Dogs suffer from skin associated issues with a disproportionate frequency, with consequent interest in providing nutrition to optimize their skin's natural defences. Linoleic acid (LA) is known as an essential nutrient in dogs and plays a critical part in the lipid component of skin barrier formation. Minimum requirements have been defined, primarily based on eliminating signs of deficiencies such as dry, flaky skin and inflammation. Zn has been shown as an important nutrient for maintaining epidermal health. This pilot study investigated whether there are skin barrier benefits from feeding both linoleic acid and Zn at levels significantly in excess of published minimum requirements. Eight Labrador retrievers were fed a diet containing 3.8 g/Mcal LA, 21 mg/Mcal Zn for 12 weeks to establish baseline conditions for all dogs (basal diet). After this period, for a further 12 weeks, the dogs were switched onto a diet containing 7.9 g/Mcal LA and 50 mg/Mcal Zn (test diet). Transepidermal water loss (TEWL measurements) were used as a measure of skin quality and integrity and were taken at the end of the initial feeding period, and at 6 and 12 weeks of the test feeding period. TEWL was reduced by 8.11 g/m2/h (P < 0.001) six weeks after instigation of the test diet, and by 7.52 g/m2/h (P < 0.005) at 12 weeks, compared to the levels (14.73 g/m2/h) at the end of the basal feeding trial period. The results showed evidence of improved barrier properties as TEWL when feeding higher levels of LA and Zn for six and 12 weeks.

Morphology of foliar trichomes was analyzed in Quercus variabilis by electron microscopy and three-dimensional surface profiling. Leaves from suppressed or dominant sprouts of the oak species were collected after a forest fire to unravel the effects of the disturbance factor on sprouting of the oak species. Scanning electron microscopy revealed two types of trichomes depending on the leaf surface. The trichomes on the adaxial surface were branched and constricted, and possessed a single row of thin-walled cells with a collapsed morphology (glandular branched uniseriate trichomes). Meanwhile, the trichomes on the abaxial surface were star-shaped, unfused with each other, and had 6 to 10 rays (nonglandular simple stellate trichomes). An apparent proliferation of trichomes was evident on the adaxial surface of the dominant sprouts. Uniseriate trichomes could be discernable as an elevation from the surface by white light scanning interferometry. By transmission electron microscopy, thin and convoluted cell wall, degenerated cytoplasm, and a single row of cells were characteristic of the trichomes on the adaxial surface. The thick cell walls of the mature trichomes on the abaxial surface represented the nonglandular nature. This is the first report on the morphological and ultrastructural characterization of foliar trichomes of the oak species.

a significant proportion of the human population suffers from some form of skin disorder, whether it be from burn injury or inherited skin anomalies. the ideal treatment for skin disorders would be to regrow skin tissue from stem cells residing in the individual patient's skin. locating these adult stem cells and elucidating the molecules involved in orchestrating the production of new skin cells are important steps in devising more-efficient methods of skin production and wound healing via the ex vivo expansion of patient keratinocytes in culture. this review focuses on the structure of the skin, the identification of skin stem cells, and the role of notch, wnt and hedgehog signalling cascades in regulating the fate of epidermal stem cells.

The host–parasite interaction between the rainbow trout Oncorhynchus mykiss and the fish louse Argulus japonicus was investigated by administering low levels of dietary cortisol before infecting the fish with low numbers of the parasite. After 24 h, the dietary cortisol treatment elevated blood cortisol and glucose levels and stimulated the synthesis of secretory granules in the upper layer of skin cells. Infection with 6 lice per fish caused skin infiltration by lymphocytes, also in areas without parasites. The lymphocyte numbers in the blood at 48 h post-parasite infection were reduced. Other changes, typical for exposure to many stressors and mediated by cortisol, were also found in the epidermis of parasitized fish, although neither plasma cortisol nor glucose levels were noticeably affected. Glucocorticoid receptors were localized immunohistochemically and found in the upper epidermal layer of pavement and filament cells, and in the leucocytes migrating in these layers. Cortisol-fed fish had reduced numbers of parasites and the changes in the host skin are likely involved in this reduction. Thus a mild cortisol stress response might be adaptive in rejecting these parasites. Further, the data suggest that this effect of cortisol is mediated by the glucocorticoid receptor in the skin epidermis, as these are located directly at the site of parasite attachment and feeding in the upper skin cells that produce more secretory granules in response to cortisol feeding.

