Influence of microgravity on root-cap regeneration and the structure of columella cells in Zea mays

We launched imbibed seeds and seedlings of Zea mays into outer space aboard the space shuttle Columbia to determine the influence of microgravity on 1) root-cap regeneration, and 2) the distribution of amyloplasts and endoplasmic reticulum (ER) in the putative statocytes (i.e., columella cells) of roots. Decapped roots grown on Earth completely regenerated their caps within 4.8 days after decapping, while those grown in microgravity did not regenerate caps. In Earth-grown seedlings, the ER was localized primarily along the periphery of columella cells, and amyloplasts sedimented in response to gravity to the lower sides of the cells. Seeds germinated on Earth and subsequently launched into outer space had a distribution of ER in columella cells similar to that of Earth-grown controls, but amyloplasts were distributed throughout the cells. Seeds germinated in outer space were characterized by the presence of spherical and ellipsoidal masses of ER and randomly distributed amyloplasts in their columella cells. These results indicate that 1) gravity is necessary for regeneration of the root cap, 2) columella cells can maintain their characteristic distribution of ER in microgravity only if they are exposed previously to gravity, and 3) gravity is necessary to distribute the ER in columella cells of this cultivar of Z. mays.     

A morphometric analysis of cellular differentiation in root caps ofCucurbita peop

In order to quantify the ultrastructural changes that occur during cellular differentiation in an “open” type of root cap, we have performed a morphometric analysis of the ultrastructures of calyptrogen, columella, and peripheral cells of the root cap ofCucurbita pepo. The relative volumes of nuclei, nucleoli, and mitochondria decrease as cells move (i.e., differentiate) through the root cap. Before cells are sloughed from the cap, the relative volume of the vacuole increases by 250%. The relative volumes of plastids and plastid starch increase as calyptrogen cells differentiate into columella cells, but decrease as columella cells differentiate into peripheral cells. Dictyosomal volumes increase only as columella cells differentiate into peripheral cells. These results indicate that the five cell types comprising the root cap ofC.pepo are each characterized by a unique structure, and that the ultrastructural changes associated with cellular differentiation in root caps are organelle specific. These results are discussed relative to the functions of the various cell types of the root cap.     

A MORPHOMETRIC ANALYSIS OF CELLULAR DIFFERENTIATION IN THE ROOT CAP OF ZEA MAYS

In order to quantify the ultrastructural changes associated with cellular differentiation, we have performed a morphometric analysis of the ultrastructure of the calyptrogen, columella, and peripheral cells of the root cap of Zea mays. The relative volumes of the nucleus, nucleolus, and mitochondria in the protoplasm gradually decrease as a cell moves through the root cap. The relative volume of plastids increases 240% during the differentiation of calyptrogen cells into columella cells. This increase is transient, however, since the relative volume of plastids as well as starch in plastids decreases markedly as columella cells differentiate into peripheral cells. Dictyosomes and spherosomes increase more gradually than plastids, peaking in relative volume in the innermost peripheral cells (PCI). The relative volume of the vacuome decreases as calyptrogen cells differentiate into columella cells, after which it increases during the differentiation of peripheral cells. By the time the outermost peripheral cells (PCIII) are sloughed from the cap, the relative volume of the vacuome has almost tripled. These results indicate that each cell type comprising the root cap of Zea mays is characterized by a distinctive ultrastructure. Furthermore, the ultrastructural changes associated with the differentiation of these cells are organelle specific. The results of this study are discussed relative to the function of the various cell types of the root cap.     

CELLULAR VOLUME AND TISSUE PARTITIONING IN CAPS OF PRIMARY ROOTS OF ZEA MAYS

Cellular and tissue volumes were measured in caps of primary roots of Zea mays. There is an 850% increase in cellular volume as cellular function changes from that of being meristematic (i.e., calyptrogen cells) to graviperception (i.e., columella cells), and a 22% increase in cellular volume during the functional transition from graviperception to the production and secretion of mucilage. Cellular volume does not change significantly after cells cease mucilage production and are sloughed from the cap. Root caps of Z. mays allocate 7.5% of their volume for regeneration, 14.9% for graviperception, 24.3% for the transition of function from graviperception to mucilage production and secretion, and 38.7% for the production and secretion of mucilage. The remaining 14.5% of the cap volume is comprised of cells being sloughed from the cap.     

