|A xylem sap retrieval pathway in rice leaf blades: evidence of a role for endocytosis?|
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|PMID: 18617505 Owner: NLM Status: MEDLINE|
|The structure and transport properties of pit membranes at the interface between the metaxylem and xylem parenchyma cells and the possible role of these pit membranes in solute transfer to the phloem were investigated. Electron microscopy revealed a fibrillar, almost tubular matrix within the pit membrane structure between the xylem vessels and xylem parenchyma of leaf blade bundles in rice (Oryza sativa). These pits are involved primarily with regulating water flux to the surrounding xylem parenchyma cells. Vascular parenchyma cells contain large mitochondrial populations, numerous dictyosomes, endomembrane complexes, and vesicles in close proximity to the pit membrane. Taken collectively, this suggests that endocytosis may occur at this interface. A weak solution of 5,6-carboxyfluorescein diacetate (5,6-CFDA) was applied to cut ends of leaves and, after a minimum of 30 min, the distribution of the fluorescent cleavage product, 5,6-carboxyfluorescein (5,6-CF), was observed using confocal microscopy. Cleavage of 5,6-CFDA occurred within the xylem parenchyma cells, and the non-polar 5,6-CF was then symplasmically transported to other parenchyma elements and ultimately, via numerous pore plasmodesmata, to adjacent thick-walled sieve tubes. Application of Lucifer Yellow, and, separately, Texas Red-labelled dextran (10 kDa) to the transpiration stream, confirmed that these membrane-impermeant probes could only have been offloaded from the xylem via the xylem vessel-xylem parenchyma pit membranes, suggesting endocytotic transmembrane transfer of these membrane-impermeant fluorophores. Accumulation within the thick-walled sieve tubes, but not in thin-walled sieve tubes, confirms the presence of a symplasmic phloem loading pathway, via pore plasmodesmata between xylem parenchyma and thick-walled sieve tubes, but not thin-walled sieve tubes.|
|C E J Botha; N Aoki; G N Scofield; L Liu; R T Furbank; R G White|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2008-07-09|
|Title: Journal of experimental botany Volume: 59 ISSN: 1460-2431 ISO Abbreviation: J. Exp. Bot. Publication Date: 2008|
|Created Date: 2008-08-11 Completed Date: 2008-11-03 Revised Date: 2013-06-05|
Medline Journal Info:
|Nlm Unique ID: 9882906 Medline TA: J Exp Bot Country: England|
|Languages: eng Pagination: 2945-54 Citation Subset: IM|
|Department of Botany, Rhodes University, Grahamstown 6140, South Africa. email@example.com|
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Fluoresceins / metabolism
Microscopy, Electron, Transmission
Phloem / physiology*, ultrastructure
Plant Leaves / physiology*, ultrastructure
Poaceae / physiology*, ultrastructure
Xylem / physiology*, ultrastructure
Journal ID (nlm-ta): J Exp Bot
Journal ID (hwp): jexbot
Journal ID (publisher-id): exbotj
Publisher: Oxford University Press
? 2008 The Author(s).
