1985
DOI: 10.1002/j.1537-2197.1985.tb08386.x
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Actin Network as a Normal Component of the Cytoskeleton in Many Vascular Plant Cells

Abstract: F‐actin was localized in cells of 17 species of vascular plants, using the F‐actin‐specific probe Rhodamine‐phalloidin. F‐actin strands formed a three‐dimensional network in these cells, and orientation of the strands varied to some extent depending on the cell shape. The strands often appeared to terminate near or at the plasma membrane. The observations presented, taken together with those from relevant literature, suggest that actin is a normal component of most, if not all, plant cells.

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Cited by 107 publications
(31 citation statements)
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“…However, details on the association between actin filaments and the nucleus are not yet known. The use of fluorescent-labelled phallotoxins revealed that actin filaments were present near the nucleus in the cells of various plants [2,10,11] including statocytes [5]. However, it was not easy to discern a physical connection.…”
Section: Discussionmentioning
confidence: 99%
“…However, details on the association between actin filaments and the nucleus are not yet known. The use of fluorescent-labelled phallotoxins revealed that actin filaments were present near the nucleus in the cells of various plants [2,10,11] including statocytes [5]. However, it was not easy to discern a physical connection.…”
Section: Discussionmentioning
confidence: 99%
“…These actin bundles are large, containing 50 to 100 microfilaments (Nagai and Rebhun, 1966) of uniform polarity (Palevitz and Hepler, 1975) in ordered, paracrystalline arrays (Nagai and Hayama, 1979). The bundles are also highly stable being resistant to breakdown during treatment with cytochalasin or during fixation with glutaraldehyde (Williamson, 1978), processes that disrupt actin filaments in other plants (Parthasarathy et al, 1985). The organisation and maintenance of actin bundles presumably requires the presence of one or several actin-bundling proteins.…”
Section: Introductionmentioning
confidence: 99%
“…Because MFs are colocalized with MTs in certain cases, and cytochalasin D (CD) interferes with the maturation of some MT arrays [Menzel and Schliwa, 1986;Kakimoto and Shibaoka, 1987;Lloyd et al, 1987;Palevitz, 1987a,b;Uyeda and Furuya, 1987;Traas et al, 1987;Kobayashi 0 1991 Wiley-Liss, Inc. Menzel and Elsner-Menzel, 1989;Pierson et al, 1989;Serlin and Ferrell, 1989;Traas et al, 19891, organizational interactions between the two seem likely. Recently, based on the presence of associated MTs during cytokinesis, it has been proposed that the nuclear envelope (NE) serves as the initiation site for the interphase array [Clayton et al, 1985;Wick, 1985al (MFs are also associated with the NE during the cell cycle [e.g., Parthasarathy et al, 1985;Palevitz, 1987a; 7-day-old cell suspension were transferred to 95 ml of fresh medium and the suspension was then incubated for 24 hr with the addition of 5 pg/ml aphidicolin (Sigma Chemical Co., St. Louis, MO). The cells were then collected by sedimentation, washed with 10 volumes of fresh medium using a glass filter, and resuspended and cultured further in fresh medium.…”
Section: Introductionmentioning
confidence: 99%