Development of cell wall modifications in the endodermis and exodermis of Allium cepa roots

2001 ◽  
Vol 79 (5) ◽  
pp. 621-634 ◽  
Author(s):  
Fengshan Ma ◽  
Carol A Peterson

The cytological events of wall modification in the endodermis and exodermis of Allium cepa L. roots were examined with fluorescence and transmission electron microscopy. In the endodermis, Casparian bands, suberin lamellae, and tertiary walls developed in succession. At the site of the future Casparian band, the plasma membrane was bound to the wall before deposition of detectable hydrophobic components in the radial wall. Suberin lamellae were deposited on the inner faces of the primary walls, first along the outer tangential walls and then the inner tangential walls. On both walls, segments of the lamellae were formed earlier in primary pit fields than at nonprimary pit field regions. Suberin lamellae then extended to the radial walls. When they reached the Casparian bands, the lamellae intruded between the bound plasma membranes and the walls, so that the cells' plasma membranes remained intact. In this way, suberin lamellae that were continuous around the cells were laid down. Later, tertiary walls were deposited internal to the suberin lamellae. None of the wall modifications interrupted the symplastic connections of the endodermis. During suberin lamella and tertiary wall formation, more dictyosomes and ER profiles appeared than during Casparian band development. In the exodermis, although Casparian bands were readily detected with fluorescence microscopy, they were rarely detected with electron microscopy. Suberin lamellae were formed in long cells severing their plasmodesmata. As in the endodermis, dictyosomes and ER were prominent during suberin lamella formation. Tertiary walls were not formed in the exodermis.Key words: Allium cepa, Casparian band, endodermis, exodermis, suberin lamella, ultrastructure.

1992 ◽  
Vol 70 (11) ◽  
pp. 2233-2237 ◽  
Author(s):  
Alban D. Barnabas ◽  
Carol A. Peterson

The endodermal Casparian band in onion (Allium cepa L.) roots is first evident 10 mm from the apex. It occupies a small region (20–30%) in the middle of the radial wall for a distance of 70 mm from the apex. However, with the development of suberin lamellae in most cells at greater distances from the root tip, the band expands symmetrically through the wall until, at 80 mm from the root tip, it fills the entire radial wall. Passage cells overlying some xylem poles have a delayed development of suberin lamellae, and in these cells the Casparian bands remain narrow. The sensitive stain, Fluorol yellow 088, detects precursors of the suberin lamellae in the outer tangential walls of the endodermal cells. The presence of complete lamellae is indicated by Sudan red 7B staining and resistance to acid digestion. Growth of the Casparian band during suberin lamella development may play a role in maintaining the apoplastic barrier in this layer by enlarging the contact area between the band and the lamellae. Key words: Casparian band, endodermis, suberin lamella, Allium cepa.


1997 ◽  
Vol 75 (7) ◽  
pp. 1188-1199 ◽  
Author(s):  
Daryl E. Enstone ◽  
Carol A. Peterson

The exodermal Casparian band in corn (Zea mays L.) was first seen 10 mm distal to the kernel 4 days after planting. From its inception, the band usually occupied most of the radial wall (as seen in a cross section of the root). Subsequent maturation of the band around the root was asynchronous into the region of emerging lateral roots. Thus, a continuous apoplastic barrier would have been absent over much of the young root surface. Suberin lamellae development was also asynchronous, as these structures formed in those cells which had Casparian bands. Frequently, a lamella was initially deposited in patches, progressing centripetally until a continuous lipid layer was formed around the cell protoplast. Many instances of band plasmolysis (typical of the endodermis) were observed in the developing uniform exodermis. It could occur in cells with no detectable Casparian bands, suggesting that the tight connection between the plasmalemma and the wall that causes this phenomenon is not due to hydrophobic attractions. The results are consistent with the idea that there are strong attractions between proteins of the membrane and wall in the region of the Casparian band. The tight connection between the plasmalemma and the wall was broken during the later stages of suberin lamella development. Key words: Zea mays L., Poaceae, band plasmolysis, exodermis, Casparian band, suberin lamella.


