The developmental anatomy of Conopholis americana (Orobancaceae) seedlings and tubercles

1986 ◽  
Vol 64 (4) ◽  
pp. 710-717 ◽  
Author(s):  
Wm. Vance Baird ◽  
James L. Riopel
Keyword(s):  
Transition Zone ◽  
Tracheary Element ◽  
Cell Types ◽  
Tracheary Elements ◽  
Cortical Cells ◽  
Developmental Anatomy ◽  
Host Root ◽  
Parenchyma Cells ◽  
First Time ◽  
Secondary Vessels

Germinated and attached seedlings of the phanerogamic parasite Conopholis americana (L.) Wallroth are described for the first time. The morphogenetic changes which characterize the transition from seedling to preflowering tubercle, as well as the anatomy of the mature tubercle, including endogenous floral buds, are also described. Conopholis seedlings were found attached only to mycorrhizal oak roots. The primary haustorium attached to and penetrated the fungal sheath, pushing aside epidermal and cortical cells of the host as it grew toward the host stele. Cells of the endophyte contacted host xylem and differentiated directly into reticulately thickened tracheary elements. Concomitantly a cambial are of parasite origin was established within the young tubercle, aligned with the vascular cambium of the host root. The cambium of the tubercle gave rise to xylem centripetally, which differentiated into tracheary elements juxtaposed to host secondary vessels, and cortical parenchyma centrifugally. Sieve elements could not be unequivocally demonstrated in seedlings or tubercles. Tissues and cell types of the parasite could be distinguished from those of the host by both morphological and histochemical criteria. The parasite to host transition zone was characterized by direct tracheary element connections and delimited by densely cytoplasmic parasite parenchyma cells that had greatly enlarged centrally located nuclei.

scholarly journals The Anatomy of the Bark of Agathis in New Zealand

IAWA Journal ◽  
1986 ◽  
Vol 7 (3) ◽  
pp. 229-241 ◽  
Author(s):  
Lek-Lim Chan
Keyword(s):  
New Zealand ◽  
Cell Types ◽  
Cortical Cells ◽  
Phloem Parenchyma ◽  
Sieve Cells ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Long Time ◽  
Crystal Sand ◽  
Resin Canals

The anatomy of the bark of Agathis australis, which is indigenous to New Zealand, is described. The phloem cell types include sieve cells, axial and ray parenchyma, fibres and sclereids. Resin canals are found in the primary cortex, phloem and phelloderm. Large crystals are found in the lumina of some sieve cells and axial parenchyma cells, while minute crystals (crystal sand) are observed in the walls of phe1- loderm cells and complementary tissue cells. The primary cortex persists on the stem for a long time. The shape of phellem and phelloderm cells cut off by phellogen derived from cortical cells are different from those cut off by phellogen derived from phloem parenchyma cells. A trabecula was observed in a radial row of phellem cells.

Torus Structure and Development in Species of Daphne

IAWA Journal ◽  
1990 ◽  
Vol 11 (4) ◽  
pp. 401-412 ◽  
Author(s):  
Roland R. Dute ◽  
Ann E. Rushing ◽  
James W. Perry
Keyword(s):  
Tracheary Element ◽  
Tracheary Elements ◽  
Bordered Pit ◽  
Fibrillar Material ◽  
Pit Membrane ◽  
Parenchyma Cells ◽  
Daphne Odora

A torus is present in intervascular pit membranes in the wood of Daphne odora and D. cneorum, but not in D. mezereum. In the two former species, each torus is surrounded by a margo consisting of fibrillar material in a tightly woven pattern. Tori are of greater diameter than pit apertures and completely occlude the apertures during aspiration. Evidence from D. odora indicates that torus deposition is spatially associated with vesicles and a plexus of microtubules, and does not begin until pit border formation is complete. The material deposited during torus synthesis also impregnates the wall of the pre-existing pit membrane. The plasmalemma often is closely appressed to the pit membrane at the site of the developing torus. In half-bordered pit pairs between tracheary elements and parenchyma cells, a torus thickening is deposited only on the side of the tracheary element. As in Osmanthus americanus, it is hypothesised that the presence of tori in species of Daphne prevents rupture of the pit membrane during aspiration.

