ArticleProtoplasma2026
Ultrastructural characterization of secretory canals in Peucedanum praeruptorum roots using microscopic sectioning, transmission electron microscopy, and computed tomography.
Article in Protoplasma, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Plant secondary metabolites are mainly synthesized and stored in secretory tissues. Secretory canal development has been mainly characterized in Apiaceae. The secretory canals of Peucedanum praeruptorum contain pharmacologically active coumarins, but their organ-specific distribution and developmental dynamics remain poorly understood. This study integrated light microscopy (LM), transmission electron microscopy (TEM), X-ray microcomputed tomography (µ-CT), and high-performance liquid chromatography (HPLC) to investigate canal development, distribution, ultrastructure, 3D architecture, and coumarin accumulation in P. praeruptorum roots. Histological analysis showed that canals adjacent to the periderm originate from pericycle cells, whereas those in secondary phloem arise from parenchyma differentiation; both develop schizogenously. Canal quantity and dimensions varied temporally. Canals located in phloem showed density increasing toward the cambial zone, where cross-sectional areas were smaller. The canal density index increased from September to November, peaking on November 15, then declined. HPLC revealed dynamic accumulation of five major coumarins: content increased from September, peaked on November 15, then gradually decreased. TEM showed that epithelial cells surrounding the canal lumen were rich in Golgi, ER, mitochondria, plastids, starch grains, and osmiophilic droplets. µ-CT volumetric analysis and segmentation generated detailed 3D models, revealing spatial organization and enabling size-based grouping of canals (1000-3000 μm). These dimensional characteristics aligned with developmental progression. This study characterizes the ontogeny, distribution, ultrastructure, and 3D architecture of secretory canals, providing a structural foundation for investigating correlations between secretory tissues and compound synthesis.
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