open-access: This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
Received Day: 11 Month: 10 Year: 2007
Revision Received Day: 6 Month: 3 Year: 2008
Accepted Day: 6 Month: 5 Year: 2008
Print publication date: Month: 8 Year: 2008
Electronic publication date: Day: 9 Month: 7 Year: 2008
pmc-release publication date: Day: 9 Month: 7 Year: 2008
Volume: 59 Issue: 11
First Page: 2945 Last Page: 2954
PubMed Id: 18617505
|A xylem sap retrieval pathway in rice leaf blades: evidence of a role for endocytosis?|
|C. E. J. Botha1*|
|G. N. Scofield3|
|R. T. Furbank3|
|R. G. White3|
1Department of Botany, Rhodes University, Grahamstown 6140, South Africa
2Department of Agricultural and Environmental Biology, Graduate School of Agricultural and Life Sciences, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, 113-8657, Japan
3CSIRO Plant Industry, GPO Box 1600, ACT 2601, Canberra, Australia
|*To whom correspondence should be addressed. E-mail: firstname.lastname@example.org
Vascular bundles in leaves are compact structures, and xylem and phloem occur in close proximity to each other. The transport of assimilates to the phloem and the recycling of water from the xylem in plant leaves are complex processes (see Canny, 1988, 1993; Evert et al., 1978, and references therein) and most, if not all, of the water entering source phloem may be taken up directly from the transpiration stream as a direct consequence of increased solute concentration within the loading sieve tubes. Transfer from the xylem involves pit membranes situated between tracheary elements and associated parenchyma cells. These pit membranes are characterized by an additional wall layer, deposited next to the plasma membrane of the xylem parenchyma cell abutting xylem vessels. The pit membrane is variously described in the literature as a ?protection? or ?additional layer? (Shaffer and Wisniewski, 1989), which is involved in the control of hydraulic resistance (Zwieniecki et al., 2001). Various free space markers used in the past have demonstrated that water and tracer ions can move from xylem vessels (see Wisniewski et al., 1991) into xylem parenchyma via interconnecting pits, and, more importantly, it has been demonstrated that these tracers end up in the phloem apoplast (Evert et al., 1985; Botha and Evert, 1986; Botha, 2006). Van Bel (1990) noted that transfer from the xylem to the phloem involved several steps including passage across this interface and ultimately uptake by the phloem.
The rice leaf blade, like many other monocotyledonous leaf blades examined to date, contains three longitudinal vein orders. All three (large, intermediate, and small) contain thin- as well as thick-walled sieve tubes which were not previously reported by Chonan and co-workers in their rice leaf blade studies (Chonan et al., 1980, 1981, 1984, 1985). The thick-walled sieve tubes, which are either in direct contact with or in close proximity to metaxylem vessels, may have functions different from those of the thin-walled sieve tubes (Botha and Evert, 1986; Evert et al., 1978, and references therein). The predominant, early metaphloem is composed of thin-walled sieve tube members and associated companion cells, as well as parenchymatous elements. In contrast, thick-walled, late-formed metaphloem sieve tube members lack companion cells and appear to be symplasmically isolated from the thin-walled sieve tube?companion cell complexes. Fossil data suggest that thick-walled sieve tubes have been present in the phloem of grasses for >5 million years (see images in Thomasson et al., 1986). This persistence during such a long period of evolution implies a likely functional role which has so far eluded researchers. For example, Heyser et al. (1978) reported the presence of a tubular substructure in the walls of the thick-walled sieve elements in maize leaves which they felt could be implicated in solute retrieval processes. Recently, Matsiliza and Botha (2002) and Botha and Matsiliza (2004) demonstrated that aphids do not preferentially feed from thick-walled sieve tubes in barley leaves. Evidence from experiments involving retrieval of [14C]sucrose (Heyser et al., 1978) as well as the distribution of cleaved polar molecules such as 5,6-carboxyfluorescein (5,6-CF) suggest that solute retrieval from the xylem could involve thin- as well as thick-walled sieve tubes.
It has been demonstrated in previous studies that the application of a weak solution of 5,6-carboxyfluorescein diacetate (5,6-CFDA) for 10?30?min to the transpiration stream resulted in the appearance of 5,6-CF in cells outside the tracheary elements of vascular bundles in the leaves, some distance from the point of application. Even though 5,6-CFDA could diffuse apoplasmically across cell walls and then enter plant cells, this is unlikely as the first point in the transport pathway where 5,6-CF was detected was always associated with the xylem vessel?xylem parenchyma interface, in the pit membrane regions. These results suggest a localized zone of xylem vessel to xylem parenchyma transfer in leaves (Botha, 2006). Cleavage of 5,6-CFDA requires metabolic activity, and thus could occur only via esterase activity within the living cells abutting metaxylem vessels in these bundles. After cleavage, the highly polar 5,6-CF molecule is not able to cross cell membranes, and cell to cell transport is then symplastic, via plasmodesmata (Wright et al., 1996; Botha, 2006, and relevant literature cited therein).
