanophycée aérienne calcifiée cavernicole:Scytonema julianum (Frank) Richter (Hormogonophycideae, Nostocales, Scytonemataceae)
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985.
Two-phase systems consisting of water, dextran and poly(ethylene glycol) have been used for partition of membranes obtained from Torpedo marmorata electric organ. The partition behaviour of the membranes could be adjusted by using a polymer with covalently-bound charged groups. By using this method, the membranes were divided into several fractions which were analyzed for nicotinic acetylcholine receptor and acetylcholinesterase content. It was found that nicotinic receptor-enriched membranes were separated from those containing esterase in a single partition step. Receptor-enriched membranes obtained by gradient centrifugation could be further separated into two receptor fractions by the two-phase technique. The results also reveal at least two types of acetylcholinesterase-rich membranes.  相似文献   
986.
For various reasons, but mainly because of reproductional constraints, cirriped arthropods have evolved less secondary soft bottom dwellers than other sessile groups of organisms. Presented examples are (1) a modern balanid that lives commensally on a small burrowing bivalve and (2) the Cretaceoous /EoceneWaiparaconus, wich is re-established as a lepadomorph whose peduncle has become transformed into a solid, horn shaped anchoring device.  相似文献   
987.
Characteristics of human chondrocyte cultures in completely defined medium   总被引:1,自引:0,他引:1  
Summary Chondrocytes derived from normal human adult articular cartilage were established and maintained for over 5 months in a completely defined medium without the addition of serum or any other growth factors. At the end of 5 months, these cells were still metabolically active. The cells incorporated [3H]thymidine into DNA, incorporated [35S]sulfate into proteoglycans, and exhibited lysosomal enzyme activities. The35S-labeled proteoglycans isolated from the culture medium had elution profiles on high pressure liquid chromatography (HPCL) similar to those observed from proteoglycans from other mammalian sources. This self-contained growth competence may reflect a need produced by the unusual avascular and alymphatic character of articular cartilage. This research was supported, in part, by Grant AM22057 from the National Institutes of Health, Bethesda, MD.  相似文献   
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