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Summary In order to demonstrate the presence of a Ca2+-activated Cl–-channel in theNitellopsis plasmalemma, tonoplast-free cells were prepared and their intracellular Ca2+ concentration was modified by internal perfusion. An increase in the Ca2+ concentration caused a large Cl– efflux with a concomitant depolarization of the membrane potential. These changes were for the most part reversible. The critical Ca2+ concentration was about 4.0 m. Neither the Cl– efflux nor the membrane depolarization showed a time-dependent inactivation. A Cl–-channel blocker, A-9-C (9-anthracenecarboxylic acid) reduced both the Cl– efflux and the magnitude of the membrane potential depolarization. A small increase in the intracellular Ca2+ concentration, which is caused by membrane excitation of tonoplast-free cells is not sufficient to activate this Ca2+-dependent Cl–-channel. 相似文献
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Eiji Kumazawa Akiko Tohgo Tsunehiko Soga Tsuneo Kusama Yasuaki Osada 《Cancer immunology, immunotherapy : CII》1992,35(5):307-314
Summary The antitumor effect of a synthetic lipid A analogue, DT-5461, was investigated using syngeneic tumor models in mice. Intravenous injection of DT-5461 into mice transplanted with solid tumors of MethA fibrosarcoma, MH134 hepatoma, MM46 mammary carcinoma, Lewis lung carcinoma (3LL), and colon adenocarcinomas 26 and 38 resulted in significant reductions in the weight of all tumors except Colon 26, with marked hemorrhagic necrosis of tumor tissues. Efficacy was almost equal to that of anEscherichia coli-type synthetic lipid A (compound 506), and also to those of some chemotherapeutics including Adriamycin, mitomycin C, fluorouracil and cisplatin. Furthermore, DT-5461 was more effective than other immunotherapeutics, including picibanil (OK-432) and lentinan. However, its antitumor effects were inferior to those of Adriamycin or OK-432 against the malignant ascites caused by intraperitoneal inoculation with MethA or with MH134 cells; life span was not prolonged by either intraperitoneal or intravenous administration. In addition, although DT-5461 showed direct inhibitory effects on the in vitro growth of MethA or MH134, these were much weaker than those of Adriamycin. These findings clearly indicated that DT-5461 with systemic administration is a highly effective antitumor agent on solid tumors, and suggest that the antitumor effect of DT-5461 with potent necrotizing activity might derive from indirect mechanisms related to the activation of host immune systems and not to the weak direct cytotoxicity. 相似文献
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Tominaga Yoshito; Kuchitsu Kazuyuki; Katsuhara Maki; Tazawa Masashi; Miyachi Shigetoh 《Plant & cell physiology》1991,32(2):261-268
Rotational streaming of the cytoplasm including chloroplastswas induced by L-histidine, as well as by light, on the anticlinalface of leaf cells of Egeria densa. In the case of treatmentwith L-histidine some of the chloroplasts remained stationaryon the periclinal face of cells after rotational cytoplasmicstreaming was initiated. However, these chloroplasts were easilydislodged and translocated to the centrifugal end of the histidine-treatedcells by application of a centrifugal force that barely affectedthe location of chloroplasts in cells incubated in the darkwithout L-histidine. This result indicates that the anchoringof chloroplasts was weakened by L-histidine. Thus only the releaseof chloroplasts from anchoring was not enough for initiationof their streaming. The cytoplasmic pH (pHc) and vacuolar pH(pHv) were noninvasively monitored by in vivo 31P-nuclear magneticresonance (NMR) spectroscopy. Compared with the dark controlvalue, both illumination and treatment with L-histidine increasedthe pHc by 0.3 units. In contrast, pHv changed only a littlewith both illumination and treatment with L-histidine. Releaseof chloroplasts from anchoring and initiation of cytoplasmicstreaming are discussed in relation to the increase in pHc inducedby both light and L-histidine.
4 Present address: Department of Cell Biology, National Instituteof Agrobiological Resources, Kannondai, Tsukuba, Ibaraki, 305Japan
5 Present address: Marine Biotechnology Institute Co., Ltd.,Head Office, 2-35-10 Hongo, Bunkyo-ku, Tokyo, 113 Japan (Received July 16, 1990; Accepted December 20, 1990) 相似文献
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Internodal cells of Chara australis were subjected to two consecutiveintracellular perfusions with a Ca2+-free EGTA medium whichdisintegrated the tonoplast within about 10 minutes and thenwith a Ca2+-buffered medium. All perfusion media usually contained1 mM ATP. To stop the electrogenic pump, the internode was depletedof intracellular ATP. The excitability of the plasmalemma wasnot significantly influenced by intracellular free Ca2+ concentrationsup to 104 M. To trigger action potentials, minimum currentdensities of 1 to 2 µA cm2 had to be applied atall tested Ca2+ concentrations. In the absence of cytoplasmicATP, excitability was completely lost at all Ca2+ concentrations.
1 Present address: Botanisches Institut der Universit?t Bonn,Venusbergweg 22, D-5300 Bonn, FRG. (Received September 22, 1984; Accepted March 6, 1985) 相似文献
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Ionic Activity Gradients across the Surface Membrane of Cytoplasmic Droplets Prepared from Chara australis 总被引:1,自引:0,他引:1
The membrane potential and the ionic activity gradients of K+and Cl across the surface membrane of cytoplasmic dropletsprepared from Chara australis internodal cells, were measuredin high and low ionic strength bathing solutions using liquidion exchange microelectrodes selective for K+ and Cl.Our results indicate that K+ is close to electrochemical equilibriumwhereas Cl is not.
1 Present address: ICI Japan, Palace Hotel Annex Building, Marunouchi,Tokyo, Japan. 相似文献
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Soichi Kojima Wakako Soga Hiromi Hagiwara Motoyuki Shimonaka Yuji Saito Yuji Inada 《Bioscience reports》1986,6(12):1029-1033
We have succeeded in corroborating the enhancing effect of vitamin A, vitamin C, sitosterol and fucosterol on the fibrinolytic activity of endothelial cells. The assay system consisted of anin situ dissolution of a fibrin layer coated onto a culture dish, over which endothelial cells were grown in a culture medium containing 10 % serum. The dissolution was enhanced by the addition of these vitamins and phytosterols to the culture medium.To whom correspondence should be addressed. 相似文献
9.
Development of human pancreas 总被引:2,自引:0,他引:2
Masashi Fukayama Michio Ogawa Yukiko Hayashi Morio Koike 《Differentiation; research in biological diversity》1986,31(2):127-133
The developmental sequence of human pancreatic secretory proteins has not previously been studied in detail. We applied immunohistochemistry to study 20 fetal and neonatal pancreas' (8th to 39th gestational weeks) using antisera against the following pancreatic secretory proteins: pancreatic secretory trypsin inhibitor (PSTI), serine proteinases (trypsin, chymotrypsin, and elastase I), and amylase. PSTI was first detected in developing buds of the pancreas during the 8th gestational week, and proteinases were observed in acinar cells during the 14th week of gestation. Immunoreactivity for both PSTI and proteinases was found in most acinar cells soon after their appearance. Immunoreactivity for amylase could not be detected in fetal or neonatal pancreas tissue. PSTI was also found in developing islets during the 14th gestational week, but the number of immunoreactive cells had decreased by term. Cells positive for serine proteinases were occasionally in contact with islets in second-trimester fetuses. In discussing these results, we give particular attention to the nonparallel appearance of secretory products in the fetal pancreas, and the significance of cells immunoreactive for secretory proteins in endocrine islets. 相似文献
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