Understanding the role of the cytoskeleton in wood formation in angiosperm trees: hybrid aspen (Populus tremula x P. tremuloides) as the model species.
Identifieur interne : 004679 ( Main/Corpus ); précédent : 004678; suivant : 004680Understanding the role of the cytoskeleton in wood formation in angiosperm trees: hybrid aspen (Populus tremula x P. tremuloides) as the model species.
Auteurs : Nigel Chaffey ; Peter Barlow ; Björn SundbergSource :
- Tree physiology [ 0829-318X ] ; 2002.
English descriptors
- KwdEn :
- Actin Cytoskeleton (physiology), Cytoskeleton (physiology), Microscopy, Confocal (MeSH), Microscopy, Fluorescence (MeSH), Microtubules (physiology), Plant Roots (growth & development), Plant Roots (ultrastructure), Plant Stems (growth & development), Plant Stems (ultrastructure), Salicaceae (growth & development), Salicaceae (physiology), Trees (growth & development), Trees (physiology), Wood (MeSH).
- MESH :
- growth & development : Plant Roots, Plant Stems, Salicaceae, Trees.
- physiology : Actin Cytoskeleton, Cytoskeleton, Microtubules, Salicaceae, Trees.
- ultrastructure : Plant Roots, Plant Stems.
- Microscopy, Confocal, Microscopy, Fluorescence, Wood.
Abstract
The involvement of microfilaments and microtubules in the development of the radial and axial components of secondary xylem (wood) in hybrid aspen (Populus tremula L. x P. tremuloides Michx.) was studied by indirect immunofluorescent localization techniques. In addition to cambial cells, the differentiated cell types considered were early- and late-wood vessel elements, axial parenchyma, normal-wood fibers and gelatinous fibers, and contact and isolation ray cells. Microfilaments were rare in ray cambial cells, but were abundant and axially arranged in their derivatives once cell elongation had begun, and persisted in that orientation in mature ray cells. Microfilaments were axially arranged in fusiform cambial cells and persisted in that orientation in all xylem derivatives of those cells. Microtubules were randomly oriented in ray and fusiform cells of the cambial zone. Dense arrays of parallel-aligned microtubules were oriented near axially in the developing gelatinous fibers, but at a wide range of angles in normal-wood fibers. Ellipses of microfilaments were associated with pit development in fiber cells and isolation ray cells. Rings of co-localized microtubules and microfilaments were associated with developing inter-vessel bordered pits and vessel-contact ray cell contact pits, and, in the case of bordered pits, these rings decreased in diameter as the over-arching pit border increased in size. Although only microtubules were seen at the periphery of the perforation plate of vessel elements, a prominent meshwork of microfilaments overlaid the perforation plate itself. A consensus view of the roles of the cytoskeleton during wood formation in angiosperm trees is presented.
DOI: 10.1093/treephys/22.4.239
PubMed: 11874720
Links to Exploration step
pubmed:11874720Le document en format XML
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<author><name sortKey="Chaffey, Nigel" sort="Chaffey, Nigel" uniqKey="Chaffey N" first="Nigel" last="Chaffey">Nigel Chaffey</name>
<affiliation><nlm:affiliation>School of Science and the Environment, Bath Spa University College, Newton Park, Newton St Loe, Bath BA2 9BN, UK. n.chaffey@bathspa.ac.uk</nlm:affiliation>
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<author><name sortKey="Barlow, Peter" sort="Barlow, Peter" uniqKey="Barlow P" first="Peter" last="Barlow">Peter Barlow</name>
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<author><name sortKey="Sundberg, Bjorn" sort="Sundberg, Bjorn" uniqKey="Sundberg B" first="Björn" last="Sundberg">Björn Sundberg</name>
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<term>Microtubules (physiology)</term>
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<term>Plant Roots (ultrastructure)</term>
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<term>Salicaceae (growth & development)</term>
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<term>Plant Stems</term>
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<front><div type="abstract" xml:lang="en">The involvement of microfilaments and microtubules in the development of the radial and axial components of secondary xylem (wood) in hybrid aspen (Populus tremula L. x P. tremuloides Michx.) was studied by indirect immunofluorescent localization techniques. In addition to cambial cells, the differentiated cell types considered were early- and late-wood vessel elements, axial parenchyma, normal-wood fibers and gelatinous fibers, and contact and isolation ray cells. Microfilaments were rare in ray cambial cells, but were abundant and axially arranged in their derivatives once cell elongation had begun, and persisted in that orientation in mature ray cells. Microfilaments were axially arranged in fusiform cambial cells and persisted in that orientation in all xylem derivatives of those cells. Microtubules were randomly oriented in ray and fusiform cells of the cambial zone. Dense arrays of parallel-aligned microtubules were oriented near axially in the developing gelatinous fibers, but at a wide range of angles in normal-wood fibers. Ellipses of microfilaments were associated with pit development in fiber cells and isolation ray cells. Rings of co-localized microtubules and microfilaments were associated with developing inter-vessel bordered pits and vessel-contact ray cell contact pits, and, in the case of bordered pits, these rings decreased in diameter as the over-arching pit border increased in size. Although only microtubules were seen at the periphery of the perforation plate of vessel elements, a prominent meshwork of microfilaments overlaid the perforation plate itself. A consensus view of the roles of the cytoskeleton during wood formation in angiosperm trees is presented.</div>
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<Title>Tree physiology</Title>
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<ArticleTitle>Understanding the role of the cytoskeleton in wood formation in angiosperm trees: hybrid aspen (Populus tremula x P. tremuloides) as the model species.</ArticleTitle>
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<Abstract><AbstractText>The involvement of microfilaments and microtubules in the development of the radial and axial components of secondary xylem (wood) in hybrid aspen (Populus tremula L. x P. tremuloides Michx.) was studied by indirect immunofluorescent localization techniques. In addition to cambial cells, the differentiated cell types considered were early- and late-wood vessel elements, axial parenchyma, normal-wood fibers and gelatinous fibers, and contact and isolation ray cells. Microfilaments were rare in ray cambial cells, but were abundant and axially arranged in their derivatives once cell elongation had begun, and persisted in that orientation in mature ray cells. Microfilaments were axially arranged in fusiform cambial cells and persisted in that orientation in all xylem derivatives of those cells. Microtubules were randomly oriented in ray and fusiform cells of the cambial zone. Dense arrays of parallel-aligned microtubules were oriented near axially in the developing gelatinous fibers, but at a wide range of angles in normal-wood fibers. Ellipses of microfilaments were associated with pit development in fiber cells and isolation ray cells. Rings of co-localized microtubules and microfilaments were associated with developing inter-vessel bordered pits and vessel-contact ray cell contact pits, and, in the case of bordered pits, these rings decreased in diameter as the over-arching pit border increased in size. Although only microtubules were seen at the periphery of the perforation plate of vessel elements, a prominent meshwork of microfilaments overlaid the perforation plate itself. A consensus view of the roles of the cytoskeleton during wood formation in angiosperm trees is presented.</AbstractText>
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