Cellular Differentiation and Tissue Partitioning in Caps of Primary and Lateral Roots of Helianthus annuus

Cellular and tissue volumes in caps of primary and lateral rootsof Helianthus annuus have been measured in order to determinequantitatively how tissues and their functions are partitionedin root caps. Patterns of change in cellular dimensions andvolumes are similar in caps of primary and lateral roots. Significantincreases in cellular dimensions and volume occur during thedifferentiation of columella cells and the innermost peripheralcells. There are no significant changes in cellular dimensionsas either (i) the production and secretion of mucilage begins,or (ii) cells are sloughed from the cap. Tissues are partitionedsimilarly in caps of primary and lateral roots. indeed, rootcaps allocate 7–8 per cent of their volume for regeneration(i.e. calyptrogen tissue), 16–19 per cent of their volumefor graviperception (i.e. columella tissue), and approx. 38per cent of their volume for the production and secretion ofmucilage. These results are discussed relative to patterns ofcellular differentiation and tissue function in root caps. Helianthus annuus, root caps, primary root, lateral root, calyptrogen, columella, peripheral cells, tissue partitioning     

Root Graviresponsiveness and Cellular Differentiation in Wild-type and a Starchless Mutant of Arabidopsis thaliana

Primary roots of a starchless mutant of Arabidopsis thalianaL. are strongly graviresponsive despite lacking amyloplastsin their columella cells. The ultrastructures of calyptrogenand peripheral cells in wild-type as compared to mutant seedlingsare not significantly different. The largest difference in cellulardifferentiation in caps of mutant and wild-type roots is therelative volume of plastids in columella cells. Plastids occupy12.3% of the volume of columella cells in wild-type seedlings,but only 3.69% of columella cells in mutant seedlings. Theseresults indicate that: (1) amyloplasts and starch are not necessaryfor root graviresponsiveness; (2) the increase in relative volumeof plastids that usually accompanies differentiation of columellacells is not necessary for root graviresponsiveness; and (3)the absence of starch and amyloplasts does not affect the structureof calyptrogen (i.e. meristematic) and secretory (i.e. peripheral)cells in root caps. These results are discussed relative toproposed models for root gravitropism. Arabidopsis thaliana, gravitropism (root), plastids, root cap, stereology, ultrastructure     

Cellular differentiation in root caps of Zea mays that do not secrete mucilage

We quantified the structural changes accompanying cellular differentiation in root caps of Zea mays cv. Ageotropic to determine the developmental basis for the nongraviresponsiveness of their primary roots. Cells of the calyptrogen and columella of primary roots of the ageotropic mutant have structures indistinguishable from those of caps of primary roots of Z. mays cv. Kys the graviresponsive, wild-type parent of Z. mays cv. Ageotropic. However, the relative volumes of dictyosomes, dictyosome-derived vesicles and starch in the outermost peripheral cells of wild-type roots were significantly lower than were those in peripheral cells of mutant roots. This corresponds to a dramatic accumulation of starch and mucilage-filled vesicles in peripheral cells of mutant roots. Cellular differentiation in root caps of graviresponsive seminal roots of the Ageotropic mutant resembled that of primary and seminal roots of the wild-type cultivar, and differed significantly from that of primary roots of the mutant. We conclude that the mutation that blocks secretion of mucilage from peripheral cells of Ageotropic roots: (1) expresses itself late in cellular differentiation in root caps; (2) is expressed only in primary (but not seminal) roots of the Ageotropic mutant; and (3) is consistent with malfunctioning dictyosomes and dictyosome-derived vesicles being the cellular basis for agravitropism of primary roots of this mutant.     

Early root cap development and graviresponse in white clover (Trifolium repens) grown in space and on a two-axis clinostat.

White clover (Trifolium repens) was germinated and grown in microgravity aboard the Space Shuttle (STS-60, 1994; STS-63, 1995), on Earth in stationary racks and in a slow-rotating two-axis clinostat. The objective of this study was to determine if normal root cap development and early plant gravity responses were dependent on gravitational cues. Seedlings were germinated in space and chemically fixed in orbit after 21, 40, and 72 h. Seedlings 96 h old were returned viable to earth. Germination and total seedling length were not dependent on gravity treatment. In space-flown seedlings, the number of cell stories in the root cap and the geometry of central columella cells did not differ from those of the Earth-grown seedlings. The root cap structure of clinorotated plants appeared similar to that of seedlings from microgravity, with the exception of three-day rotated plants, which displayed significant cellular damage in the columella region. Nuclear polarity did not depend on gravity; however, the positions of amyloplasts in the central columella cells were dependent on both the gravity treatment and the age of the seedlings. Seedlings from space, returned viable to earth, responded to horizontal stimulation as did 1 g controls, but seedlings rotated on the clinostat for the same duration had a reduced curvature response. This study demonstrates that initial root cap development is insensitive to either chronic clinorotation or microgravity. Soon after differentiation, however, clinorotation leads to loss of normal root cap structure and plant graviresponse while microgravity does not.     

