Glycogen Distribution in Relation to Epidermal Cell Differentiation During Embryonic Scale Morphogenesis in the Lizard Anolis lineatopus

The differentiation of the epidermis during scale morphogenesis in the lizard Anolis lineatopus has been studied by autoradiographic and immunocytochemical techniques and by electron microscopy, in relation to mitotic activity and to the distribution of glycogen. The flat embryonic epidermis of the early embryo is transformed into symmetric epidermal papillae which progressively become asymmetric and eventually form scales with stratified epidermal and peridermal layers. Papilla asymmetrization and epidermal stratification derive from cell hypertrophy and multiplication in the “basal hypertrophic layer of the forming outer side of scales” (BLOS). Glycogen is scarce or absent during early stages of epidermis development. In the dermis no glycogen is found at any stage of scale morphogenesis. Glycogen particles 25–40 nm in size accumulate in hypertrophic basal cells and peridermal cells during scale development. Conversely cells in the forming inner side of scales do not accumulate glycogen, divide less frequently than in the outer side and do not form a β–keratinized layer. It is suggested that an osmotic effect related to glycogen deposition causes increased hydration of the BLOS, whose cells become swollen and contribute to the asymmetrization of the epidermal papillae. Glycogen decreases in suprabasal differentiating cells and disappears from the BLOS at the stage of complete keratinization of the scale, around the period of hatching. Terminal differentiation in the peridermis and suprabasal epidermal layers takes place by cell flattening and condensation of the nucleus and cytoplasm as typical for apoptotic cells.     

Histology,ultrastructure, and pigmentation in the horny scales of growing crocodilians

Alibardi L. 2011. Histology, ultrastructure, and pigmentation in the horny scales of growing crocodilians. —Acta Zoologica (Stockholm) 92 : 187–200. The present morphological study describes the color of hatchling, juvenile, and adult crocodilian skin and the origin of its pigmentation. In situ hybridization and immunostaining indicate that crocodilian scales grow as an expansion of the proliferating epidermis of the hinge region that form thin lateral rings. In more central areas of growing scales, new epidermal layers contribute to increase the thickness of the stratum corneum. The dark pigmentation and color pattern derive from the different distribution of epidermal and dermal chromatophores. The more intensely pigmented stripes, irregular patches and dot‐like spots, especially numerous in dorsal scales, derive from the incorporation of the eumelanosomes of epidermal melanocytes in differentiating beta cells of the epidermis. Dermal melanophores, mainly localized in the loose upper part of the dermis, also contribute to the formation of the dark or gray background of crocodilian scales. The eumelanosomes of dermal melanophores determine the darkening of the skin pattern in association with the epidermal melanocytes. Iridophores are infrequent, while xantophores are present in the species analyzed with a sparse distribution in the superficial dermis among melanophores. The presence of xantophores and of the few iridophores in areas where epidermal melanocytes are absent appear to determine the brown or the light yellow‐orange background observed among the darker regions of crocodilian scales.     

Secondary phenolic products in isolated guard cell,epidermal cell and mesophyll cell protoplasts from pea (Pisum sativum L.) leaves: Distribution and determination

Summary Guard cells and epidermal cells of the abaxial (lower) and adaxial (upper) epidermis ofPisum sativum L., mutant Argenteum, are the predominant sites of flavonoid accumulation within the leaf. This was demonstrated by the use of a new method of simultaneous isolation and separation of intact, highly-purified guard cell and epidermal cell protoplasts from both epidermal layers and of protoplasts from the mesophyll. Isolated guard and epidermal protoplasts retained flavonoid patterns of the parent epidermal tissue; quercetin 3-triglucoside and its p-coumaric acid ester as major constituents, kaempferol 3-triglucoside and its p-coumaric acid ester as minor compounds. Total flavonoid content in the lower epidermis was estimated to be ca. 80 fmol per guard cell protoplast and 500 fmol per epidermal cell protoplast. Protoplasts isolated from the upper epidermis had about 20–30% as much of these flavonoids. Mesophyll protoplasts retained only about 25 fmol total flavonoid per protoplast.By fluorescence microscopy, using the alkaline-induced yellow-green fluorescence characteristics of flavonols, we suggest that these flavonol glycosides are present in cell vacuoles. There was no indication for the presence of flavine-like compounds.Abbreviations uE adaxial (upper) epidermis - IE abaxial (lower) epidermis - GCP guard cell protoplasts - ECP epidermal cell protoplasts - MCP mesophyll cell protoplasts - PP protoplasts - HPLC high performance liquid chromatography - TLC thin layer chromatography - CC column chromatography - HOAc acetic acid     