The epidermis of snakes produces two types of keratinocytes containing an alpha (soft) and a beta (hard) form of keratin. During epidermal renewal, which allows body growth, six types of epidermal layers are produced before moulting: oberhautchen, beta-, mesos, alpha-, lacunar, and clear. The precise layers in which beta-keratin, alpha-keratin and matrix proteins (loricrin and filaggrin) are produced, have been studied by light and ultrastructural immunocytochemistry. An antibody against chick scale beta-keratin recognizes also snake beta-keratin only in the oberhautchen and beta-layer. This confirms the phylogenetic relationships between avian and reptilian hard (beta) keratins. Beta-keratin rapidly disappears in mesos-cells, where little beta-keratin is present. Antibodies that recognize alpha-keratins (AE1, AE2, AE3) show that acidic keratins (AE1 positive) mainly localize in the most basal layers and basic keratins (AE3 positive) in all layers but disappear in those layers that are keratinized, especially in the beta-layer. The AE2 immunolabelling (a marker of keratinization in mammalian epidermis) is localized in the compact alpha-layer. This pattern is similar to that for loricrin and filaggrin, although in the latter the reaction is less intense and located mainly in the hinge regions among scales. Alpha-keratins and associated proteins disappear in the oberhautchen and beta-cells where beta-keratin is produced instead. This study suggests that the shedding mechanism in snakes evolved after the hard beta-keratin was compartmentalized beneath the soft alpha-keratin to create an intra-epidermal weakness region. The study also suggests that some common mechanism of alpha-keratinization is present in snakes, and the other amniotes in general.

The morphological transition from the simple epidermis that contacts the amniotic fluid of embryonic crocodilians to the adult epidermis required in a terrestrial environment has never been described. We used light and electron microscopy to study the development, differentiation and keratinisation of the epidermis of the American alligator, Alligator mississippiensis, between early and late stages of embryonic skin formation. In early embryonic development, the epidermis consists of a flat bilayer. As it develops, the bilayered epidermis comes to lie beneath the peridermis. Glycogen is almost absent from the bilayered epidermis but increases in basal and suprabasal cells when scales form. Glycogen disappears from suprabasal cells that accumulate keratin. The peridermis and 1 or 2 subperidermal layers form an embryonic epidermis that is partially or totally lost before hatching. These cells accumulate coarse filaments and form reticulate bodies. Mucous and lamellate granules are produced in the Golgi apparatus and are partly secreted extracellularly. The embryonic cells darken with the formation of larger reticulate bodies that aggregate with intermediate filaments and other cell organelles, as their nuclear chromatin condenses. Thin β-cells resembling those of scutate scales of birds develop beneath the embryonic epidermis and form a stratified β-layer that varies in thickness in different body regions. The epidermis differentiates first in the back, tail and belly. At the beginning of β-cell differentiation, the cytoplasm contains sparse bundles of α-keratin filaments, glycogen and lipid droplets or vacuoles apparently derived from the endoplasmic reticulum and Golgi apparatus. These organelles disappear rapidly as irregular bundles of electron-dense β-keratin filaments accumulate and form larger bundles. The larger bundles consist of 3 nm thick electron-pale keratin microfibrils and are derived from the assemblage of β-keratin molecules produced by ribosomes. While in mammals the epidermal barrier is formed by α-keratinocytes, in the alligator the barrier is formed by β-keratin cells. The β-layer is reduced or absent from the small hinge region between scales. In the latter areas the barrier is made of a or a mixture of α/β keratinocytes. Thus alligators resemble birds where the β-keratin molecules are deposited directly over an α-keratin scaffold, rather than an initial production of β-keratin packets which then merge with α-keratin, as occurs in the Chelonia and Lepidosauria. The pigmentation of the epidermis of embryos is mostly derived from epidermal melanocytes.

Introduction. The fruit of `Encore' mandarin (Citrus deliciosa × Citrus nobilis) usually shows chlorotic spots in the epicarp from the first stages of development. Thispeel disorder triggers off, thereafter, the occurrence of a large quantity of dark stains (pre-harvest`peel pitting'). Materials and methods. A biochemical and ultra-structural study of the flavedo,using epicarp with and without stains, was carried out. Quality assays were assessed on the edible portionof the fruit or on juice. Results. The cell structure of pitted and unpitted epicarp analysed byelectron microscopy revealed that dark spots were associated with the degradation of cellular membranes.The peroxidase system that shields the epicarp against photooxidative stress showed an inhibition ofcatalase activity and an increase of superoxide dismutase functioning. Moreover, the activities ofascorbate peroxidase and glutathione reductase remained unaffected in stained tissues. In sunshade trees,it was also found that the number of dark stains per fruit decreased but the internal quality of theendocarp was not significantly affected. The weight and the caliber of the fruit also slightly decreased.Discussion. High light intensities induce an oxidative stress in the epicarp, which is characterized by anincreased peroxidation and degradation of biological membranes. On the other hand, protection againstsolar radiation alleviates the stress, but, although not affecting the internal quality of the fruit,slightly decreases the fruit weight and size.