The Influence of Gravity on the Formation of Amyloplasts in Columella Cells of Zea mays L

Columella (i.e., putative graviperceptive) cells of Zea mays seedlings grown in the microgravity of outer space allocate significantly less volume to putative statoliths (amyloplasts) than do columella cells of Earth-grown seedlings. Amyloplasts of flight-grown seedlings are significantly smaller than those of ground controls, as is the average volume of individual starch grains. Similarly, the relative volume of starch in amyloplasts in columella cells of flight-grown seedlings is significantly less than that of Earth-grown seedlings. Microgravity does not significantly alter the volume of columella cells, the average number of amyloplasts per columella cell, or the number of starch grains per amyloplast. These results are discussed relative to the influence of gravity on cellular and organellar structure.     

The Involvement of Glucose-6-Phosphatase in Mucilage Secretion by Root Cap Cells of Zea mays

In order to determine the involvement of glucose-6-phosphatasein mucilage secretion by root cap cells, we have cytochemicallylocalized the enzyme in columella and peripheral cells of rootcaps of Zea mays. Glucose-6-phosphatase is associated with theplasmalemma and cell wall of columella cells. As columella cellsdifferentiate into peripheral cells and begin to produce andsecrete mucilage, glucose-6-phosphatase staining intensifiesand becomes associated with the mucilage and, to a lesser extent,the cell wall. Cells being sloughed from the cap are characterizedby glucose-6-phosphatase staining being associated with thevacuole and plasmalemma. These changes in enzyme localizationduring cellular differentiation in root caps suggest that glucose-6-phosphataseis involved in the production and/or secretion of mucilage byperipheral cells of Z. mays. Zea mays, corn, glucose-6-phosphatase, columella cell, peripheral cell, mucilage, secretion, cytochemistry     

Morphometric analysis of epidermal differentiation in primary roots of Zea mays

Epidermal differentiation in primary roots of Zea mays was divided into six cell types based on cellular shape and cytoplasmic appearance. These six cell types are: 1) apical protoderm, located at the tip of the root pole and characterized by periclinally flattened cells; 2) cuboidal protoderm, located approximately 230 microns from the root pole and characterized by cuboidal cells; 3) tabular epidermis, located approximately 450 microns from the root pole and characterized by anticlinally flattened cells; 4) cuboidal epidermis, located approximately 900 microns from the root pole and characterized by cuboidal cells having numerous small vacuoles; 5) vacuolate cuboidal epidermis, located approximately 1,500 microns from the root pole and characterized by cuboidal cells containing several large vacuoles; and 6) columnar epidermis, located approximately 2,200 microns from the root pole (i.e., at the beginning of the zone of elongation) and characterized by elongated cells. We also used stereology to quantify the cellular changes associated with epidermal differentiation. The quiescent center and the apical protoderm have significantly different ultrastructures. The relative volume of dictyosomes increases dramatically during the early stages of epidermal differentiation. This increase correlates inversely with the amount of coverage provided by the root cap and mucilage.     

Influence of Microgravity on Cellular Differentiation of Root Apical Meristematic Cap in Rice Seedling

Three groups of experimental treatment of rice seeds were designed: (1) As control,the seeds were germinated(1–3 days after imbibition) and sprouted (4–7 days after imbibition) at static state, (2) Seeds were germinated under microgravity simulated by the horizontal clinostat,and (3) Seeds were germinated at the static state and sprouted under microgravity. The differentiation of the apical meristematic cap of the seedling was observed. 1. Germination and sprouting in the static state (CK), the root apical meristematic cap cells could differentiate into statocysts which could sense the least irritation of the gravity. The amyloplasts of statocysts deposited in the distal region,later changed into secretory cells ,and finally resulted in exocytosis which led the root tip cells to fall off during the cap growth. 2. The rice seedlings germinating and sprouting under microgravity,the apical meristematic cap cells differentiated into statocysts but the amyloplasts in the statocyst were distributed throughout the cell and a central vacuole was formed. The statocysts could form nonsecretory cells similar to the cells in the dividing and elongating area without exocytosis. The number of the root cap cell layers increased and root cap elongated. 3. The rice seedlings germinating in the static state and sprouting under micro-gravity,the amyloplasts of the statocyst were scattered in the cell. The statocysts became vacuolized quickly but remaind on the root cap.     