The focus of this study includes the pit membranes which form the boundary between the apoplast (xylem vessels) and the symplast (xylem parenchyma) in Oryza sativa as in other grass species (Botha, 2006). These pits, and their associated membranes, are considered to be a vital physiological barrier (Zwieniecki et al., 2001) between the apoplasmic and symplasmic compartments. The transmission electron microscopy (TEM) and transport study reported here focuses on the following specific questions:
- Are the xylem vessel?xylem parenchyma pits structurally significant in terms of facilitating solute exchange across this interface?
- Do xylem parenchyma cells have the capacity to take up 5,6-CFDA and cleave the diacetate to form membrane-impermeable 5,6-CF?
- If so, what pathways are involved in the movement of 5,6-CF from xylem parenchyma cells?
- Can it be demonstrated that membrane-impermeant phloem-mobile, symplasmically transported fluorophores, such as 5,6-CF, Texas Red?dextran (TRD) and Lucifer Yellow (LYCH), are transported via the xylem, offloaded into vascular parenchyma elements, and subsequently taken up by thin-walled and/or thick-walled sieve tubes?
- Does the xylem vessel?xylem parenchyma interface provide a solute retrieval pathway?
Rice plants of O. sativa L. cv. Nipponbare were grown to maturity in flooded paddy tanks in a glasshouse, in pots containing 75% compost and 25% perlite supplemented with Osmocote slow-release fertilizer. Growth was under natural light with a daytime temperature of 28??C and a night-time temperature of 25??C. Mature leaves from pre- or post-flowering plants were used in experiments.
Segments from the mid-lamina region of mature vegetative leaves were cut from O. sativa cv. Nipponbare plants directly into cold primary fixative (composed of 2.5% glutaraldehyde and 0.5% paraformaldehyde in 0.1?M sodium cacodylate buffer), and immediately placed in vials containing the fixative in an ice bucket. After 30?min, leaf segments were carefully trimmed to remove edge material damaged during initial specimen preparation. Retrimmed segments were returned to fresh primary fixative. Trimmed segments were fixed in several changes of the primary fixative overnight at 4??C. After several buffer rinses, the leaf tissue was post-fixed in 1% OsO4 in 0.1?M sodium cacodylate buffer, left overnight at 4??C, subsequently dehydrated through a cold ethanol series, followed by several changes of propylene oxide, and embedded in Spurr's resin (hard grade). Ultrathin sections (silver) were stained with uranyl acetate and lead citrate before TEM observation using a JEOL 1210 (Tokyo, Japan) electron microscope. High resolution analogue images were taken on cut film, and selected regions were digitized directly from the negatives using a scanner at 2400?2400 dpi.
A 188?mM stock solution of 5,6-CFDA (Sigma C8166) was prepared in dimethylsulphoxide (DMSO) and was diluted with distilled water to provide a working solution with a final concentration of 0.188?mM. A 40?mM stock solution of sulphorhodamine-101 HCl [Texas Red (TR) Sigma, S3388] was made up in DMSO and diluted with distilled water to a final concentration of 0.04?mM. In dual-probe experiments, 500??l of this working strength solution was diluted further by adding 500??l of distilled water. A 54.7?mM solution of Lucifer Yellow CH (LYCH; dilithium salt Sigma-Aldrich, L0259) was prepared in distilled water and diluted to a 0.547?mM working solution. An aqueous stock solution of 2.5?mM TRD (D1828 neutral, molecular weight 10?000?Da, Molecular Probes) was diluted to a working strength of 0.156?mM in distilled water. Stock and working strength solutions were kept foil-wrapped and stored at ?4??C until needed. Prior to use, the working strength probes were centrifuged at 14?000?g for 15?min, using Microcon 3000?Da or 10?000?Da microconcentrators (Amicon Inc., Beverly, MA, USA) to ensure removal of free fluorochromes.
