Evidence map›Paper›PMID 23969761›Full record

ArticleAnnals of botany2013

Early local differentiation of the cell wall matrix defines the contact sites in lobed mesophyll cells of Zea mays.

E Giannoutsou, P Sotiriou, P Apostolakos, B Galatis

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Article in Annals of botany, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

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17citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Novel resources to investigate leaf plasmodesmata formation in CThe Plant journal : for cell and molecular biology · 2024
    Article
  4. Auxin as an architect of the pectin matrix.Journal of experimental botany · 2023
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. CPlant, cell & environment · 2017
    Article
  15. Article
  16. Article
  17. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

E GiannoutsouDepartment of Botany, Faculty of Biology, University of Athens, Athens 15784, Greece.
P Sotiriou
P Apostolakos
B Galatis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe morphogenesis of lobed mesophyll cells (MCs) is highly controlled and coupled with intercellular space formation. Cortical microtubule rings define the number and the position of MC isthmi. This work investigated early events of MC morphogenesis, especially the mechanism defining the position of contacts between MCs. The distributions of plasmodesmata, the hemicelluloses callose and (1 → 3,1 → 4)-β-d-glucans (MLGs) and the pectin epitopes recognized by the 2F4, JIM5, JIM7 and LM6 antibodies were studied in the cell walls of Zea mays MCs.

methodsMatrix cell wall polysaccharides were immunolocalized in hand-made sections and in sections of material embedded in LR White resin. Callose was also localized using aniline blue in hand-made sections. Plasmodesmata distribution was examined by transmission electron microscopy.

resultsBefore reorganization of the dispersed cortical microtubules into microtubule rings, particular bands of the longitudinal MC walls, where the MC contacts will form, locally differentiate by selective (1) deposition of callose and the pectin epitopes recognized by the 2F4, LM6, JIM5 and JIM7 antibodies, (2) degradation of MLGs and (3) formation of secondary plasmodesmata clusterings. This cell wall matrix differentiation persists in cell contacts of mature MCs. Simultaneously, the wall bands between those of future cell contacts differentiate with (1) deposition of local cell wall thickenings including cellulose microfibrils, (2) preferential presence of MLGs, (3) absence of callose and (4) transient presence of the pectins identified by the JIM5 and JIM7 antibodies. The wall areas between cell contacts expand determinately to form the cell isthmi and the cell lobes.

conclusionsThe morphogenesis of lobed MCs is characterized by the early patterned differentiation of two distinct cell wall subdomains, defining the sites of the future MC contacts and of the future MC isthmi respectively. This patterned cell wall differentiation precedes cortical microtubule reorganization and may define microtubule ring disposition.

Indexed as

Cell DifferentiationAntibodiesCell WallEpitopesGlucansMesophyll CellsMicroscopy, Electron, TransmissionMicrotubulesPectinsPlasmodesmataPolysaccharidesSeedlingsZea maysAntibodiescalloseEpitopesGlucanshemicellulosePectinsPolysaccharidesCallosecell contactslobed cell morphogenesismicrotubulesmixed-linkage glucanspectin epitopesZea mays

Identifiers

PMID23969761
PMCPMC3783239

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.