Localization of partially methylated flavonol glucosides in Chrysosplenium americanum. II. Immunofluorescence

Chrysosplenium americanum Schwein. ex Hooker (Saxifragaceae) accumulates a variety of partially methylated flavonol glucosides. Specific antibodies to tri- and tetramethylated flavonol-2′-O-glucosides, located using fluorescein isothiocyanate (FITC) goat antirabbit antibody, were used for the localization of the flavonol glucosides in leaf epidermis, cross sections and protoplasts. The results indicated that flavonoid accumulation occurred mainly in the walls of epidermal cells and, to a much lesser extent, in mesophyll cell walls. The weak fluorescence observed in the vacuoles of protoplasts suggested a minor role of this compartment in the accumulation process. The significance of flavonoid deposition within epidermal cell walls is discussed in relation to the lipophilic nature of these compounds and their possible role in the physiology of the plant.     

Flavonol content of guard cell and mesophyll cell protoplasts isolated from Vicia faba leaves

Guard cells of the lower epidermis of leaflets of Vicia faba L. cv. Weißkernige Hangdown contain several kaempferol 3,7-O-glycosides. This was demonstrated for the first time by the use of isolated, highly purified guard cell protoplasts for flavonol estimation and quantitation. From a total of ca 12 kaempferol glycosides, three were identified by comparative thin layer chromatography and high performance liquid chromatography as kaempferol 3-O-glucoside 7-O-rhamnoside (major component), 3-O-rhamnogalactoside 7-O-rhamnoside and 3,7-O-bisglucoside (minor components). On average, the total flavonol content was estimated to be 85 fmol protoplast⁻¹. From comparative investigations including alkaline-induced (green) fluorescence characteristics of flavonols and UV-microscopical studies we suggest that kaempferol glycosides are present in guard cells and epidermal cells in similar quantities, and that these compounds are in the vacuole.
By contrast, mesophyll protoplasts have a low flavonol content (one sixth that of guard cells). In spite of the different total flavonol contents, individual components of each cell-type are the same. However, they show differences in their quantitative distribution.     

Expression of the HB9 homeobox gene concomitant with proliferation accompanying epidermal stratification during development of chick embryonic tarsometatarsal skin

A homeobox gene, HB9, has been isolated from the tarsometatarsal skin of 13-day-old chick embryos using a degenerate RT-PCR-based screening method. In situ hybridization analysis revealed that, during development of chick embryonic skin, the HB9 gene was expressed in epidermal basal cells of the placodes, but not in those of interplacodes, and in the dermal cells under the placodes at 9 days before addition of an intermediate layer by proliferation of the basal cells in the placodes. With the onset of epidermal stratification, the direction of the basal cell mitosis changed, with the axis becoming vertical to the epidermal surface. Placodes and interplacodes form outer and inner scales, respectively, after they have elongated distally (Tanaka S, Kato Y (1983b) J Exp Zool 225: 271–283). During scale ridge elongation at 12–15 days, HB9 was strongly expressed in the epidermis of the outer scale face, where the cell proliferation is more active than in the epidermis of the inner scale face; hence, stratification of the outer scale face is more prominent than that of the inner scale face. After 16 days, when mitotic activity in the epidermal basal cells decreases and the thickness of the epidermis is maintained at a constant level, the HB9 expression decreases with the onset of epidermal keratinization. These results suggest that HB9 may be involved in the proliferation of the epidermal basal cells that accompanies epidermal stratification.     

Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians

Alibardi, L. 2011. Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians. —Acta Zoologica (Stockholm) 00 :1–11. The cytology and distribution of chromatophores responsible for skin pigmentation in chelonians is analyzed. Epidermal melanocytes are involved in the formation of dark spots or stripes in growing shelled and non‐shelled skin. Melanocytes rest in the basal layer of the epidermis and transfer melanosomes into keratinocytes during epidermal growth. Dermal melanophores and other chromatophores instead remain in the dermis and form the gray background of the skin. When dermal melanophores condense, they give origin to the dense spots or stripes in areas where no epidermal melanocytes are present. In the latter case, the epidermis and the corneous layer are transparent and reveal the dermal distribution of melanophores and other chromatophores underneath. As a result of this basic process of distribution of pigment cells, the dark areas visible in scales can have a double origin (epidermal and dermal) or a single origin (epidermal or dermal). Xanthophores, lipophores, and a cell containing both pterinosomes and lipid droplets are sparse in the loose dermis while iridophores are rarely seen in the skin of chelonians analyzed in the present study. Xanthophores and lipophores contribute to form the pale, yellow or oranges hues present among the dark areas of the skin in turtles.     

Cell adhesion and junctional proteins in the developing skin of snakes indicate they coordinate the differentiation of the epidermis

The development of scales and the sequence of epidermal layers during snake embryogenesis has been studied by immunofluorescence for the localization of cell adhesion, adherens, and communicating cell junctional proteins. At about 2nd/3rd of embryonic development in snakes the epidermis forms symmetric bumps at the beginning of scale formation, and they rapidly become asymmetric and elongate forming outer and inner surfaces of the very overlapped scales seen at hatching. The dermis separates a superficial loose from a deeper dense part; the latter is joined to segmental muscles and nerves, likely acting on scale orientation during snake movements. N-cam is present in the differentiating epidermis and mesenchyme of forming scales while L-cam is only/mainly detected in the periderm and epidermis. Mesenchymal N-cam is associated with the epidermis of the elongating dorsal scale surface and with the beta-differentiation that occurs in the overlapping outer surface of scales. Beta-catenin and Connexin-43 show a similar distribution, and they are mainly present in the periderm and differentiating suprabasal keratinocytes likely forming an intense connectivity during epidermal differentiation. Beta-catenin also shows nuclear localization in differentiating cells of the shedding and beta-layers at late stages of scale morphogenesis, before hatching. The study suggests that intensification of adhesion and gap junctions allows synchronization of the differentiation of suprabasal cells to produce the ordered sequence of epidermal layers of snake scales, starting from the shedding complex and the beta-layer.

     

Cell migration and differentiation during wound healing and regeneration in Microstomum lineare (Turbellaria)

Using transmission electron microscopy and serial sections with light-microscopic autoradiography, I have investigated the ultrastructure of wound healing, the distribution of cells preparing for proliferation, and the fates of cells labelled with exogenous tritiated thymidine ([³H]T) in Microstomum lineare undergoing wound healing and regeneration. Immediately after decapitation the open wound was reduced to a minimum by strong contraction of circular muscle fibers. The wound epidermis was cellular, consisting of thin parts of epidermal cells from the epidermis around the wound. These epidermal cells maintained close adhesive contact with one another through zonulae adherentes and septate junctions. No proliferating cells were found in the old epidermis. The only cells taking up [³H]T were mesenchymal and gastrodermal neoblasts which proliferated and migrated towards the surface. The final epidermis was formed by conjunction of the wound epidermis and newly differentiated epidermal cells. Regeneration in Microstomum, in contrast to that of planarians, occurs mainly by morphallaxis, without the formation of a regeneration blastema, but also through continuous cell proliferation, migration, and differentiation.     

