The input of terrestrial invertebrates from tree canopies to a stream

SUMMARY. The input of terrestrial invertebrates from different tree canopies to a trout stream was determined for a 28-week period from April to October, 1980. Sycamore produced the greatest number of animals, followed by oak and alder. Ash was not significantly different from the controls. Coleoptera, Diptera, Homoptera and Arachnida made up the greatest number of animals caught, with Lepidoptera larvae important beneath oak. The input of biomass (g m^-2 dry wt) was also greatest beneath sycamore (35.80), followed by oak (27.76), alder (20.39), ash (11.15) and control (9.92). The input of biomass was bimodal. The significance of terrestrial invertebrates as food for salmonids is discussed.     

Philopatry in the alpine grasshopper, Podisma pedestris: a novel experimental and analytical method

Abstract.

• 1 Local dispersal and philopatric behaviour of the alpine grasshopper, Podisma pedestris, were studied at two sites in the Alpes Maritimes using a new mark—release—resight technique featuring marking in situ, and multiple resighting without handling. The time-consuming nature of the design was justified by the quantity and quality of the data yielded.
• 2 Philopatry is defined independently of any concept of home range as a phenomenon by which movements over longer periods are less than would be expected by extrapolation of measures over shorter periods.
• 3 By this definition, the grasshoppers are shown to exhibit philopatry. Nymphs comprise two heterogenous classes of those which move little and those which move considerable distances.
• 4 Daily dispersal estimates were obtained from movements of 1055 nymphs and adults at one site, and of 593 adults at another.
• 5 Differences are demonstrated in daily dispersal distances for age, sex and site combinations.
• 6 Some differences in microhabitat preference were observed.
• 7 The findings are compared with previous measurements of dispersal in this species, and the merits of the new technique are discussed.

     

Characterizing the normal proteome of human ciliary body

Background

The ciliary body is the circumferential muscular tissue located just behind the iris in the anterior chamber of the eye. It plays a pivotal role in the production of aqueous humor, maintenance of the lens zonules and accommodation by changing the shape of the crystalline lens. The ciliary body is the major target of drugs against glaucoma as its inhibition leads to a drop in intraocular pressure. A molecular study of the ciliary body could provide a better understanding about the pathophysiological processes that occur in glaucoma. Thus far, no large-scale proteomic investigation has been reported for the human ciliary body.

Results

In this study, we have carried out an in-depth LC-MS/MS-based proteomic analysis of normal human ciliary body and have identified 2,815 proteins. We identified a number of proteins that were previously not described in the ciliary body including importin 5 (IPO5), atlastin-2 (ATL2), B-cell receptor associated protein 29 (BCAP29), basigin (BSG), calpain-1 (CAPN1), copine 6 (CPNE6), fibulin 1 (FBLN1) and galectin 1 (LGALS1). We compared the plasma proteome with the ciliary body proteome and found that the large majority of proteins in the ciliary body were also detectable in the plasma while 896 proteins were unique to the ciliary body. We also classified proteins using pathway enrichment analysis and found most of proteins associated with ubiquitin pathway, EIF2 signaling, glycolysis and gluconeogenesis.

Conclusions

More than 95% of the identified proteins have not been previously described in the ciliary body proteome. This is the largest catalogue of proteins reported thus far in the ciliary body that should provide new insights into our understanding of the factors involved in maintaining the secretion of aqueous humor. The identification of these proteins will aid in understanding various eye diseases of the anterior segment such as glaucoma and presbyopia.     

Characterization of dental pulp stem/stromal cells of Huntington monkey tooth germs

Background

Activation by extracellular ligands of G protein-coupled (GPCRs) and tyrosine kinase receptors (RTKs), results in the generation of second messengers that in turn control specific cell functions. Further, modulation/amplification or inhibition of the initial signalling events, depend on the recruitment onto the plasma membrane of soluble protein effectors. High throughput methodologies to monitor quantitatively second messenger production, have been developed over the last years and are largely used to screen chemical libraries for drug development. On the contrary, no such high throughput methods are yet available for the other aspect of GPCRs regulation, i.e. protein translocation to the plasma membrane, despite the enormous interest of this phenomenon for the modulation of receptor downstream functions. Indeed, to date, the experimental procedures available are either inadequate or complex and expensive.

Results

Here we describe the development of a novel conceptual approach to the study of cytosolic proteins translocation to the inner surface of the plasma membrane. The basis of the technique consists in: i) generating chimeras between the protein of interests and the calcium (Ca²⁺)-sensitive, luminescent photo-protein, aequorin and ii) taking advantage of the large Ca²⁺ concentration [Ca²⁺] difference between bulk cytosolic and the sub-plasma membrane rim.

Conclusion

This approach, that keeps unaffected the translocation properties of the signalling protein, can in principle be applied to any protein that, upon activation, moves from the cytosol to the plasma membrane. Thus, not only the modulation of GPCRs and RTKs can be investigated in this way, but that of all other proteins that can be recruited to the plasma membrane also independently of receptor activation. Moreover, its automated version, which can provide information about the kinetics and concentration-dependence of the process, is also applicable to high throughput screening of drugs affecting the translocation process.