The Ultrastructure and Ontogeny of Pollen in Helleborus Foetidus L

1968 ◽  
Vol 3 (2) ◽  
pp. 161-174
Author(s):  
P. ECHLIN ◽  
H. GODWIN

The ontogeny of the tapetum and Ubisch bodies in Helleborus foetidus L. has been examined at the ultrastructural level, and their development has been closely linked with that of the sporogenous cell and pollen grains. During development the tapetum passes through successive phases of synthesis, maturity and senescence, ending in complete dissolution. During the anabolic phase of growth, precursors of the Ubisch bodies are formed as spheroidal vesicles of medium electron density within the tapetal cytoplasm; they are associated with a zone of radiating ribosomes, which, as development proceeds, can clearly be seen to be situated on strands of endoplasmic reticulum. The callose special wall round the microspores and the tapetal cell wall now disintegrate and the pro-Ubisch bodies are extruded through the cell membrance of the tapetal cells, where they remain on the surface of the anther cavity and soon become irregularly coated with sporopollenin. Deposition of sporopollenin continues on the Ubisch bodies at the same time as upon the exines of the developing pollen grains. In both cases, the later stages of sporopollenin deposition are associated with electron-transparent layers of unit-membrane dimensions appearing in section as white lines of uniform thickness. Continuing deposition of sporopollenin leads to the formation of compound or aggregate Ubisch bodies. It is conjectured that the sporopollenin is synthesized from the compounds of low molecular weight released into the anther loculus by the breakdown of the callose special wall and the tapetal cell wall. The final stages of tapetal autolysis involve the disappearance of all the cell organelles. An attempt is made to relate the findings to those described in other recent studies on Ubisch body formation and to combine them in a common ontogenetic pattern.

2018 ◽  
Author(s):  
Joseph R. Jacobowitz ◽  
Jing-Ke Weng

AbstractPollen and microspore development is an essential step in the life cycle of all land plants that generate male gametes. Within flowering plants, pollen development occurs inside of the anther. Here, we report the identification of two class III peroxidase-encoding genes, PRX9 and PRX40, that are genetically redundant and essential for proper anther and pollen development in Arabidopsis thaliana. Arabidopsis double mutants devoid of functional PRX9 and PRX40 are male-sterile. The mutant anthers display swollen, hypertrophic tapetal cells and pollen grains, suggesting disrupted cell wall integrity. These phenotypes ultimately lead to nearly 100%-penetrant pollen degeneration upon anther maturation. Using immunochemical and biochemical approaches, we show that PRX9 and PRX40 are likely extensin peroxidases that contribute to the establishment of tapetal cell wall integrity during anther development. This work identifies PRX9 and PRX40 as the first extensin peroxidases to be described in Arabidopsis and highlights the importance of extensin cross-linking during plant development.


1972 ◽  
Vol 11 (1) ◽  
pp. 111-129
Author(s):  
P. ECHLIN

The final stages of Helleborus pollen-grain ontogeny, which culminate in maturation and germination of the grain, have been investigated at the ultrastructural level. Following the deposition of primary and secondary exine, and during the early stages of intine formation, the microspore passes through a vacuolate phase, in which the cytoplasm appears devoid of most organelles other than the prominent nucleus. The formation of the vacuole results in the displacement of the nucleus to one side of the pollen grain. The vacuole quickly disappears and a number of organelles reappear in the cytoplasm, in particular the dictyosomes and strands of endoplasmic reticulum, with associated grey bodies. Following mitotic division of the pollen grain, the first signs of the generative cell wall appear as a pair of tightly appressed unit membranes in the narrow strand of cytoplasm separating the two newly formed generative and vegetative nuclei. As development proceeds, the space between the two membranes gradually fills with an electron-transparent material similar to the substance found in the numerous dictyosome-derived vesicles which, together with the endoplasmic reticulum, are both closely associated with the developing cell wall. The generative cell wall fuses with the cellulosic intine, which has gradually increased in amount during these stages, and the cell division is complete. The smaller generative cell contains a prominent nucleus and a small amount of cytoplasm devoid of plastids and most other organelles. The larger vegetative cell also contains a prominent nucleus and a large amount of cytoplasm containing amyloplasts, mitochondria, dictyosomes and endoplasmic reticulum, and abundant ribosomes, many of which are in a polysome configuration. The final stages in development are characterized by a progressive decrease in the amount of starch in the vegetative cell and an increase in the size of grey bodies, many of which are invested in multilayered shrouds of endoplasmic reticulum. The generative cell wall disappears and a multivesicular/granular body gradually appears at the periphery of the pollen grain. The granular-vesicular material, which is formed from the dictyosomes and/or the degenerating plastids, is thought to represent metabolic reserves necessary for pollen-tube formation. One or more pollen tubes emerge from the apertural sectors of the pollen grain, and maturation of the grain is complete.


Author(s):  
M.C. Castillo-Jessen ◽  
A. González-Angulo

Information regarding the normal morphology of uterine blood vessels at ultrastructural level in mammals is scarce Electron microscopy studies dealing with endometrial vasculature despite the functional implications due to hormone priming are not available. Light microscopy observations with combined injection of dyes and microradiography along with histochemical studies does not enable us to know the detailed fine structure of the possible various types of blood vessels in this tissue. The present work has been designed to characterize the blood vessels of endometrium of mice as well as the behavior of the endothelium to injection of low molecular weight proteins during the normal estrous cycle in this animal. One hundred and forty female albino mice were sacrificed after intravascular injection of horse radish peroxidase (HRP) at 30 seconds, 5, 15, 30 and 60 minutes.