1996 ◽  
Vol 74 (8) ◽  
pp. 1220-1226 ◽  
Author(s):  
Carol A. Peterson ◽  
Janet L. Waite

The onion exodermis is made up of two cell types, i.e., long and short cells. Both form Casparian bands, but suberin lamella development is absent or delayed in the short cells. Long cells did not accumulate fluorescein, a common test for cell vitality, because of reduced wall permeability due to suberin lamella development. Immature, long cells without lamellae stained in 15 min, whereas mature cells with lamellae required a 3.5- to 4-h treatment before staining was visible. Long exposure to fluorescein was needed to show that mature long cells were alive. Their vitality appeared to decline slowly with age but was not affected by drought stress. Fluorescein staining was apparent in the long cells only after treatment of paradermal sections; when dye was applied only externally to root segments, it did not enter the long cells from the epidermis or from the neighbouring short cells. This result indicates that the long cells were connected symplasmically to the cells of the cortex but were either unconnected, or connected by plasmodesmata of small functional diameter, to the epidermal and short cells. If they were unconnected, they would not form part of the symplasmic path of ion transfer into the root. Keywords: Allium cepa L., drought, exodermis, suberin lamella, vitality.


1986 ◽  
Vol 64 (9) ◽  
pp. 1873-1878 ◽  
Author(s):  
C. J. Perumalla ◽  
Carol A. Peterson

The Casparian band of the exodermis of corn and onion roots matures further from the root tip than its counterpart in the endodermis. A complete suberin lamella in the exodermal cells usually develops about 10 mm proximal to the exodermal Casparian band. The distance between the exodermal Casparian band and suberin lamella in the endodermis was usually much greater than in the exodermis. Both the exodermal Casparian band and suberin lamella matured closer to the tip in onion than in corn roots. The distance from the root tip at which the exodermal Casparian band matured increased with root age during the 5-day period studied in corn grown in hydroponics and vermiculite, and onion grown in hydroponics. This difference was most pronounced in corn, in which the Casparian band matured 20 mm from the root tip when the root was 20 mm long but matured 120 mm from the tip 4 days later when the root was 170 mm long. When the growth rate of corn roots was drastically inhibited by adding polyethylene glycol to the hydroponic medium, the exodermal Casparian band and suberin lamellae were present within 10 mm of the root tip. The position in the root at which the exodermis matures is thus highly variable and can depend on the plant species, and the age and growth rate of the individual root.


1995 ◽  
Vol 73 (9) ◽  
pp. 1436-1450 ◽  
Author(s):  
Norman Thomson ◽  
Ray F. Evert ◽  
Arthur Kelman

Healing was investigated in whole tubers wounded by cuts and bruises and compared with core, disc, and slice wounds. Bright-field, fluorescence, and transmission electron microscopy were used in conjunction with cytochemical analyses. Wound reaction cells bordering a wound site responded to wounding initially with deposition of callose at the primary pit fields followed by intussusception of lignin in the middle lamellae and primary walls and suberization along the inner surfaces of the primary walls. Suberization was initially detected by the presence of a prosuberin lamella in which suberin lamellae subsequently developed. Both lignin and the prosuberin lamella were first detected in wound reaction cells of the cortex at 4 h in cut, core, disc, and slice wounds and at 8 h in bruise wounds. Healing was completed with formation of a continuous wound cork cambium beneath the wound site. With lignification and suberization, wounded potato tubers apparently develop specialized barriers against potential pathogens and water loss. The overall healing process proceeds more slowly in bruise wounds than in cut wounds. Moreover, the capacity for wound healing decreases with increasing age of the tuber, or time in storage. Key words: lignin, prosuberin lamella, Solanum tuberosum, suberin, suberization, wound healing.


1986 ◽  
Vol 64 (8) ◽  
pp. 1606-1610 ◽  
Author(s):  
A. R. Biggs ◽  
L. W. Stobbs

Bark on the scaffold limbs of 6-year-old peach (Prunus persica (L.) Batsch cv. Redhaven) trees was mechanically wounded and tissue samples for ultrastructural study were taken after 6, 8, 12, and 14 days. Examination with light and fluorescence microscopy revealed lignification of boundary zone cell walls after 6 days followed by suberization of the lignified cell walls after 8 days. Necrophylactic periderm was present by day 12 and, by day 14, three to five cells of the new phellem were observed. Examination of tissues with transmission electron microscopy revealed suberin lamellae on the inner wall of boundary zone cells. These cells contained senescing cytoplasm with fragments of undifferentiated dense material that formed a thin, discontinuous granular deposit inside the suberin layer. Suberin lamellae did not occlude plasmodesmata. Cells of the new phellem were radially compressed, heavily suberized, and lacked pits or plasmodesmata.


