皮肤的屏障作用英文文献(7页).doc

-皮肤的屏障作用英文文献-第 7 页Moisturization and skin barrier functionABSTRACT: Over the past decade，great progress has been made toward elucidating the structure and function of the stratum corneum (SC),the outermost layer of the epidermis. SC cells (corneocytes) protect against desiccation and environmental by the SC is largely dependent on several factors. First, intercellular lamellar lipids, organized predominantly in an orthorhombic gel phase, provide an effective barrier to the passage of water through the tissue. Secondly, the diffusion path length also retards water loss, since water must traverse the tortuous path created by the SC layers and corneocyte envelopes. Thirdly, and equally important, is natural moisturizing factor (NMF), a complex mixture of low-molecular-weight, water-soluble compounds first formed within thee corneocytes by degradation of the histidine-rich protein known as filaggrin. Each maturation step leading to the formation of an effective moisture barrierincluding corneocyte strengthening, lipid processing, and NMF generationis influenced by the level of SC hydration. These processes, as well as the final step of corneodesmolysis that mediates exfoliations, are often disturbed upon environmental challenge, resulting in dry, flaky skin conditions. The present paper reviews our current understanding of the biology of the SC, particularly its homeostatic mechanisms of hydration.Keywords: corneocyte, corneodesmolysis, filaggrin, natural moisturizing factor, stratum corneum.IntroductionFor humans to survive in a terrestrial environment, the loss of water from the skin must be carefully regulated by the epidermis, a function dependent on the complex nature of its outer layer, the stratum corneum (SC) (1)。 The SC is a selectively permeable, heterogeneous, composite outer layer of the epidermis that protects against desiccation and environmental challenge, and retains sufficient water to allow it to function in arid environments. The small amount of water loss that does occur hydrates the outer layers of the SC, maintaining its flexibility and facilitating the enzymatic reactions that drive the SCs maturation (24). The water-retaining capacity of the SC is highly dependent upon the phenotype of the corneocytes, their spatial arrangement, the precise composition and physical packing of extracellular lipids, and the presence of highly hygroscopic compounds found largely within the corneocytes (Fig. 1).Under conditions of normal humidity (> 80%), a steep water gradient exists in the SC, which can be viewed by a variety of elegant techniques (Fig. 2) (5,6). The gradient is established, in part, by a discontinuity in the water-binding capacities between different corneocyte cell layers, as demonstrated via cryo-scanning electron microscopy (Fig. 3) (7). Briey, corneocytes do not appear to be swollen at low hydration levels (1826% w/w), suggesting that only bound water is present in the SC. However, at higher hydration levels (57 87% w/w), the corneocytes are more swollen in the central portion of the SC compared with the supercial and deeper layers. The corneocyte cell thickness is shown to increase linearly in a direction perpendicular to the skin surface with increasing hydration. Extracellular pools of water are only observed at very high hydration levels (> 300% w/w). The explanation of these differential hydration levels is rooted in the mechanisms involved in SC moisturization.The present review describes the most recent research that reveals the complexity and intricacy of the everyday functioning of the SC to maintain hydration in relation to ever-changing environmental conditions. It shows that skin is involved in a constant battle to maintain optimal moisture barrier and protective functions. As discussed throughout this supplement, different elements of fundamental skin care exercised as a daily routine truly help the skin to achieve its healthiest state.Stratum corneum moisturization at the molecular levelStratum corneumThe SC consists of terminally differentiated keratinocytes (corneocytes) and the secreted contents of lamellar bodies (2,8). Each corneocyte originates from an actively proliferating keratinocyte in the epidermis beneath the SC. Corneocyte proteins are generally sequestered to the cytosol, while ceramides and other lipids are enriched in the extracellular space, where they form a continuous phase (8). The physical packing of the corneocytes creates a tortuous path for molecules to traverse, effectively increasing the diffusion length and thereby improving the SC barrier function. Extracellular lipids, tightly arranged as a covalently bound matrix in a crystalline phase called an orthorhombic packing state further reduce the rate of water ux through the tissue (9). The constitution, and thus the effectiveness, of the lipid barrier are dependent on the absolute concentrations and the relative