Structure of the integument of a fresh-water teleost,Bagarius bagarius (Ham.) (Sisoridae,pisces)

The skin of Bagarius bagarius (Ham.) is devoid of scales but is rough due to the presence of numerous pentagonal epidermal elevations, which are separated by deep furrows at regular intervals. These elevated pentagonal regions of the epidermis are covered by dead cornified cells in the form of caps. As the old cap goes off a new one is formed by the death of the underlying epidermal cells. The middle layer of the epidermis is mainly composed of well defined polygonal cells. Their cytoplasm is granular in nature and give reactions for protein bound sulphydryl groups. The stratum germinativum is composed of two types of basal cells, the columnar cells and the spherical cells. The flask shaped mucous glands are restricted to the epidermal furrows and secrete either neutral or acidic mucopolysaccharides. Certain large specialysed granular cells are found in the epidermis which are grouped around the taste buds. These specialysed cells may be the photocytes. Two layers of the dermis can be distinguished—the relatively thin stratum laxum and the thick stratum compactum. Dermal papillae mainly support the taste buds. The pigment cells are arranged in two layers in the dermis. The subcutis is composed of loose connective tissues, richly infiltrated with the fat cells, nerves and blood capillaries.     

中国早熟禾属植物部分种叶下表皮微形态的研究

通过光学显微镜及扫描电子显微镜对中国早熟禾属20种、6亚种及2变种植物的叶下表皮微形态特征进行了观察, 以明确叶表皮微形态特征在早熟禾属植物中的分类学意义。结果显示：(1)早熟禾属植物的叶下表皮长细胞多为长筒状或纺锤形,少数短筒状,细胞壁波状弯曲或近平直;脉间具有短细胞或缺如;气孔器多数常见,副卫细胞平行形至低圆屋顶形;脉上具有刺细胞或缺如,脉间刺细胞多为缺如;脉上硅细胞单生或对生,椭圆形、肾形、新月形、近方形、长方形边缘波状弯曲或结节形;部分早熟禾属植物叶下表皮存在冠细胞。(2)早熟禾属植物叶下表皮微形态特征在长细胞的形状及其细胞壁的弯曲与否、短细胞的有无及其形状、气孔器的分布与副卫细胞的形状、刺细胞的分布、脉上硅细胞的形状、冠细胞的有无这些方面存在着一定的差异,可为该属植物种间分类提供参考依据。叶表皮微形态证据支持高原早熟禾、细叶早熟禾作为草地早熟禾亚种的处理意见。     

Spectral dependence of flavonol and betacyanin accumulation in Mesembryanthemum crystallinum under enhanced ultraviolet radiation

Mesembryanthemum crystallinum L. (Aizoaceae) is a drought‐ and salt‐tolerant halophyte that is able to endure harsh environmental conditions. Upon irradiation with high light irradiance (1200–1500 µmol m^?2 s^?1) it displays a rapid cell‐specific accumulation of plant secondary metabolites in the upper leaf epidermis; a phenomenon that is not detectable with salt or drought treatment. The accumulation of these compounds, the betacyanins and acylated flavonol glycosides, increases if the plants are exposed to polychromatic radiation with a progressively decreasing short‐wave cut‐off in the ultraviolet range. The response is localized in the epidermal bladder cells on the tips of young leaves and epidermal layers of fully expanded leaves. It is demonstrated that the accumulation of flavonols and betacyanins can be described by a weakly sigmoid dose function in combination with an exponential decrease of the response function of the plant with increasing wavelength.     

Morphological characters of leaf epidermis in schisandraceae and their systematic significance

The leaf epidermis of 23 species belonging to 2 genera within Schisandraceae was investigated using light and scanning electron microscopy. Many characters of the leaf epidermis in Schisandraceae, such as shape of epidermal cells, type of stomata, and cuticular ornamentation, are usually constant within species and thus helpful for elucidating the relationship between and within genera. Leaf epidermal cells are usually irregular or polygonal in shape. The patterns of anticlinal walls are straight, sinuolate, sinuous or sinuate. The stomatal apparatus belong to paracytic or laterocytic type and the latter is subdivided into various subtypes based on the number and arrangement of subsidiary cells. Under scanning electron microscopy observation, the cuticular membrane is often striated, sometimes squamulate or granular; the inner margin of the outer stomatal rim is nearly smooth or denticulate. Evidences from shape of epidermal cells, patterns of cuticular intrusions between the ends of each guard cell of a pair and distribution of stomatal apparatuses support the viewpoint thatKadsura is more primitive thanSchisandra. Study on leaf epidermis also shows thatKadsura interior deserves the rank of a distinct species and the treatment of the evergreen groups, includingS. propinqua andS. plena, as distinct from the deciduous species of the genus is quite natural.     

