A tarsal spinning organ in glomeridesmid millipedes (Diplopoda: Pentazonia: Glomeridesmida)

The production of sticky threads from spinnerets is known from various myriapod groups including some representatives of the millipedes (Diplopoda). In Diplopoda the thread-producing glands are mostly seta-like and positioned terminally on the telson, and the secretion product is typically used to build molting chambers or egg sacs. So far, no such secretions or organs have been documented for the subgroup Pentazonia. Here we describe thread-producing glands from the species-poor Glomeridesmida. These putative spinning organs are single circular fields of small pores (spinning fields) positioned on the outer side of the tarsi of all walking legs of mature and juvenile individuals of both sexes. These pores are the openings of cuticular tubuli (conducting canals), which extend from the tarsus to an aggregation of cells, a putative gland, within the femur. In several specimens thin threads were observed to be extruded from the pores. The tarsal spinning fields are present in all 21 investigated Glomeridesmida morphospecies, including Termitodesmidae and Glomeridesmidae from South East Asia, the Indian subcontinent, Oceania, and South and Central America. These organs might constitute an apomorphic character of the Glomeridesmida, as similar organs are absent in other Myriapoda. The function of the extruded threads in Glomeridesmida remains speculative, because observations of living specimens of the group are almost non-existing. We suggest that the secretion might be used for defense, to build molting chambers or to secure tunnels burrowed in the substrate.

Detection of endogenous lipids in chicken feathers distinct from preen gland constituents

Bird feather lipids are usually attributed to the oily secretion product of the uropygial (preen) gland. We have observed, however, that feathers exhibit a strong reaction with osmium tetroxide (OsO4), even after treatment with detergents. This leads us to postulate the existence of endogenous feather lipids distinct from preen gland lipids. In order to substantiate our hypothesis, we investigated down feathers from a 1-day-old chicken as their uropgygial gland is not functionally active. The results confirmed the osmiophilic reaction, which was concentrated in the center of barbs and strongly reduced after lipid extraction. In these lipid extracts, we identified using thin layer chromatography, cholesterol, various ceramides, glycolipids, phospholipids, and fatty acids, which closely resembled the lipid composition of the water barrier in the chicken-cornified epidermal envelope. This composition is clearly distinct from chicken uropygeal gland secretion (UGS) known to consist of fatty alcohols as part of aliphatic monoester waxes and of free, predominantly saturated, fatty acids. A filter assay showed a strong reactivity between OsO4 and the fatty acids C18:1 and C18:2 and with feather lipid extracts, but not with UGS. These observations were confirmed by gas chromatography detecting unsaturated fatty acids including C18:1 and C18:2 as well as cholesterol exclusively in chicken feathers. Our results indicate that (1) endogenous lipids are detectable in chicken feathers and distinct from UGS and (2) in analogy to the morphogenesis of the cornified envelope of chicken feather lipids that may have derived from cellular feather-precursors, apparently enduring the specific cell death during developmental feather cornification.

Human Synovia Contains Trefoil Factor Family (TFF) Peptides 1–3 Although Synovial Membrane Only Produces TFF3: Implications in Osteoarthritis and Rheumatoid Arthritis

Objective: Trefoil factor family peptide 3 (TFF3) has been shown to support catabolic functions in cases of osteoarthritis (OA). As in joint physiology and diseases such as OA, the synovial membrane (SM) of the joint capsule also plays a central role. We analyze the ability of SM to produce TFF compare healthy SM and its secretion product synovial fluid (SF) with SM and SF from patients suffering from OA or rheumatoid arthritis (RA). Methods: Real-time PCR and ELISA were used to measure the expression of TFFs in healthy SM and SM from patients suffering from OA or RA. For tissue localization, we investigated TFF1-3 in differently aged human SM of healthy donors by means of immunohistochemistry, real-time PCR and Western blot. Results: Only TFF3 but not TFF1 and -2 was expressed in SM from healthy donors as well as cases of OA or RA on protein and mRNA level. In contrast, all three TFFs were detected in all samples of SF on the protein level. No significant changes were observed for TFF1 at all. TFF2 was significantly upregulated in RA samples in comparison to OA samples. TFF3 protein was significantly downregulated in OA samples in comparison to healthy samples and cases of RA significantly upregulated compared to OA. In contrast, in SM TFF3 protein was not significantly regulated. Conclusion: The data demonstrate the production of TFF3 in SM. Unexpectedly, SF contains all three known TFF peptides. As neither articular cartilage nor SM produce TFF1 and TFF2, we speculate that these originate with high probability from blood serum.

Histological Aspects of Brunner’s Glands in Chinchillas (Chinchilla lanigera)

Since their discovery, Brunner’s glands have been an attractive subject of research. The study aimed to investigate the structure, the topography, and the degree of development of the Brunner’s glands in chinchillas through light microscopy. Transversal fragments from the duodenum of 5 chinchilla males were histologically processed by classical paraffin technique. Brunner glands are much more developed and proportionally, they occupy at least three times more space than the Lieberkuhn glands. In many places, Brunner glands are clustered, suggesting that more than one such gland spills its secretion product through a common Lieberkuhn gland in the space between villi. We can affirm that Brunner glands, after their disposition, appearance and absence of distinct muscularis mucosae, are disposed into the thickness of the mucosa and submucosa in chinchilla (together with the Lieberkuhn glands) and not strictly in the submucosa as in other mammals.