Fully expanded source (assimilate exporting) leaves were rapidly cut from pre- and post-flowering rice, and immediately transferred into a beaker containing water. As needed, excised leaves were transferred directly into a mixture usually containing equal volumes of working strength 5,6-CFDA and TR. The fluorophore 5,6-CFDA was co-transported with TR. TR is transported in the xylem and remains principally attached to lignified cell walls; it thus revealed the position of the translocating xylem very effectively. Non-polar, non-fluorescent 5,6-CFDA is cleaved only within living cells to form highly fluorescent, strongly polar 5,6-CF once it exits the tracheary elements.
Cut leaves, with their cut ends in dye solution, were illuminated (?150??mol m?2 s?1) using a small 15?W table lamp. Experiments were run for a minimum of 30?min, after which time the position of the 5,6-CF fluorescence front was detected using a green fluorescent protein (GFP) filter set on a Leica MZFLIII or MZ6 stereo fluorescence microscope, and its location carefully marked on the edge of the leaves using a permanent fine point marker pen. Under the experimental conditions described, the fluorescence front was usually 10?cm or more from the cut base of the leaf. The spread of 5,6-CF was monitored in more detail by examining intact leaf tissue and tissue sections taken progressively further from the cut leaf base using an Olympus BX-51 (Olympus, Wirsam Scientific, Johannesburg, South Africa) widefield fluorescence microscope, and multiple fluorescence (m-FIP) images were captured using Analysis 5 (Olympus, Tokyo Japan) imaging software and either a high-resolution F-View, or colourview FX Peltier cooled camera (Olympus, Wirsam Scientific, Johannesburg, South Africa). In all cases, fluorescent probes were detected only in the longitudinal or cross-veins, except in the immediate vicinity of the cut base of the leaf.
Due to the inherent difficulties associated with cutting longitudinal sections of living tissue and still retaining cell integrity, thick (50?200??m) transverse sections were routinely prepared. Leaves were examined not less than 10?cm from the cut end of the leaf to ensure that transport in undamaged tissue was observed. Using single-edge razor blades, transverse sections were cut directly into silicone oils (to minimize loss of the fluorophore from exposed cells) and transferred directly to microscope slides. Sections were mounted in silicone oil under coverslips and examined immediately using a Leica TCS SP2 confocal laser scanning microscope (CLSM). The 5,6-CF was excited by the 488?nm line from an argon?ion laser, whilst TR was excited with the 543?nm line from a He?Ne laser. Fluorescence emission was collected over 500?530?nm for 5,6-CF, 610?635?nm for TR, and 680?720?nm for chlorophyll autofluorescence. In experiments using LYCH, fluorescence emission was collected over 500?580?nm following excitation at 405?nm. The confocal images presented here are representative of many replicate experiments.
The xylem of the intermediate leaf blade vascular bundles is composed of metaxylem vessels and parenchyma (Fig. 1a?d), and the phloem contains two types of sieve tube?early metaphloem (S; described as thin-walled), associated with companion cells (CC), and late-formed metaphloem (described as thick-walled; arrowheads in Fig. 1a indicate two thick-walled sieve tubes). These thick-walled sieve tubes lacked companion cells (Fig. 1a, c), but were in symplasmic contact with vascular parenchyma (details of pore-plasmodesmata not shown). Xylem vascular parenchyma (XVP; Fig. 1a, d) was connected via plasmodesmata (Fig. 1b) to other vascular parenchyma (VP) and by pore-plasmodesmata (paired arrowheads, Fig. 1c) to thick-walled sieve tubes. Of interest were the thin-walled structures between the metaxylem vessels and XVP (arrows, Fig. 1d). This pit structure has been described elsewhere as a hydrolysed wall (Evert et al. 1978).
