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PubMed1985

Imunohistochemical Localization of alpha-Amylase in Cotyledons of Vigna mungo Seedlings.

We studied the localization of alpha-amylase with indirect fluorescence microscopy in transversely sectioned cotyledons of Vigna mungo seedlings. Tissue sections were fixed in periodate-lysine-paraformaldehyde and treated with anti-alpha-amylase immunoglobulin G followed by fluorescein isothiocyanate labeled goat anti-rabbit immunoglobulin G. alpha-Amylase appeared in the cells farthest from vascular bundles on the second day of growth and appeared gradually closer to the vascular bundles as growth progressed. The pattern of alpha-amylase appearance was similar in detached cotyledons, indicating that attachment of the embryonic axis has no effect on this pattern. However, in attached cotyledons, alpha-amylase disappeared from the regions where starch grains had been digested, but in detached cotyledons there was no disappearance of alpha-amylase, and digestion was slower than in intact cotyledons.

Journal Article↗
PubMed2006

[Ultracytochemical studies of aloin in Aloe arborescens leaves].

Lead acetate precipitation method was used for ultracytochemical localization of aloin. The processes of aloin production, transport and storage were studied by transmission electron microscope. Results showed that aloin was produced in the plastids of the assimilating tissue. The aloin was transported through the plastid membrane to the surrounding endoplasmic reticulum and enveloped in the vesicles by the endoplasmic reticulum elements, the vesicles approached and later fused with the plasmalemma. Some vesicles of the plastid membrane directly fused with the plasmalemma. The vesicles released their contents into the apoplast through exocytosis, and finally reached the vascular bundle sheath by apoplastic translocation. Aloin was transported to the internal tangential wall of vascular bundle sheath cell through endoplasmic reticulum vesicles, and reached the cytoplasm of aloin cell by means of plasmodesmata. Finally, aloin was stored in the vacuoles of aloin cell.

Aloe↗
PubMed1998

Leiomyomatous nodules and bundles of vascular origin in the fibrosarcomatous variant of dermatofibrosarcoma protuberans.

We report 5 cases of the fibrosarcomatous variant of dermatofibrosarcoma protuberans, 4 of which presented a morphologic change of intraneoplastic blood vessels not previously recognized. This change consisted of focal proliferation of smooth muscle cells, resulting in hypertrophy, generally eccentric, of vascular walls with reduction and collapsing of vascular lumina. In 3 cases the proliferation was so intense it formed leiomyomatous nodules and bundles. This proliferation may originate in the smooth muscle cells of the vessel walls either by means of a hyperplastic mechanism or in the pericytes via a line of differentiation leading to mature smooth muscle cells. In either case, we believe that it concerns a reactive process of the vessel walls very probably induced by adjacent neoplastic cells. The cases recently reported by Calonje and Fletcher as "myoid differentiation" of neoplastic cells in dermatofibrosarcoma protuberans (DFSP) may well be an expression of the same phenomenon, and therefore the presence of leiomyomatous areas in this tumor should not be used to support the theory of a fibroblastic/myofibroblastic line of differentiation for DFSP.

Actins↗
PubMed2000

Organ and cellular localization of asparagine synthetase in rice plants.

DNA gel blot analysis suggested that asparagine synthetase (AS; EC 6.3.5.4) occurred as a single gene in rice. A fusion protein consisting of 17 kDa tagged-region from pET32a(+) expression plasmid and 42 kDa N-terminal region of rice AS was first expressed in Escherichia coli. The resulting polypeptide was purified and a mono-specific antibody for rice AS was prepared after affinity-purification with the antigen. Immunoblotting revealed a high content of AS protein in the leaf sheath at the second position from the fully expanded top leaf and in grains at the middle stage of ripening. Accumulation of mRNA for AS was also observed in these organs. During the ripening of the spikelets, the AS protein contents increased during the first 21 days after flowering, then declined rapidly. Immunolocalization analysis revealed signals for AS protein in the companion cells of vascular bundles of leaf sheath and phloem-parenchyma cells, nucellar projection, and nucellar epidermis of dorsal vascular bundles of grains.

Aspartate-Ammonia Ligase↗
PubMed2005

Unusual metaxylem tracheids in petioles of Amorphophallus (Araceae) giant leaves.

