Gradients and the Specification of Planar Polarity in the Insect Cuticle

In addition to specifying cell fate, there is a wealth of evidence that molecular gradients are also primarily responsible for specifying cell polarity, particularly in the plane of epithelial sheets (“planar polarity”). The first compelling evidence of a role for gradients in specifying planar polarity came from transplantation experiments in the insect cuticle. More recent molecular genetic analyses in the fruit fly Drosophila have begun to give insights into the molecular nature of the gradients involved, and how they are interpreted at the cellular level.Development requires the coordinated specification of at least three attributes: cell fate, tissue size, and cell polarity. In both theory and practice, all three can be specified by the action of gradients. This article examines the experimental evidence for gradients acting to specify cell polarity in developing tissues, considers the mechanisms by which they are thought to act, and discusses what remains unknown. The problem of how cell polarity is specified in the plane of a tissue (“planar polarity”) is addressed. The tissues discussed are all formed from epithelial sheets that also show apicobasal cell polarity.For more than half a century, the preeminent system for studying the regulation of planar polarity in epithelia has been the insect cuticle. This lends itself to the study of the problem by virtue of often being adorned by structures such as hairs, scales, ridges, or other protrusions that reveal the polarity of the underlying cells. However, the lack of polarized structures on the surface of other epithelial-derived tissues should not be taken as evidence that the cells are not planar polarized, because often such polarity is cryptically expressed and only becomes apparent when the cells participate in a polarized process, such as cell division or cell intercalation.     

Sites of Synthesis and Transport Pathways of Insect Hydrocarbons: Cuticle and Ovary as Target Tissues

SYNOPSIS. The outer surface of insects is covered with a lipidlayer that provides water-proofing and protection against environmentalstresses. Hydrocarbons (HC) are major constituents of this epicuticularwax and they also serve as semiochemicals. In some insects HCare also exploited as biosynthetic precursors for pheromones.HC are synthesized by oenocyteswhich are situated in the integumentor hemocoel. Shuttling of HC to the epicuticie, fat body, andgonads requires transport through an aqueous medium. Insects,unlike vertebrates, use a versatile lipoprotein to effect lipidtransport and to selectively deliver lipids to specific tissues.A high-density hemolymph lipoprotein (lipophorin [Lp]) servesthis function.In adult females of the German cockroach (Blattellagermanica), Lp carries both HC and a contact sex pheromone.Lipophorin is a multi-functional lipid carrier serving alsoas a juvenile hormone binding protein in many insects. Studiesofthe interactions between Lp and HC are beginning to unravelthe routes used in delivering HC to target tissues. We discussthepathways and dynamics of loading of Lp with HC and HC-derivedpheromones, their transport through the hemolymph, and depositionin various tissues, including the epicuticie, ovaries, and pheromone-emittingglands.     

Cuticle differentiation during Drosophila embryogenesis

The constitutive criterion for the evolutionary successful clade of ecdysozoans is a protective exoskeleton. In insects the exoskeleton, the so-called cuticle consists of three functional layers, the waterproof envelope, the proteinaceous epicuticle and the chitinous procuticle that are produced as an extracellular matrix by the underlying epidermal cells. Here, we present our electron-microscopic study of cuticle differentiation during embryogenesis in the fruit fly Drosophila melanogaster. We conclude that cuticle differentiation in the Drosophila embryo occurs in three phases. In the first phase, the layers are established. Interestingly, we find that establishment of the layers occurs partially simultaneously rather than in a strict sequential manner as previously proposed. In the second phase the cuticle thickens. Finally, in the third phase, when secretion of cuticle material has ceased, the chitin laminae acquire their typical orientation, and the epicuticle of the denticles and the head skeleton darken. Our work will help to understand the phenotypes of embryos mutant for genes encoding essential cuticle factors, in turn revealing mechanisms of cuticle differentiation.     

Partitioning Yield Loss on Yellow Squash into Nematode and Insect Components

The effect of a contplex of several insect and nematode pests on yield of yellow squash (Cucurbita pepo L.) was examined in two field tests in southern Florida. Applications of permethrin for insect control and oxamyl primarily for nematode control plus some insect control were made alone and in combination to achieve differential reduction of various insect and nematode components contributing to yield loss. The effect of these components on yield was further analyzed by multiple regression. Yield losses in weight of small fruit to nematode and insect pests together were estimated at 23.4% and 30.4% in each of the two tests, respectively. In the first test, this loss was attributed to the melonworm, Diaphania hyalinata, while in the second test, it was attributed to D. hyalinata and the nematodes Quinisulcius acutus and particularly Rotylenchulus reniforrnis. D. hyalinata accounted for further losses of 9.0% and 10.3%, respectively, from direct damage to the fruit. Despite the presence of low levels of Diabrotica balteata, Liriomyza sativae, and Myzus persicae, yields were little affected by these pests. Prediction of yield loss by multiple regression analysis was more accurate when both insect and nematode populations were present in the plots than when nematodes alone were present.     