In a more detailed examination of the pit region between metaxylem vessels and the xylem parenchyma (Fig. 2a?f), the wall appeared porous, with a complex substructure (Fig. 2a, b). Furthermore, the inner face of the wall (nearest the vascular parenchyma) appeared more electron-dense than the outer face associated with the metaxylem vessel. This interface contained numerous vesicles (short arrows, Fig. 2d) between the parenchyma cell plasma membrane and the hydrolysed pit membrane. Stalked vesicles (Fig. 2c, arrow) were appressed to the outer plasma membrane leaflet, and were apparently encapsulated by a double unit membrane (V, Fig. 2e). Occasionally, large, distinctly granular plasma membrane blebs (Fig. 2f) were observed in the pit membrane region. Pit-containing xylem parenchyma cells always contained large mitochondrial populations (M; Fig. 2a, b), which were, in turn, closely associated with dictyosomes and endoplasmic reticulum (D and ER respectively, Fig. 2b). Although not quantified, all vascular parenchyma cells examined were well connected by plasmodesmata (Fig. 1b), which is in agreement with previous studies of monocotyledonous leaves (Botha, 2006). When examined at higher magnification, the wall structure in the pit regions appeared sponge-like with numerous narrow tubular substructures (Fig. 2c?e).
Previous work showed rapid movement of 5,6-CFDA through the xylem and rapid appearance of its cleavage product, 5,6-CF, within leaf vascular parenchyma (Botha, 2006). This observation and the TEM study described above led to examination of the potential transport pathway from xylem vessels to xylem parenchyma cells in more detail.
Upon supplying 5,6-CFDA to the transpiration stream, it was first determined that within 30?min, the 5,6-CF produced by cleavage of 5,6-CFDA at the cut surface of the leaf diffused no more than 1?cm through basal leaf tissues (Fig. 3a). Close to the cut surface, cross-sections showed a wide distribution of 5,6-CF throughout all leaf tissues (Fig. 3b); however, as close as 1?mm from the surface (Fig. 3c), the dye was largely restricted to living cells, indicating diffusion of dye cleaved by esterases within living cells rather than diffusion of cleaved dye in the external solution and apoplast. A more detailed examination of single vascular bundles showed TR in cell walls of xylem vessels and vascular parenchyma 20?cm from the cut surface 30?min after supply to the cut end of the leaf (Fig. 4). In contrast, 5,6-CF was seen only in the cytoplasm of vascular parenchyma at 10?cm from the cut surface, and was absent from the phloem by 3?cm from the cut. It was concluded that 5,6-CF seen in living cells of leaf cross-sections taken at least 10?cm from the cut surface of the leaf represented intracellular cleavage of intact 5,6-CFDA supplied by the xylem.
Confocal images (Fig. 5) confirmed that the localization of 5,6-CF was clearly intracellular, and associated with living cells only (this is most clearly demonstrated in Fig. 5a). Some parenchymatous elements adjacent to the protoxylem lacuna contained 5,6-CF (Fig. 5d), but there was no evidence of back-leakage of the fluorophore into the protoxylem cavity. 5,6-CF fluorescence was never observed within xylem vessels, in either large (Fig. 5a, d), intermediate (Fig. 5b, c), or small (Fig. 5f) vascular bundles. The fluorophore only occasionally appeared in sieve tubes. Phloem parenchyma cells also contained 5,6-CF (see Fig. 5e for detail), but none was evident in the companion cells or the metaphloem sieve tubes (S) in images from this series of sections. Of note was that 5,6-CF was taken up by the thick-walled sieve tubes (paired arrowheads, Fig. 5c, f) and transported laterally to a connected thin-walled sieve tube (TST) within the transverse vein. Some 5,6-CF fluorescence was seen occasionally outside the vascular bundle (Fig. 5b). Given that there are plasmodesmata along the interfaces from the vascular parenchyma through the bundle sheath and into the mesophyll, this result is not surprising as water diffuses rapidly and presumably can make use of the symplasmic pathway that exists from vascular parenchyma to the mesophyll. It is clear that the results presented here are in line with earlier findings (Botha, 2006; Wright et al., 1996) that cleavage of 5,6-CFDA occurs within the living (symplasmic), rather than the non-living (apoplasmic) domain.
The uptake and distribution of a relatively small (LYCH) or large (10?kDa TRD) apoplasmic fluorophore was assessed to make a comparison with the symplastic movement of 5,6-CF. It was assumed that these dyes would differ mainly in the extent of their migration through the apoplast. Figure 6 shows that LYCH (Fig. 6a) was taken up into the symplast of xylem parenchyma around the metaxylem (MX) and protoxylem (PX), and spread throughout the vascular parenchyma and thick-walled sieve tubes (S). The TRD spread rapidly from the MX (Fig 6a, b) and PX (inset) in both large (Fig. 6b) and small (Fig. 6c) intermediate veins. The dye was detected throughout vascular parenchyma and in thick-walled sieve tubes and, as illustrated here, within some thin-walled metaphloem sieve tubes (arrow in Fig. 6c). Neither LYCH nor TRD was detected in any xylem vessels.