BACKGROUND AND AIMS: Petioles of huge solitary leaves of mature plants of Amorphophallus resemble tree trunks supporting an umbrella-like crown. Since they may be 4 m tall, adaptations to water transport in the petioles are as important as adaptations to mechanical support of lamina. The petiole is a cylindrical shell composed of compact unlignified tissue with a honeycomb aerenchymatous core. In both parts numerous vascular bundles occur, which are unique because of the scarcity of lignified elements. In the xylemic part of each bundle there is a characteristic canal with unlignified walls. The xylem pecularities are described and interpreted. MATERIAL: Vascular bundles in mature petioles of Amorphophallus titanum and A. gigas plants were studied using light and scanning electron microscopy. KEY RESULTS: The xylemic canal represents a file of huge metaxylem tracheids (diameter 55-200 microm, length >30 mm) with unlignified lateral walls surrounded by turgid parenchyma cells. Only their end walls, orientated steeply, have lignified secondary thickenings. The file is accompanied by a strand of narrow tracheids with lignified bar-type secondary walls, which come into direct contact with the wide tracheid in many places along its length. CONCLUSIONS: The metaxylem tracheids in A. petioles are probably the longest and widest tracheids known. Only their end walls have lignified secondary thickenings. Tracheids are long due to enormous intercalary elongation and wide due to a transverse growth mechanism similar to that underlying formation of aerenchyma cavities. The lack of lignin in lateral walls shifts the function of 'pipe walls' to the turgid parenchyma paving the tracheid. The analogy to carinal canals of Equisetum, as well as other protoxylem lacunas is discussed. The stiff partitions between the long and wide tracheids are interpreted as structures similar to the end walls in vessels.

Amorphophallus↗
PubMed2006

Spatio-temporal accumulation of microRNAs is highly coordinated in developing plant tissues.

MicroRNAs (miRNAs) are an abundant class of small, endogenous non-protein-coding RNAs, approximately 21 nucleotides in length, that modulate the expression of animal and plant target genes at the post-transcriptional level. Recent work has shown that miRNA-based gene regulation plays a crucial role in pathways involved in plant growth and development. However, knowledge about the timing and spatial regulation of plant miRNA expression is still limited. Here we used in situ analysis to demonstrate that miRNAs accumulate spatially and temporally in a highly restricted manner in Nicotiana benthamiana and Arabidopsis thaliana. The presence of the seven investigated miRNAs was characteristic of the developing organs, implying a role in cell-fate establishment, differentiation and cell-cycle progression. Spatial analyses revealed that six of the studied miRNAs were present in vascular bundles, suggesting that mobile miRNAs in the phloem could contribute to the coordination of organogenesis and development. The obvious absence of miR167 in vascular bundles represented an exception to this observation, implying an active process in regulating the presence of miRNAs in the vascular system. Taken together, our results imply that the spatially and temporally organized accumulation of miRNAs plays a pivotal role in fine-tuning of target gene expression in plant development.

Arabidopsis↗
PubMed2002

Tissue-specific silencing of a transgene in rice.

In a transgenic rice line, a beta-glucuronidase reporter gene under the control of the rice tungro bacilliform virus promoter became gradually methylated, and gene activity was lost concomitantly. Methylation was observed only in the homozygous offspring and was initially restricted to the promoter region and accompanied by loss of expression in the vascular bundle tissue only. This expression pattern was similar to that of a promoter with a deletion of a vascular bundle expression element. The gene activity could be reestablished by treatment with 5-azacytidine. Methylation per se did not inhibit the binding to the promoter region of protein factors which also bound to the unmethylated sequence. Instead, promoter methylation enabled the alternative binding of a protein with specificity for sequence and methylation. In further generations of homozygous offspring the methylation spread into the transcribed region and gene activity was completely repressed also in nonvascular cells. The results indicate that different stages are involved in DNA methylation-correlated gene inactivation, and that at least one of them may involve the attraction of a sequence and methylation-specific DNA-binding protein.

Badnavirus↗
PubMed2003

Three differentially expressed basic peroxidases from wound-lignifying Asparagus officinalis.

The activity of ionically bound peroxidases from an asparagus spear increased from 5-24 h post-harvest. Isoelectric focusing showed that the post-harvest increase of the total peroxidase activity was due to the increase of several distinct isoperoxidases. Concomitantly, a decrease in the activity of two anionic peroxidases was observed. Peroxidases with pI 5.9, 6.4 and 9.2 were detected only at 24 h post-harvest, whereas four peroxidases, with pI 8.7, 8.1, 7.4, and 6.7, detected throughout the time-course, increased in their activity. Histochemical staining demonstrated that lignin and peroxidase activity were located in the vascular bundles throughout the period of measurement. Lignin was detected in the cell walls of the protoxylem in the vascular bundles of the asparagus stem. A cDNA library of mRNA isolated from asparagus spears 24 h post-harvest was screened for peroxidases using homologous and heterologous probes. Three clones were isolated and the corresponding mature asparagus peroxidases displayed 70%, 76% and 81% amino acid sequence identity to each other. These new asparagus peroxidases are typical class III plant peroxidases in terms of conserved regions with a calculated pI >9.2, which is consistent with most basic peroxidases. One of the genes was shown to be a constitutively expressed single-copy gene, whereas the others showed an increased expression at post-harvest. The highest similarity in the amino acid sequence (71-77%) was found in peroxidases from roots of winter grown turnip TP7, to Arabidopsis AtP49, to an EST sequence from cotton fibres and to TMV-infected tobacco.

