Growth Pattern and Movement of Epidermal Cells within Leaves of Asphodelus tenuifolius Cav.

The pattern of growth (velocity field) in the intercalary growthzones of monocotyledon leaves can be determined from patternsof cell number density (number per unit length of cell file)and leaf elongation rates using theory based on a cell numberconservation equation. The case where elongation rate is non-steadywhile the pattern of cell number density is steady is discussedand a method for extending calculations into the meristem usingobservations of numbers of mitotic cells is outlined. Applicationof these methods is illustrated using data for epidermal cellsin the first leaf of Asphodelus tenuifolius Cav. During earlyleaf development, leaf elongation rate increased exponentiallybut cell number density and mitotic number density were steady.Cells 0.1 mm from the base of the leaf when leaves were 3.2mm long took 8.3 d to move through the growth zone. In leavesthat were 4 d older, similar cells took 5.1 d to traverse thegrowth zone. Increases in the rates of leaf elongation and ofcell movement appeared to be associated mainly with increasesin total rates of cell production in the epidermal meristem. Asphodelus tenuifolius Cav., Asphodelus fistulosus L., velocity field, meristem, mitotic cell number density, extension-only zone     

Structure and Histochemistry of Stomata and Epidermal Cells in Five Species of Polypodiaceae

The epidermal structure of the five species of ferns, Arthromeriswallichiana (Spr.) Ching., Drymoglossum piloselloides (Prest.),Drynaria quercifolia (L.) J. Smith, Lepisorus nudus (Hook.)Ching. and Pyrrosia nuda (Gies.) Ching., has been investigated.Fifteen types of stomatal structures have been identified ofwhich copolo-desmocytic and coperi-desmocytic are new types.Four more possible stomatal structures: ccpolo-peri-, codesmo-polo-,codesmo-peri- and duplodesmocytic, are suggested. Localizationof starch, insoluble polysaccharides, protein and lipids hasbeen examined histochemically in the guard cells, subsidiarycells and epidermal cells. In Drynaria starch plastids and plastidscontaining both starch and protein are present in guard cells.Starch plastids are present in the subsidiary cells of all speciesexcept in Arthromeris, whereas, they are present in epidermalcells of only Drymoglossum and Lepisorus. Granular or amorphousinsoluble polysaccharides (other than starch) are present inguard cells of all the species, in the subsidiary cells of Arthromeris,Drynaria and Pyrrosia, and in the epidermal cells of Pyrrosia.Except in Pyrrosia lipids are present in the guard cells. Subsidiarycells of Drynaria and the epidermal cells of Arthromeris andDrynaria show lipid bodies. The presence of plasmodesmata andectodesmata is demonstrated in the epidermal cells of Drymoglossum.     

Stomatal Characteristics of Four Native Herbs Following Exposure to Elevated CO2

Contrasting effects on the stomatal index (SI), stomatal density,epidermal cell size and number were observed in four chalk grasslandherbs (Sanguisorba minor Scop., Lotus corniculatus L., Anthyllisvulneraria L. and Plantago media L.) following exposure to elevatedcarbon dioxide concentrations (CO₂) in controlled environmentgrowth cabinets. SI of S. minor increased for both leaf surfaces,whilst in A. vulneraria and P. media SI decreased on one surfaceonly. In L. corniculatus , no differences in SI were observedas epidermal cell density changed in parallel with stomataldensity. In L. corniculatus and S. minor stomatal density increasedon both surfaces, whereas in P. media it decreased; in A. vulnerariastomatal density decreased on the abaxial leaf surface alonefollowing exposure to elevated CO₂. In the latter three species,SI changed because stomatal density did not change in parallelwith epidermal cell density. The results suggest elevated CO₂is either directly or indirectly affecting cell differentiationand thus stomatal initiation in the meristem. In S. minor and P. media leaf growth increased in elevated CO₂,because of increased cell expansion of epidermal cells, whereasin L. corniculatus, epidermal cell size decreased and greaterleaf growth was because of an increase in epidermal cell divisions.In A. vulneraria, leaf size did not change, but increased cellexpansion on the adaxial surface suggests CO₂ affects leaf surfacesdifferently, either directly or indirectly at the cell differentiationstage or as the leaf grows. These results suggest component species of a plant communitymay differ in their response to elevated CO₂. Predicting theeffect of environmental change is therefore difficult.Copyright1994, 1999 Academic Press Elevated CO₂, Sanguisorba minor (salad burnet), Lotus corniculatus (birdsfoot trefoil), Anthyllis vulneraria (kidney vetch), Plantago media (hoary plantain), stomatal index, stomatal density, epidermal cell size     

