ReviewProtoplasma2026
Microscopic probing into plasmodesmata (PD) and PD-derived intercellular gateways (PdIGs): Beyond morphology.
Review in Protoplasma, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- How cells overcome egoism.Protoplasma · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Plasmodesmata (PD) are nano-channels in plant cell walls that connect adjacent cells, facilitating the symplastic transport of micro- and macromolecules. In certain tissues, specialized transport requirements drive the formation of intercellular channels in diverse morphologies, compositions and functions, including sieve plate pores, plasmodesmo-pore units, lateral sieve area pore, and flexible gateways. These channels, derived from PD, are referred to as PD-derived intercellular gateways (PdIGs) in this review. Studies of PD and PdIGs are crucial for understanding how plants achieve cell-to-cell and long-distance transport of specific cargos under various physiological conditions. Multiple types of specialized microscopy are essential for studying these nano-channels, enabling elucidating their structures, compositions, distribution patterns, frequencies, and permeability. In particular, transmission electron microscopy (TEM), scanning electron microscopy (SEM), laser scanning confocal microscopy (LSCM), and structural illumination microscopy (SIM) offer advantages for such specialized analysis. With the aid of antibodies, fluorescent dyes, custom-built molecules, and image processing technologies, microscopy can also capture dynamic details of PD/PdIGs beyond morphology features. This review examines the application of these microscopy in studying specific aspects of PD/PdIGs, discusses the merits and limitations of these methods, and evaluate their suitability in PD studying the results obtained from these microscopy studies enhance our knowledge of PD/PdIGs and form the basis of the current paradigm of PD-based plant communication.
Indexed as
Identifiers
40646286What OpenQuestion holds
Registered trials
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.