Matches in SemOpenAlex for { <https://semopenalex.org/work/W2036783366> ?p ?o ?g. }
- W2036783366 endingPage "630" @default.
- W2036783366 startingPage "615" @default.
- W2036783366 abstract "An analysis of the epithelial cell ultrastructure of secretory ducts in the primary phloem of Rhus toxicodendron was performed quantitatively using stereological techniques. The quantitative parameters were volume densities and absolute volumes per cell of nine epithelial cell components. The linear dimensions, individual volumes, and total numbers of plastids, mitochondria, peroxisomes, and Golgi zones were also calculated. In addition, the surface densities of membranes were calculated for plastids, mitochondria, and rough ER (RER) and smooth ER (SER). Parameters of the Golgi apparatus and frequencies of cytoplasmic, plastid, and mitochondrial ribosomes, as well as the frequencies of plasmodesmata, were also determined. Four stages of epithelial cell development were recognized, i.e., procambial, RER, SER, and postsecretory stages. Epithelial cells begin secretion at the procambial stage, together with the differentiation of the first elements of the protophloem and protoxylem. At this stage they contain well‐developed SER and RER and a hypersecretory Golgi apparatus. The RER stage is marked by the proliferation of the RER cisternae and an increase in the number of dictyosomes and Golgi vesicles. Tubular SER becomes a dominant cell component at the next stage. The surface area of its membranes per cell is 6.5 times larger than that of membranes of plastids and mitochondria combined and similar to that of steroidogenic animal cells. There is also a proliferation of peroxisomes at this stage. The leucoplasts of epithelial cells appear to be blocked in their development. At the postsecretory stage, the epithelial cells become highly vacuolated and lose any signs of secretory activity. I conclude that the RER and Golgi apparatus are involved in glycoprotein secretion, which occurs by means of exocytosis of large granular vesicles. The SER is the main component responsible for terpene synthesis and intracellular transport. Peroxisomes are proposed to be involved in the regulation of terpene synthesis, which is most active in the third stage. Plastids do not appear to participate actively in the secretory processes. Before segregation within the canal, secretory glycoproteins and terpenoids are accumulated in the extraplasmic phase of the cytoplasm, i.e., in the intermembraneous spaces of the Golgi apparatus, ER, mitochondria, and plastids, rather than in the protoplasmic phase (cytosol and organelle’s matrix). The synthesis of glycoproteins and terpenes occurs at all three stages of secretion, though the rate of glycoprotein production is highest at the second stage, while terpene synthesis is maximal at the third stage." @default.
- W2036783366 created "2016-06-24" @default.
- W2036783366 creator A5052608127 @default.
- W2036783366 date "2000-07-01" @default.
- W2036783366 modified "2023-09-25" @default.
- W2036783366 title "Quantitative Ultrastructural Data of Secretory Duct Epithelial Cells in <i>Rhus toxicodendron</i>" @default.
- W2036783366 cites W1528760252 @default.
- W2036783366 cites W1966146364 @default.
- W2036783366 cites W1966988636 @default.
- W2036783366 cites W1973535199 @default.
- W2036783366 cites W1985593477 @default.
- W2036783366 cites W1993495322 @default.
- W2036783366 cites W1996694105 @default.
- W2036783366 cites W2002316663 @default.
- W2036783366 cites W2004338398 @default.
- W2036783366 cites W2005783040 @default.
- W2036783366 cites W2006816772 @default.
- W2036783366 cites W2009854160 @default.
- W2036783366 cites W2027171464 @default.
- W2036783366 cites W2032396761 @default.
- W2036783366 cites W2034101766 @default.
- W2036783366 cites W2035547390 @default.
- W2036783366 cites W2041532767 @default.
- W2036783366 cites W2053201199 @default.
- W2036783366 cites W2053785195 @default.
- W2036783366 cites W2053790022 @default.
- W2036783366 cites W2060697628 @default.