Amino Acid Sequence↗
PubMed1998

Functional magnetic resonance imaging in intact plants--quantitative observation of flow in plant vessels.

Quantitative magnetic resonance (MR) images of flow velocities in intact corn plants were acquired using magnetization-prepared MR microscopy. A phase contrast flow imaging technique was used to quantitate water flow velocities and total volume flow rates in small xylem vessels. The simultaneous measurement of the transpiration of the whole plant was achieved by using a closed climate chamber within the MR magnet. The total volume flow rate and the transpiration values were in close correlation. Functional magnetic resonance imaging in intact plants was performed by light stimulation of the transpiration inside of the magnet. The change in the flow velocities in the xylem vessels of single vascular bundles was in correlation with the changes in the transpiration. Significant differences were observed between the xylem vessels in different vascular bundles. Furthermore, flow velocity measurements were performed on excised plant stems and visualized by the uptake of the MR contrast agent, gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA). A comparison between the phase contrast flow imaging and the contrast media uptake showed to be in good agreement with each other.

Hydroponics↗
PubMed2002

Lignification and lignin heterogeneity for various age classes of bamboo (Phyllostachys pubescens) stems.

The lignification process and lignin heterogeneity of fibre, vessel and parenchyma cell walls for various age classes of bamboo stems of Phyllostachys pubescens Mazel were investigated. It was shown that protoxylem vessels lignified in the early stage of vascular bundle differentiation, metaxylem vessel and fibre walls initiated lignification from the middle lamella and cell corners after the completion of vascular bundle differentiation. Most of the parenchyma cell walls lignified after the stem reached its full height, while a few parenchyma cells remained non-lignified even in the mature culm. The cell walls of fibres and most parenchyma cells thickened further during the stem growth to form polylamellate structure and the lignification process of these cells may last even up to 7 years. The fibre walls were rich in guaiacyl lignin in the early stage of lignification, and lignin rich in syringyl units were deposited in the later stage. Vessel walls mainly contained guaiacyl lignin, while both guaiacyl and syringyl lignin were present in the fibre and parenchyma cell walls.

Journal Article↗
PubMed2003

A sucrose transporter, LjSUT4, is up-regulated during Lotus japonicus nodule development.

LjSUT4, encoding a putative sucrose transporter, was identified in a Lotus japonicus nodule cDNA library. The deduced amino acid sequence showed a high degree of identity with sucrose transporters from other plants. Semi-quantitative RT-PCR analysis demonstrated that the L. japonicus SUT4 gene was expressed at high levels in both roots and nodules. In situ hybridization revealed that, in young nodules, SUT4 mRNA transcripts are present in vascular bundles, inner cortex and both infected and uninfected cells while, in mature nodules, accumulation of transcripts was restricted only in vascular bundles and the inner cortex. The results indicated that LjSUT4 codes for a putative sucrose transporter, and its expression pattern suggests a possible shift in the mechanism of sugar transport during nodule development. The role of this polypeptide in sucrose transport and metabolism is discussed.

Amino Acid Sequence↗
PubMed1986

Accumulation and Conversion of Sugars by Developing Wheat Grains : VI. Gradients Along the Transport Pathway from the Peduncle to the Endosperm Cavity during Grain Filling.

Gradients along the transport pathway from the peduncle to the endosperm cavity were examined during grain filling in wheat. Sieve tube exudate was collected from severed aphid stylets established on the peduncle and rachis and on the vascular bundles in the creases of grains. Phloem exudate could also be collected from broken grain pedicels, and by puncturing the vascular bundle in the grain crease with a needle. Stylets on excised grains persisted exuding, indicating that grain sieve tubes are capable of loading solutes. There was little, if any, discernible gradient in osmolality or solute composition (sucrose, total amino acids) of sieve tube contents along the phloem pathway from the peduncle to the rachis or along the rachis itself. Neither was a gradient detected in osmolality along the sieve tube pathway from the rachis through the rachilla and grain stalk to the crease. Demonstrable solute gradients occurred only across those tissues of the grain crease between the crease sieve tubes and the endosperm cavity, a distance of just 1 millimeter. However, while the sucrose concentration in the sieve tubes was almost tenfold that in the endosperm cavity sap, total amino acids were only threefold higher, and the potassium concentrations of the two were equal. Our observations strongly implicate the movement of assimilates from the sieve tubes and across the crease tissues as important control points in grain filling.

