2013
DOI: 10.1007/s11738-013-1235-8
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Immunogold method evidences that kinesin and myosin bind to and couple microtubules and actin filaments in lipotubuloids of Ornithogalum umbellatum ovary epidermis

Abstract: Lipotubuloids in ovary epidermis of Ornithogalum umbellatum which are a domain of cytoplasm containing a lot of lipid bodies, microtubules and actin filaments, ribosomes, endoplasmic reticulum as well as scarce mitochondria, microbodies, dictyosomes, autolytic vacuoles, exhibit progressive-rotary motion. The immunogold method demonstrated that microtubules and actin filaments of lipotubuloids might be connected with one another by myosin and kinesin. It was supposed that collaboration of motor proteins with ac… Show more

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Cited by 6 publications
(7 citation statements)
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“…The fact that lipotubuloids are able to move in a cell together with the cytoplasm streaming (progressive movement) as well as dynamically, autonomously rotate with a speed sixfold greater than that of cyclosis (Kwiatkowska 1972b ; Kwiatkowska et al 2009 ), undoubtedly facilitates cutinsome release from lipotubuloids and their subsequent transport to a cell wall. Our latest immunogold studies seemed to show that the lipotubuloid’s ability to rotate autonomously resulted from the fact that kinesin and myosin formed the link between microtubules and actin filaments in lipotubuloids (Kwiatkowska et al 2013 ).…”
Section: Discussionmentioning
confidence: 99%
“…The fact that lipotubuloids are able to move in a cell together with the cytoplasm streaming (progressive movement) as well as dynamically, autonomously rotate with a speed sixfold greater than that of cyclosis (Kwiatkowska 1972b ; Kwiatkowska et al 2009 ), undoubtedly facilitates cutinsome release from lipotubuloids and their subsequent transport to a cell wall. Our latest immunogold studies seemed to show that the lipotubuloid’s ability to rotate autonomously resulted from the fact that kinesin and myosin formed the link between microtubules and actin filaments in lipotubuloids (Kwiatkowska et al 2013 ).…”
Section: Discussionmentioning
confidence: 99%
“…Sections were treated with 10% hydrogen peroxide for 15 min to remove osmium and washed in distilled water and in phosphatebuffered saline (PBS) buffer (0.01 M, pH 7.4) (Kwiatkowska et al, 2013). Samples were then blocked with small drops of PBS buffer containing 3% bovine serum albumin for 1 h at room temperature and later washed three times in PBS buffer.…”
Section: Tissue Sectioning and Immunolabeling For Temmentioning
confidence: 99%
“…They are rich in ribosomes forming numerous polysomes and rough endoplasmic reticulum (RER). Moreover, they contain numerous lipid bodies entwined with microtubules, which in turn are connected by myosin and kinesin to actin filaments (Kwiatkowska et al, 2013). In LMs, there are also very few mitochondria, Golgi structures, or microbodies (peroxisomes and glyoxysomes).…”
Section: Structure and Function Of Lipotubuloids As Lmsmentioning
confidence: 99%