恒河猴皮肤干细胞的体外培养纯化与鉴定

探索恒河猴皮肤干细胞的体外培养及纯化条件,为进一步的研究奠定基础. 通过组织块培养法和消化培养法 在体外培养恒河猴表皮细胞,然后用Ⅳ型胶原吸附法吸附20 min,获得快吸附细胞. 对快吸附细胞进行克隆培养,并进行免疫细胞化学双标染色、RT PCR鉴定 β1 整合素和角蛋白15的表达,用流式细胞仪鉴定纯化前后的细胞中 β1 整合素和角蛋白15的阳性细胞比例,并通过透射电镜观察细胞的超微结构. 组织块培养法和消化培养法均可获得表皮细胞,Ⅳ型胶原纯化后的细胞胞体较小,饱满,核/浆比例大,细胞镶嵌状排列. 细胞克隆分析显示,细胞全克隆生长率高. 细胞免疫荧光显示,分选后的细胞显示 β1 整合素和角蛋白15阳性. RT PCR检查呈现 β1 整合素和角蛋白15的特异性片段. 流式细胞仪检查显示,纯化前的细胞中角蛋白15阳性细胞占总细胞中的比例为8％, β1 整合素阳性细胞的比例为10.7％;纯化后,角蛋白15阳性细胞的比例为89.4％, β1 整合素阳性细胞的比例为88.5％. 通过组织块培养法和消化培养法均可培养获得活性良好的表皮细胞,Ⅳ型胶原吸附法是一种简便、有效的皮肤干细胞分离方法,可以为进一步的眼表上皮替代重建眼表提供足量的高纯度的干细胞建立可靠的物质基础.     

Arrangement of Cortical Microtubules in Avena Coleoptiles and Mesocotyls and Pisum Epicotyls

Cortical microtubules (MTs) in coleoptiles and mesocotyls ofAvena sativa and epicotyls of Pisum sativum were examined byimmunofluorescence. In elongating Avena coleoptiles whose elongationis less localized, the orientations of cortical MTs of parenchymaand adaxial epidermal cells, and abaxial epidermal cells aretransverse, and oblique or longitudinal, respectively, and doesnot differ between the upper, middle and lower parts. The transverseMTs in parenchyma and adaxial epidermal cells turns to obliqueor longitudinal ones after elongation stops. The obliquity ofMTs in abaxial epidermal cells also tends to become steeperas elongation comes to a stop. In Avena mesocotyls and Pisumepicotyls whose elongation is localized, the orientation ofcortical MTs of cortical cells in the elongating region is relativelytransverse. The epidermis has intermingling cells of transverseor oblique MTs. In the non-elongating region, MT orientationbecomes steeper both in the cortex and epidermis. The present results indicate that whatever the degree of localizationof the elongation, the obliquity of MTs in these organs is steeperin epidermal than in inner tissue cells and becomes steeperas elongation stops in both tissues. (Received October 26, 1987; Accepted April 19, 1988)     

Stomatal Characteristics at Different Ploidy Levels inCoffeaL.