Initiation of adventitious root primordia in very young Pinusbanksiana seedling cuttings

1983 ◽  
Vol 13 (1) ◽  
pp. 191-195 ◽  
Author(s):  
Cheryl R. Montain ◽  
Bruce E. Haissig ◽  
John D. Curtis
Keyword(s):  
Transition Zone ◽  
Adventitious Root ◽  
Secondary Xylem ◽  
Vascular Cambium ◽  
Root Initiation ◽  
Secondary Phloem ◽  
Root Primordia ◽  
Cortical Cells ◽  
Parenchyma Cells ◽  
Resin Canals

The present work describes the anatomy of adventitious root initiation in 20-day-old Pinusbanksiana Lamb, seedling cuttings propagated under intermittent mist. Shortly after cuttings were made, basal necrosis occurred in all tissues (epidermis, periderm, cortex, primary and secondary phloem, and vascular cambium) that surrounded the central xylem cylinder. Thereafter, a relatively small "callus complex" composed of parenchyma cells, a few secondary xylem tracheids, and incompletely differentiated callus vascular cambium and periderm developed at the base of cuttings. One or sometimes two root primordia initiated in the transition zone between the lowermost cortical cells of the hypocotyl and the uppermost callus parenchyma cells. Primordia invariably arose just outside one of the four axial resin canals in the hypocotyl. Results suggested that adventitious root primordia may be initiated in P. banksiana cuttings only in association with differentiated or differentiating resin canals.

Annulate lamellae in the Sertoli cells of guinea pig testis after unilateral torsion of the spermatic cord

1984 ◽  
Vol 42 ◽  
pp. 196-197
Author(s):  
J. Chakraborty ◽  
A. P. Sinha Hikim ◽  
J. S. Jhunjhunwala
Keyword(s):  
Sertoli Cells ◽  
Guinea Pigs ◽  
Spermatic Cord ◽  
Present Report ◽  
Cell Types ◽  
Annulate Lamellae ◽  
Spermatogenic Cells ◽  
Electron Microscopic ◽  
Structural Details ◽  
First Time

Although the presence of annulate lamellae was noted in many cell types, including the rat spermatogenic cells, this structure was never reported in the Sertoli cells of any rodent species. The present report is based on a part of our project on the effect of torsion of the spermatic cord to the contralateral testis. This paper describes for the first time, the fine structural details of the annulate lamellae in the Sertoli cells of damaged testis from guinea pigs.One side of the spermatic cord of each of six Hartly strain adult guinea pigs was surgically twisted (540°) under pentobarbital anesthesia (1). Four months after induction of torsion, animals were sacrificed, testes were excised and processed for the light and electron microscopic investigations. In the damaged testis, the majority of seminiferous tubule contained a layer of Sertoli cells with occasional spermatogonia (Fig. 1). Nuclei of these Sertoli cells were highly pleomorphic and contained small chromatinic clumps adjacent to the inner aspect of the nuclear envelope (Fig. 2).

Structural aspects of tracheary element differentiation in suspension cultures of Zinnia elegans

1989 ◽  
Vol 47 ◽  
pp. 768-769
Author(s):  
C. H. Haigler ◽  
A. W. Roberts
Keyword(s):  
Tracheary Element ◽  
Vesicle Fusion ◽  
Zinnia Elegans ◽  
Cellulose Synthesis ◽  
Tracheary Elements ◽  
Animal Cells ◽  
Mesophyll Cells ◽  
Fixation Techniques ◽  
Localized Patterns ◽  
Structural Aspects