Holzforschung ◽  
2011 ◽  
Vol 65 (2) ◽  
Author(s):  
Rahime Bag ◽  
Johnny Beaugrand ◽  
Patrice Dole ◽  
Bernard Kurek

Abstract The aim of this study was to determine the effect of removing extractives from the woody core of hemp (chènevotte) on the chain mobility of hemicelluloses and lignins, which can react during technological transformation such as de-fibering and/or composite materials production. Extractives are molecules with low molecular weight, which are present in the cell wall matrix and can be readily removed by solvents. In the present paper, the nature and amounts of extractives, removed under different conditions and with solvents of different polarities, were determined. The mobility and structural relaxations of lignins and hemicelluloses were stu-died in situ by dynamic mechanical analysis and dielectric analysis under controlled moisture content. Extractions at low temperature led to rigidification of lignins and plasticizing of hemicelluloses, probably due to local changes by the selective removal of molecules interacting with the polymers. Probably, the accessibility of hemicelluloses to plasticizing water was increased at controlled humidity. In contrast, hot extractions including water induced rigidification of the hemi-celluloses and plasticizing of lignins. This could be related to a combination of molecule extractions and chemical modi-fications of both polymers. This interpretation is supported by the variation of activation energy for relaxation of hemi-celluloses. It can be concluded that each type of extraction has a clear specific effect on the relaxation properties of the amorphous cell wall polymers.


2019 ◽  
Vol 20 (12) ◽  
pp. 2946 ◽  
Author(s):  
Xiao Han ◽  
Li-Jun Huang ◽  
Dan Feng ◽  
Wenhan Jiang ◽  
Wenzhuo Miu ◽  
...  

Plant cells are separated by cellulose cell walls that impede direct cell-to-cell contact. In order to facilitate intercellular communication, plant cells develop unique cell-wall-spanning structures termed plasmodesmata (PD). PD are membranous channels that link the cytoplasm, plasma membranes, and endoplasmic reticulum of adjacent cells to provide cytoplasmic and membrane continuity for molecular trafficking. PD play important roles for the development and physiology of all plants. The structure and function of PD in the plant cell walls are highly dynamic and tightly regulated. Despite their importance, plasmodesmata are among the few plant cell organelles that remain poorly understood. The molecular properties of PD seem largely elusive or speculative. In this review, we firstly describe the general PD structure and its protein composition. We then discuss the recent progress in identification and characterization of PD-associated plant cell-wall proteins that regulate PD function, with particular emphasis on callose metabolizing and binding proteins, and protein kinases targeted to and around PD.


Author(s):  
María Flores-Tornero ◽  
Lele Wang ◽  
David Potěšil ◽  
Said Hafidh ◽  
Frank Vogler ◽  
...  

Abstract Key message Analyses of secretomes of in vitro grown pollen tubes from Amborella, maize and tobacco identified many components of processes associated with the cell wall, signaling and metabolism as well as novel small secreted peptides. Abstract Flowering plants (angiosperms) generate pollen grains that germinate on the stigma and produce tubes to transport their sperm cells cargo deep into the maternal reproductive tissues toward the ovules for a double fertilization process. During their journey, pollen tubes secrete many proteins (secreted proteome or secretome) required, for example, for communication with the maternal reproductive tissues, to build a solid own cell wall that withstands their high turgor pressure while softening simultaneously maternal cell wall tissue. The composition and species specificity or family specificity of the pollen tube secretome is poorly understood. Here, we provide a suitable method to obtain the pollen tube secretome from in vitro grown pollen tubes of the basal angiosperm Amborella trichopoda (Amborella) and the Poaceae model maize. The previously published secretome of tobacco pollen tubes was used as an example of eudicotyledonous plants in this comparative study. The secretome of the three species is each strongly different compared to the respective protein composition of pollen grains and tubes. In Amborella and maize, about 40% proteins are secreted by the conventional “classic” pathway and 30% by unconventional pathways. The latter pathway is expanded in tobacco. Proteins enriched in the secretome are especially involved in functions associated with the cell wall, cell surface, energy and lipid metabolism, proteolysis and redox processes. Expansins, pectin methylesterase inhibitors and RALFs are enriched in maize, while tobacco secretes many proteins involved, for example, in proteolysis and signaling. While the majority of proteins detected in the secretome occur also in pollen grains and pollen tubes, and correlate in the number of mapped peptides with relative gene expression levels, some novel secreted small proteins were identified. Moreover, the identification of secreted proteins containing pro-peptides indicates that these are processed in the apoplast. In conclusion, we provide a proteome resource from three distinct angiosperm clades that can be utilized among others to study the localization, abundance and processing of known secreted proteins and help to identify novel pollen tube secreted proteins for functional studies.


2014 ◽  
Vol 56 (2) ◽  
pp. 215-227 ◽  
Author(s):  
John R. Rowley ◽  
Björn Walles

In <em>Pinus sylvestris</em> Ubisch bodies are produced repeatedly, and each crop is formed at a distinct phase in the secretory cycles of tapetal cells. While each production has a Ubisch body wall similar to the then current state of the exine with regard to thickening and ornamentation, the survivers of previous productions do not change. Examples of all the structurally different Ubisch body wall forms can be seen when terminally, at the time of pollen shedding, the relict Ubisch bodies become spatially concentrated on the minimal surface area of the senescent cells of the tapetum. In angiosperms after one or a few periods of initiation Ubisch bodies may remain in association with the surface of tapetal cells where the Ubisch body wall undergoes changes like those of the maturing pollen exine. We conclude that as a consequence of Ubisch body detachment from the plasma membrane of tapetal cells there is in <em>Pinus sylvestris</em> no updated information for modification of the wall and the Ubisch body wall remains static.


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