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The ultrastructure of the tegumental cytoskeleton of Fasciola hepatica has been examined following various extraction fixations. Microtubules were found throughout the tegument. They run parallel to the basal and apical tegumental borders, and have a pre-dominant basal-to-apical orientation in the central parts of the distal cytoplasm. Microtubules are also found in the cytoplasmic bridges which connect the distal and perikaryal tegumental parts.
Changes in the microtubular cytoskeleton of Dactylorhiza majalis (Rchb.) Hunt et Summerh. (Orchidaceae) during microsporogenesis were investigated by the immunofluorescence method. Dactylorhiza microsporocytes in microsporangia divide into tetrads after a regular meiosis, which is completed with simultaneous cytokinesis. Three typical configurations of the microtubular cytoskeleton appear during microsporogenesis: the microtubular system in the cytoplasm and at the nuclear envelope, meiotic spindles, and phragmoplasts. Microtubules of the early prophase I microsporocyte are dispersed throughout the cortical cytoplasm, and later the arrays of microtubules are visible at the nuclear envelope. During metaphase I, the microtubules form the spindle which also acts during anaphase I. At telophase I, interzonal microtubules of the first meiotic spindle disappear, and new microtubular arrays extend from the nuclei towards the equatorial plane of the microsporocyte. There, these microtubules form the phragmoplast, which disintegrates before the second meiotic division. During the second meiotic division, the microtubular cytoskeleton repeats the configurations from the first meiotic division. The microtubular arrays emanating from the telophase II nuclei form interconnections of all non-sister and sister nuclei. During the formation of the cell plates between the future microspores, these microtubular arrays disappear. The results support the view that cytoskeletal configurations participate in the formation of the nuclear-cytoplasmic domains of the dividing microsporocyte in its transition from mononucleate microsporocyte to undivided dyad, and to four microspore domains after the second meiotic division.
A detailed description of the fine structure of Balantidium ctenopharyngodoni Chen, 1955 with an emphasis on its vestibulum is given in the present paper. As to the vestibular kinetids, special attention is paid to the characters of T1, T2 microtubules and nematodesmata. Serving as the major skeleton to the vestibular cortex, the T1, T2 and Pc microtubules are described herein and their support function is also discussed. Moreover, the well-developed nematodesmata of the vestibular kinetids that form a large basket-like complex are described in detail.
The microtubular cytoskeleton in dividing microsporocytes and developing pollen grains of Gagea lutea (L.) Ker.-Gaw. (Liliaceae) was investigated with a modified indirect immunofluorescence method. Meiotic and mitotic stages were identified by DAPI staining. The microtubular cytoskeleton was compared in plants originating from natural localities and others grown in the laboratory. In natural conditions, microsporocytes and pollen grains of wild early-spring Gagea lutea plants are subjected to abiotic factors including cold exposure and lack of water. The persistent influence of these factors can disturb microtubular cytoskeleton functioning. The following disturbances were observed in the course of microsporogenesis and pollen development: abnormal chromosome configurations in the metaphase of meiosis I; abnormally divided dyads with irregular, radial microtubule systems around the nuclei; the formation of differently sized microspores with irregular shapes, and irregular division; and the formation of pollen grains with vacuoles abnormal for their development stage. Similar kinds of disturbances were observed after 1.5 months of cold treatment (4°C) and drying in the laboratory. These abiotic factors simulated in laboratory conditions caused more disturbances in the course of microsporogenesis and produced more frequent defective pollen grains than in the sample that had experienced cold and drying in natural conditions.
This study investigated patterns of cytoskeletal organization during microsporogenesis in Chondrilla juncea L., an autonomous apomict with a triploid chromosome number (2n = 15). The distribution of microtubules and organelles is not typical. The microtubules do not form a normal phragmoplast and consequently the organelle equatorial plate observed in many taxons is not present. The organelles are dispersed randomly in both the central and peripheral parts of the cytoplasm.
The distribution of plastids at the time of microspore and pollen grain development in Gagea lutea (L.) Ker.-Gaw. was analyzed using electron microscopy. It was shown that plastids are not transmitted to the forming generative cell of this species during microspore division. At the vacuolate microspore stage, preceding division, the microspore nucleus takes an acentric position and the plastids gather at the opposite side of the cell. In the highly polarized microspore at prophase of mitosis, all plastids are aggregated at one side of the nucleus, whereas mitochondria are dispersed throughout the cytoplasm. Numerous profiles of endoplasmic reticulum (ER) are present between the clustered plastids. Some of the ER profiles are attached by their ends to the outer membrane of plastid envelopes and join the distant plastids. The outer membrane of the microspore plastids may form long and thin evaginations contacting with other plastids. Microtubules are visible in plastid aggregations occasionally. In dividing microspores, long ER cisterns surround the area of the mitotic spindle and separate it from the region containing plastids. There are no plastids in the young generative cell: all plastids remain clustered in the region of the microspore that now forms the vegetative cell of the bicellular pollen grain. Later the connections between plastids and ER cisterns gradually disappear and plastids disperse in the cytoplasm of the whole vegetative cell. The results of our study are not sufficient to define the mechanism causing selective aggregation of plastids at the vegetative pole of the Gagea microspore, nor to say whether the microtubular cytoskeleton plays a role. However, the participation of ER in these processes, at least in holding the special arrangement of microspore plastids, seems certain.
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