- W2036783366 cites W2063134378 @default.
- W2036783366 cites W2065973473 @default.
- W2036783366 cites W2071838542 @default.
- W2036783366 cites W2072844774 @default.
- W2036783366 cites W2076651414 @default.
- W2036783366 cites W2081770121 @default.
- W2036783366 cites W2083216590 @default.
- W2036783366 cites W2092423868 @default.
- W2036783366 cites W2170955721 @default.
- W2036783366 cites W2171128695 @default.
- W2036783366 cites W2176603852 @default.
- W2036783366 cites W2269724892 @default.
- W2036783366 cites W2275031561 @default.
- W2036783366 cites W2337086300 @default.
- W2036783366 cites W2594218414 @default.
- W2036783366 cites W2795851934 @default.
- W2036783366 cites W2795923765 @default.
- W2036783366 cites W2913156532 @default.
- W2036783366 cites W292860081 @default.
- W2036783366 cites W4239206045 @default.
- W2036783366 cites W4246706866 @default.
- W2036783366 cites W4251695548 @default.
- W2036783366 cites W1981057203 @default.
- W2036783366 doi "https://doi.org/10.1086/314288" @default.
- W2036783366 hasPublicationYear "2000" @default.
- W2036783366 type Work @default.
- W2036783366 sameAs 2036783366 @default.
- W2036783366 citedByCount "23" @default.
- W2036783366 countsByYear W20367833662012 @default.
- W2036783366 countsByYear W20367833662016 @default.
- W2036783366 countsByYear W20367833662017 @default.
- W2036783366 countsByYear W20367833662018 @default.
- W2036783366 countsByYear W20367833662019 @default.
- W2036783366 countsByYear W20367833662020 @default.
- W2036783366 countsByYear W20367833662021 @default.
- W2036783366 countsByYear W20367833662022 @default.
- W2036783366 crossrefType "journal-article" @default.
- W2036783366 hasAuthorship W2036783366A5052608127 @default.
- W2036783366 hasConcept C104317684 @default.
- W2036783366 hasConcept C119062480 @default.
- W2036783366 hasConcept C127078168 @default.
- W2036783366 hasConcept C130316041 @default.
- W2036783366 hasConcept C1491633281 @default.
- W2036783366 hasConcept C158617107 @default.
- W2036783366 hasConcept C169727747 @default.
- W2036783366 hasConcept C176080148 @default.
- W2036783366 hasConcept C190062978 @default.
- W2036783366 hasConcept C206052861 @default.
- W2036783366 hasConcept C28859421 @default.
- W2036783366 hasConcept C41625074 @default.
- W2036783366 hasConcept C49039625 @default.
- W2036783366 hasConcept C55493867 @default.
- W2036783366 hasConcept C59822182 @default.
- W2036783366 hasConcept C69305403 @default.
- W2036783366 hasConcept C86803240 @default.
- W2036783366 hasConcept C87555872 @default.
- W2036783366 hasConcept C93829228 @default.
- W2036783366 hasConcept C95444343 @default.
- W2036783366 hasConceptScore W2036783366C104317684 @default.
- W2036783366 hasConceptScore W2036783366C119062480 @default.
- W2036783366 hasConceptScore W2036783366C127078168 @default.
- W2036783366 hasConceptScore W2036783366C130316041 @default.
- W2036783366 hasConceptScore W2036783366C1491633281 @default.
- W2036783366 hasConceptScore W2036783366C158617107 @default.
- W2036783366 hasConceptScore W2036783366C169727747 @default.
- W2036783366 hasConceptScore W2036783366C176080148 @default.
- W2036783366 hasConceptScore W2036783366C190062978 @default.
- W2036783366 hasConceptScore W2036783366C206052861 @default.
- W2036783366 hasConceptScore W2036783366C28859421 @default.
- W2036783366 hasConceptScore W2036783366C41625074 @default.
- W2036783366 hasConceptScore W2036783366C49039625 @default.