Plasmodesmata display dynamic local and systemic redox responses during plant stress

Clicks: 2
ID: 318223
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #294 of 310 articles by views in The Plant cell

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 310 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Hydrogen peroxide (H2O2) is a potent reactive oxygen species (ROS) that plays a crucial role as a versatile signaling molecule for cellular function and vitality. Recent experimental evidence indicates that H2O2 affects cell-to-cell communication through plasmodesmata, tiny cytoplasmic nanopores connecting adjacent plant cells. H2O2-dependent systemic signaling has also been reported to involve plasmodesmal function in some contexts, although the dominant routes and messengers underlying rapid long-distance signaling remain under active debate. Nevertheless, direct monitoring of redox dynamics at plasmodesmata in live tissues has remained challenging. In this study, we developed a plasmodesmata-localized HyPer7 (Pd-HyPer7) reporter to investigate H2O2 dynamics at plasmodesmata in response to exogenous redox stressors and plant stresses, including cold and mechanical wounding. Pd-HyPer7 showed response characteristics that differed from the HyPer7 reporters localized to the cytosol, plasma membrane, and chloroplasts under the conditions tested, indicating that redox responses at plasmodesmata are distinguishable from these compartments. Notably, during mechanical wounding, both the cytosol and plasmodesmata showed transient redox responses with broadly similar temporal profiles in local tissues. In systemic tissues, however, the responses were temporally separated, with plasmodesmal oxidation peaking well after the cytosolic response. This timing relationship is consistent with plasmodesmata acting downstream of early systemic wound signaling, rather than simply mirroring cytosolic redox dynamics. Together, our results establish Pd-HyPer7 as a tool for monitoring plasmodesmal redox dynamics and support a model in which plasmodesmata participate in spatially and temporally regulated redox responses during plant stress.
Reference Key
openalex_W7165591212 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Niraj Kumar Vishwakarma, Md Abdur Razzak, Vishnu Mishra, Timothy Chaya, Jeffrey L. Caplan, Jung‐Youn Lee
Journal The Plant cell
Year 2026
DOI
10.1093/plcell/koag192
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.