Tracheary elements, the water-conducting cells in plants, are characterized by their reinforced walls that became thickened in localized patterns during differentiation (Fig. 1). The synthesis of this localized wall involves abundant secretion of Golgi vesicles that export preformed matrix polysaccharides and putative proteins involved in cellulose synthesis. Since the cells are not growing, some kind of endocytotic process must also occur. Many researchers have commented on where exocytosis occurs in relation to the thickenings (for example, see), but they based their interpretations on chemical fixation techniques that are not likely to provide reliable information about rapid processes such as vesicle fusion. We have used rapid freezing to more accurately assess patterns of vesicle fusion in tracheary elements. We have also determined the localization of calcium, which is known to regulate vesicle fusion in plant and animal cells.Mesophyll cells were obtained from immature first leaves of Zinnia elegans var. Envy (Park Seed Co., Greenwood, S.C.) and cultured as described previously with the following exceptions: (a) concentration of benzylaminopurine in the culture medium was reduced to 0.2 mg/l and myoinositol was eliminated; and (b) 1.75ml cultures were incubated in 22 x 90mm shell vials with 112rpm rotary shaking. Cells that were actively involved in differentiation were harvested and frozen in solidifying Freon as described previously. Fractures occurred preferentially at the cell/planchet interface, which allowed us to find some excellently-preserved cells in the replicas. Other differentiating cells were incubated for 20-30 min in 10(μM CTC (Sigma), an antibiotic that fluoresces in the presence of membrane-sequestered calcium. They were observed in an Olympus BH-2 microscope equipped for epi-fluorescence (violet filter package and additional Zeiss KP560 barrier filter to block chlorophyll autofluorescence).

scholarly journals Interactome Analysis of KIN (Kin17) Shows New Functions of This Protein

2021 ◽  
Vol 43 (2) ◽  
pp. 767-781
Author(s):  
Vanessa Pinatto Gaspar ◽  
Anelise Cardoso Ramos ◽  
Philippe Cloutier ◽  
José Renato Pattaro Junior ◽  
Francisco Ferreira Duarte Junior ◽  
...  
Keyword(s):  
Dna Replication ◽  
Protein Interactions ◽  
Ribosome Biogenesis ◽  
Cell Metabolism ◽  
Cell Types ◽  
Protein Protein Interactions ◽  
Cellular Mechanisms ◽  
Cancerous Cell ◽  
First Time

KIN (Kin17) protein is overexpressed in a number of cancerous cell lines, and is therefore considered a possible cancer biomarker. It is a well-conserved protein across eukaryotes and is ubiquitously expressed in all cell types studied, suggesting an important role in the maintenance of basic cellular function which is yet to be well determined. Early studies on KIN suggested that this nuclear protein plays a role in cellular mechanisms such as DNA replication and/or repair; however, its association with chromatin depends on its methylation state. In order to provide a better understanding of the cellular role of this protein, we investigated its interactome by proximity-dependent biotin identification coupled to mass spectrometry (BioID-MS), used for identification of protein–protein interactions. Our analyses detected interaction with a novel set of proteins and reinforced previous observations linking KIN to factors involved in RNA processing, notably pre-mRNA splicing and ribosome biogenesis. However, little evidence supports that this protein is directly coupled to DNA replication and/or repair processes, as previously suggested. Furthermore, a novel interaction was observed with PRMT7 (protein arginine methyltransferase 7) and we demonstrated that KIN is modified by this enzyme. This interactome analysis indicates that KIN is associated with several cell metabolism functions, and shows for the first time an association with ribosome biogenesis, suggesting that KIN is likely a moonlight protein.

scholarly journals Morphological and Ultrastructural Characterization of Hemocytes in an Insect Model, the Hematophagous Dipetalogaster maxima (Hemiptera: Reduviidae)

Insects ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 640
Author(s):  
Natalia R. Moyetta ◽  
Fabián O. Ramos ◽  
Jimena Leyria ◽  
Lilián E. Canavoso ◽  
Leonardo L. Fruttero
Keyword(s):  
Cell Biology ◽  
Cell Types ◽  
Transmission Electron ◽  
Ultrastructural Characterization ◽  
Current Classification ◽  
Contrast Microscopy ◽  
First Time ◽  
Controversial Aspect