Roots of angiosperms differ in the behaviour of their apical meristems, and this diversity has been studied through the patterns of differentiation in a range of families. Except for three families of the Nymphaeales, all dicotyledons derive the epidermis wholly or partially with the root cap. In closed meristems the inner cell layer of the cap complex forms the epidermis; in open meristems, where cortex and cap are intermittently of common origin, linkages between the epidermis and the cap predominate. Roots of most monocotyledons derive the epidermis as the outer layer of the cortex. Nymphaeaceae, Cabombaceae and Barclayaceae resemble monocotyledons in this respect, and this applies even in the species with open meristems, in which a cleft forms between the cap and the rest of the apex. This feature fits with the close relationship between the Nymphaeales and monocotyledons revealed by other data. But none of the other Magnoliidae with close links to Liliidae has this type of epidermis. The Nymphaeales are also almost unique among dicotyledons in having trichoblasts in a vertical pattern. This results from transverse divisions of epidermal cells giving two conspicuously different daughters. The smaller and most densely staining one later bears a root hair. This is the way trichoblasts develop in many monocotyledons. The only other dicotyledons found with trichoblasts in vertical patterns are in the Piperaceae, though their closed meristems derive the epidermis in the normal dicotyledon pattern. All other dicotyledons that bear trichoblasts develop them in radial patterns probably related to the radial disposition of cells across the cortex. This pattern is more widespread than was previously known, though it can occur only in roots with closed meristems. In plants of both subclasses with vertical patterns of trichoblasts, it is usually the proximal daughter of the initiating mitosis which becomes the trichoblast. But it is the distal daughter in Juncaceae, Restionaceae, Cyperaceae and Poaceae. Vertical patterns differ further as to whether the atrichoblast daughters divide after initiation, thus changing the alternation of trichoblasts and atrichoblasts along a file of epidermal cells. Monocotyledons and the Nymphaeaceae can produce trichoblasts in open or closed meristems. In some embryos and root primordia the epidermis becomes discrete from cortex and cap and remains so in the meristems. This has now been found in six aquatic genera of the Liliidae, but reports of it occurring elsewhere are probably due to misinterpretation of sections. Discrete epidermises differentiate into trichoblasts and atrichoblasts in Hydrocharitaceae, but not in Araceae or Lemnaceae.

During the initial phases of elongation of pea internodes, oat and rice coleoptiles, oat mesocotyls, soybean hypocotyls and dandelion peduncles, net transverse orientation of cellulose wall microfibrils (Mfs) was found in the outer epidermal wall. This paper demonstrates that in all these axes, with the exception of rice coleoptile, net longitudinal orientation of microfibrils occurs in the outer epidermal wall in portions of the axes that were still elongating at the time of sampling. The timing of the transition to net longitudinal orientation and whether the transition proceeded acropetally or basipetally varied with the type of axis under study. The variability of the relationship between extension and the transition from net transverse to net longitudinal orientation suggests that factors other than extension are important in determining the transition. Layers of longitudinal wall microfibrils may be added to the extending epidermal wall to bolster its tensile strength commensurate with its function during and after extension. Attention is drawn to the parallels between the concept of tissue tension in growing axes and the concept that the epidermis functions as a stressed skin in the support of mature plant parts in primary growth.

The activity and distribution of the lysosomal marker enzyme acid phosphatase have been studied in the epidermis during tail regeneration in the lizard Podarcis muralis. This study gives information both on the mechanism of separation of the old from the new epidermal generation and on the involvement of lysosomes in β- and α-keratinization in lepidosaurians. The biochemical analysis shows that the activity of acid phosphatase was higher in the regenerating tail than in the normal tail until the stage of skin shedding at around 25–30 days post-amputation. The enzyme was present in keratinizing layers of epidermis, and particularly in the shedding layer. The shedding layer followed the outline of the regenerating scales beneath the wound in the epidermis showing that lysosomal enzymes are involved in epidermal shedding. The ultrastructural study showed that acid phosphatase was initially localized within the lysosomes but, with the progress of differentiation, it also appeared free within the cytoplasm of the cornifying cells of the shedding complex and of the β-keratinizing cells, and in the intercellular space among them. The role of lysosomal enzymes in the shedding process and their involvement in the mechanism of β-keratinization is discussed. While the process of β-keratinization has an intracellular and extracellular localization of acid phosphatase, the process of α-keratinization shows that most acid phosphatase is localized within the cell. Lysosomes and mesos granules containing acid phosphatase were concentrated in the cytoplasm of differentiating mesos cells. Some mesos granules later discharged their contents into the extracellular space. The α-layer was partially formed in proximal regenerated scales around 30 days post-amputation. Lysosomes appeared to concentrate within pre-keratinizing cells of the α-keratin layer and little reactivity was seen extracellularly.