Stomatal frequency, epidermal cell frequency, stomatal guardcell length and stomatal index were examined at different ploidylevels inCoffea. In general, stomatal and epidermal cell frequencyper unit leaf area decreased while stomatal guard cell lengthincreased with an increase in ploidy. The reduction in stomatalfrequency at higher ploidy levels was mainly a result of largerepidermal cells. In the case ofC. canephora(cultivar S.274)a significant reduction in stomatal frequency was noticed fromdiploid to tetraploid level which was due to both larger epidermalcell size and less stomatal differentiation at the tetraploidlevel. Besides the effect of ploidy on stomatal frequency andguard cell length, genotypic differences in stomatal frequencyand stomatal guard cell length were also observed among cultivarsof the same ploidy level. Although variation in stomatal frequencyamong cultivars was found to be associated with the differencein stomatal to epidermal cell ratio, variation in guard celllength was attributed to differential genetic architecture.In the present study a highly significant positive correlation(r=0.82) between stomatal and epidermal cell frequency and highnegative correlations between stomatal frequency and guard celllength (r=-0.91) and epidermal cell frequency and stomatal guardcell length (r=-0.93) were obtained. The study also indicatedthat stomatal frequency can be predicted with 83 and 87% accuracy,respectively, by measuring stomatal guard cell length in coffee.Copyright1997 Annals of Botany Company Coffea; ploidy level; stomatal characteristics     

Epidermal Abscisic Acid as Detected by Immunofluorescence. Effect of Proline

The effect of proline supplied to detached young leaves of Viciafaba L. var. major on the level of epidermal ABA was investigated.After 1 h treatment with 5 min proline, fluorescent isothiocyanate(FITC) labeling of sonicated epidermal peelings indicated asignificant increase in the level of endogenous ABA. In a simultaneousexperiment on the same material, the effect of 10^–7 MABA on epidermal FITC. fluorescence labeling was also studied.A marked increase in epidermal FITC fluorescence was observed.These results suggest an involvement of proline in the enhancementof ABA bound to the plasma membrane of epidermal cells. (Received April 11, 1986; Accepted September 1, 1986)     

Characterization of membrane-bound Mg++-activated ATPase isolated from the lower epidermis of tobacco leaves

Membrane-bound Mg⁺⁺-activated ATPase was separated from thelower epidermis of tobacco leaves (Nicotiand tabacum L. SamsunNN) on stepwise sucrose density gradient centrifugation. Membrane-bound epidermal ATPase was localized in the interfaceof densities in sucrose of 1.12 to 1.16 in the sedimentary fractionbetween 1,500?g to 10,000?g from the homogenate of the lowerepidermis. The epidermal ATPase activity was activated by divalentcations (Mg⁺⁺>Mn⁺⁺Co⁺⁺>Fe⁺⁺>Zn⁺⁺>Ca⁺⁺) and furtherstimulated by KCl by ca. 20%. The pH optimum for Mg⁺⁺-activationof the epidermal ATPase was ca. 6.0. The enzyme hydrolyzed ATPmore rapidly than other nucleoside triphosphates. The optimumtemperature for activation of the epidermal ATPase activitywas ca. 40?C. 50% of the epidermal ATPase activity was lostin 18 min at 55?C and in 2.5 days at 2.5?C. The apparent Kmvalue of the epidermal ATPase was 4.7?10^–4 M and Vmaxwas 65.4 nmoles Pi/mg protein/min. The epidermal ATPase wasstrongly inhibited by N, N'-dicyclohexylcarbodiimide (DCCD)in vitro whereas oligomycin, carbonyl cyanide m-chlorophenylhydrazone(CCGP), indoleacetic acid (IAA) and abscisic acid (ABA) wereinsensitive to the epidermal ATPase activity. (Received May 23, 1978; )     

The Electrical Potential Difference Across the Tonoplast of Root Cells

Changes in electrical potential, measured as a microelectrodewas advanced into epidermal cells and from cell to cell in rootsof Lolium multiflorum and Zea mays, are described. The recordingssuggest that the electrical potential difference between thecytoplasm and vacuole, E_vc is of the order of a few millivolts,the vacuole tending to be the more positive. E_vc appeared tobe approximately the same for epidermal, cortical, endodermal,and pericycle cells.     