1999 ◽  
Vol 77 (1) ◽  
pp. 113-121
Author(s):  
James L Seago, Jr. ◽  
Carol A Peterson ◽  
Daryl E Enstone

Tissues in adventitious roots of Hydrocharis morsus-ranae L. developed from a four-tiered apical meristem. A set of periclinal divisions in the outermost layer of the ground meristem produced a hypodermis, which was normally uniformly biseriate. Aerenchyma formed from the adjacent inner layer of the cortex by a series of cell divisions and cell lyses; three- to five-celled, radial aerenchyma strands formed by periclinal divisions in radial cell files 0.3-5 mm behind the apex. Intervening cells underwent anticlinal and periclinal divisions followed by cell lyses within 1 mm of the apex to produce air spaces. Aerenchyma formation in this species is unusual and presents a unique system suitable for a study of developmentally programmed cell death in parenchyma cells. The endodermis formed a complete Casparian band about 10 mm behind the root apex and did not develop further; it had neither suberin lamellae nor secondary walls. The hypodermis was parenchymatous and was without Casparian bands, suberin lamellae, and secondary walls. Following acid digestion, the wavy walls of the endodermis and the walls of the epidermis remained.Key words: aerenchyma, cell death, endodermis, Hydrocharis, hypodermis, root development.


Development ◽  
1977 ◽  
Vol 40 (1) ◽  
pp. 125-141
Author(s):  
James Hogan ◽  
J. P. Trinkaus

The fine structure of motile deep cells of the gastrula stage of Fundulus hetewclitus was studied with transmission electron microscopy, using both thin sectioning and freeze-cleave techniques. Gastrula deep cells form extensive non-junctional appositions with each other, in which the apposed plasma membranes are parallel and separated by a distance of 26–28 nm. They also form gap junctions. Tight junctions, desmosomes, and extensive interdigitations of apposed plasma membranes were not observed. The plasma membranes of deep cells contain numerous unclustered intramembranous particles. Cytoplasmic microtubules were found, but they appear to be small in number, sparsely distributed, and mainly randomly oriented. Microfilaments are also present and are localized largely in the cortical cytoplasm and in thin cell extensions. The significance of these findings for the contact and locomotory behavior of deep cells is discussed.


1981 ◽  
Vol 49 (1) ◽  
pp. 383-399
Author(s):  
R.D. Lang ◽  
M.V. Nermut ◽  
L.D. Williams

Sheep erythrocyte plasma membrane monolayers were formed on positively charged supports by means of controlled lysis and squirting of cells so that the original protoplasmic or inner surfaces (PS) were exposed. The appearance of the surface was studied by transmission electron microscopy of platinum/carbon replicas following freeze-drying of the membranes. After gentle washing with water or dilute buffer, a network of filaments and particles was found to cover the surface. Whole cells bound to positively charged supports were treated with Triton X-100 and hypertonic KCl, which left the protein components of the cytoskeleton on the support. Stereo electron microscopy of Pt/C replicas of these residues showed complex networks of filaments, similar to those seen on the cytoplasmic surfaces of the intact membranes. In both cases the lengths of the filaments correspond to that of the spectrin dimer. Removal of spectrin, actin and other proteins by alkaline treatment led to loss of this network and revealed 15.4-nm particles on the membranes PS. These particles, which were also visible after negative staining, could be removed by treatment with trypsin and were found to correspond to band 4 protein (the equivalent of human erythrocyte band 3 protein). Membranes freeze-fractured following treatment with alkali showed normal intramembranous particles with frequencies similar to those of native membranes. This indicates that band 4 protein spans the sheep erythrocyte membrane and forms a very high proportion of the intramembranous particles. The protoplasmic portions of these particles may be membrane binding sites for the cytoskeleton in sheep erythrocytes.


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