Nectary ultrastructure and secretory modes in three species of Tillandsia (Bromeliaceae) that have different pollinators

The floral nectaries of three Tillandsia L. spp. having different pollinators were investigated with transmission electron microscopy (TEM) to describe the previously unstudied ultrastructure of the nectar-producing tissues (primarily the epidermis) and also to determine if any differences in the ultrastructural features could be correlated to pollination mode. We determined that there were variations in nectaries among the three species, and that these may be linked to pollinator choice. Tillandsia seleriana Mez, which has a strict relationship with ants, had a nectary epithelium characterized by abundant dictyosomes and endoplasmic reticulum (ER), and a final degeneration stage possibly leading to holocrine secretion. The presence of protein crystals in epithelial plastids was correlated to a nectar enriched with amino acids and proteins, likely functioning to provide a protein-enriched diet and possibly defence against pathogens. Epithelial cells of the hummingbird-pollinated Tillandsia juncea (Ruiz et Pav.) Poir. nectary displayed cell wall ingrowths and dictyosomes and also contained cytoplasmic lipid droplets and protein crystals within plastids, both of which would enrich the nectar for hummingbirds. The nectary epithelium and the parenchyma of bat-pollinated Tillandsia grandis Schltdl. possessed a few cubic protein crystals in the plastids and its secretion product appeared electron transparent.

Structural features of Rhododendron luteum flower

The flower of Rhododendron luteum (L.) Sweet has a pentamerous structure with radial symmetry. The anthers filament surface is covered by dense non-glandular hairs to the half of the height. The tubular anther dehisces along creating two openings in the anther-sac walls and the viscous pollen is released through two splits along the anther lobes. The pistil is pentamerous and the axial channel is filled with a mucilaginous secretion product which is continuous with the exudate on the stigma surface. The stigmatic papillae are densely packed and their exudate is stained intensively red for carbohydrates, while pollen grains are stained positively for lipids. The five-locular ovary has isomerous carpels (syncarpous gynoecium) and the ovary surface is covered by numerous, densely-packed glandular and non-glandular hairs protecting the nectar against transpiration. Numerous ovules per locule occur with one integument and a thin-walled megasporiangium. In carpels, oil cells occur sporadically as solitary idioblasts, located around the vascular bundles. Transmitting tissue cells contain a large central, electron translucent vacuole, filling most of the cell containing dark osmiophilic bodies homogenous or granular in appearance.

Comparative analysis of two fatty acid binding proteins fromFasciola gigantica

SUMMARYFatty acid binding proteins are considered to be promising vaccine candidates against trematodiasis. In order to provide additional information about their function inFasciola giganticawe performed a comparative analysis of FgFABP1 and FgFABP3, two isoforms with quite different isoelectric points of 4·9 and 9·9 and 67% sequence identity. Both are expressed in the juvenile and adult parasite but differ in their tissue-specific distribution. In addition, the sequence of FABP3 is identical inF. hepaticaandF. giganticaindicating the protein's functional importance in this genus. Immune sera produced against soluble recombinant FgFABPs reacted with 14 kDa antigens in crude worm, soluble egg, cirrus sac extracts, and excretion/secretion product. Both FgFABPs were located in the parenchyma of the parasite but in addition, FgFABP1 was abundant in testes and spermatozoa while FgFABP3 was abundant in vitelline cells, eggs, and caecal epithelium. Mass spectrometry identified FgFABP1 and FgFABP3 in the ES product whereas only FgFABP3 was identified in egg extract. Serum samples of an experimentally infected rabbit reacted from week 6 post-infection with FgFABP3 and from week 12 with FgFABP1 while sera of infected sheep were not reactive. The results suggest differences in the biological functions of these 2 isoforms and differences in the host/parasite interaction that should be considered for their potential as vaccines against fascioliasis.

De Novo Alanine Synthesis by Bacteroids of Mesorhizobium loti Is Not Required for Nitrogen Transfer in the Determinate Nodules of Lotus corniculatus

ABSTRACT Deletion of both alanine dehydrogenase genes (aldA) in Mesorhizobium loti resulted in the loss of AldA enzyme activity from cultured bacteria and bacteroids but had no effect on the symbiotic performance of Lotus corniculatus plants. Thus, neither indeterminate pea nodules nor determinate L. corniculatus nodules export alanine as the sole nitrogen secretion product.

New Products of Defense Secretion in South East Asian Whip Scorpions (Arachnida: Uropygi: Thelyphonida)

Secretion products from the opisthosomal defense gland of south east Asian whip scorpions were identified for the first time by gas-chromatography and mass-spectrometry. Specimens of the genera Hypoctonus, Typopeltis and Ginosigma were tested. While some ingredients are present in large concentrations, others are possibly only side products and may be synthesized more incidentally. For this reason no important functional role is attributed to them. There are considerable individual differences concerning the concentrations of various ingredients. While the secretion products of most species of the genus Typopeltis - similar to Mastigoproctus - are characterized by acetic and octanoic acid in large concentrations, the secretion product of Hypoctonus siamensis provides octanoic acid only in a very low concentration but it is characterized by hexyl acetate.