The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Wounding in the plant tissue: the defense of a dangerous passage
Open accessAbstract
Plants are continuously exposed to agents such as herbivores and environmental mechanical stresses that cause wounding and open the way to the invasion by microbial pathogens. Wounding provides nutrients to pathogens and facilitates their entry into the tissue and subsequent infection. Plants have evolved constitutive and induced defense mechanisms to properly respond to wounding and prevent infection. The constitutive defenses are represented by physical barriers, i.e., the presence of cuticle or lignin, or by metabolites that act as toxins or deterrents for herbivores. Plants are also able to sense the injured tissue as an altered self and induce responses similar to those activated by pathogen infection. Endogenous molecules released from wounded tissue may act as Damage-Associated Molecular Patterns (DAMPs) that activate the plant innate immunity. Wound-induced responses are both rapid, such as the oxidative burst and the expression of defense-related genes, and late, such as the callose deposition, the accumulation of proteinase inhibitors and of hydrolytic enzymes (i.e., chitinases and gluganases). Typical examples of DAMPs involved in the response to wounding are the peptide systemin, and the oligogalacturonides, which are oligosaccharides released from the pectic component of the cell wall. Responses to wounding take place both at the site of damage (local response) and systemically (systemic response) and are mediated by hormones such as jasmonic acid, ethylene, salicylic acid, and abscisic acid.
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Citations
Cites
Emerging MAP kinase pathways in plant stress signalling
Nakagami, H., Pitzschke, A., & Hirt, H. (2005) · Trends in Plant Science · doi:10.1016/j.tplants.2005.05.009 · Cited by 676
Ferrari, S. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00049 · Cited by 573
Molecular Identification of a Eukaryotic, Stretch-Activated Nonselective Cation Channel
Kanzaki, M., Nagasawa, M., Kojima, I., Sato, C., Naruse, K., Sokabe, M., & Iida, H. (1999) · Science · doi:10.1126/science.285.5429.882 · Cited by 213 · cited 1×
“…and MCA2 in yeast complements the lethal effect of loss-of-function mutations in the MID1 and MID2 genes encoding stretch-activated calcium channels (Kanzaki et al., 1999; Ketela et al., 1999) and promote calcium influx upon mechanical stimulation (Nakagawa et al., 2007; Yamanaka et al., 2010).”
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Cited by
Avellan, A., Yun, J., Morais, B. P., Clement, E. T., Rodrigues, S. M., & Lowry, G. V. (2021) · Environmental Science & Technology · doi:10.1021/acs.est.1c00178 · Cited by 412
Electrical Wiring and Long-Distance Plant Communication
Hedrich, R., Salvador-Recatalà, V., & Dreyer, I. (2016) · Trends in Plant Science · doi:10.1016/j.tplants.2016.01.016 · Cited by 249
Multidimensional role of silicon to activate resilient plant growth and to mitigate abiotic stress
Mir, R. A., Bhat, B. A., Yousuf, H., Islam, S. T., Raza, A., Rizvi, M. A., Charagh, S., Albaqami, M., Sofi, P. A., & Zargar, S. M. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.819658 · Cited by 178
Specificity Influences in (1→3)-β-d-Glucan-Supported Diagnosis of Invasive Fungal Disease
Finkelman, M. A. (2020) · Journal of Fungi · doi:10.3390/jof7010014 · Cited by 76
Metadata
- Authors
- Savatin, D. V., Gramegna, G., Modesti, V., & Cervone, F.
- Venue
- Frontiers in Plant Science
- Publisher
- Frontiers Media SA
- Published
- 2014-09-16
- Volume
- 5
- Pages
- 470-470
- ISSN
- 1664-462X (ISSN-L)
- OpenAlex
- W2153154562
- Cited by
- 389
- References
- 3
- FWCI
- 19.10
- Type
- journal article
- Language
- en
- Open access
- gold
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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