Journal Article↗
PubMed2002

Kidney of giraffes.

This study focuses on certain aspects of the renal structure of the giraffe, with some implications as to its function. About 4,000 collecting ducts open at the truncated end of a curved crest that juts into the renal pelvis as the inner medulla (IM). Extensions of the pelvis pass between the medullary (MP) and vascular (VP) processes almost to the corticomedullary border. The MPs contain an IM and an outer medulla (OM) containing clusters of capillaries (vascular bundles). The VPs contain the interlobar arteries and veins. All of the IM and almost all of the OM, with its vascular bundles, are bathed with pelvic urine. The cortex comprises 63% of the parenchyma. The OM has nine times the mass of the IM. The IM comprises 4% of the parenchyma. The ratio of mass of the adult cortex to the medulla is 1.7:1.0, and the number of glomeruli per kidney is 6.6 x 10(6). Glomerular mass is 6.2-6.7% of renal mass in the adult and 5.2% in the 6-month-old calf. The dimensions of the glomerular capsules are the same across the thickness of the cortex. Every terminal collecting duct drains an estimated 1,650 nephrons. In the adult giraffe the ratio of thickness of the muscularis of the main renal artery (RA) to its diameter is 0.117 (right RA) and 0.132 (left RA). These ratios are close to those in rhinoceros and ox but greater than in man. The visceral arteries (celiac, anterior mesenteric, and renal) have about the same muscularis : diameter ratio. Giraffes have arterial hypertension, but atherosclerosis is apparently absent and serum lipid fractions are low.

Animals↗
PubMed2004

Expression analysis of the NgORF13 promoter during the development of tobacco genetic tumors.

We investigated the expression pattern of the promoter of Nicotiana glauca (Ng) ORF13 in the hybrids between N. glauca and N. langsdorffii harboring the NgORF13-beta-glucuronidase (GUS) chimeric gene. The promoter of NgORF13 of N. glauca had lower activities than the promoter of RiORF13 of Agrobacterium rhizogenes agropine-type root-inducing (Ri) plasmid. However, the localization of GUS activity in the NgORF13 transgenic plants was similar to that in the RiORF13 transgenic plants. The GUS activity of NgORF13-GUS was high in genetic tumors cultured in vitro or developed spontaneously on F1 plants with aging or by wounding. The GUS activity in tumors was observed in bud primordia, vascular bundles and leaves in the buds. While the activity was lower than in tumors, NgORF13-GUS was also expressed in vascular bundles and the parenchymatous tissues in plants regenerated from tumors. Furthermore, the promoter activity of NgORF13 was induced by wounding and activated by exogenous application of methyl jasmonate. During tumorization, NgORF13 was induced at an early stage and showed expression patterns similar to both NgrolB and NgrolC whose expression were investigated by Nagata et al. (1996) Plant Cell Physiol. 37: 489-498. It is thought that Ngrol genes might be involved in the formation of genetic tumors, and, moreover, NgORF13 might work in cooperation with NgrolB and NgrolC.

Acetates↗
PubMed1980

An integrated light and electron microscopic study on the existence of intramedullary lymphatics in the dog kidney.

The existence of intramedullary lymphatics was investigated in canine kidneys by two detailed morphological approaches. The first used a combined light and electron microscopic analysis of medullary tissue fixed in vivo and obtained from animals with dilated as well as freely-flowing intrarenal lymphatics. Examination of 100 vascular bundles and 100 interbundle areas from 90 medullary tissue strips elicited only one strip containing lymphatic vessels. These lymphatics, in a vascular bundle, were confirmed ultrastructurally and were followed in serial one micron sections which revealed their course to be immediately adjacent to or within the arcuate region. The dearth of medullary lymphatics was in marked contrast to the existence of cortical lymphatics found in similarly processed tissue. By the second approach sections of arcuate lymphatics were examined for medullary tributaries. In serial sections from 60 tissue blocks arcuate lymphatics received only cortical tributaries. Reconstruction diagrams made from 8 blocks showed 14 tributaries from the cortex and none from the medulla. It was concluded from this study that an intramedullary system of lymphatics does not exist within the dog kidney. It is proposed that a meduallary contribution to renal lymph occurrs by movement of fluid through the medullary interstitium to lymphatics associated with arcuate or possibly interlobar blood vessels.