An Experimental Study of Cell and Nuclear Growth and Their Relation to Cell Diversification within a Plant Tissue

Roots of Zea mays were grown for four days in a solution of colchicine that inhibits cell division. During this period the amount of cell growth and nuclear DNA replication was measured in different regions of the root cap. The rates at which cell volume and nuclear DNA content double are similar in the first cell-tier of the cap (the meristematic stem-cell) but in more distal cells the rate of cell growth outstrips the rate of nuclear DNA increase. It is suggested that the degree of coordination between cell and nuclear growth regulates meristematic activity and can influence the onset of cell differentiation.
The pattern of endopolyploidy changes in the different regions of the colchicine-treated root cap. It is suggested that the degree of endopolyploidy normally characteristic of cells at particular locations within this tissue is not a response to a positional signal alone; it is more likely to be due to some rate-limiting control of DNA synthesis.     

Effects of light on protein patterns in gravitropically stimulated root caps of corn

In certain cultivars of corn (Zea mays var. Merit), light stimulates gravitropic bending of the root by influencing events in the root cap. In this paper, we report on changes in root cap proteins which occur as a result of the light treatment and single out specific proteins as potentially having a role in mediating the gravitropic response. For this work, we have used root caps maintained aseptically in culture media supplemented with auxin. If auxin is deleted from the culture medium, the protein profiles observed following illumination differ from that seen in caps provided light while in auxin-supplemented media. We also report that several of the proteins for which synthesis is stimulated by light appear to turn over rapidly, usually within 0.5 hour of formation.     

Sloughing of root cap cells decreases the frictional resistance to maize (Zea mays L.) root growth

Root caps provide a protective layer in front of the meristemthat protects the meristem from abrasion by soil particles.The continuous production and sloughing of the root cap cellsmay be an adaptation to decrease the friction at the soil-rootinterface by acting as a low-friction lining to the channelformed by the root. Experiments were performed which providethe first direct evidence that such cell sloughing decreasesfrictional resistance to root penetration. The penetration resistance (force per unit crosssectional area)to maize roots, which were pushed mechanically into the soil,was compared with the penetration resistance to growing rootsand to 1 mm diameter metal probes (cone semi-angles of 7.5or 30). The pushed roots experienced only about 40% of thepenetration resistance experienced by the 7.5 metal probe thatwas pushed into the soil at the same rate. Thus, the frictionbetween the soil and the pushed root was much smaller than betweenthe soil and the metal probe. The penetration resistance tothe growing root was between 50% and 100% of that to the pushedroot, indicating that the relief of friction and slower rateof soil compression were more efficient around the growing root.SEM examination of the surface of roots pushed or grown intothe soil showed that numerous root cap cells had detached fromthe cap and slid for several millimetres relative to the root.The low friction properties of roots may be due largely to thelow coefficient of friction between sloughing root cap cells,and may be decreased further by intracellular mucilage secretions. Key words: Zea mays, root cap, frictional resistance, root penetration, cell sloughing     

How Effectively Does a Clinostat Mimic the Ultrastructural Effects of Microgravity on Plant Cells?

Columella cells of seedlings of Zea mays L. cv. Bear Hybridgrown in the microgravity of orbital flight allocate significantlylarger relative-volumes to hyaloplasm and lipid bodies, andsignificantly smaller relative-volumes to dictyosomes, plastids,and starch than do columella cells of seedlings grown at I g.The ultrastructure of columella cells of seedlings grown atI g and on a rotating clinostat is not significantly different.However, the ultrastructure of cells exposed to these treatmentsdiffers significantly from that of seedlings grown in microgravity.These results indicate that the actions of a rotating clinostatdo not mimic the ultrastructural effects of microgravity incolumella cells of Z. mays. Zea mays L., gravity, microgravity, ultrastructure, clinostat, space shuttle, space biology     

Actin microfilaments in presumptive statocytes of root caps and coleoptiles

Rhodamine-phalloidin was used to determine the distribution of actin microfilament bundles (mfb) in cells thought to be the site of gravity perception (statocytes) in coleoptiles and root caps of Zea mays and Hordeum vulgare. In coleoptile cells, amyloplasts were usually observed in close proximity to thick mfb, which often appeared to divide into finer mfb adjacent to individual amyloplasts. The nucleus in these cells was surrounded by an extensive network of mfb, which were connected to thicker transvacuolar mfb. Columella cells of the root cap contained an extensive reticulum of fine mfb throughout the protoplast, but lacked the much thicker mfb seen in coleoptile cells. The distribution and extent of mfb observed in fixed cells correlates with patterns of streaming and amyloplast movement seen in living cells. A possible role for actin mfb in the perception of gravity is discussed.     