The Effects of Light Irradiation on the Orientation of Microtubules in Seedlings of Avena sativa L. and Pisum sativum L.

The effects of light irradiation on the arrangement of corticalmicrotubules (MTs) were examined in etiolated A vena mesocotylsand coleoptiles, and in Pisum epicotyls. Elongation of A venamesocotyls ceased as a result of irradiation with white lightwithin 1 h. The predominant orientation of MTs became more longitudinalwithin 1 h in epidermal cells and changed from transverse tooblique, after the elongation ceased, in parenchymal cells.Irradiation with red and with blue light also caused cessationof cell elongation and the same changes in the orientation ofMTs. Elongation of Avena coleoptiles ceased as a result of irradiationwith white light within 24 h. The predominant orientation ofMTs became more longitudinal in epidermal cells and changedfrom transverse to oblique in parenchymal cells. The changein orientation of MTs in epidermal cells preceded that in parenchymalcells. In Pisum epicotyls, elongation ceased as a result ofirradiation with white light within 1 h. Although the orientationsof MTs in epidermal cells did not show any remarkable change,those in parenchymal cells changed from transverse to obliqueafter cell elongation ceased. The change in orientation of MTs and the cessation of cell elongationof A vena mesocotyls induced by white-light irradiation wereboth significantly retarded by treatment with IAA. This resultsuggests that IAA is involved in maintaining the transverseorientation of MTs in Avena mesocotyls. (Received February 22, 1989; Accepted August 2, 1989)     

Intracellular localization of capsaicin and its analogues, capsaicinoid, in Capsicum fruit 1. Microscopic investigation of the structure of the placenta of Capsicum annuum var. annuum cv. Karayatsubusa

Transverse sections of the placenta of hot pepper, Capsicumannuum var. annuum cv. Karayatsubusa, at different stages afterflowering were examined microscopically. Examination of thecellular structure of the placenta using a light microscoperevealed that some morphological changes took place mainly inthe epidermal tissue of the placenta during maturation. Elongationof the epidermal cells and many osmiophilic granules were recognizedin the epidermal cells of the placenta in which capsaicinoidwas being formed and actively accumulated. Moreover, a granule-likestructure having an absorption at 280 nm was also recognizedby ultraviolet microscopy around the same region where the osmiophilicgranules were observed. By electron microscopy, many electron-densegranules stained with glutaraldehyde and osmium tetroxide wereobserved both in the small vesicles and vacuoles of epidermalcells of the placenta. The electron-dense granules varied insize from smaller than 1 µm to larger than 2 µmin diameter. They were thought to be capsaicinoid and were observedonly in the epidermal cells. Therefore, the epidermal tissueappeared to be the site of capsaicinoid accumulation. ¹Formation and metabolism of pungent principle of Capsicum fruits.Part V. (Received December 27, 1979; )     

Histochemical Localization of Phenolic Deposits in Leaf Blades of Eragrostis racemosa

The distribution of phenolic deposits in the leaves of Eragrostisracemosa from different habitats was investigated during cultivationunder uniform environmental conditions. The plants retainedtheir leaf phenolic distribution pattern over a period of 8months. Plants from dry habitats had phenolic inclusions inboth epidermal layers, whereas phenolic deposits were absentor only occurred in the abaxial epidermal layers of plants occupyingmoist habitats. Eragrostis racemosa, narrow-heart love grass, Poaceae, phenolic deposits, epidermis, histochemistry, anatomy     

The Effect of Temperature Changes on the Expansion of Individual Leaves of Vicia faba L

The growth in area of the sixth leaf of field bean plants wasinvestigated in growth room experiments. Temperatures were variedduring the periods from appearance to unfolding and from unfoldingto full expansion. The effects on the duration of growth weregreater than those on absolute growth rates. Counts of epidermalcell number showed that the changes in final leaf area couldbe explained by changes in epidermal cell size for these temperaturesand these times of treatment. Epidermal cell number was notaffected by the treatments. Vicia faba, leaf expansion, temperature, growth, cell division     