Sectioning Insects with Sclerotized Cuticle

Adult insects of different orders including beetles were fixed in a mixture of a saturated solution of picric acid in 90% alcohol, 75 parts; formalin, 25 parts; nitric acid (cone), 8 parts, 4-6 days and even up to 10 days depending upon the hardness of the cuticle (addition of 5% mercuric chloride to this mixture is recommended when prolonged immersion is required), or in Carnoy and Lebruns' fluid 24-48 hours and then transferred to a solution of 3-6 parts of nitric acid in 100 parts of 90% alcohol (3-6 days). After dehydration in different grades of alcohol, the insects were double embedded in celloidin and paraffin, either by (1) clove oil for 1 day, then to a saturated solution of celloidin in clove oil matured for at least 2 months for 20-40 days, or (2) the conventional ether-alcohol-celloidin mixture for 7 days; followed by hardening in chloroform. The difficulty in the proper infiltration of paraffin into celloidin hardened by chloroform around the insect is avoided by keeping the block overnight in a mixture of paraffin, 1 part; chloroform, 5 parts. The rest of the technic is essentially the same as that followed in cutting sections after double embedding.     

Effect of Abrading the Cuticle Using Emery

Abrading the cuticle is sometimes required in order to measureauxin-stimulated acidification. We have determined, however,that the process should be used with caution. The diameter ofthe Edmund Scientific emery No. 305 particles was found to benear 40 times greater than cuticle thickness (0 –14 µm).Thus it was not surprising to find that even gentle abrasionmight cause damage to the epidermal cells. The resultant woundingmay complicate interpretastion of experimental results becausethe healing process shown to follow the wounding is likely tohave an auxin – regulated component. Experiments shouldbe designed to differentiate wound – related auxin effectsfrom elongation-related auxin effects.     

The Structure and Calcification of the Crustacean Cuticle

The integument of decapod crustaceans consists of an outer epicuticle,an exocuticle, an endocuticle and an inner membranous layerunderlain by the hypodermis. The outer three layers of the cuticleare calcified. The mineral is in the form of calcite crystalsand amorphous calcium carbonate. In the epicuticle, mineralis in the form of spherulitic calcite islands surrounded bythe lipid-protein matrix. In the exo- and endocuticles the calcitecrystal aggregates are interspersed with chitin-protein fiberswhich are organized in lamellae. In some species, the organizationof the mineral mirrors that of the organic fibers, but suchis not the case in certain cuticular regions in the xanthidcrabs. Thus, control of crystal organization is a complex phenomenonunrelated to the gross morphology of the matrix. Since the cuticle is periodically molted to allow for growth,this necessitates a bidirectional movement of calcium into thecuticle during postmolt and out during premolt resorption ofthe cuticle. In two species of crabs studied to date, thesemovements are accomplished by active transport effected by aCa-ATPase and Na/Ca exchange mechanism. The epi- and exocuticular layers of the new cuticle are elaboratedduring premolt but do not calcify until the old cuticle is shed.This phenomenon also occurs in vitro in cuticle devoid of livingtissue and implies an alteration of the nucleating sites ofthe cuticle in the course of the molt.     

Fine Structure of the Archiannelid Cuticle and Remarks on the Evolution of the Cuticle Within the Spiralia*

The fine structure of the cuticle in the archiannelids Polygordius, Protodrilus, Trilobodrilus, and Diurodrilus is described. Polygordius and Protodrilus are unique with respect to the filiform microvilli penetrating through the cuticle. Basically all forms conform to the most common type of cuticular structure in the Annelida: a fibrous matrix of varying complexity penetrated by micro-villar-like cell processes. Following the ideas expressed by Lyons (1970), a hypothesis on the evolution of the cuticle within the vermiform Spiralia (e.g. Turbellaria, Nemertea, Annelida) is proposed. New data on interstitial Turbellaria and other new forms of interstitial worms suggest a morphological and functional sequence from the multiciliated epidermis of Turbellaria to the cuticularized hypodermis of Annelida.     

Rheological Properties of Enzymatically Isolated Tomato Fruit Cuticle

Rheological properties were determined for cuticular membranes (CMs) enzymatically isolated from mature tomato (Lycopersicon esculentum Mill. cv Pik Red) fruit. The cuticle responded as a viscoelastic polymer in stress-strain studies. Both CM and dewaxed CM expanded and became more elastic and susceptible to fracture when hydrated, suggesting that water plasticized the cuticle. Dewaxing of the CM caused similar changes in elasticity and fracturing, indicating that wax may serve as a supporting filler in the cutin matrix. Exposure of the cuticle to the surfactant Triton X-100 did not significantly affect its rheological properties.     

植物的虫瘿与成瘿昆虫

虫瘿是植物组织遭受昆虫取食或产卵的刺激后,细胞加速分裂和异常分化而长成的畸形瘤状物或突起,它们是昆虫生活的"房子".介绍了虫瘿的形态多样性和形成过程,成瘿昆虫的多样性、生活史、寄生、食性和寄食现象,成瘿昆虫与寄主植物的关系以及人类对虫瘿的利用.