Influence of a weak DC electric field on root meristem architecture

BACKGROUND AND AIMS: Electric fields are an important environmental factor that can influence the development of plants organs. Such a field can either inhibit or stimulate root growth, and may also affect the direction of growth. Many developmental processes directly or indirectly depend upon the activity of the root apical meristem (RAM). The aim of this work was to examine the effects of a weak electric field on the organization of the RAM. METHODS: Roots of Zea mays seedlings, grown in liquid medium, were exposed to DC electric fields of different strengths from 0.5 to 1.5 V cm(-1), with a frequency of 50 Hz, for 3 h. The roots were sampled for anatomical observation immediately after the treatment, and after 24 and 48 h of further undisturbed growth. KEY RESULTS: DC fields of 1 and 1.5 V cm(-1) resulted in noticeable changes in the cellular pattern of the RAM. The electric field activated the quiescent centre (QC): the cells of the QC penetrated the root cap junction, disturbing the organization of the closed meristem and changing it temporarily into the open type. CONCLUSIONS: Even a weak electric field disturbs the pattern of cell divisions in plant root meristem. This in turn changes the global organization of the RAM. A field of slightly higher strength also damages root cap initials, terminating their division.     

Stage-dependent border cell and carbon flow from roots to rhizosphere

Rising CO(2) levels in the atmosphere have drawn attention to the important role of soil in sequestering carbon. This project goal was to quantify soil carbon deposition associated with border cell release and exudation from root growth zones. Carbon was measured with a Carlo Erba C/N analyzer in soil from the rhizosphere of mature grasses and, in separate experiments, in soil collected around root growth zones. Root border cells in "rhizosphere soil" (silica sand) were counted using a compound microscope after soil sonication and extraction with surfactant. For sand-grown Bromus carinatus, Zea mays, and Cucumis sativus, young seedlings (with roots shorter than 2 cm) released thousands of border cells, while older root tips released only hundreds. For a variety of native annual and perennial grasses and invasive annual grasses (Nassella pulchra, B. carinatus, B. diandrus, B. hordeaceus, Vulpia microstachys, Aegilops triuncialis, Lolium multiflorum, Zea mays), the rhizosphere of mature root systems contained between 18 and 32 μg C g(-1) sand more than that of the unplanted controls. Spatial analysis of the rhizosphere around the cucumber growth zone confirmed C enrichment there. The root tip provided C to the rhizosphere: 4.6 μg C in front of the growing tip, with the largest deposition, 20.4 μg C, to the rhizosphere surrounding the apical 3 mm (root cap/meristem). These numbers from laboratory studies represent the maximum C that might be released during flooding in soils. Scaling up from the organ scale to the field requires a growth analysis to quantify root tip distributions in space and time.     

Cytochemical localization of calcium in cap cells of primary roots of Zea mays L

The distribution of calcium (Ca) in caps of vertically- and horizontally-oriented roots of Zea mays was monitored to determine its possible role in root graviresponsiveness. A modification of the antimonate precipitation procedure was used to localize Ca in situ. In vertically-oriented roots, the presumed graviperceptive (i.e., columella) cells were characterized by minimal and symmetric staining of the plasmalemma and mitochondria. No precipitate was present in plasmodesmata or cell walls. Within 5 min after horizontal reorientation, staining was associated with the portion of the cell wall adjacent to the distal end of the cell. This asymmetric staining persisted throughout the onset of gravicurvature. No staining of lateral cell walls of columella cells was observed at any stage of gravicurvature, suggesting that a lateral flow of Ca through the columella tissue of horizontally-oriented roots does not occur. The outermost peripheral cells of roots oriented horizontally and vertically secrete Ca through plasmodesmata-like structures in their cell walls. These results are discussed relative to proposed roles of root-cap Ca in root gravicurvature.