This study, in part, addresses a fundamental question in plant water relations physiology: what is the fate of material transported passively in the xylem? Clearly, these substances must be retrieved and recycled for distribution to regions where they are required. The current TEM study shows that the major interface between xylem vessels and associated xylem parenchyma is the pit membrane. At this interface, the fenestrated xylem vessel wall with its complex compartmented membrane structure and associated membrane-bound vesicles (Fig. 5a?f) suggests an active transmembrane transport process other than simple diffusion. Vesiculation in close proximity to dictyosomes, together with large mitochondrial populations, suggest that this interface may play an important physiological role in apoplast to symplast transfer, which could be regulated through ion-mediated and dynamic changes in hydrogels (Zwieniecki et al., 2001). LYCH crossed the interface between the xylem vessel and xylem parenchyma, implying that active membrane transport may be involved. LYCH has previously been shown to enter the vacuole of a range of plant cell protoplasts from the external medium (Wright and Oparka, 1989). That LYCH as well as TRD could cross the interface between the xylem vessels and xylem parenchyma is good evidence for a complex interchange process (endo- and/or exocytosis) between the apoplast and the symplast in the rice leaf.
It has been demonstrated, using CLSM, that 5,6-CFDA, LYCH, and TRD can exit the xylem and that, in the case of 5,6-CFDA, its polar fluorescent cleavage product, 5,6-CF, appears first in the xylem parenchyma cells abutting the xylem vessels (Figs 3?6). Beyond the zone of damaged cells at the cut base of the leaf (500??m to no more than 1000??m, Fig. 3), the xylem parenchyma are the first receiver cells for cleaved 5,6-CF (Fig. 4). Examination of whole leaf material confirmed that fluorescent areas were discrete and sometimes patchy in distribution (data not shown), suggesting that the 5,6-CF was trafficked symplasmically from discrete locations rather than simply leaking from the xylem. Taken together, the data presented here strongly support a localized pathway for retrieval of materials from the xylem (apoplasm) into the living parenchyma cells (symplasm) via pit membranes, after which the fluorescent, highly polar 5,6-CF can be transported away from the xylem parenchyma. Lack of diffuse fluorescence across multiple cell types of the leaf after 5,6-CFDA feeding indicates that lateral diffusion of the uncleaved dye followed by later cleavage in cells distant from xylem parenchyma was unlikely in these experiments. The same conclusion was reached by previous groups using this dye (see discussion in Wright et al., 1989, 1996).
Data for LYCH and TRD transport suggest that the highly complex pit membrane region may be a site of uptake from xylem apoplast to xylem parenchyma symplast, via transfer across the permeable cell wall and parenchyma plasma membrane. The membrane vesiculation in this region suggests a role for endocytosis in uptake of these normally membrane-impermeant dyes. Earlier TEM analysis demonstrated a distinct export pathway of lanthanum and lead nitrate, as well as Prussian blue, from the transpiration stream to the mesophyll (Botha and Evert, 1986, and references therein). Larger tracers, such as the TRD used here, are not usually transported readily across cell walls; thus the loose cell wall structure of the pit membrane seen in the TEM images probably reflects a high capacity for transfer across this wall. Hence, the xylem parenchyma and specialized pit membranes appear to contain specific features for uptake and transfer of small and large solutes from the xylem into the vascular symplasm.