proportions of the different lipids (e.g., ceramides, cholesterol, and fatty acids). Lectins and desmosomes found in the SC also help to maintain the structural cohesiveness of the SC. The reduction of water ux and loss through the tissue is not the sole cause of the apparent discontinuity in hydration between different corneocyte layers, however. Selective retention of water is required as well, central to which is SC natural moisturizing factor (NMF).Natural moisturizing factor Found exclusively in the SC, NMF consists primarily of amino acids or their derivatives, such as pyrrolidone carboxylic acid (PCA) and urocanic acid, together with lactic acid, urea, citrate, and sugars (10) (Table 1). Natural moisturizing factor compounds are present in high concentrations within corneocytes and represent up to 2030% of the dry weight of the SC (11). By absorbing atmospheric water and dissolving in their own water of hydration, hygroscopic NMF components act as very efcient humectants (2). Biologically, this humectancy allows the outermost layers of the SC to remain hydrated despite the desiccating action of the environment. Corneocytes that possess the highest concentration of NMF retain more water and appear more swollen when viewed under cryo-scanning electron microscopy (7). However, NMF is much more important than this. As our understanding of the terminal differentiation and SC maturation process has increased, it has become clear that, by maintaining free water in the SC, NMF also facilitates critical biochemical events. The most striking example of this is the regulation of several corneocyte proteases that are ultimately responsible for the very generation of NMF itself.Origin of NMF. The components of NMF are derived from laggrin, a 37-kDa SC protein initially synthesized in keratohyalin granules of the epidermis as prolaggrin, a large (> 500 kDa), highly basic, heavily phosphorylated, histidinerich protein (2,1215) (Fig. 4). First expressed in the granular layer of the SC during the nal stages of epidermal differentiation, prolaggrin consists of multiple laggrin repeats (1012 in humans) joined by short hydrophobic linker peptides (15). Extensive phosphorylation of internal serine residues renders prolaggrin extremely insoluble. Prolaggrin is, in effect, synthesized and then precipitated within the keratohyalin granule as an insoluble, osmotically inactive precursor of NMF. During the transition of the mature granular cell into the corneocyte, prolaggrin is rapidly dephosphorylated to form laggrin, a transient component that does not persist beyond the two to three deepest layers of the SC (16). As corneocyte maturation and progression through the upward layers of the SC proceeds, the complete proteolysis of laggrin generates NMF. The timing of the entire process is controlled, in part, by the association of laggrin with keratin, which is thought to shield laggrin from premature proteolysis (15). Although the proteases catalyzing laggrin breakdown in the SC remain to be identied, the “signal” that initializes the proteolysis at a dened stage of SC maturation was found to be the water gradient within the SC itself (17).Filaggrins relatively short life span is dependent on the turnover time of the SC. The protease activity that results in the sudden release of a concentrated NMF pool is delayed until the corneocytes have attened, moved far enough out into the dryer areas of the SC, and the cornied cell envelopes have strengthened. Once these conditions have been met, the SC can withstand the resulting osmotic effects of NMF generation (15). Other NMF components that may be extracellular to the corneocytes include sugars, hyaluronic acid, urea, and especially lactate (18). Since lactate is derived from eccrine sweat, its gradient is different from the amino-acid-derived NMF components (6). Age-related decline in NMF. There is a signicant age-related decline in the level of NMF. Electron microscopy studies show decreased numbers of keratohyalin granules in senile xerosis (19); this suggests that the intrinsically lower levels of NMF present in aged skin, compared with the levels in young skin, reect a generally reduced synthesis of prolaggrin. Furthermore, it is likely that the loss of NMF is exacerbated by the age-related decline in barrier function (20). The decline in NMF production probably reects the cumulative effects of actinic damage since it was observed in SC recovered from the back of the hand (photodamaged), but not from the inner aspect of the biceps (photo-protected). Typical proles of SC depth versus NMF concentration (obtained by sequential tape stripping of elderly individuals) show a decline toward the surface of the skin of elderly subjects compared to young individuals (2). This is typical of normal skin exposed to routine soap washing, during which much of the readily soluble NMF is washed out of the supercial SC (21). Indeed, recent