Distribution of Secondary Plant Metabolites and Their Biosynthetic Enzymes in Pea (Pisum sativum L.) Leaves : Anthocyanins and Flavonol Glycosides

Leaves of a novel strain of peas (Pisum sativum L.) were used to determine the distribution of secondary metabolites and their biosynthetic enzymes. Leaf epidermal layers in this strain are easily separated from the parenchyma. Anthocyanins and flavonol glycosides were localized in epidermal vacuoles only. Among the biosynthetic enzymes studied, phenylalanine ammonia-lyase (PAL, EC 4.3.1.5), S-adenosyl-1-methionine (SAM):caffeic acid and SAM:quercetin methyltransferases (o-dihydric phenol methyltransferase, EC 2.1.1.42) and a flavonoid 7-O-glucosyltransferase (EC 2.4.1.91) were chiefly localized in the parenchyma, whereas trans-cinnamate 4-monooxygenase (EC 1.14.13.11), hydroxycinnamate:CoA ligases (EC 6.2.1.12) and a flavonoid 3-O-glucosyltransferase (EC 2.4.1.91) were found mainly in the epidermis. Flavanone (chalcone) synthase activity was found only in the epidermis, whereas chalcone isomerase (EC 5.5.1.6) was evenly distributed in epidermal and parenchyma tissues.     

Heterogeneity of epidermal cells in relation to nickel accumulation in hyperaccumulator plants belonging to the genus <Emphasis Type="Italic">Alyssum</Emphasis> L.

Epidermal cells of some plants are able to accumulate high levels of heavy metals (Zn, Ni, Cd). We studied this ability in plants in the genus Alyssum L. distinguished by tolerance to nickel (Ni). It was established that the predominant Ni accumulation occurred in epidermis, whereas in other tissues lower concentrations of the metal were revealed. It was also found that epidermal cells were characterized by heterogeneity in relation to Ni accumulation. The highest metal amount was accumulated in ordinary epidermal cells and in trichomes. Species-specific features of Ni distribution in leaf tissues in Alyssum spp. were shown. The reasons for the heterogeneity of epidermal cells in relation to Ni accumulation were discussed. We have attempted to resolve the contradictions encountered in the literature concerning the distribution and accumulation of Ni in the leaf tissues of plants belonging to the genus Alyssum L.     

Two ways to skin a plant: The analysis of root and shoot epidermal development in Arabidopsis

The post-embryonic architecture of higher plants is derived from the activity of two meristems that are formed in the embryo: the shoot meristem and the root meristem. The epidermis of the shoot is derived from the outermost layer of cells covering the shoot meristem through repeated anticlinal divisions. By contrast, the epidermis of the root is derived from an internal ring of cells, located at the centre of the root meristem, by a precise series of both periclinal and anticlinal divisions. Each epidermis has an independent origin. In Arabidopsis the mature shoot epidermis is composed of a small number of cell types: hair cells (trichomes), stomatal guard cells and other epidermal cells. In shoots, hairs take the form of branched trichomes that are surrounded at their base by a ring of accessory cells in a sheet of epidermal cells. The root epidermis is composed of two cell types: trichoblasts that form root hair cells and atrichoblasts that form non-hair cells. Mutations affecting both the patterning and the morphogenesis of cells in both shoot and root epidermis have recently been described. Most of these mutations affect development in a single epidermis, but at least one, ttg, is involved in development in both epidermal systems.     