Hemocytes, the cells present in the hemolymph of insects and other invertebrates, perform several physiological functions, including innate immunity. The current classification of hemocyte types is based mostly on morphological features; however, divergences have emerged among specialists in triatomines, the insect vectors of Chagas’ disease (Hemiptera: Reduviidae). Here, we have combined technical approaches in order to characterize the hemocytes from fifth instar nymphs of the triatomine Dipetalogaster maxima. Moreover, in this work we describe, for the first time, the ultrastructural features of D. maxima hemocytes. Using phase contrast microscopy of fresh preparations, five hemocyte populations were identified and further characterized by immunofluorescence, flow cytometry and transmission electron microscopy. The plasmatocytes and the granulocytes were the most abundant cell types, although prohemocytes, adipohemocytes and oenocytes were also found. This work sheds light on a controversial aspect of triatomine cell biology and physiology setting the basis for future in-depth studies directed to address hemocyte classification using non-microscopy-based markers.

scholarly journals Characterization of the inositol 1,4,5-trisphosphate-induced calcium release from permeabilized endocrine cells and its inhibition by decavanadate and p-hydroxymercuribenzoate

1989 ◽  
Vol 262 (1) ◽  
pp. 83-89 ◽  
Author(s):  
K J Föhr ◽  
J Scott ◽  
G Ahnert-Hilger ◽  
M Gratzl
Keyword(s):  
Endocrine Cells ◽  
Calcium Release ◽  
Cell Types ◽  
Inhibitory Effect ◽  
Maximal Effect ◽  
Thiol Compounds ◽  
Inositol 1,4,5 Trisphosphate ◽  
Dependent Inhibition ◽  
Pheochromocytoma Pc12 ◽  
First Time

The inositol 1,4,5-trisphosphate (IP3)-sensitive Ca2+ compartment of endocrine cells was studied with alpha-toxin- and digitonin-permeabilized rat insulinoma (RINA2) and rat pheochromocytoma (PC12) cells. The Ca2+ uptake was ATP-dependent, and submicromolar concentrations of IP3 specifically released the stored Ca2+. Half-maximal Ca2+ release was observed with 0.25-0.5 mumol of IP3/l, and the amount of Ca2+ released due to IP3 could be enhanced by additional loading of the Ca2+ compartment. Consecutive additions of the same concentration of IP3 for 1-2 h always released the same amount of Ca2+ without desensitization, providing an ideal basis to further characterize the IP3-induced Ca2+ release. Here we describe for the first time a reversible inhibitory effect of decavanadate on the IP3-induced Ca2+ release. Among the vanadium species tested (decavanadate, oligovanadate and monovanadate), only decavanadate was inhibitory, with a half-maximal effect at 5 mumol/l in both cell types. The effect of decavanadate could be overcome by increasing the amount of sequestered Ca2+ or added IP3. Decavanadate did not affect the ATP-driven Ca2+ uptake but oligovanadate was inhibitory on Ca2+ uptake. p-Hydroxymercuribenzoate (pHMB) at concentrations between 10 and 30 mumol/l also inhibited the Ca2+ release due to IP3. Thiol compounds such as dithiothreitol (DTT; 1 mmol/l) added before pHMB removed all its inhibitory effect on the IP3-induced Ca2+ release, whereas the inhibition caused by decavanadate was unaffected by DTT. Thus, the decavanadate-dependent inhibition functions by a distinctly different mechanism than pHMB and could serve as a specific tool to analyse various aspects of the IP3-induced Ca2+ release within endocrine cells.