Animals↗
PubMed1998

[Histological studies on the roots of eighteen species of sect. microdiscus of the genus Adenophora].

The Chinese materia medica "Nanshasheng" (Radix Adenophorae) specified in Chinese Pharmacopoeia (1995) is the dried root of Adenophora tetraphylla (Thunb.) Fisch. or A. stricta Miq. (Fam. Campanulaceae). Results of an investigation on the botanical origin of the drug showed that the roots of 30 species (subspecies, varieties) of the genus Adenophora are also used in certain districts in China. Thus, it is necessary to study and compare the histological characters of these roots. In this paper, the root structure of 18 species from Sect. Microdiscus are reported, viz. Adenophora brevidiscifera Hong, A. coelestis Diels, A. stricta Miq., A. stricta Miq. var. qinglongshanica P. F. Tu et G. J. Xu, A. stricta Miq. var. nanjingensis P. F. Tu et G. J. Xu, A. stricta Miq. subsp. henanica P. F. Tu et G. J. Xu, A. stricta Miq. subsp. sessilifolia Hong, A. longipedicellata Hong, A. gmelinii (Spreng.) Fisch., A. polyantha Nakai, A. micrantha Hong, A. stenophylla Hemsl., A. potaninii Korsh., A. bockiana Diels, A. wawreana Zahlbr., A. tricuspidata (Fisch. ex Roem. et Schult.) A. DC., A. pereskiifolia (Fisch. ex Roem. et Schult.) G. Don and A. divaricata Franch. et Sav.. According to the presence, arrangement and thickening of cell walls of sclerified cork cell (SCC) in cork tissue and the rate of secondary and anomalous structures, the histological structures of Adenophora roots are classified into types A, B and C. In type A, SCC are arranged in ring shape. Type A can be further classified into subtypes A1 and A2. Only the outer and anticlinal walls of SCC are thickened in subtype A1, and all cell walls of SCC are thickened in subtype A2. In type B, SCC are arranged scatteredly, not in ring shape. In type C, there is no SCC. Type C can be classified into subtypes C1, C2 and C3. In type C1, the secondary structure occupies more than 50% of the root diameter. In type C2, the anomalous structure is more than 50% of the root diameter, and the anomalous vascular bundles are in band form. The anomalous structure occupies more than 50% of the root diameter in subtype C3, and the anomalous vascular bundles are branched.

Campanulaceae↗
PubMed2003

Occurrence of the allene oxide cyclase in different organs and tissues of Arabidopsis thaliana.

Occurrence of an essential enzyme in jasmonate (JA) biosynthesis, the allene oxide cyclase, (AOC) was analyzed in different developmental stages and various organs of Arabidopsis thaliana plants by immuno blot analysis and immunocytological approaches. Levels of AOC and of the two preceding enzymes in JA biosynthesis increased during seedling development accompanied by increased levels of JA and 12-oxophytodienoic acid levels after 4 and 8 weeks. Most tissues including all vascular bundles and that of flower buds contain AOC protein. Flowers shortly before opening, however, contain AOC protein preferentially in ovules, stigma cells and vascular bundles, whereas in anthers and pollen AOC could not be detected. The putative roles of AOC and JA in development are discussed.

Arabidopsis↗
PubMed1981

Structural organization of the renal medulla: comparative and functional aspects.

The renal medulla develops very differently among species, being more prominent in those with a high urinary concentrating capacity. Attempts to correlate structure and function must consider loops of Henle, collecting ducts, vessels, interstitium, and pelvis. Two types of loops of Henle, long and short, are distinguished. Numerical relationships between both differ among species. Based on the epithelial lining a short loop consists of a thick descending limb (pars recta of proximal tubule), a thin descending limb, and a thick ascending limb. Long loops, in addition, have a thin ascending limb; their descending thin limbs are different from those of short loops and are site of considerable interspecies differences. Collecting ducts form in the cortex by joining several nephrons. Patterns with and without arcade formation are distinguished. On entering inner medulla, collecting ducts fuse successively. Collecting duct epithelium consists of principal and intercalated cells whose individual functions are subject to debate. Blood vessels are arranged in a very strict pattern reflecting that, in addition to nourishment, unique requirements in maintaining the corticomedullary osmotic gradient are to be met. Ultrastructural organization of medullary vessels is less specific compared to cortical vessels. Two types of renal medulla are distinguished. The simple type has vascular bundles consisting only of de- and ascending vasa recta; in the complex type, descending thin limbs of short loops are also integrated into vascular bundles. Functional implications of this difference are considerable. Striking interspecies differences also occur in the renal pelvis.

Animals↗