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排序方式: 共有123条查询结果,搜索用时 19 毫秒
1.
金黄滴虫细胞核微丝系统的初步观察 总被引:2,自引:0,他引:2
金黄滴虫细胞核内经常存在着许多直径约为7nm的微丝。这些徽丝大多组合成走向不定的徽丝束,微丝束交织而成遍布核内的网架。核被下面微丝束较多,它们的存在常使核被外凸而成隆脊。核内微丝与核内结构如核仁、染色质等似乎都是相连的。有些微丝横跨核被,一端位于核内,另一端位于核周腔中,并靠近叶绿体。核周腔和内质网腔中也存在着微丝和另一种纤维,印管状纤维。用细胞松弛素B处理后,细胞核、核周腔和内质网腔中的微丝均消失,细胞核的形态也发生变化,似乎微丝网架有支持细胞核的作用。核内微丝可能是在内质网中组装,然后经核周腔进入核内的。 相似文献
2.
William D. Meek Walter L. Davis 《In vitro cellular & developmental biology. Plant》1986,22(12):725-737
Summary The potent fungal metabolite cytochalasin D (CD) and cationized ferritin (CF) are used in combination to test for negative
charge distribution on blebs (knobs). Two established human epithelial cell lines, WISH and HeLa, that display blebs in various
phases of the cell cycle or under certain culture conditions (37,46) are investigated. CD alone, applied at a low concentration
(1.0 μg/ml) and for a short time period (3 min), causes blebs to appear as the prevalent surface feature. These are filled
mainly with free ribosomes. Additionally, feltlike mats, presumed to be disorganized, compacted microfilaments, are formed
directly beneath the cell membrane. These are especially evident in the cortical cytoplasm below the blebs or bleb clusters.
CF (0.345 mg/ml), applied for a 5-min period after CD administration (1.0 μg/ml) for 3 min, appears along the surface of microvilli,
at the base of blebs, and in vesicles beneath the bleb clusters. In some cases, microfilaments (6 nm in diameter) are closely
related to the vesicles. CF does not preferentially bind to the apical cell membrane of blebs. Above areas of the subplasmalemmal
microfilaments, CF membrane binding is apparent, even under circumstances where the filaments are disorganized by cytochalasin
treatment. These results seem to show the following: (a) bleb membranes are different from the remainder of the cell and do
exhibit a loss of negative charge and (b) surface charge may be dependent on the presence or structural integrity of membrane-related
6-nm microfilaments.
The support of this research by a grant from the Baylor College of Dentistry and The Oklahoma College of Osteopathic Medicine
and Surgery is gratefully acknowledged. The assistance of Dr. J. H. Martin, Department of Pathology, Baylor University Medical
Center, is also greatly appreciated. 相似文献
3.
Abstract The structural polarity of statocytes from cress roots is changed by centrifugation. Upon low- dose centrifugation (3000 g min), the extent of stratification depends on statocyte position, i.e., central statocytes are affected more than lateral ones. Upon higher doses of centrifugation (60,000 and 360,000 g min), a uniform density gradient is established in all statocytes. If, after centrifugation, the roots are exposed to gravity again, the endoplasmic reticulum (ER) cisternae are relocated parallel to the periclinal cell walls within a few minutes; this relocation is independent of the direction of gravity in relation to the root axis, and independent of the previously applied centrifugation dose. This supports the notion that polarity is determined genetically. Cytochalasin B treatment, before and during centrifugation, totally inhibits the relocation of ER. After removing the drug by rinsing the roots, the statocytes restore cell polarity and relocate ER. These results indicate that relocation of ER cisternae may be mediated by microfilaments. When centrifuged roots are exposed to 1 g in the horizontal position, the latent period of gravitropism increases by 8–10 min relative to controls, regardless of the previously applied centrifugation doses. The kinetics of curvature are virtually identical. Since the increase in the latent period coincides with the time needed for most statocytes to restore the distal cell pole, it is evident that perception of gravity is correlated to the integrity of the distal cell pole. 相似文献
4.
Heide Schatten Calvin Simerly Gerd Maul Gerald Schatten 《Molecular reproduction and development》1989,23(3):309-322
Microtubule assembly is required for the formation of the male and female pronuclei during mouse, but not sea urchin, fertilization. In mouse oocytes, 50 μM colcemid prevents the decondensation of the maternal meiotic chromosomes and of the incorporated sperm nucleus during in vitro fertilization. Nuclear lamins do not associate with either of the parental chromatin sets although peripherin, the PI nuclear peripheral antigen, appears on both. DN A synthesis docs not occur in these fertilized, colcemid-arrested oocytes. This effect is limited to the first hours after ovulation, since colcemid added 4–6 hours later no longer prevents pronuclear development, lamin acquisition, or DNA synthesis. Neither microtubule stabilization with 10 μM taxol nor microfilament inhibition with 10 μM cytochalasin D or 2.2 μg/ml lalrunculin A prevent these pronuclear events; these drugs will inhibit the apposition of the pronuclei at the egg center. In sea urchin eggs, colcemid or griseofulvin treatment doe? not result in the same effect and the male pronucleus forms with the attendant accumulation of the nuclear lamins. The differences in the requirement for microtubule assembly during pronucleus formation may be related to the cell cycle: In mice the sperm enters a meiotic cytoplasm, whereas in sea urchin eggs it enters an interphase cytoplasm. Refertilization of mitotic sea urchin eggs was performed to test the possibility that this phenomenon is related to whether the sperm enters a meiotic/mitotic cytoplasm or one at interphase; during refertilization at first mitosis, the incorporated sperm nucleus is unable to decondense and acquire lamins. These results indicate a requirement for microtubule assembly for the progression from meiosis to first interphase during mouse fertilization and suggest that the cytoskeleton is required for changes in nuclear architecture necessary during fertilization and the cell cycle. 相似文献
5.