Interpolation of microtubules into cortical arrays during cell elongation and differentiation in roots of Azolla pinnata

1979 ◽  
Vol 37 (1) ◽  
pp. 411-442
Author(s):  
A.R. Hardham ◽  
B.E. Gunning
Keyword(s):  
Cell Differentiation ◽  
Cell Walls ◽  
Unit Length ◽  
Cell Types ◽  
High Rate ◽  
Wall Thickening ◽  
Cortical Microtubules ◽  
Azolla Pinnata ◽  
Outer Cortex ◽  
Cortical Cells

Longitudinal sections of roots of Azolla pinnata R. Br. were prepared for electron microscopy so that cortical microtubules could be counted along the longitudinal walls in cell files in the endodermis, pericycle, and inner and outer cortex, and in sieve and xylem elements. With the exception of the xylem, where there are no transverse cell divisions, each file of cells commences with its initial cell and then possesses a zone of concomitant cell expansion and transverse cell division, followed, after completion of the divisions, by a zone of terminal cell differentiation. The cells augment their population of cortical microtubules as they elongate and divide, showing a net increase of up to 0.6 micron of polymerized microtubule length per min. Two main sub-processes were found: (i) When a longitudinal wall is first formed it is supplied with a higher number of microtubules per unit length of wall than it will have later, when it is being expanded. This initial quota becomes diluted as the second sub-process commences. (ii) The cells interpolate new microtubules at a rate which is characteristic of the cell, and, in the endodermis, of the face of the cell, while the cell elongates. Most cell types thus maintain a set density of cortical microtubules while they elongate and divide. Comparisons of endodermal cells in untreated controls, and roots that had been treated with colchicine, low temperature, or high pressure indicate that the initial quota of microtubules, and the later interpolations, and differentially sensitive to microtuble perturbations. Three types of behaviour, all related to changes in the cell walls, were noted as cortex, xylem and sieve element cells entered their respective phases of cell differentiation. The cortical cells expanded in all dimensions, and the interpolation of microtubules diminished or ceased. The sieve elements continued to elongate, and interpolated at a high rate, reaching unusually high densities of microtubules when the cell walls were being thickened. During this period a net increase of 2.0 micron of polymerized microtubule length per min was calculated. Thereafter interpolation ceased and the density of microtubules declined. The sample applied to developing xylem except that, because wall-thickening is localized rather than widespread, the rise and subsequent fall in the density of microtubules was less marked. The data are discussed in relation to the participation of microtubules in wall deposition and to the hypothesis that cortical microtubules arise in discrete zones along the edges of cells.

scholarly journals Ants (Hymenoptera: Formicidae) from an Amazonian fragmented landscape, Juara, Mato Grosso, Brazil, with new records of ant species

2018 ◽  
Vol 58 ◽  
pp. e20185840
Author(s):  
Ricardo Eduardo Vicente ◽  
Alexandre Casadei Ferreira ◽  
Rogério Conceição Lima dos Santos ◽  
Lívia Pires do Prado
Keyword(s):  
Transition Zone ◽  
New Records ◽  
The State ◽  
Fragmented Landscape ◽  
General Knowledge ◽  
Pitfall Traps ◽  
Mato Grosso ◽  
Brazilian State ◽  
First Time

The state of Mato Grosso is the 3rd largest Brazilian state, is covered with three major Brazilian biomes, including the Pantanal, Cerrado, and Amazonia. To date, 449 ant species are recorded in literature for the state. In the present work, we documented the ants sampled along a fragmented landscape, in the municipality of Juara, in the Cerrado-Amazon transition zone in the state of Mato Grosso, Brazil. The ant species were captured with Pitfall traps installed in 20 trails with 10 traps in each (totaling 200). Our results show 151 species, belonging to 43 genera and eight subfamilies, of which 28 species were recorded for the first time in the state and five species recorded for the first time in Brazil. Most genera collected were Pheidole Westwood, 1839 (45 species) followed by Crematogaster Lund, 1831 (11 species). By highlighting species recorded for the first time in state of Mato Grosso and Brazil, we hope to encourage new discoveries and increase the general knowledge of the ant fauna of different biomes in the region.

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