Beyond the xylem parenchyma, symplasmic communication occurs through functional plasmodesmata, but grasses have been generally shown to have low connectivity between vascular parenchyma cells and the companion cell?sieve tube (CC?ST) complexes (Botha, 1992, 2006; van Bel, 1993, and references therein), and more than one operational pathway may be involved in cell?cell transport. The confocal images showing movement of these fluorophores from xylem parenchyma through phloem parenchyma to the CC?ST complexes unequivocally demonstrate the presence of a symplasmic pathway connecting these cells. Free space markers, in contrast, remain confined to the apoplasmic pathway, intercellular spaces, and cell walls, and their movement is, for the most part, along lignified walls (Botha and Evert, 1986). Once the fluorophores reach the CC?ST complexes, they may be transported laterally across the leaf via the transverse connecting strands common in cereal leaves (Fig. 5f), and then into surrounding tissues.
The CLSM study clearly shows fluorescence within a few sieve tubes in vascular bundles (see Fig. 5f). However, the disjunction between vascular parenchyma and the CC?ST (thin-walled ST; Botha, 1992, 2006; Botha and van Bel, 1992) would seem to preclude significant 5,6-CF symplasmic movement and subsequent accumulation in the thin-walled sieve tubes (see Fig. 5e). In contrast, pore-plasmodesmata between vascular parenchyma and thick-walled sieve tubes may provide a pathway for 5,6-CF entry (see Fig. 5f). There may not be a high flux through this transport pathway as dye feeding experiments demonstrate symplasmic connectivity rather than dynamic transport rates. Moreover, the reported low osmotic potential within (Evert et al., 1978), and the lack of interest of aphids in thick-walled sieve tubes (Botha and Matsiliza, 2004), together with the low plasmodesmatal frequencies reported at the interface between vascular parenchyma and either thick-walled sieve tubes or companion cells, is further evidence that this is not a major assimilate accumulation pathway. Nevertheless, the retrieval of 5,6-CF by thick-walled sieve tubes, together with earlier results by Fritz et al. (1983) showing that the thick-walled sieve tubes in leaf blade veins of Zea are involved in [14C]sucrose retrieval by these sieve tubes, demonstrates a functional symplasmic pathway to thick-walled sieve tubes in grasses.
A model of assimilate and solute flow consistent with the data presented here is shown in Fig. 7. Water, ions, and dissolved substances are carried in the xylem and offloaded in transpiring, photosynthesizing leaves, via hydrolysed pit membranes into xylem parenchyma cells. Transfer from the apoplast to the symplast involves passage through the pit membrane between xylem vessels and xylem parenchyma, across the vascular parenchyma cell plasma membrane, where porosity may be enhanced in pectin-rich walls (Baron-Epel et al., 1988). The present TEM and dye transport data provide evidence that this interface is also important in retrieval of larger solutes, possibly via endocytosis. It has been suggested that interface permeability may be regulated by calcium flux, in effect acting to regulate passage of substances, whether secretion via Golgi-related vesicles (Benayoun, 1983) or the control of xylem physiology (Schaffer and Wisniewski, 1989) including changes in diameters of microchannels in the pit membranes (Zwieniecki et al., 2001), or the movement of virus particles through calcium-mediated disruption of the pit membrane (Opalka et al., 1998).
In this study, a pathway for the recovery of material from the apoplast to the symplast in O. sativa leaf blades was demonstrated. It was concluded that all xylem parenchyma cells are potentially involved in this recovery/transport pathway, as demonstrated by their ability to take up membrane-impermeant fluorophores. It is proposed that the pit membranes in rice leaf blade vascular bundles?specifically those at the interface with xylem parenchyma cells?are potentially a major traffic pathway and that they are probably involved in retrieval, regulating resorption and movement across the apoplast?symplast interface of a wide range of material within leaves.
|CLSM||confocal laser scanning microscopy|
|LYCH||Lucifer Yellow carbonyl hydrazine|
|TEM||transmission electron microscopy|
We thank Celia Miller for assistance with the preparation of some of the initial samples for TEM. The National Research Foundation Pretoria is acknowledged for grants to CEJB for travel to CSIRO, Canberra, where the confocal study was undertaken.
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Keywords: Apoplasmic and symplasmic transport, companion cell, exo- and endocytosis, Oryza sativa, pit membrane, rice, thick-walled sieve tube, thin-walled sieve tube, xylem parenchyma.
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