2022
DOI: 10.3389/fpls.2022.971235
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Laticifer growth pattern is guided by cytoskeleton organization

Abstract: Laticifers are secretory structures that produce latex, forming a specialized defense system against herbivory. Studies using anatomical approaches to investigate laticifer growth patterns have described their origin; however, their mode of growth, i.e., whether growth is intrusive or diffuse, remains unclear. Studies investigating how cytoskeleton filaments may influence laticifer shape establishment and growth patterns are lacking. In this study, we combined microtubule immunostaining and developmental anato… Show more

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Cited by 2 publications
(3 citation statements)
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References 49 publications
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“…In other cases, pectinase and cellulase activities were related to secretion release into the duct lumen, as described in Protium [26]. The participation of the cytoskeleton has never been identified during the splitting off of the epithelial cells, but its reorganization to promote diffuse or polarized growth is well-known in several cell types [23,27]. The cytoskeleton arrangement may also be involved in the secretory process, especially in granulocrine secretion, due to its coordination of vesicle trafficking within the cell during exocytosis [28].…”
Section: Discussionmentioning
confidence: 99%
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“…In other cases, pectinase and cellulase activities were related to secretion release into the duct lumen, as described in Protium [26]. The participation of the cytoskeleton has never been identified during the splitting off of the epithelial cells, but its reorganization to promote diffuse or polarized growth is well-known in several cell types [23,27]. The cytoskeleton arrangement may also be involved in the secretory process, especially in granulocrine secretion, due to its coordination of vesicle trafficking within the cell during exocytosis [28].…”
Section: Discussionmentioning
confidence: 99%
“…The protocol of Medina et al [23] was used for microtubule labeling. Free-hand sections of shoot apices were fixed in PMET buffer (100 mM PIPES, 5 mM EGTA, 1 mM magnesium sulfate, pH 6.9) containing 0.5% glutaraldehyde, 1.5% formaldehyde fixative solution for 40 min.…”
Section: Microtubule Immunolocalizationmentioning
confidence: 99%
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