Epidermal and Guard Cell Interactions on Stomatal Aperture in Epidermal Strips and Intact Leaves

Despite the observation first made by von Mohl in 1856, thatepidermal cells greatly influence stomatal aperture, subsequentstudies have failed to pay adequate attention to epidermal cellviability or to quantify the degree of its influence on aperturein epidermal strips and leaf sections. Using Vicia faba stripsand leaf sections we found the following: (i) a non-linear relationshipbetween aperture and guard cell contact with live epidermalcells; (ii) epidermal cell viability on isolated strips hada threshold at about 25 °C; (iii) epidermal strips withdead epidermal cells had wider apertures and lower variabilitythan strips with live cells or intact leaf sections; (iv) afterepidermal cell viability was accounted for, stomatal aperturesshowed no significant differences between isolated strips orstrips removed from leaf sections treated in the same manner;(v) highly variable apertures appeared to be the normal conditionof the intact leaf. Caution should therefore be used in interpretingstomatal behaviour from epidermal strips without first takinginto account mechanical interactions between the guard and surroundingepidermal cells. Vicia faba L, broad bean, epidermal strips, leaf impressions, stomata, guard cells, temperature effects     

Tentoxin Suppresses Stomatal Opening by Inhibiting Photophosphorylation

Tentoxin and, to a lesser extent, dihydrotentoxin (both at 10mmol m^–3) reduce stomatal opening in epidermal stripsof Commelina communis in the light but not in darkness. Thiseffect was significantly greater in normal air than in CO₂-freeair. Fusicoccin overcame the tentoxin effect. However, tentoxindid not inhibit stomatal opening in the light in epidermal stripsof Paphiopedilum harrisianum, a species which lacks guard cellchloroplasts. It is concluded that tentoxin exerts its actionon stomata not by an ionophorous effect in the plasmalemma ofguard cells but by the inhibition of photophosphorylation intheir chloroplasts. The effects of DCMU and tentoxin on guardcells are discussed in terms of their effects on chloroplastsand the extent to which energy is supplied from this organelleduring stomatal opening in the light. The results indicate thatneither photophosphorylation nor non-cyclic electron transportin guard cell chloroplasts are essential for stomatal opening. Key words: Commelina, epidermal strips, Paphiopedilum, photophosphorylation, stomata, tentoxin     

Stomatal Pattern in Four Species of Monocotyledons

The distribution of stomata has been investigated in the leafepidermis of Chlorophytum comosum, Galanthus nivalis, Schizostyliscoccinea and Scilla lancifolia. The epidermis was consideredto consist of units of construction of two kinds: type A, along epidermal cell with a stoma at its distal end, and typeB, a long epidermal cell without an associated stoma. Exceptin Scilla, the probability of an epidermal unit being type Aincreases approximately with its length. Considering the epidermisas rows of units, alternating sequences of type A and type Bdo not occur randomly along the rows. In Chlorophytum, Galanthusand Schizostylis, both type A and B units tend to be aggregatedinto longer sequences than would be expected on a random basis.It is suggested that homoeogenetic induction (i.e. of like bylike) may be occurring during development. No case can be madefor homoeogenetic induction of units in Scilla. There is a slighttendency to periodicity of distribution of type A units in Galanthus,Schizostylis and Scilla, but this does not seem to representa primary element of pattern. There is interaction between rowsin the sense that unit ends (transverse walls) tend to avoidthose in neighbour rows; this affects the relative distributionof stomata, but there is no evidence of any direct interactionbetween stomata in different rows. Chlorophytum comosum, Galanthus nivalis, Schizostylis coccinea, Scilla lancifolia, leaf, epidermis, stomata, pattern     

Effects of an Epidermal Growth Factor on Growth of Zea Primary Roots and Mesocotyls