Cultured steroidogenic cells derived from the adrenal glands of duck embryos were used to study changes in the distribution of actin associated with the corticotropic responsiveness. Actin-containing components were identified by rhodamine-phalloidin staining. The actin in most of the unstimulated cells occurred as stress fibers that either ran parallel throughout the cell or were present as domains of parallel fibers at angles to one another. When incubated in Krebs-Henseleit buffer containing 1–24 ACTH, the cells released approximately equal amounts of corticosterone and aldosterone. Incubation of the cells in buffer containing cytochalasin D caused the cells to lose their stress fibers, and the actin became distributed at the periphery in what appeared to be fragments of stress fibers and clumps of fibrous material in the central cytoplasm. Although cytochalasin D did not affect the basal output of corticosterone and aldosterone, the 1–24 ACTH-induced rates of both hormones were suppressed significantly. After the cells had been washed in unadulterated buffer, the normal distribution of actin stress fibers was restored and the cells responded normally when incubated in buffer containing 1–24 ACTH. These results suggest that the actin components of the cytoskeleton are important determinants of corticotropin-induced steroidogenic responsiveness. 相似文献
6.
The aim of this study was to delineate the flow patterns in a non-unidirectional flow field inside a ventricle-shaped cell
culture chamber, and examine the resulting morphology and integrity of the endothelium in select regions of the monolayer.
The chamber was perfused by pulsatile flow, and the coherent motion of the fluid was studied using flow visualization aided
by image analysis. Four distinct flow patterns were discerned and examined: central jet, flow impingement, flow separation,
and recirculating eddies. The influence of these patterns on endothelial cell morphology was assessed after 20 h of exposure
to flow. There were no signs of damage to the endothelium in the jet region nor was there evidence of cell alignment with
the flow. Yet, there were changes in cell morphology and cytoskeletal architecture as compared to control. By contrast, within
the eddies where the flow was highly disturbed, there was apparent damage to the endothelium. Thus, exposure of cells to random
velocity fluctuations in regions of quasi-static flow compromises the integrity of the monolayer. Identification of such sites
and acquisition of the knowledge necessary to protect the cells from denudation will be valuable for the endothelialization
efforts of cardiac prostheses. 相似文献
7.
以蚕豆叶片下表皮条为材料,研究了微丝在气孔运动中的作用。利用肌动蛋白纤丝专一性抑制剂──细胞松弛素B(CB)预处理后,再用诱导气孔运动的因子处理表皮条,在显微镜下观测气孔孔径的变化。结果显示,用CB处理开放或关闭状态气孔,其开度均不发生变化;CB处理使微丝解聚,气孔运动被抑制;且CB处理后气孔的运动是可以恢复的。实验进一步表明,开放气孔经10mg/L的CB预处理后,ABA、Ca2+及暗诱导气孔关闭的作用均不同程度地受到抑制,推测微丝可能参与ABA、Ca2+及暗诱导的气孔关闭过程;关闭气孔经10mg/L的CB预处理后,K+和(或)光诱导气孔开放的作用受到抑制,推测微丝可能参与光及K+诱导的气孔开放过程。 相似文献
8.
P. Binarova C. Cihalikova J. Dolezel S. Gilmer L. C. Fowke 《In vitro cellular & developmental biology. Plant》1996,32(2):59-65
Summary Examination of unfixed immature somatic embryos of white spruce (Picea glauca) with fluorescent rhodamine-labeled phalloidin revealed an extensive network of fine actin microfilaments (MFs) in the embryonal
region which were not detected in specimens fixed with formaldehyde. Transition cells linking the embryonal region and suspensor
cells contained fine MFs as well as bundles of MFs. The large, highly vacuolated suspensor cells were characterized by actin
MF cables only. Treatment of embryos with cytochalasin B (CB) removed the fine MFs from the embryonal region and transition
cells, but many MF cables in suspensor cells were resistant. Full recovery from CB treatment was observed in most somatic
embryos. Embryogenic protoplasts capable of regenerating to somatic embryos in culture were released from only the embryonal
region of somatic embryos. Both uninucleate and multinucleate embryogenic protoplasts retained the extensive network of fine
actin MFs. In contrast, protoplasts derived from vacuolated suspensor cells and vacuolated free-floating cells contained thick
MF bundles and were not embryogenic. Distinct MF cages enclosed nuclei in multinucleate protoplasts and may be responsible
for preventing nuclear fusion. Microspectrophotometric analyses showed that the DNA contents of embryonal cells in the embryo
and embryogenic protoplasts were similar and characteristic of rapidly dividing cell populations. However, transition and
suspensor cells which released nonembryogenic protoplasts appeared to be arrested in G1, and suspensor cells showed signs of DNA degradation. 相似文献
9.
This is the first report of intranuclear microfilaments within gametangial nuclei of oömycetous fungi. Longitudinal sections of four to six microfilaments were frequently observed in meiotic antheridial nuclei of Achlya ambisexualis. Each microfilament measured approximately 7–10 nm in diameter. Spindle tubules (25 nm in diameter) were also observed within some of the nuclei possessing microfilaments. 相似文献
10.