The skin structure of 2 Bathyergid rodents, the naked mole-rat (Heterocephalus glaber) and the common mole-rat (Cryptomys hottentotus) is compared, to investigate whether thermoregulatory differences may be attributed to different skin features. Histological and ultrastructural studies of the dorsal skin of these closely related species show morphological and structural similarities but differences in the degree of skin folding, thickness of the integument and dermal infrastructure were evident. The skin of the common mole-rat conforms with expected morphological/histological arrangements that are commonly found in mammalian skin. Many features of the skin of the naked mole-rat, such as the lack of an insulating layer and the loosely folded morphological arrangement contribute to poikilothermic responses to changing temperatures of this mammal. Further evidence for poikilothermy in the naked mole-rat is indicated by the presence of pigment containing cells in the dermis, rather than the epidermis, as commonly occurs in homeotherms. Lack of fur is compensated by a thicker epidermal layer and a marked reduction in sweat glands. Differences in skin morphology thus contribute substantially to the different thermoregulatory abilities of the 2 Bathyergids. The skin morphology is related to the poor thermoinsulatory ability of the animals while simultaneously facilitating heat transfer from the environment to the animal by thigmothermy and/or other behavioural means.

The epidermal layer of the skin of the cartilaginous fish Raja clavata taken from a suitable place on the ventral side of the head was examined by light and electron microscopy. Cells of the basal layer divide and differentiate as epithelial cells of the mid-epidermis, characterized by numerous electron-dense, membrane-bound vesicles; their content is assumed to be mucus. Cells at the superficial layer of the epidermis lose these vesicles but have a palisade of mucous vesicles below the apical membrane. A modified glycocalyx coats the outer leaflet of the apical membrane.

In addition to epithelial cells, there are epidermal cells differentiated as two kinds of mucous goblet cells, sacciform cells similar to those found in teleost fish epidermis, holocrine cells with some resemblance to the club cells of teleosts but differing in their cytology, and chemosensory cells similar to those found in the oral epithelium of Raja. Merkel cells were not found. Cells that might be interpreted as ionocytes were seen but their nature was not confirmed. The epidermis is penetrated by numerous nerve fibres; swellings contain mitochondria and glycogen granules. The nerve fibres also contain 50–70 nm vesicles with an indistinct core. Cells intrusive to the epidermis include melanocytes, lymphocytes, macrophages, and several types of granular leucocyte. The cytology of the various epidermal elements is generally similar to that known in teleost fishes.

Sclerophylly and synthesis of phenolic compounds are active responses of plants subjected to environmental stress (drought, low nutrient supply, u.v.-B radiation, ozone). Here we describe the morphological and histochemical alterations occurring in field-grown leaves of Fagus sylvatica L. from three sites located along an ecological gradient: from a site in cool and protected conditions to one located on a mountain ridge, where the trees grow on a thin layer of soil and are exposed to the wind and to intense solar radiation in summer. The morphological data show that, as the ecological conditions of the stand worsen, individual leaf surface decreases, while the thickness of the leaves and their specific d. wt (i.e. d. wt per unit leaf area) increases. Histochemical and ultrastructural tests show a marked increase of phenolics during the course of the year. These substances, present primarily in the leaves of trees growing in stress conditions, have been identified mainly as tannins. They accumulate in the vacuoles, especially those of the upper epidermal layer and the palisade mesophyll; at a later stage they appear to be solubilized in the cytoplasm and retranslocated, eventually impregnating the outer wall of the epidermal cells amidst the cellulose fibrils, where they cluster together and form an electron-opaque layer between the wall and the cuticle. Observation of the epidermal cells also reveals that the outer cell wall is thicker. The paper discusses the roles of secondary metabolites in protection and detoxification processes; the possible ecological significance of these alterations in the ecophysiology of beech trees.

After cooling the roots and shoot apex of barley, there is a reduction in sucrose export from, and an increased total accumulation of carbohydrate and induction of fructan synthesis in, source leaves. We investigated carbohydrate accumulation in individual leaf cells. Using the microsampling technique and microfluorometric enzymatic assay, the amounts of various carbohydrates were measured in mesophyll, bundle sheath and epidermal cells. Epidermal cells take no part in carbohydrate partitioning and have very low concentrations of sugars even when leaf export is reduced. Even without cooling, however, there are remarkable changes in sucrose concentration (up to 200 mM) in mesophyll and bundle sheath cells during the photoperiod. The activity of acid invertase in samples from individual cells was very low, c. 3 μmol sucrose (g f. wt)−1 h−1. Interrelationships between these cell types and the control of fructan metabolism are discussed.