Sections of the elongation zones of primary roots and mesocotylsof Zea mays L. were incubated with various concentrations ofhuman epidermal growth factor (EGF). The growth rates of rootsections incubated with 1,000, 100 and 10 µg liter^–1EGF were higher than that of control by 15%, 26% and 14%, respectively.The rates of mesocotyl sections incubated with 100, 10, 1.0and 0.1µg liter^–1 EGF were 23%, 31%, 24% and 22%higher than that of control. (Received August 8, 1994; Accepted November 1, 1994)     

Cell Potentials and Turgor Pressures in Epidermal Cells of Tradescantia and Commelina

Cell membrane potentials have been measured both in epidermalstrips and intact leaf sections of Tradescantia virginiana andCommelina communis, and in epidermal cells over green and overalbino mesophyll cells of T. albiflora var. albovittata. Membranepotentials (_cell) in strips were considerably lower than thosein intact sections and were insensitive to light and to theabsence or presence of calcium. Their response to external cationlevels was indifferent to ionic species. However, in intactleaf sections incubated with calcium present, membrane potentialsresponded to K⁺ levels but not to Na⁺. were more negative thancells in epidermal strips, and responded to changes in illumination. Long-term recordings of _cell and vacuolar K⁺ levels in T. virginianaduring stomatal closure suggest that the fluctuations of _cellwere unrelated to K⁺ movement (which we could not detect) andthus probably to stomatal movement as well. Turgor pressures measured in epidermal cells of intact leafsections of T. virginiana were found to be of the same magnitudeas those previously reported for epidermal strips. It is concludedthat epidermal cells maintain their solute contents during strippingwithout the involvement of an electrophysiological transportsystem. With the possible exception of lateral subsidiary cells,there was no evidence suggesting that ordinary epidermal cellsare capable of osmotic adjustment even when additional KCI wassupplied in the osmoticum. Absolute turgor levels in intactleaf sections kept at constant external KCI were unrelated tosteady state _cell.     

The Cuticle, Epidermis and Stomatal Ontogeny of Casuarina equisetifolia Forst

The cuticle, epidermis and stomatal ontogeny of Casuarina equisetifoliaForst. is described. The cuticle shows well marked impressionsof the epidermal cells and stomata. The epidermis of leaf andstem shows transversely oriented, tetracytic, mesoperigenousstomata with two lateral mesogene subsidiaries and two polarperigene neighbouring cells. Although the epidermal structureof Casuarina shows a good deal of resemblance with that of theBennettitales, it may not indicate any phylogenetic relationshipssince there are important differences in the structure and reproductionof the plants of these two groups.     

Orientation of Wall Microfibrils in Avena Coleoptiles and Mesocotyls and in Pisum Epicotyls

Microfibrils (MFs) on the inner surface of the walls of Avenacoleoptile and mesocotyl cells and of Pisum epicotyl cells wereexamined by a replica method. In the elongating epidermis ofthese three organs, cells having MFs that were transverse, obliqueor longitudinal to the elongation axis were intermingled. Inthe elongating parenchymal tissues, all cells deposited MFstransversely. In non-elongating cells of Avena coleoptiles andPisum epicotyls, the orientation of MFs on the inner wall surfaceof both epidermal and parenchymal cells was more longitudinalthan in elongating cells. These observations on the orientationsof MFs are compatible with those our previously reported observationson the orientations of microtubules (MT) (Iwata and Hogetsu1988). Disruption of MTs of Avena coleoptiles by treatment withamiprophosmethyl caused changes in the orientation of depositionof MFs. These results support the idea that MFs are usuallyco-aligned with MTs in organ cells and that the orientationof MFs is controlled by MTs. The averaged direction of MFs, visualized under polarized light,showed a clear difference between the epidermal and inner-tissuecell walls in the elongating regions of the three organs. Inalmost all elongating and non-elongating epidermal cells, theaveraged direction of MFs was longitudinal, while it was transversein all inner-tissue cells. (Received December 16, 1988; Accepted April 28, 1989)