15种蹄盖蕨科植物叶表皮形态特征的研究

利用光学显微镜对蹄盖蕨科15种植物的叶表皮形态特征进行观察和研究。结果表明:蹄盖蕨科15种植物的上、下表皮细胞均为无规则型,垂周壁为凹凸状或深波状;上表皮细胞长宽比在1.0~3.2之间,下表皮细胞长宽比在1.0~2.6之间;在这15种植物中共观察到6种气孔器类型,即极细胞型、腋下细胞型、聚合极细胞型、聚腋下细胞型、无规则四细胞型和无规则型,每种植物具有3~4种气孔器类型,气孔均为下生型,多呈椭圆形。气孔的长宽比在1.3~2.1之间;气孔密度在32~90个/mm2之间;气孔指数为17.7%~40.9%。依据上述叶表皮形态特征将15种蹄盖蕨科植物分为3类,即双盖蕨类、蹄盖蕨类和对囊蕨类。该研究在一定程度上支持Christenhusz分类系统对蹄盖蕨科的划分,为蹄盖蕨科植物的系统分类及演化研究提供基础资料。     

On the existence of non-cycling germinative cells in human epidermis in vivo and cell cycle aspects of psoriasis

Abstract. This report deals with the controversies of whether all germinative epidermal cells in human epidermis are in the cycling state and whether stimulated hyperproliferation of psoriatic epidermis is due to a shortening of the cell cycle time or to a recruitment of non-cycling germinative epidermal cells. Experiments were performed on human subjects in vivo . Continuous infusion of [³H]thymidine for 8½ days indicated that 40% of germinative epidermal cells reside in the non-cycling state. Proliferative stimulation by tape stripping indicated recruitment of non-cycling (G₀) germinative epidermal cells in both normal and psoriatic skin, and a prolongation (rather than a shortening) of cell cycle traverse in activated psoriatic epidermal cells.     

中国伞形科矮泽芹属植物叶表皮形态特征的研究

利用光学显微镜、扫描电镜对伞形科矮泽芹属8种植物叶表皮形态进行观察与研究。结果表明:(1)矮泽芹属8种植物上下表皮细胞均为不规则形或规则多边形,垂周壁为近平直状或波状,上表皮细胞长宽比在1.3~2.4之间,下表皮细胞长宽比在1.5~2.5之间;在近轴面,有细叶矮泽芹、聂拉木矮泽芹和绿花矮泽芹3种植物没有气孔器的存在,其余物种气孔密度在20~74个/mm2之间,气孔指数为6.0%~17.7%;在远轴面,所有物种都具有丰富的气孔器,气孔密度为100~183个/mm2,气孔指数为16.1%~23.6%。(2)聚类分析结果显示,矮泽芹、大苞矮泽芹、粗棱矮泽芹为类群Ⅰ,鹤庆矮泽芹为类群Ⅱ,聂拉木矮泽芹、细叶矮泽芹、绿花矮泽芹为类群Ⅲ,松潘矮泽芹则单独聚为类群Ⅳ;聚类分析结果大体上支持形态学分类的结果。(3)叶表皮形态特征对于区分矮泽芹属不同物种具有十分重要的分类学价值。     

Origin of feathers: Feather beta (beta) keratins are expressed in discrete epidermal cell populations of embryonic scutate scales

The feathers of birds develop from embryonic epidermal lineages that differentiate during outgrowth of the feather germ. Independent cell populations also form an embryonic epidermis on scutate scales, which consists of peridermal layers, a subperiderm, and an alpha stratum. Using an antiserum (anti-FbetaK) developed to react specifically with the beta (beta) keratins of feathers, we find that the feather-type beta keratins are expressed in the subperiderm cells of embryonic scutate scales, as well as the barb ridge lineages of the feather. However, unlike the subperiderm of scales, which is lost at hatching, the cells of barb ridges, in conjunction with adjacent cell populations, give rise to the structural elements of the feather. The observation that an embryonic epidermis, consisting of peridermal and subperidermal layers, also characterizes alligator scales (Thompson, 2001. J Anat 198:265-282) suggests that the epidermal populations of the scales and feathers of avian embryos are homologous with those forming the embryonic epidermis of alligators. While the embryonic epidermal populations of archosaurian scales are discarded at hatching, those of the feather germ differentiate into the periderm, sheath, barb ridges, axial plates, barbules, and marginal plates of the embryonic feather filament. We propose that the development of the embryonic feather filament provides a model for the evolution of the first protofeather. Furthermore, we hypothesize that invagination of the epidermal lineages of the feather filament, namely the barb ridges, initiated the formation of the follicle, which then allowed continuous renewal of the feather epidermal lineages, and the evolution of diverse feather forms.