results from in vivo confocal methods have demonstrated reductions in the amount of all NMF amino acids in the supercial layers of the SC (6), largely as a result of damage from bathing or ultraviolet light. Improvements in corneodesmolysis are necessary to rapidly alleviate the scaling and aking associated with this condition.Structural changes in corneocyte envelopesDry skin is further characterized by structural changes in corneocyte envelopes (CE) that are a result of reduced transglutaminase activity. This bifunctional enzyme transforms a soft or fragile corneocyte envelope (CEf) into a rigid corneocyte envelope (CEr) by mediating the gamma-glutamyl lysine crosslinking of specialized corneocyte proteins, and in addition, the esterication of ceramides and fatty acids to the cornied envelope (22). Fragile corneocyte envelopes predominate in dry skin.Inuence of external humidity on barrier functionThe processes involved in the maintenance of SC hydration appear to be under the profound inuence of external humidity. Denda and colleagues (23) analyzed cutaneous barrier function, epidermal morphology, and lipid content of the SC in hairless mice maintained for 2 weeks in high relative humidity (RH > 80%) and low relative humidity (RH < 10%). Basal transepidermal water loss was reduced by 31% in animals maintained in a dry environment. Moreover, the number of lamellar bodies in stratum granulosum cells, the extent of lamellar body exocytosis, and the number of layers of SC signicantly increased in animals kept in a dry environment, as did the dry weight of the SC and the thickness of the epidermis. In addition, the amount of total SC lipids increased, but lipid analysis revealed no signicant differences in lipid distribution. Lastly, barrier recovery following either acetone treatment or tape stripping was accelerated after prolonged prior exposure to a dry environment, but was delayed by prior exposure to a humid environment. Importantly, Declerq et al. (24) reported a similar adaptive response in human barrier function. Individuals living in a dry climate like that of Arizona, USA, compared with those in a humid climate like that of New York, USA, have less scaly skin, perhaps because of increased desquamatory enzyme levels and elevated ceramide levels, which improve barrier function. Similar increases in scalp lipid levels are observed between the wet and dry seasons in Thailand (25), and in the summer and winter months in the UK (26). In the latter studies, reductions in the levels of linoleatecontaining ceramide with omega-hydroxy fatty acid (O), ester-linked (E) to linoleic acid and amide linked to sphingosine (S) Cer(EOS), and increasing levels of oleate-containing Cer(EOS) were found in the SC in winter.Inuence of external humidity on laggrin hydrolysis, desquamation, and cutaneous disordersScott and Harding (1315,17) found that laggrin hydrolysis during development of rat SC is controlled by environmental humidity as well. Filaggrin distribution in the rat SC, as shown by immunouorescence, changed dramatically during the rst hours of postnatal life. During late fetal development, laggrin accumulated through the entire thickness of the SC, suggesting an inhibition of its proteolytic degradation to free amino acids. Immediately after birth, laggrin proteolysis occurred in the outer part of the SC and followed the normal adult pattern. Thus, activation of laggrin proteolysis was dependent on the drop in external water activity caused by the transition from an aqueous environment in utero to a dryer environment after birth. Filaggrin proteolysis could be blocked by maintaining a 100% humidity atmosphere around the newborn rat after birth. Interestingly, prolaggrin levels vary inversely with humidity, indicating yet another homeostatic regulatory mechanism that balances the SC hydration state (23). To clarify the effects of environmental humidity on skin pathology, Katagiri and coworkers (27) studied skin surface conductance (a measure of surface hydration using a skin surface hygrometer; Skicon 200 I.B.S. Co., Ltd., Japan), free amino acid content, and the immunoreactivity of laggrin in the epidermis of hairless mice subjected to varying levels of humidity. In this study, the skin surface conductance in the SC of mice was signicantly lower 37 days after transfer from a humid environment (RH > 80%) to a dry environment (RH < 10%), as compared to mice transferred from a normal environment (RH = 4070%) to a dry environment. Furthermore, the free amino acid content in the SC, while reduced 24 h after the mice had been transferred from a normal to a dry condition, recovered to the original level within 3 days. By contrast, mice transferred from a humid to a dry condition showed a signicantly lower amino acid content even 7 days after the transfer. The immunoreactivity of laggrin became faint in the epidermis of the mice transferred from a humid or nor